Criticalkare Pharma

Bdpazo 200mg tablet contains the active substance pazopanib. It is an antineoplastic drug that belongs to the class tyrosine kinase inhibitor. It is used in adults to treat advanced kidney cancer or has spread to other organs. It is also indicated to treat certain forms of soft-tissue sarcoma, a type of cancer affecting the supportive tissues of the body. This medicine works by preventing the activity of proteins involved in the growth and spread of cancer cells. 

Do not take Bdpazo 200mg tablet if you are allergic to Pazopanib or any other ingredients of this medicine. Before initiating the treatment, inform your physician if you have kidney, heart, lung, or liver problems, bleeding disorders, stomach or bowel problems, and thyroid problems. This tablet can raise your blood pressure. It is necessary to check your blood pressure regularly during the treatment. No dose adjustments are required for patients with kidney diseases. 

Your doctor will advise you to stop Bdpazo 200mg tablet at least 7 days before any surgeries or dental operations that you are undergoing, as it may affect wound healing. This medicine is not recommended for people aged under 18. This medicine can cause infertility; consult your doctor before taking this medicine. The most common side effects are diarrhea, hypertension, hair color changes, nausea, and vomiting.

Uses of Bdpazo 200mg Tablet

• Advanced renal cell carcinoma
• Advanced soft tissue sarcoma

 

More Information

• Store Bdpazo 200mg tablet in room temperature (25°C)
• Keep the injection away from the reach of children and pets.
• If you forgot to take a dose, take it as soon as you remember. However, skip the missed dose if it is nearly time for the next dose.
• Do not take a double dose to make up for a forgotten dose.

Safety Advices  Pregnancy  

Bdpazo 200mg tablet is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for at least 2 weeks after your last dose is necessary.    

Breast Feeding  

Breastfeeding is not recommended in patients taking Bdpazo 200mg  tablet because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs  

It is unknown whether Bdpazo 200mg tablet can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Bdpazo 200mg tablet is unsafe when administered in patients with severe liver diseases. Dose adjustments are necessary for moderate liver failure. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol  

It is unknown whether it is safe to consume alcohol when taking Bdpazo 200mg tablet. Consult your doctor for more advice.  

Driving  

Driving or operating heavy machinery is unsafe after taking Bdpazo 200mg  tablet because you may feel dizzy, drowsy, or have blurred vision.

Side Effects

• Hypertension
• Hair color change
• Increased glucose levels
• Decreased weight, decrease in appetite
• Diarrhea
• Nausea, vomiting
• Muscle and joint pain
• Headache
• Shortness of breath
• Tiredness

• Heart problems
• Bleeding from the anus, mouth
• Hypothyroidism
• Interstitial lung disease
• Infections

Pazinib 200mg tablet contains the active substance pazopanib. It is an antineoplastic drug that belongs to the class tyrosine kinase inhibitor. It is used in adults to treat advanced kidney cancer or has spread to other organs. It is also indicated to treat certain forms of soft-tissue sarcoma, a type of cancer affecting the supportive tissues of the body. This medicine works by preventing the activity of proteins involved in the growth and spread of cancer cells. 

Do not take Pazinib 200mg tablet if you are allergic to Pazopanib or any other ingredients of this medicine. Before initiating the treatment, inform your physician if you have kidney, heart, lung, or liver problems, bleeding disorders, stomach or bowel problems, and thyroid problems. This tablet can raise your blood pressure. It is necessary to check your blood pressure regularly during the treatment. No dose adjustments are required for patients with kidney diseases. 

Your doctor will advise you to stop Pazinib 200mg tablet at least 7 days before any surgeries or dental operations that you are undergoing, as it may affect wound healing. This medicine is not recommended for people aged under 18. This medicine can cause infertility; consult your doctor before taking this medicine. The most common side effects are diarrhea, hypertension, hair color changes, nausea, and vomiting.

Uses of Pazinib 200mg Tablet

• Advanced renal cell carcinoma
• Advanced soft tissue sarcoma

 

More Information

• Store Pazinib 200mg tablet in room temperature (25°C)
• Keep the injection away from the reach of children and pets.
• If you forgot to take a dose, take it as soon as you remember. However, skip the missed dose if it is nearly time for the next dose.
• Do not take a double dose to make up for a forgotten dose.

Safety Advices Pregnancy  

Pazinib 200mg tablet is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for at least 2 weeks after your last dose is necessary.    

Breast Feeding  

Breastfeeding is not recommended in patients taking Pazinib 200mg  tablet because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs  

It is unknown whether Pazinib 200mg tablet can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Pazinib 200mg tablet is unsafe when administered in patients with severe liver diseases. Dose adjustments are necessary for moderate liver failure. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol  

It is unknown whether it is safe to consume alcohol when taking Pazinib 200mg tablet. Consult your doctor for more advice.  

Driving  

Driving or operating heavy machinery is unsafe after taking Pazinib 200mg  tablet because you may feel dizzy, drowsy, or have blurred vision.

Side Effects

• Hypertension
• Hair color change
• Increased glucose levels
• Decreased weight, decrease in appetite
• Diarrhea
• Nausea, vomiting
• Muscle and joint pain
• Headache
• Shortness of breath
• Tiredness

• Heart problems
• Bleeding from the anus, mouth
• Hypothyroidism
• Interstitial lung disease
• Infections

Zyceva 100mg Tablet is an anticancer medicine containing the active constituent erlotinib. It is used to treat non-small lung cancer (NSCLC) and pancreatic cancer. Cancer is a disorder in which cells multiply in an uncontrolled and abnormal manner. It is usually given in combination with another anticancer medicine, gemcitabine, for patients with metastatic or advanced pancreatic cancers.

Patients need to inform your doctor if you use contact lenses, have an intolerance to sugars, have a history of eye problems or clotting disorders, or if you take medicines for clotting disorders or cholesterol. Zyceva 100mg Tablet is not recommended for adolescents and children under the age of 18. Do not take this medication with food. Use effective birth control during the treatment and for at least 2 weeks after the last dose. 

Patients are advised not to smoke while being treated with Zyceva 100mg Tablet, as smoking may decrease the amount of medicine in the blood. Wear protective clothing and sunscreen while going outside. Inform your physician if patients develop pain in the eye, blurred vision, cough, fever, shortness of breath, severe abdominal pain, and persistent diarrhea while taking this medicine. 

Uses of Zyceva 100mg Tablet

• Advanced or metastatic non-small lung cancer (NSCLC)
• Advanced or metastatic pancreatic cancer

Therapeutic Effects of Zyceva 100mg Tablet

Zyceva 100mg Tablet prevents the activity of a protein called epidermal growth factor receptor (EFGR), a protein involved in the spread and growth of cancer cells.

Interaction of Zyceva 100mg Tablet with other drugs

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional and vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with Zyceva 100 mg tablet and cause undesirable side effects. 

More Information about Zyceva 100mg Tablet

Keep out of sight and reach of children. Store at a controlled room temperature between 15°C to 30°C. Do not freeze.

Safety Advices  Pregnancy  

Taking Zyceva 100mg tablets while pregnant can harm the baby. You should not take this medicine during pregnancy unless your doctor recommends taking it. Inform your doctor if you are pregnant or planning to be pregnant before taking this medicine.  

Breast Feeding  

You must not take Zyceva 100mg Tablet if you are breastfeeding. Consult your doctor for risks and benefits.  

Lungs  

It is unknown whether Zyceva 100 mg Tablets affect the lungs. Please consult your doctor.  

Liver  

This medicine is not recommended in patients with severe liver diseases. Inform your physician if you have any liver disorders.   

Alcohol  

It is unknown whether it is safe to consume alcohol with Zyceva 100 mg Tablets. Please consult your doctor.  

Driving  

It is not known whether Zyceva 100 mg Tablet alters the ability to drive. Do not drive if you experience symptoms affecting your ability to concentrate and react.

Side Effects

• Persistent or severe diarrhea
• Pain in the eye, blurred vision
• Sudden difficulty in breathing accompanied by cough and fever
• Severe pain in your abdomen
• Liver failure

• Rash, worsened in sun-exposed areas
• Loss of appetite decreased weight
• Infection
• Headache
• Depression
• Nausea
• Mouth irritation
• Indigestion
• Hair loss, dry skin, itching, acne, cracked skin
• Tiredness
• Inflammation around fingernail
• Bleeding from nose, stomach, intestines
• Reduced kidney function

Tepmetko 225mg Tablet is a medication that contains Tepotinib as an active agent. The primary benefit of this medication is its ability to slow down or stop the growth and prevent the spread of cancer cells in the body, particularly in patients with non-small cell lung cancer (NSCLC) that has a mutation in the MET gene (surface of certain cancer cells). Another potential benefit of Tepmetko 225mg Tablet is that it may have fewer side effects when compared to traditional chemotherapy. However, it can still cause side effects like nausea, vomiting, and fatigue. Patients who are allergic to Tepmetko 225mg Tablet or its components should not use this medication. 

Patients with previous heart, kidney, lung, and liver disease should talk to a doctor before taking this medication. This medicine has not been studied in elderly patients, so its use in this population requires careful monitoring. Patients receiving it are monitored for signs of bleeding, such as hemoptysis (coughing up blood), melena (dark, tarry stools), or hemorrhagic shock. It is recommended to avoid consuming large amounts of grapefruit or grapefruit juice, as it can increase the risk of adverse reactions or interactions with some medications.

Uses of Tepmetko 225mg Tablet

• Treatment of non-small cell lung cancer (NSCLC)

Therapeutic Effects

In patients with NSCLC and the specific MET mutation, Tepmetko 225mg Tablet has been shown to have an anti-tumor effect, leading to tumor shrinkage and improved disease control. Studies have demonstrated that this medicine can significantly improve progression-free survival (PFS) in patients with NSCLC compared to standard chemotherapy.

More Information

• Store in a refrigerator between 20-25°C (68-77°F).
• Keep away from moisture, heat, and light.
• It should not be frozen.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.

Safety Advices  Pregnancy  

Pregnant women should consult their healthcare provider about their pregnancy status before receiving Tepmetko 225mg Tablet.  

Breast Feeding  

It is unknown if Tepmetko 225mg Tablet is excreted in human breast milk, so breastfeeding women should consult a healthcare provider before taking this medication.  

Lungs  

Tepmetko 225mg Tablet can cause lung problems, such as interstitial lung disease (ILD) or pneumonitis. Patients with a history of lung disease or pre-existing lung damage may be at increased risk for these side effects.  

Liver  

Tepmetko 225mg Tablet can cause liver toxicity, so it should be avoided in patients who have severe liver disease.  

Alcohol  

Individuals should avoid consuming alcohol before or immediately after receiving Tepmetko 225mg Tablet, as alcohol can impair the immune system and potentially reduce the effectiveness of the treatment.  

Driving  

Patients should always monitor their response to the Tepmetko 225mg Tablet medication and be cautious when driving or operating machinery if they experience any side effects that may impair their ability to do so safely.

Side Effects

• Hepatotoxicity
• Interstitial lung disease (ILD)
• Severe skin reactions
• Perforation or fistula formation in the gastrointestinal tract
• Bleeding, including severe or fatal bleeding

• Edema (swelling)
• Nausea
• Diarrhea
• Fatigue
• Anorexia (loss of appetite)
• Vomiting
• Increased blood creatinine levels
• Increased alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels
• Rash or itching
• Muscle pain or weakness

Pazib 200mg tablet contains the active substance pazopanib. It is an antineoplastic drug that belongs to the class tyrosine kinase inhibitor. It is used in adults to treat advanced kidney cancer or has spread to other organs. It is also indicated to treat certain forms of soft-tissue sarcoma, a type of cancer affecting the supportive tissues of the body. This medicine works by preventing the activity of proteins involved in the growth and spread of cancer cells. 

Do not take Pazib 200mg tablet if you are allergic to Pazopanib or any other ingredients of this medicine. Before initiating the treatment, inform your physician if you have kidney, heart, lung, or liver problems, bleeding disorders, stomach or bowel problems, and thyroid problems. This tablet can raise your blood pressure. It is necessary to check your blood pressure regularly during the treatment. No dose adjustments are required for patients with kidney diseases. 

Your doctor will advise you to stop Pazib 200mg tablet at least 7 days before any surgeries or dental operations that you are undergoing, as it may affect wound healing. This medicine is not recommended for people aged under 18. This medicine can cause infertility; consult your doctor before taking this medicine. The most common side effects are diarrhea, hypertension, hair color changes, nausea, and vomiting.

Uses of Pazib 200mg Tablet

• Advanced renal cell carcinoma
• Advanced soft tissue sarcoma

 

More Information

• Store Pazib 200mg tablet in room temperature (25°C)
• Keep the injection away from the reach of children and pets.
• If you forgot to take a dose, take it as soon as you remember. However, skip the missed dose if it is nearly time for the next dose.
• Do not take a double dose to make up for a forgotten dose.

Safety Advices  Pregnancy  

Pazib 200mg tablet is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for at least 2 weeks after your last dose is necessary.    

Breast Feeding  

Breastfeeding is not recommended in patients taking Pazib 200mg  tablet because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs  

It is unknown whether Pazib 200mg tablet can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Pazib 200mg tablet is unsafe when administered in patients with severe liver diseases. Dose adjustments are necessary for moderate liver failure. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol  

It is unknown whether it is safe to consume alcohol when taking Pazib 200mg tablet. Consult your doctor for more advice.  

Driving  

Driving or operating heavy machinery is unsafe after taking Pazib 200mg  tablet because you may feel dizzy, drowsy, or have blurred vision.

Side Effects

• Hypertension
• Hair color change
• Increased glucose levels
• Decreased weight, decrease in appetite
• Diarrhea
• Nausea, vomiting
• Muscle and joint pain
• Headache
• Shortness of breath
• Tiredness

• Heart problems
• Bleeding from the anus, mouth
• Hypothyroidism
• Interstitial lung disease
• Infections

Azashine 300 mg tablet consists of the active ingredient Azacitidine. It is used for treating adults with blood conditions, namely Myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia, and Acute myeloid leukemia (AML), if they are considered ineligible for stem cell transplant. In Myelodysplastic Syndrome, the bone marrow does not produce healthy blood cells due to its lack of function. Acute Myeloid Leukemia is a type of bone marrow cancer caused by the release of incompletely formed blood cells into the bloodstream. Chronic myelomonocytic leukemia is a rare form of blood cancer caused by an increased number of monocytes of the white blood cells.

Uses of Azashine 300mg Tablet

• Acute Myeloid Leukemia with 20-30% blasts in patients who are not eligible for Haemopoietic stem cell transplant
• High-risk Myelodysplastic syndrome (MDS)

Therapeutic Effects of Azashine 300mg Tablet

Azashine 300 mg tablet binds to RNA and DNA, interrupts their activity in actively multiplying cells, and exhibits a toxic effect on cancer cells.

Interaction of Azashine 300mg Tablet with other drugs

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional and vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with Azashine 300 mg tablet and cause undesirable side effects.

More Information about Azashine 300mg Tablet

Store at 25°C. Keep out of reach of children.

How to consume Azashine 300mg Tablet

Take Azashine 300 mg only under the supervision of your physician. Your physician will decide the dose based on your height, weight and general condition. The tablet is orally administered. Take it as a whole with water. Do not break, chew or crush the tablet. 

Safety Advices Pregnancy  

Azashine 300 mg tablets is not intended for use during pregnancy. Talk to your physician if you are pregnant or think you could be pregnant.  

Breast Feeding  

Consult your physician for advice on taking Azashine 300 mg tablets if you are a breastfeeding mother  

Lungs  

Inform your physician before taking Azashine 300 mg tablets if you have any lung problems.   

Liver  

Inform your physician before you take Azashine 300 mg tablets if you are diagnosed with a tumor in the liver cells.  

Alcohol  

It is not known whether it is safe to consume alcohol with Azashine 300 mg tablets. Please consult your doctor.  

Driving  

It is unsafe to drive after taking this injection as it causes dizziness and patients lack concentration and alertness. So, avoid driving and handling heavy machinery after taking Azashine 300 mg tablets.

Side Effects

• Drowsiness
• Shivering
• Jaundice
• Stomach bloating
• Unusual bleeding or bruising
• Reduced urination
• Increased thirst
• Dizziness
• Confusion
• Chest pain
• Breathlessness
• Allergies

• Disturbances in the blood count (RBC, WBC, Platelets)
• Nausea, vomiting, diarrhea
• Constipation
• Tiredness
• Skin reactions like redness and pain at the site of the tablet
• Decreased appetite
• Dizziness
• Pain in extremities
• Joint pain
• Stomach pain
• Headache
• Sore nose and throat
• Rashes and bruising

Pazokast 400mg tablet contains the active substance pazopanib. It is an antineoplastic drug that belongs to the class tyrosine kinase inhibitor. It is used in adults to treat advanced kidney cancer or has spread to other organs. It is also indicated to treat certain forms of soft-tissue sarcoma, a type of cancer affecting the supportive tissues of the body. This medicine works by preventing the activity of proteins involved in the growth and spread of cancer cells. 

Do not take Pazokast 400mg tablet if you are allergic to Pazopanib or any other ingredients of this medicine. Before initiating the treatment, inform your physician if you have kidney, heart, lung, or liver problems, bleeding disorders, stomach or bowel problems, and thyroid problems. This tablet can raise your blood pressure. It is necessary to check your blood pressure regularly during the treatment. No dose adjustments are required for patients with kidney diseases. 

Your doctor will advise you to stop Pazokast 400mg tablet at least 7 days before any surgeries or dental operations that you are undergoing, as it may affect wound healing. This medicine is not recommended for people aged under 18. This medicine can cause infertility; consult your doctor before taking this medicine. The most common side effects are diarrhea, hypertension, hair color changes, nausea, and vomiting.

Uses of Pazokast 400mg Tablet

• Advanced renal cell carcinoma
• Advanced soft tissue sarcoma

More Information

• Store Pazokast 400mg tablet in room temperature (25°C)
• Keep the injection away from the reach of children and pets.
• If you forgot to take a dose, take it as soon as you remember. However, skip the missed dose if it is nearly time for the next dose.
• Do not take a double dose to make up for a forgotten dose.

Safety Advices   Pregnancy  

Pazokast 400mg tablet is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for at least 2 weeks after your last dose is necessary.  

Breast Feeding  

Breastfeeding is not recommended in patients taking Pazokast 400mg  tablet because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs  

It is unknown whether Pazokast 400mg tablet can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Pazokast 400mg tablet is unsafe when administered in patients with severe liver diseases. Dose adjustments are necessary for moderate liver failure. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol  

It is unknown whether it is safe to consume alcohol when taking Pazokast 400mg tablet. Consult your doctor for more advice.  

Driving  

Driving or operating heavy machinery is unsafe after taking Pazokast 400mg  tablet because you may feel dizzy, drowsy, or have blurred vision.

Side Effects

• Hypertension
• Hair color change
• Increased glucose levels
• Decreased weight, decrease in appetite
• Diarrhea
• Nausea, vomiting
• Muscle and joint pain
• Headache
• Shortness of breath
• Tiredness

• Heart problems
• Bleeding from the anus, mouth
• Hypothyroidism
• Interstitial lung disease
• Infections

Bderlo 100mg Tablet is an anticancer medicine containing the active constituent erlotinib. It is used to treat non-small lung cancer (NSCLC) and pancreatic cancer. Cancer is a disorder in which cells multiply in an uncontrolled and abnormal manner. It is usually given in combination with another anticancer medicine, gemcitabine, for patients with metastatic or advanced pancreatic cancers.

Patients need to inform your doctor if you use contact lenses, have an intolerance to sugars, have a history of eye problems or clotting disorders, or if you take medicines for clotting disorders or cholesterol. Bderlo 100mg Tablet is not recommended for adolescents and children under the age of 18. Do not take this medication with food. Use effective birth control during the treatment and for at least 2 weeks after the last dose. 

Patients are advised not to smoke while being treated with Bderlo 100mg Tablet, as smoking may decrease the amount of medicine in the blood. Wear protective clothing and sunscreen while going outside. Inform your physician if patients develop pain in the eye, blurred vision, cough, fever, shortness of breath, severe abdominal pain, and persistent diarrhea while taking this medicine. 

Uses of Bderlo 100mg Tablet

• Advanced or metastatic non-small lung cancer (NSCLC)
• Advanced or metastatic pancreatic cancer

Therapeutic Effects of Bderlo 100mg Tablet

Bderlo 100mg Tablet prevents the activity of a protein called epidermal growth factor receptor (EFGR), a protein involved in the spread and growth of cancer cells.

Interaction of Bderlo 100mg Tablet with other drugs

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional and vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with Bderlo 100 mg tablet and cause undesirable side effects. 

More Information about Bderlo 100mg Tablet

Keep out of sight and reach of children. Store at a controlled room temperature between 15°C to 30°C. Do not freeze.

Safety Advices Pregnancy  

Taking Bderlo 100mg tablets while pregnant can harm the baby. You should not take this medicine during pregnancy unless your doctor recommends taking it. Inform your doctor if you are pregnant or planning to be pregnant before taking this medicine.  

Breast Feeding  

You must not take Bderlo 100mg Tablet if you are breastfeeding. Consult your doctor for risks and benefits.  

Lungs  

It is unknown whether Bderlo 100 mg Tablets affect the lungs. Please consult your doctor.  

Liver  

This medicine is not recommended in patients with severe liver diseases. Inform your physician if you have any liver disorders.   

Alcohol  

It is unknown whether it is safe to consume alcohol with Bderlo 100 mg Tablets. Please consult your doctor.  

Driving  

It is not known whether Bderlo 100 mg Tablet alters the ability to drive. Do not drive if you experience symptoms affecting your ability to concentrate and react.

Side Effects

• Persistent or severe diarrhea
• Pain in the eye, blurred vision
• Sudden difficulty in breathing accompanied by cough and fever
• Severe pain in your abdomen
• Liver failure

• Rash, worsened in sun-exposed areas
• Loss of appetite decreased weight
• Infection
• Headache
• Depression
• Nausea
• Mouth irritation
• Indigestion
• Hair loss, dry skin, itching, acne, cracked skin
• Tiredness
• Inflammation around fingernail
• Bleeding from nose, stomach, intestines
• Reduced kidney function

Pazib 400mg tablet contains the active substance pazopanib. It is an antineoplastic drug that belongs to the class tyrosine kinase inhibitor. It is used in adults to treat advanced kidney cancer or has spread to other organs. It is also indicated to treat certain forms of soft-tissue sarcoma, a type of cancer affecting the supportive tissues of the body. This medicine works by preventing the activity of proteins involved in the growth and spread of cancer cells. 

Do not take Pazib 400mg tablet if you are allergic to Pazopanib or any other ingredients of this medicine. Before initiating the treatment, inform your physician if you have kidney, heart, lung, or liver problems, bleeding disorders, stomach or bowel problems, and thyroid problems. This tablet can raise your blood pressure. It is necessary to check your blood pressure regularly during the treatment. No dose adjustments are required for patients with kidney diseases. 

Your doctor will advise you to stop Pazib 400mg tablet at least 7 days before any surgeries or dental operations that you are undergoing, as it may affect wound healing. This medicine is not recommended for people aged under 18. This medicine can cause infertility; consult your doctor before taking this medicine. The most common side effects are diarrhea, hypertension, hair color changes, nausea, and vomiting.

Uses of Pazib 400mg Tablet

• Advanced renal cell carcinoma
• Advanced soft tissue sarcoma

More Information

• Store Pazib 400mg tablet in room temperature (25°C)
• Keep the injection away from the reach of children and pets.
• If you forgot to take a dose, take it as soon as you remember. However, skip the missed dose if it is nearly time for the next dose.
• Do not take a double dose to make up for a forgotten dose.

Safety Advices Pregnancy  

Pazib 400mg tablet is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for at least 2 weeks after your last dose is necessary.    

Breast Feeding  

Breastfeeding is not recommended in patients taking Pazib 400mg  tablet because the medicine passes into the breast milk in small amounts and may harm your baby.  

Lungs  

It is unknown whether Pazib 400mg tablet can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Pazib 400mg tablet is unsafe when administered in patients with severe liver diseases. Dose adjustments are necessary for moderate liver failure. Inform your physician if you have liver problems before initiating the therapy.    

Alcohol  

It is unknown whether it is safe to consume alcohol when taking Pazib 400mg tablet. Consult your doctor for more advice.  

Driving  

Driving or operating heavy machinery is unsafe after taking Pazib 400mg  tablet because you may feel dizzy, drowsy, or have blurred vision.

Side Effects

• Hypertension
• Hair color change
• Increased glucose levels
• Decreased weight, decrease in appetite
• Diarrhea
• Nausea, vomiting
• Muscle and joint pain
• Headache
• Shortness of breath
• Tiredness

• Heart problems
• Bleeding from the anus, mouth
• Hypothyroidism
• Interstitial lung disease
• Infections

Tykerb 250mg Tablet contains the active ingredient lapatinib. It is indicated to treat advanced breast cancer and it may be used alone or in combination with other medications. It is effective against cells sensitive to hormones and rapidly multiplying cancer cells that produce most of the protein called human epidermal growth receptor -2.

The common side effects that are likely to occur while you are on the treatment with Tykerb 250mg Tablet are nausea, vomiting, tiredness, weakness, itching, dry skin, loss of appetite, indigestion, constipation, mouth ulcers, stomach pain, difficulty in sleeping, joint or back pain, cough, breathing problems, headache, etc. If you experience severe allergic reactions, skin rashes, heart, liver, and lung problems, report your physician immediately.

Inform your healthcare provider at the first sign of diarrhea or dehydration. Monitor your blood pressure regularly while taking Tykerb 250mg Tablet. If you have diarrhea while taking this medication, drink plenty of fluids, eat low-fat, high-protein foods, and avoid milk and its products and herbal supplements.

Uses of Tykerb 250mg Tablet

• Treats advanced or HER2 Positive metastatic breast cancer.

Therapeutic Effects of Tykerb 250mg Tablet

Tykerb 250mg Tablet acts against the enzyme called tyrosine kinase. It prevents the Human epidermal growth factor receptor protein (HER2) and Epidermal growth factor receptors (EGFRs) from signaling, which are produced by breast cancer cells. It kills cancer cells and slows down their growth. 

Interaction of Tykerb 250mg Tablet with other drugs

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional and vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with Tykerb 250mg Tablet Injection and cause undesirable side effects.

More Information about Tykerb 250mg Tablet

Store below 30°C and away from light.

Safety Advices Pregnancy  

It is not safe to consume Tykerb 250mg Tablet while you are pregnant. Consult your doctor and use a reliable contraception method to avoid becoming pregnant during this treatment.  

Breast Feeding  

Tykerb 250mg Tablet is unsafe during breastfeeding as this medication tends to pass into the breast milk and affect the baby.  

Lungs  

Talk to your doctor if you have any lung conditions before starting treatment with Tykerb 250mg Tablet.  

Liver  

Tykerb 250mg Tablet should be used with caution in patients with severe liver disease. Consult your physician for advice.  

Alcohol  

Avoid drinking alcohol while taking Tykerb 250mg Tablet as it may cause dizziness.  

Driving  

Tykerb  250mg Tablet may affect your ability to drive or perform activities that require focus. Exercise caution while driving or using machines.

Side Effects

• Diarrhea
• Severe allergic reactions
• Skin rash
• Heart problems

• Loss of appetite
• Nausea, vomiting
• Tiredness, weakness
• Indigestion
• Constipation
• Sore mouth or mouth ulcers
• Stomach pain
• Trouble sleeping
• Back pain
• Pain in the hands and feet
• Joint or back pain
• Cough, breathlessness
• Headache
• Nose bleed
• Hot flush
• Unusual hair loss
• Dry skin and itching

Zocitab 500mg Tablet contains the active ingredient Capecitabine. It belongs to the category of medicines known as antimetabolites. This medication is used in combination with other anticancer drugs for the treatment of Metastatic colorectal cancer and breast cancer. Cancer is a disease in which cells multiply in an abnormal and uncontrolled manner. It is also used for the prevention of new occurrences of cancer in the colon after the complete removal of the tumor by surgery. 

The common side effects that are likely to occur with this medicine are loss of appetite, headache, runny nose, fever, hair loss, and dry mouth. During the treatment, your doctor may periodically monitor your complete blood counts, prothrombin time, INR, to prevent serious complications. Report to your doctor if you have been diagnosed with stomach ulcers, cataract, lung disease, problems in your heart, liver, skin, kidneys. Tell your physician before you undergo eye surgery or dental procedures.  Inform your doctor if you have experienced any allergic or unusual reactions after taking this tablet. This medicine can cause fertility issues, inform your doctor about any fertility concerns you may have before starting treatment with this medicine. 

Uses

• Adjuvant colon cancer
• Metastatic colorectal cancer
• Metastatic breast cancer

More Information

• Store Zocitab 500mg Tablet in the original package at room temperature (20°C to 25°C). Do not freeze.
• Keep it out of reach from children and pets.
• It is important to get the dose at the scheduled time. If you missed the schedule, contact your doctor and reschedule the dose.

Safety Advices  Pregnancy  

Zocitab 500mg Tablet is not recommended for pregnant women as it may cause fetal harm.  

Breast Feeding  

It is not known if Zocitab 500mg passes into your breast milk or if it will affect your baby or your breast milk. Talk to your doctor about the best way to feed your baby if you receive this drug.  

Lungs  

It is not known whether Zocitab 500mg can be prescribed to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your doctor if you have any liver disorders before taking Zocitab 500mg. Regular monitoring of liver function tests is recommended.  

Alcohol  

It is unknown whether consuming alcohol interacts with Zocitab 500mg. Please consult your doctor for more advice.  

Driving  

Zocitab 500mg Tablet may cause drowsiness which can affect the patient’s ability to drive or use machines. Consult your doctor before you resume driving. 

Side Effects

• Severe bloody diarrhoea, abdominal pain
• Heart problems (chest pain, shortness of breath, feeling faint, irregular heartbeat, sudden weight gain)
• Loss of too much body fluid, kidney failure
• Serious skin and mouth reactions (skin peeling, blisters)
• Hand and foot syndrome (swelling, changes in sensation of hands and feet)
• Liver problems
• Decreased blood count

• Loss of appetite
• Weight loss
• Insomnia, depression
• Headache, dizziness
• Eye irritation, redness, increased tears
• Inflammation of veins
• Runny nose, fever
• Infections
• Hair loss
• Pain in joints, back
• Dry mouth, indigestion
• Constipation

Enzalutasun 40mg Capsule contains the active ingredient enzalutamide. It is an antineoplastic drug that belongs to the category of medicines known as androgen receptor inhibitors. This medication is used in the treatment of advanced prostate cancer in patients who do not respond to surgical or hormonal treatments. 

It is not recommended to take Enzalutasun 40mg Capsule if you are allergic to enzalutamide or any of its ingredients. During this treatment, your doctor may periodically monitor for Prostate-specific antigen (PSA) tests. This blood test measures the level of PSA, a protein produced by the prostate gland that can be elevated in men with prostate cancer. PSA levels can help monitor the progression of the disease and the response to treatment. Other tests also include liver function tests and complete blood count(CBC) to prevent serious complications.

This medicine can cause seizures, so patients with a history of seizures should use caution when taking this medication. Avoid grapefruit and grapefruit juice while taking Enzalutasun 40mg Capsule, as it can increase the levels of the medication in the body. This drug is not recommended during pregnancy as it causes harm to the unborn baby, and it also causes fertility issues, inform your doctor about any fertility concern you may have before starting treatment with this medicine. Before beginning this treatment, tell your healthcare provider if you are pregnant or planning to have a baby. It is advised for both men and women to follow proper contraceptive methods during and for 3 months after the last dose of Enzalutasun 40mg Capsule.

Uses of Enzalutasun 40mg Capsule

• Advanced prostate cancer

More Information

• Store Enzalutasun 40mg Capsule in the original package at room temperature (20°C to 25°C).
• Keep it out of reach from children and pets.

Safety Advices Pregnancy  

Enzalutasun 40mg Capsule are not recommended for pregnant women as they may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment.  

Breast Feeding  

It is not known if Enzalutasun 40mg Capsule passes into your breast milk or if it will affect your baby or your breast milk. Talk to your doctor about the best way to feed your baby if you receive this drug.  

Lungs  

It is not known whether Enzalutasun 40mg Capsule can be prescribed to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your doctor if you have any liver disorders before taking Enzalutasun 40mg Capsule. Regular monitoring of liver function tests is recommended.  

Alcohol  

It is unknown whether consuming alcohol interacts with Enzalutasun 40mg Capsule. Please consult your doctor for more advice.  

Driving  

Enzalutasun 40mg Capsule may cause drowsiness which can affect the patient’s ability to drive or use machines. Consult your doctor before you resume driving.

Side Effects

• Hypersensitivity
• Seizures
• Posterior reversible encephalopathy syndrome
• Heart disease
• Falls and fractures

• Tiredness
• Back pain
• Constipation
• Arthralgia
• Decreased appetite
• Diarrhea
• High BP
• Headache
• Anxiety
• Dry skin
• Enlarged breasts in men
• Inability to concentrate

Enuta 40mg Capsule contains the active ingredient enzalutamide. It is an antineoplastic drug that belongs to the category of medicines known as androgen receptor inhibitors. This medication is used in the treatment of advanced prostate cancer in patients who do not respond to surgical or hormonal treatments. 

It is not recommended to take Enuta 40mg Capsule if you are allergic to enzalutamide or any of its ingredients. During this treatment, your doctor may periodically monitor for Prostate-specific antigen (PSA) tests. This blood test measures the level of PSA, a protein produced by the prostate gland that can be elevated in men with prostate cancer. PSA levels can help monitor the progression of the disease and the response to treatment. Other tests also include liver function tests and complete blood count(CBC) to prevent serious complications.

This medicine can cause seizures, so patients with a history of seizures should use caution when taking this medication. Avoid grapefruit and grapefruit juice while taking Enuta 40mg Capsule, as it can increase the levels of the medication in the body. This drug is not recommended during pregnancy as it causes harm to the unborn baby, and it also causes fertility issues, inform your doctor about any fertility concern you may have before starting treatment with this medicine. Before beginning this treatment, tell your healthcare provider if you are pregnant or planning to have a baby. It is advised for both men and women to follow proper contraceptive methods during and for 3 months after the last dose of Enuta 40mg Capsule.

Uses of Enuta 40mg Capsule

• Advanced prostate cancer

 

More Information

• Store Enuta 40mg Capsule in the original package at room temperature (20°C to 25°C).
• Keep it out of reach from children and pets.

Safety Advices  Pregnancy  

Enuta 40mg Capsule are not recommended for pregnant women as they may cause fetal harm. Consult your doctor if you are pregnant or planning for pregnancy during the treatment.  

Breast Feeding  

It is not known if Enuta 40mg Capsule passes into your breast milk or if it will affect your baby or your breast milk. Talk to your doctor about the best way to feed your baby if you receive this drug.  

Lungs  

It is not known whether Enuta 40mg Capsule can be prescribed to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your doctor if you have any liver disorders before taking Enuta 40mg Capsule. Regular monitoring of liver function tests is recommended.  

Alcohol  

It is unknown whether consuming alcohol interacts with Enuta 40mg Capsule. Please consult your doctor for more advice.  

Driving  

Enuta 40mg Capsule may cause drowsiness which can affect the patient’s ability to drive or use machines. Consult your doctor before you resume driving.

Side Effects

• Hypersensitivity
• Seizures
• Posterior reversible encephalopathy syndrome
• Heart disease
• Falls and fractures

• Tiredness
• Back pain
• Constipation
• Arthralgia
• Decreased appetite
• Diarrhea
• High BP
• Headache
• Anxiety
• Dry skin
• Enlarged breasts in men
• Inability to concentrate

Afayro 20mg Tablet is an anticancer medicine containing Afatinib dimaleate as an active ingredient. It is used to treat patients with non-small cell lung cancer (NSCLC) whose tumors have certain (non-resistant) abnormal epidermal growth factor receptor (EGFR) genes and patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy. Cancer is a disorder in which cells multiply in an abnormal and uncontrolled manner. Talk to your doctor if you have kidney disorders, breathing problems, liver disorders, heart problems, intolerance to sugars, severe dry eye, or other eye problems before taking this medicine. 

Afayro 20mg Tablet can delay disease progression and improve overall survival, it can also help patients maintain a better quality of life for a longer period of time. This includes improved physical functioning, reduced pain, and better mental and emotional health. Tell your doctor if you are wearing contact lenses or breastfeeding before taking this medication. Limit your time in the sun as this medicine may make your skin sensitive to the sun. It is not recommended for children and adolescents under the age of 18.  Do not stop taking this medicine without consulting your doctor.

Uses

• Non-small cell lung cancer (NSCLC)

More Information

• Afayro 20mg Tablet should be stored at room temperature, between 20°C to 25°C (68°F to 77°F).
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices  Pregnancy  

Afayro 20mg Tablet is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feeding  

It is unknown, whether Afayro 20mg Tablet is excreted in human milk or not, and the potential risks to a nursing infant are unknown. So nursing women should consult a healthcare provider before taking it.  

Lungs  

Afayro 20mg Tablet is primarily used to treat non-small cell lung cancer (NSCLC). Patients should consult healthcare providers if they have any other lung disease before taking it.  

Liver  

Afayro 20mg Tablet is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Afayro 20mg Tablet, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Afayro 20mg Tablet should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Interstitial lung disease (ILD)
• Severe diarrhea or dehydration
• Liver problems
• Eye problems, such as corneal erosion or ulceration
• Hemorrhage or bleeding problems
• Kidney problems
• Cardiac problems

• Diarrhea
• Mouth sores
• Acne or skin rash
• Nausea and vomiting
• Fatigue
• Loss of appetite
• Abdominal pain
• Nail changes, such as nail bed infections or inflammation
• Dry skin or itching
• Eye irritation or dryness
• Respiratory infections

Afayro 40mg Tablet is an anticancer medicine containing Afatinib dimaleate as an active ingredient. It is used to treat patients with non-small cell lung cancer (NSCLC) whose tumors have certain (non-resistant) abnormal epidermal growth factor receptor (EGFR) genes and patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy. Cancer is a disorder in which cells multiply in an abnormal and uncontrolled manner. Talk to your doctor if you have kidney disorders, breathing problems, liver disorders, heart problems, intolerance to sugars, severe dry eye, or other eye problems before taking this medicine. 

Afayro 40mg Tablet can delay disease progression and improve overall survival, it can also help patients maintain a better quality of life for a longer period of time. This includes improved physical functioning, reduced pain, and better mental and emotional health. Tell your doctor if you are wearing contact lenses or breastfeeding before taking this medication. Limit your time in the sun as this medicine may make your skin sensitive to the sun. It is not recommended for children and adolescents under the age of 18.  Do not stop taking this medicine without consulting your doctor.

Uses

• Non-small cell lung cancer (NSCLC)

More Information

• Afayro 40mg Tablet should be stored at room temperature, between 20°C to 25°C (68°F to 77°F).
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices Pregnancy  

Afayro 40mg Tablet is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feeding  

It is unknown, whether Afayro 40mg Tablet is excreted in human milk or not, and the potential risks to a nursing infant are unknown. So nursing women should consult a healthcare provider before taking it.  

Lungs  

Afayro 40mg Tablet is primarily used to treat non-small cell lung cancer (NSCLC). Patients should consult healthcare providers if they have any other lung disease before taking it.  

Liver  

Afayro 40mg Tablet is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Afayro 40mg Tablet, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Afayro 40mg Tablet should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Interstitial lung disease (ILD)
• Severe diarrhea or dehydration
• Liver problems
• Eye problems, such as corneal erosion or ulceration
• Hemorrhage or bleeding problems
• Kidney problems
• Cardiac problems

• Diarrhea
• Mouth sores
• Acne or skin rash
• Nausea and vomiting
• Fatigue
• Loss of appetite
• Abdominal pain
• Nail changes, such as nail bed infections or inflammation
• Dry skin or itching
• Eye irritation or dryness
• Respiratory infections

Afzeta 30mg Tablet is an anticancer medicine containing Afatinib dimaleate as an active ingredient. It is used to treat patients with non-small cell lung cancer (NSCLC) whose tumors have certain (non-resistant) abnormal epidermal growth factor receptor (EGFR) genes and patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy. Cancer is a disorder in which cells multiply in an abnormal and uncontrolled manner. Talk to your doctor if you have kidney disorders, breathing problems, liver disorders, heart problems, intolerance to sugars, severe dry eye, or other eye problems before taking this medicine. 

Afzeta 30mg Tablet can delay disease progression and improve overall survival, it can also help patients maintain a better quality of life for a longer period of time. This includes improved physical functioning, reduced pain, and better mental and emotional health. Tell your doctor if you are wearing contact lenses or breastfeeding before taking this medication. Limit your time in the sun as this medicine may make your skin sensitive to the sun. It is not recommended for children and adolescents under the age of 18.  Do not stop taking this medicine without consulting your doctor.

Uses

• Non-small cell lung cancer (NSCLC)

More Information

• Afzeta 30mg Tablet should be stored at room temperature, between 20°C to 25°C (68°F to 77°F).
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices  Pregnancy  

Afzeta 30mg Tablet is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feeding  

It is unknown, whether Afzeta 30mg Tablet is excreted in human milk or not, and the potential risks to a nursing infant are unknown. So nursing women should consult a healthcare provider before taking it.  

Lungs  

Afzeta 30mg Tablet is primarily used to treat non-small cell lung cancer (NSCLC). Patients should consult healthcare providers if they have any other lung disease before taking it.  

Liver  

Afzeta 30mg Tablet is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Afzeta 30mg Tablet, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Afzeta 30mg Tablet should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Interstitial lung disease (ILD)
• Severe diarrhea or dehydration
• Liver problems
• Eye problems, such as corneal erosion or ulceration
• Hemorrhage or bleeding problems
• Kidney problems
• Cardiac problems

• Diarrhea
• Mouth sores
• Acne or skin rash
• Nausea and vomiting
• Fatigue
• Loss of appetite
• Abdominal pain
• Nail changes, such as nail bed infections or inflammation
• Dry skin or itching
• Eye irritation or dryness
• Respiratory infections

Afanat 20mg Tablet is an anticancer medicine containing Afatinib dimaleate as an active ingredient. It is used to treat patients with non-small cell lung cancer (NSCLC) whose tumors have certain (non-resistant) abnormal epidermal growth factor receptor (EGFR) genes and patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy. Cancer is a disorder in which cells multiply in an abnormal and uncontrolled manner. Talk to your doctor if you have kidney disorders, breathing problems, liver disorders, heart problems, intolerance to sugars, severe dry eye, or other eye problems before taking this medicine. 

Afanat 20mg Tablet can delay disease progression and improve overall survival, it can also help patients maintain a better quality of life for a longer period of time. This includes improved physical functioning, reduced pain, and better mental and emotional health. Tell your doctor if you are wearing contact lenses or breastfeeding before taking this medication. Limit your time in the sun as this medicine may make your skin sensitive to the sun. It is not recommended for children and adolescents under the age of 18.  Do not stop taking this medicine without consulting your doctor.

Uses

• Non-small cell lung cancer (NSCLC)

More Information

• Afanat 20mg Tablet should be stored at room temperature, between 20°C to 25°C (68°F to 77°F).
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices Pregnancy  

Afanat 20mg Tablet is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feeding  

It is unknown, whether Afanat 20mg Tablet is excreted in human milk or not, and the potential risks to a nursing infant are unknown. So nursing women should consult a healthcare provider before taking it.  

Lungs  

Afanat 20mg Tablet is primarily used to treat non-small cell lung cancer (NSCLC). Patients should consult healthcare providers if they have any other lung disease before taking it.  

Liver  

Afanat 20mg Tablet is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Afanat 20mg Tablet, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Afanat 20mg Tablet should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Interstitial lung disease (ILD)
• Severe diarrhea or dehydration
• Liver problems
• Eye problems, such as corneal erosion or ulceration
• Hemorrhage or bleeding problems
• Kidney problems
• Cardiac problems

• Diarrhea
• Mouth sores
• Acne or skin rash
• Nausea and vomiting
• Fatigue
• Loss of appetite
• Abdominal pain
• Nail changes, such as nail bed infections or inflammation
• Dry skin or itching
• Eye irritation or dryness
• Respiratory infections

Afanat 30mg Tablet is an anticancer medicine containing Afatinib dimaleate as an active ingredient. It is used to treat patients with non-small cell lung cancer (NSCLC) whose tumors have certain (non-resistant) abnormal epidermal growth factor receptor (EGFR) genes and patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy. Cancer is a disorder in which cells multiply in an abnormal and uncontrolled manner. Talk to your doctor if you have kidney disorders, breathing problems, liver disorders, heart problems, intolerance to sugars, severe dry eye, or other eye problems before taking this medicine. 

Afanat 30mg Tablet can delay disease progression and improve overall survival, it can also help patients maintain a better quality of life for a longer period of time. This includes improved physical functioning, reduced pain, and better mental and emotional health. Tell your doctor if you are wearing contact lenses or breastfeeding before taking this medication. Limit your time in the sun as this medicine may make your skin sensitive to the sun. It is not recommended for children and adolescents under the age of 18.  Do not stop taking this medicine without consulting your doctor.

Uses

• Non-small cell lung cancer (NSCLC)

More Information

• Afanat 30mg Tablet should be stored at room temperature, between 20°C to 25°C (68°F to 77°F).
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices Pregnancy  

Afanat 30mg Tablet is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feeding  

It is unknown, whether Afanat 30mg Tablet is excreted in human milk or not, and the potential risks to a nursing infant are unknown. So nursing women should consult a healthcare provider before taking it.  

Lungs  

Afanat 30mg Tablet is primarily used to treat non-small cell lung cancer (NSCLC). Patients should consult healthcare providers if they have any other lung disease before taking it.  

Liver  

Afanat 30mg Tablet is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Afanat 30mg Tablet, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Afanat 30mg Tablet should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Interstitial lung disease (ILD)
• Severe diarrhea or dehydration
• Liver problems
• Eye problems, such as corneal erosion or ulceration
• Hemorrhage or bleeding problems
• Kidney problems
• Cardiac problems

• Diarrhea
• Mouth sores
• Acne or skin rash
• Nausea and vomiting
• Fatigue
• Loss of appetite
• Abdominal pain
• Nail changes, such as nail bed infections or inflammation
• Dry skin or itching
• Eye irritation or dryness
• Respiratory infections

Afanat 40mg Tablet is an anticancer medicine containing Afatinib dimaleate as an active ingredient. It is used to treat patients with non-small cell lung cancer (NSCLC) whose tumors have certain (non-resistant) abnormal epidermal growth factor receptor (EGFR) genes and patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy. Cancer is a disorder in which cells multiply in an abnormal and uncontrolled manner. Talk to your doctor if you have kidney disorders, breathing problems, liver disorders, heart problems, intolerance to sugars, severe dry eye, or other eye problems before taking this medicine. 

Afanat 40mg Tablet can delay disease progression and improve overall survival, it can also help patients maintain a better quality of life for a longer period of time. This includes improved physical functioning, reduced pain, and better mental and emotional health. Tell your doctor if you are wearing contact lenses or breastfeeding before taking this medication. Limit your time in the sun as this medicine may make your skin sensitive to the sun. It is not recommended for children and adolescents under the age of 18.  Do not stop taking this medicine without consulting your doctor.

Uses

• Non-small cell lung cancer (NSCLC)

More Information

• Afanat 40mg Tablet should be stored at room temperature, between 20°C to 25°C (68°F to 77°F).
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices  Pregnancy  

Afanat 40mg Tablet is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feeding  

It is unknown, whether Afanat 40mg Tablet is excreted in human milk or not, and the potential risks to a nursing infant are unknown. So nursing women should consult a healthcare provider before taking it.  

Lungs  

Afanat 40mg Tablet is primarily used to treat non-small cell lung cancer (NSCLC). Patients should consult healthcare providers if they have any other lung disease before taking it.  

Liver  

Afanat 40mg Tablet is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Afanat 40mg Tablet, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Afanat 40mg Tablet should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Interstitial lung disease (ILD)
• Severe diarrhea or dehydration
• Liver problems
• Eye problems, such as corneal erosion or ulceration
• Hemorrhage or bleeding problems
• Kidney problems
• Cardiac problems

• Diarrhea
• Mouth sores
• Acne or skin rash
• Nausea and vomiting
• Fatigue
• Loss of appetite
• Abdominal pain
• Nail changes, such as nail bed infections or inflammation
• Dry skin or itching
• Eye irritation or dryness
• Respiratory infections

AB-Taxomed 100 mg Injection is an anticancer medicine. It treats breast cancer, non-small cell lung cancer, ovarian cancer, and AIDS (Acquired Immuno-Deficiency Syndrome). Cancer is a condition in which cells are dividing and growing fast and in an uncontrolled manner. This Injection may be given alone or in combination with other anticancer medicines. It should not be used for severe liver problems, uncontrolled infection, and low white blood cell or platelet count.

This injection is not recommended for adolescents and children under the age of 18. Talk to your doctor if you have heart disorders before taking this medicine. Administration of this medicine can cause serious allergic reactions. Use effective birth control during the treatment and for at least six months after the last dose. This Injection may harm patients suffering from alcoholism as this medicine contains alcohol.

Uses of Ab-taxomed 100mg Injection

• Ovarian cancer
• Breast cancer
• Non-small cell lung cancer
• AIDS-related Kaposi’s sarcoma

Therapeutic Effects of Ab-taxomed 100mg Injection

AB-Taxomed 100 mg Injection binds to β-tubulin subunits of microtubules, interferes with interphase (a process involving cell growth) and mitotic functions (a process of cell division), and prevents the growth of cancer cells.

Interaction of Ab-taxomed 100mg Injection with other drugs

Inform your doctor about any prescribed medicines, over-the-counter medications, nutritional and vitamin supplements, or herbal products that you are taking or have taken before the treatment. Certain medications may interact with AB-Taxomed 100 mg injection and cause undesirable side effects.

More Information about Ab-taxomed 100mg Injection

• Keep AB-Taxomed 100 mg Injection out of sight and reach of children.
• Do not store above 25°C.

Safety Advices   Pregnancy  

AB-Taxomed 100 mg Injection can harm your unborn baby. Tell your doctor if you are pregnant or planning to get pregnant before taking this Injection.   

Breast Feeding  

Stop breastfeeding during the treatment with AB-Taxomed 100 mg Injection. Consult your doctor for potential risks.  

Lungs  

It is unknown whether AB-Taxomed 100 mg injection can be given to patients with lung disorders. Please consult your physician for more advice.  

Liver  

It is contraindicated in patients with severe liver disorders. Inform your doctor if you have any liver disorders before taking AB-Taxomed 100 mg Injection.  

Alcohol  

It is unsafe to consume alcohol with AB-Taxomed 100 mg Injection.  

Driving  

The alcohol present in AB-Taxomed 100 mg Injection may affect your ability to drive. Avoid driving if you feel unwell.

Side Effects

• Serious allergic reactions (rash, swelling of face, lips, throat, or tongue, trouble breathing, and swallowing)
• Severe diarrhea
• Severe stomach pain

• Anemia, feeling tired
• Hair loss
• Burning, tingling, or numbness in your feet or hands
• Muscle and joint pain
• Vomiting, nausea
• Mouth or lip sores
• Infections
• Swelling of hands, feet, and face
• Bleeding
• Irritation at the injection site
• Low blood pressure

Paclicad N 100 mg Injection is an anticancer medicine. It treats breast cancer, non-small cell lung cancer, ovarian cancer, and AIDS (Acquired Immuno-Deficiency Syndrome). Cancer is a condition in which cells are dividing and growing fast and in an uncontrolled manner. This Injection may be given alone or in combination with other anticancer medicines. It should not be used for severe liver problems, uncontrolled infection, and low white blood cell or platelet count.

This injection is not recommended for adolescents and children under the age of 18. Talk to your doctor if you have heart disorders before taking this medicine. Administration of this medicine can cause serious allergic reactions. Use effective birth control during the treatment and for at least six months after the last dose. This Injection may harm patients suffering from alcoholism as this medicine contains alcohol.

Uses of Paclicad N 100mg Injection

• Ovarian cancer
• Breast cancer
• Non-small cell lung cancer
• AIDS-related Kaposi’s sarcoma

Therapeutic Effects of Paclicad N 100mg Injection

Paclicad N 100 mg Injection binds to β-tubulin subunits of microtubules, interferes with interphase (a process involving cell growth) and mitotic functions (a process of cell division), and prevents the growth of cancer cells.

Interaction of Paclicad N 100mg Injection with other drugs

Inform your doctor about any prescribed medicines, over-the-counter medications, nutritional and vitamin supplements, or herbal products that you are taking or have taken before the treatment. Certain medications may interact with Paclicad N 100 mg injection and cause undesirable side effects.

More Information about Paclicad N 100mg Injection

• Keep Paclicad N 100 mg Injection out of sight and reach of children.
• Do not store above 25°C.

How to consume Paclicad N 100mg Injection

It will be given to you by a doctor or nurse. Do not self-administer. Your doctor will decide the dose and dosage of the Paclicad N 100 mg injection.

Safety Advices Pregnancy  

Paclicad N 100 mg Injection can harm your unborn baby. Tell your doctor if you are pregnant or planning to get pregnant before taking this Injection.   

Breast Feeding  

Stop breastfeeding during the treatment with Paclicad N 100 mg Injection. Consult your doctor for potential risks.  

Lungs  

It is unknown whether Paclicad N 100 mg injection can be given to patients with lung disorders. Please consult your physician for more advice.  

Liver  

It is contraindicated in patients with severe liver disorders. Inform your doctor if you have any liver disorders before taking Paclicad N 100 mg Injection.  

Alcohol  

It is unsafe to consume alcohol with Paclicad N 100 mg Injection.  

Driving  

The alcohol present in Paclicad N 100 mg Injection may affect your ability to drive. Avoid driving if you feel unwell.

Side Effects

• Serious allergic reactions (rash, swelling of face, lips, throat, or tongue, trouble breathing, and swallowing)
• Severe diarrhea
• Severe stomach pain

• Anemia, feeling tired
• Hair loss
• Burning, tingling, or numbness in your feet or hands
• Muscle and joint pain
• Vomiting, nausea
• Mouth or lip sores
• Infections
• Swelling of hands, feet, and face
• Bleeding
• Irritation at the injection site
• Low blood pressure

Azadine-O 300 mg tablet consists of the active ingredient Azacitidine. It is used for treating adults with blood conditions, namely Myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia, and Acute myeloid leukemia (AML), if they are considered ineligible for stem cell transplant. In Myelodysplastic Syndrome, the bone marrow does not produce healthy blood cells due to its lack of function. Acute Myeloid Leukemia is a type of bone marrow cancer caused by the release of incompletely formed blood cells into the bloodstream. Chronic myelomonocytic leukemia is a rare form of blood cancer caused by an increased number of monocytes of the white blood cells.

Uses of Azadine O 300mg Tablet

• Acute Myeloid Leukemia with 20-30% blasts in patients who are not eligible for Haemopoietic stem cell transplant
• High-risk Myelodysplastic syndrome (MDS)

Therapeutic Effects of Azadine O 300mg Tablet

Azadine-O 300 mg tablet binds to RNA and DNA, interrupts their activity in actively multiplying cells, and exhibits a toxic effect on cancer cells.

Interaction of Azadine O 300mg Tablet with other drugs

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional and vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with Azadine-O 300 mg tablet and cause undesirable side effects.

More Information about Azadine O 300mg Tablet

Store at 25°C. Keep out of reach of children.

How to consume Azadine O 300mg Tablet

Take Azadine-O 300 mg only under the supervision of your physician. Your physician will decide the dose based on your height, weight and general condition. The tablet is orally administered. Take it as a whole with water. Do not break, chew or crush the tablet. 

Safety Advices for Azadine O 300mg Tablet

 

Pregnancy

Azadine-O 300 mg tablets is not intended for use during pregnancy. Talk to your physician if you are pregnant or think you could be pregnant.

 

Breast Feeding

Consult your physician for advice on taking Azadine-O 300 mg tablets if you are a breastfeeding mother

 

Lungs

Inform your physician before taking Azadine-O 300 mg tablets if you have any lung problems. 

 

Liver

Inform your physician before you take Azadine-O 300 mg tablets if you are diagnosed with a tumor in the liver cells.

 

Alcohol

It is not known whether it is safe to consume alcohol with Azadine-O 300 mg tablets. Please consult your doctor.

 

Driving

It is unsafe to drive after taking this injection as it causes dizziness and patients lack concentration and alertness. So, avoid driving and handling heavy machinery after taking Azadine-O 300 mg tablets.

Side Effects of Azadine O 300mg Tablet

Side effects are unwanted symptoms caused by medicines. Even though all drugs cause side effects, not everyone gets them. 

Serious:

• Drowsiness
• Shivering
• Jaundice
• Stomach bloating
• Unusual bleeding or bruising
• Reduced urination
• Increased thirst
• Dizziness
• Confusion
• Chest pain
• Breathlessness
• Allergies

Common:

• Disturbances in the blood count (RBC, WBC, Platelets)
• Nausea, vomiting, diarrhea
• Constipation
• Tiredness
• Skin reactions like redness and pain at the site of the tablet
• Decreased appetite
• Dizziness
• Pain in extremities
• Joint pain
• Stomach pain
• Headache
• Sore nose and throat
• Rashes and bruising

Hemazide O 300 mg tablet consists of the active ingredient Azacitidine. It is used for treating adults with blood conditions, namely Myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia, and Acute myeloid leukemia (AML), if they are considered ineligible for stem cell transplant. In Myelodysplastic Syndrome, the bone marrow does not produce healthy blood cells due to its lack of function. Acute Myeloid Leukemia is a type of bone marrow cancer caused by the release of incompletely formed blood cells into the bloodstream. Chronic myelomonocytic leukemia is a rare form of blood cancer caused by an increased number of monocytes of the white blood cells.

Uses of Hemazide O 300mg Tablet

• Acute Myeloid Leukemia with 20-30% blasts in patients who are not eligible for Haemopoietic stem cell transplant
• High-risk Myelodysplastic syndrome (MDS)

Therapeutic Effects of Hemazide O 300mg Tablet

Hemazide O 300 mg tablet binds to RNA and DNA, interrupts their activity in actively multiplying cells, and exhibits a toxic effect on cancer cells.

Interaction of Hemazide O 300mg Tablet with other drugs

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional and vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with Hemazide O 300 mg tablet and cause undesirable side effects.

More Information about Hemazide O 300mg Tablet

Store at 25°C. Keep out of reach of children.

How to consume Hemazide O 300mg Tablet

Take Hemazide O 300 mg only under the supervision of your physician. Your physician will decide the dose based on your height, weight and general condition. The tablet is orally administered. Take it as a whole with water. Do not break, chew or crush the tablet. 

Safety Advices  Pregnancy  

Hemazide O 300 mg tablets is not intended for use during pregnancy. Talk to your physician if you are pregnant or think you could be pregnant.  

Breast Feeding  

Consult your physician for advice on taking Hemazide O 300 mg tablets if you are a breastfeeding mother  

Lungs  

Inform your physician before taking Hemazide O 300 mg tablets if you have any lung problems.   

Liver  

Inform your physician before you take Hemazide O 300 mg tablets if you are diagnosed with a tumor in the liver cells.  

Alcohol  

It is not known whether it is safe to consume alcohol with Hemazide O 300 mg tablets. Please consult your doctor.  

Driving  

It is unsafe to drive after taking this injection as it causes dizziness and patients lack concentration and alertness. So, avoid driving and handling heavy machinery after taking Hemazide O 300 mg tablets.

Side Effects

• Drowsiness
• Shivering
• Jaundice
• Stomach bloating
• Unusual bleeding or bruising
• Reduced urination
• Increased thirst
• Dizziness
• Confusion
• Chest pain
• Breathlessness
• Allergies

• Disturbances in the blood count (RBC, WBC, Platelets)
• Nausea, vomiting, diarrhea
• Constipation
• Tiredness
• Skin reactions like redness and pain at the site of the tablet
• Decreased appetite
• Dizziness
• Pain in extremities
• Joint pain
• Stomach pain
• Headache
• Sore nose and throat
• Rashes and bruising

MDS O 300 mg tablet consists of the active ingredient Azacitidine. It is used for treating adults with blood conditions, namely Myelodysplastic syndrome (MDS), chronic myelomonocytic leukemia, and Acute myeloid leukemia (AML), if they are considered ineligible for stem cell transplant. In Myelodysplastic Syndrome, the bone marrow does not produce healthy blood cells due to its lack of function. Acute Myeloid Leukemia is a type of bone marrow cancer caused by the release of incompletely formed blood cells into the bloodstream. Chronic myelomonocytic leukemia is a rare form of blood cancer caused by an increased number of monocytes of the white blood cells.

Uses of MDS O 300mg Tablet

• Acute Myeloid Leukemia with 20-30% blasts in patients who are not eligible for Haemopoietic stem cell transplant
• High-risk Myelodysplastic syndrome (MDS)

Therapeutic Effects of MDS O 300mg Tablet

MDS O 300 mg tablet binds to RNA and DNA, interrupts their activity in actively multiplying cells, and exhibits a toxic effect on cancer cells.

Interaction of MDS O 300mg Tablet with other drugs

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional and vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with MDS O 300 mg tablet and cause undesirable side effects.

More Information about MDS O 300mg Tablet

Store at 25°C. Keep out of reach of children.

How to consume MDS O 300mg Tablet

Take MDS O 300 mg only under the supervision of your physician. Your physician will decide the dose based on your height, weight and general condition. The tablet is orally administered. Take it as a whole with water. Do not break, chew or crush the tablet. 

Safety Advices   Pregnancy  

MDS O 300 mg tablets is not intended for use during pregnancy. Talk to your physician if you are pregnant or think you could be pregnant.  

Breast Feeding  

Consult your physician for advice on taking MDS O 300 mg tablets if you are a breastfeeding mother  

Lungs

Inform your physician before taking MDS O 300 mg tablets if you have any lung problems.   

Liver

Inform your physician before you take MDS O 300 mg tablets if you are diagnosed with a tumor in the liver cells.  

Alcoho

It is not known whether it is safe to consume alcohol with MDS O 300 mg tablets. Please consult your doctor.  

Driving

It is unsafe to drive after taking this injection as it causes dizziness and patients lack concentration and alertness. So, avoid driving and handling heavy machinery after taking MDS O 300 mg tablets.

Side Effects

• Drowsiness
• Shivering
• Jaundice
• Stomach bloating
• Unusual bleeding or bruising
• Reduced urination
• Increased thirst
• Dizziness
• Confusion
• Chest pain
• Breathlessness
• Allergies

• Disturbances in the blood count (RBC, WBC, Platelets)
• Nausea, vomiting, diarrhea
• Constipation
• Tiredness
• Skin reactions like redness and pain at the site of the tablet
• Decreased appetite
• Dizziness
• Pain in extremities
• Joint pain
• Stomach pain
• Headache
• Sore nose and throat
• Rashes and bruising

Cadilap 250mg Tablet contains the active ingredient lapatinib. It is indicated to treat advanced breast cancer and it may be used alone or in combination with other medications. It is effective against cells sensitive to hormones and rapidly multiplying cancer cells that produce most of the protein called human epidermal growth receptor -2.

The common side effects that are likely to occur while you are on the treatment with Cadilap 250mg Tablet are nausea, vomiting, tiredness, weakness, itching, dry skin, loss of appetite, indigestion, constipation, mouth ulcers, stomach pain, difficulty in sleeping, joint or back pain, cough, breathing problems, headache, etc. If you experience severe allergic reactions, skin rashes, heart, liver, and lung problems, report your physician immediately.

Inform your healthcare provider at the first sign of diarrhea or dehydration. Monitor your blood pressure regularly while taking Cadilap 250mg Tablet. If you have diarrhea while taking this medication, drink plenty of fluids, eat low-fat, high-protein foods, and avoid milk and its products and herbal supplements.

Uses of Cadilap 250mg Tablet

• Treats advanced or HER2 Positive metastatic breast cancer.

Therapeutic Effects of Cadilap 250mg Tablet

Cadilap 250mg Tablet acts against the enzyme called tyrosine kinase. It prevents the Human epidermal growth factor receptor protein (HER2) and Epidermal growth factor receptors (EGFRs) from signaling, which are produced by breast cancer cells. It kills cancer cells and slows down their growth. 

Interaction of Cadilap 250mg Tablet with other drugs

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional and vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with Cadilap 250mg Tablet Injection and cause undesirable side effects.

More Information about Cadilap 250mg Tablet

Store below 30°C and away from light.

Safety Advices Pregnancy  

It is not safe to consume Cadilap 250mg Tablet while you are pregnant. Consult your doctor and use a reliable contraception method to avoid becoming pregnant during this treatment.  

Breast Feeding  

Cadilap 250mg Tablet is unsafe during breastfeeding as this medication tends to pass into the breast milk and affect the baby.  

Lungs  

Talk to your doctor if you have any lung conditions before starting treatment with Cadilap 250mg Tablet.  

Liver  

Cadilap 250mg Tablet should be used with caution in patients with severe liver disease. Consult your physician for advice.  

Alcohol  

Avoid drinking alcohol while taking Cadilap 250mg Tablet as it may cause dizziness.  

Driving  

Cadilap  250mg Tablet may affect your ability to drive or perform activities that require focus. Exercise caution while driving or using machines.

Side Effects

• Diarrhea
• Severe allergic reactions
• Skin rash
• Heart problems

• Loss of appetite
• Nausea, vomiting
• Tiredness, weakness
• Indigestion
• Constipation
• Sore mouth or mouth ulcers
• Stomach pain
• Trouble sleeping
• Back pain
• Pain in the hands and feet
• Joint or back pain
• Cough, breathlessness
• Headache
• Nose bleed
• Hot flush
• Unusual hair loss
• Dry skin and itching

HER Tinib 250mg Tablet contains the active ingredient lapatinib. It is indicated to treat advanced breast cancer and it may be used alone or in combination with other medications. It is effective against cells sensitive to hormones and rapidly multiplying cancer cells that produce most of the protein called human epidermal growth receptor -2.

The common side effects that are likely to occur while you are on the treatment with HER Tinib 250mg Tablet are nausea, vomiting, tiredness, weakness, itching, dry skin, loss of appetite, indigestion, constipation, mouth ulcers, stomach pain, difficulty in sleeping, joint or back pain, cough, breathing problems, headache, etc. If you experience severe allergic reactions, skin rashes, heart, liver, and lung problems, report your physician immediately.

Inform your healthcare provider at the first sign of diarrhea or dehydration. Monitor your blood pressure regularly while taking HER Tinib 250mg Tablet. If you have diarrhea while taking this medication, drink plenty of fluids, eat low-fat, high-protein foods, and avoid milk and its products and herbal supplements.

Uses of HER Tinib 250mg Tablet

• Treats advanced or HER2 Positive metastatic breast cancer.

Therapeutic Effects of HER Tinib 250mg Tablet

HER Tinib 250mg Tablet acts against the enzyme called tyrosine kinase. It prevents the Human epidermal growth factor receptor protein (HER2) and Epidermal growth factor receptors (EGFRs) from signaling, which are produced by breast cancer cells. It kills cancer cells and slows down their growth. 

Interaction of HER Tinib 250mg Tablet with other drugs

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional and vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with HER Tinib 250mg Tablet Injection and cause undesirable side effects.

More Information about HER Tinib 250mg Tablet

Store below 30°C and away from light.

Safety Advices Pregnancy  

It is not safe to consume HER Tinib 250mg Tablet while you are pregnant. Consult your doctor and use a reliable contraception method to avoid becoming pregnant during this treatment.  

Breast Feeding  

HER Tinib 250mg Tablet is unsafe during breastfeeding as this medication tends to pass into the breast milk and affect the baby.  

Lungs  

Talk to your doctor if you have any lung conditions before starting treatment with HER Tinib 250mg Tablet.  

Liver  

HER Tinib 250mg Tablet should be used with caution in patients with severe liver disease. Consult your physician for advice.  

Alcohol  

Avoid drinking alcohol while taking HER Tinib 250mg Tablet as it may cause dizziness.  

Driving  

HER Tinib  250mg Tablet may affect your ability to drive or perform activities that require focus. Exercise caution while driving or using machines.

Side Effects

• Diarrhea
• Severe allergic reactions
• Skin rash
• Heart problems

• Loss of appetite
• Nausea, vomiting
• Tiredness, weakness
• Indigestion
• Constipation
• Sore mouth or mouth ulcers
• Stomach pain
• Trouble sleeping
• Back pain
• Pain in the hands and feet
• Joint or back pain
• Cough, breathlessness
• Headache
• Nose bleed
• Hot flush
• Unusual hair loss
• Dry skin and itching

Xeloda 500mg Tablet contains the active ingredient Capecitabine. It belongs to the category of medicines known as antimetabolites. This medication is used in combination with other anticancer drugs for the treatment of Metastatic colorectal cancer and breast cancer. Cancer is a disease in which cells multiply in an abnormal and uncontrolled manner. It is also used for the prevention of new occurrences of cancer in the colon after the complete removal of the tumor by surgery. 

The common side effects that are likely to occur with this medicine are loss of appetite, headache, runny nose, fever, hair loss, and dry mouth. During the treatment, your doctor may periodically monitor your complete blood counts, prothrombin time, INR, to prevent serious complications. Report to your doctor if you have been diagnosed with stomach ulcers, cataract, lung disease, problems in your heart, liver, skin, kidneys. Tell your physician before you undergo eye surgery or dental procedures.  Inform your doctor if you have experienced any allergic or unusual reactions after taking this tablet. This medicine can cause fertility issues, inform your doctor about any fertility concerns you may have before starting treatment with this medicine. 

Uses

• Adjuvant colon cancer
• Metastatic colorectal cancer
• Metastatic breast cancer

More Information

• Store Xeloda 500mg Tablet in the original package at room temperature (20°C to 25°C). Do not freeze.
• Keep it out of reach from children and pets.
• It is important to get the dose at the scheduled time. If you missed the schedule, contact your doctor and reschedule the dose.

Safety Advices Pregnancy  

Xeloda 500mg Tablet is not recommended for pregnant women as it may cause fetal harm.  

Breast Feeding  

It is not known if Xeloda 500mg passes into your breast milk or if it will affect your baby or your breast milk. Talk to your doctor about the best way to feed your baby if you receive this drug.  

Lungs  

It is not known whether Xeloda 500mg can be prescribed to patients with lung problems. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Inform your doctor if you have any liver disorders before taking Xeloda 500mg. Regular monitoring of liver function tests is recommended.  

Alcohol  

It is unknown whether consuming alcohol interacts with Xeloda 500mg. Please consult your doctor for more advice.  

Driving  

Xeloda 500mg Tablet may cause drowsiness which can affect the patient’s ability to drive or use machines. Consult your doctor before you resume driving. 

Side Effects

• Severe bloody diarrhoea, abdominal pain
• Heart problems (chest pain, shortness of breath, feeling faint, irregular heartbeat, sudden weight gain)
• Loss of too much body fluid, kidney failure
• Serious skin and mouth reactions (skin peeling, blisters)
• Hand and foot syndrome (swelling, changes in sensation of hands and feet)
• Liver problems
• Decreased blood count

• Loss of appetite
• Weight loss
• Insomnia, depression
• Headache, dizziness
• Eye irritation, redness, increased tears
• Inflammation of veins
• Runny nose, fever
• Infections
• Hair loss
• Pain in joints, back
• Dry mouth, indigestion
• Constipation

Afayro 30mg Tablet is an anticancer medicine containing Afatinib dimaleate as an active ingredient. It is used to treat patients with non-small cell lung cancer (NSCLC) whose tumors have certain (non-resistant) abnormal epidermal growth factor receptor (EGFR) genes and patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy. Cancer is a disorder in which cells multiply in an abnormal and uncontrolled manner. Talk to your doctor if you have kidney disorders, breathing problems, liver disorders, heart problems, intolerance to sugars, severe dry eye, or other eye problems before taking this medicine. 

Afayro 30mg Tablet can delay disease progression and improve overall survival, it can also help patients maintain a better quality of life for a longer period of time. This includes improved physical functioning, reduced pain, and better mental and emotional health. Tell your doctor if you are wearing contact lenses or breastfeeding before taking this medication. Limit your time in the sun as this medicine may make your skin sensitive to the sun. It is not recommended for children and adolescents under the age of 18.  Do not stop taking this medicine without consulting your doctor.

Uses

• Non-small cell lung cancer (NSCLC)

More Information

• Afayro 30mg Tablet should be stored at room temperature, between 20°C to 25°C (68°F to 77°F).
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices

  Pregnancy  

Afayro 30mg Tablet is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feedin  

It is unknown, whether Afayro 30mg Tablet is excreted in human milk or not, and the potential risks to a nursing infant are unknown. So nursing women should consult a healthcare provider before taking it.  

Lungs  

Afayro 30mg Tablet is primarily used to treat non-small cell lung cancer (NSCLC). Patients should consult healthcare providers if they have any other lung disease before taking it.  

Liver  

Afayro 30mg Tablet is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Afayro 30mg Tablet, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Afayro 30mg Tablet should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Interstitial lung disease (ILD)
• Severe diarrhea or dehydration
• Liver problems
• Eye problems, such as corneal erosion or ulceration
• Hemorrhage or bleeding problems
• Kidney problems
• Cardiac problems 

• Diarrhea
• Mouth sores
• Acne or skin rash
• Nausea and vomiting
• Fatigue
• Loss of appetite
• Abdominal pain
• Nail changes, such as nail bed infections or inflammation
• Dry skin or itching
• Eye irritation or dryness
• Respiratory infections

Afzeta 20mg Tablet is an anticancer medicine containing Afatinib dimaleate as an active ingredient. It is used to treat patients with non-small cell lung cancer (NSCLC) whose tumors have certain (non-resistant) abnormal epidermal growth factor receptor (EGFR) genes and patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy. Cancer is a disorder in which cells multiply in an abnormal and uncontrolled manner. Talk to your doctor if you have kidney disorders, breathing problems, liver disorders, heart problems, intolerance to sugars, severe dry eye, or other eye problems before taking this medicine. 

Afzeta 20mg Tablet can delay disease progression and improve overall survival, it can also help patients maintain a better quality of life for a longer period of time. This includes improved physical functioning, reduced pain, and better mental and emotional health. Tell your doctor if you are wearing contact lenses or breastfeeding before taking this medication. Limit your time in the sun as this medicine may make your skin sensitive to the sun. It is not recommended for children and adolescents under the age of 18.  Do not stop taking this medicine without consulting your doctor.

Uses

• Non-small cell lung cancer (NSCLC)

More Information

• Afzeta 20mg Tablet should be stored at room temperature, between 20°C to 25°C (68°F to 77°F).
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices Pregnancy  

Afzeta 20mg Tablet is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feeding  

It is unknown, whether Afzeta 20mg Tablet is excreted in human milk or not, and the potential risks to a nursing infant are unknown. So nursing women should consult a healthcare provider before taking it.  

Lungs  

Afzeta 20mg Tablet is primarily used to treat non-small cell lung cancer (NSCLC). Patients should consult healthcare providers if they have any other lung disease before taking it.  

Liver  

Afzeta 20mg Tablet is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Afzeta 20mg Tablet, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Afzeta 20mg Tablet should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Interstitial lung disease (ILD)
• Severe diarrhea or dehydration
• Liver problems
• Eye problems, such as corneal erosion or ulceration
• Hemorrhage or bleeding problems
• Kidney problems
• Cardiac problems

• Diarrhea
• Mouth sores
• Acne or skin rash
• Nausea and vomiting
• Fatigue
• Loss of appetite
• Abdominal pain
• Nail changes, such as nail bed infections or inflammation
• Dry skin or itching
• Eye irritation or dryness
• Respiratory infections

Afzeta 40mg Tablet is an anticancer medicine containing Afatinib dimaleate as an active ingredient. It is used to treat patients with non-small cell lung cancer (NSCLC) whose tumors have certain (non-resistant) abnormal epidermal growth factor receptor (EGFR) genes and patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy. Cancer is a disorder in which cells multiply in an abnormal and uncontrolled manner. Talk to your doctor if you have kidney disorders, breathing problems, liver disorders, heart problems, intolerance to sugars, severe dry eye, or other eye problems before taking this medicine. 

Afzeta 40mg Tablet can delay disease progression and improve overall survival, it can also help patients maintain a better quality of life for a longer period of time. This includes improved physical functioning, reduced pain, and better mental and emotional health. Tell your doctor if you are wearing contact lenses or breastfeeding before taking this medication. Limit your time in the sun as this medicine may make your skin sensitive to the sun. It is not recommended for children and adolescents under the age of 18.  Do not stop taking this medicine without consulting your doctor.

Uses

• Non-small cell lung cancer (NSCLC)

More Information

• Afzeta 40mg Tablet should be stored at room temperature, between 20°C to 25°C (68°F to 77°F).
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices  Pregnancy  

Afzeta 40mg Tablet is unsafe during pregnancy as it can cause fetal harm. It is recommended to avoid this medication during pregnancy.  

Breast Feeding  

It is unknown, whether Afzeta 40mg Tablet is excreted in human milk or not, and the potential risks to a nursing infant are unknown. So nursing women should consult a healthcare provider before taking it.  

Lungs  

Afzeta 40mg Tablet is primarily used to treat non-small cell lung cancer (NSCLC). Patients should consult healthcare providers if they have any other lung disease before taking it.  

Liver  

Afzeta 40mg Tablet is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Afzeta 40mg Tablet, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Afzeta 40mg Tablet should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Interstitial lung disease (ILD)
• Severe diarrhea or dehydration
• Liver problems
• Eye problems, such as corneal erosion or ulceration
• Hemorrhage or bleeding problems
• Kidney problems
• Cardiac problems

• Diarrhea
• Mouth sores
• Acne or skin rash
• Nausea and vomiting
• Fatigue
• Loss of appetite
• Abdominal pain
• Nail changes, such as nail bed infections or inflammation
• Dry skin or itching
• Eye irritation or dryness
• Respiratory infections

Nabpac 100 mg Injection is an anticancer medicine. It treats breast cancer, non-small cell lung cancer, ovarian cancer, and AIDS (Acquired Immuno-Deficiency Syndrome). Cancer is a condition in which cells are dividing and growing fast and in an uncontrolled manner. This Injection may be given alone or in combination with other anticancer medicines. It should not be used for severe liver problems, uncontrolled infection, and low white blood cell or platelet count.

This injection is not recommended for adolescents and children under the age of 18. Talk to your doctor if you have heart disorders before taking this medicine. Administration of this medicine can cause serious allergic reactions. Use effective birth control during the treatment and for at least six months after the last dose. This Injection may harm patients suffering from alcoholism as this medicine contains alcohol.

Uses of Nabpac 100mg Injection

• Ovarian cancer
• Breast cancer
• Non-small cell lung cancer
• AIDS-related Kaposi’s sarcoma

Therapeutic Effects of Nabpac 100mg Injection

Nabpac 100 mg Injection binds to β-tubulin subunits of microtubules, interferes with interphase (a process involving cell growth) and mitotic functions (a process of cell division), and prevents the growth of cancer cells.

Interaction of Nabpac 100mg Injection with other drugs

Inform your doctor about any prescribed medicines, over-the-counter medications, nutritional and vitamin supplements, or herbal products that you are taking or have taken before the treatment. Certain medications may interact with Nabpac 100 mg injection and cause undesirable side effects.

More Information about Nabpac 100mg Injection

• Keep Nabpac 100 mg Injection out of sight and reach of children.
• Do not store above 25°C.

How to consume Nabpac 100mg Injection

It will be given to you by a doctor or nurse. Do not self-administer. Your doctor will decide the dose and dosage of the Nabpac 100 mg injection.

Safety Advices Pregnancy  

Nabpac 100 mg Injection can harm your unborn baby. Tell your doctor if you are pregnant or planning to get pregnant before taking this Injection.   

Breast Feeding  

Stop breastfeeding during the treatment with Nabpac 100 mg Injection. Consult your doctor for potential risks.  

Lungs  

It is unknown whether Nabpac 100 mg injection can be given to patients with lung disorders. Please consult your physician for more advice.  

Liver  

It is contraindicated in patients with severe liver disorders. Inform your doctor if you have any liver disorders before taking Nabpac 100 mg Injection.  

Alcohol  

It is unsafe to consume alcohol with Nabpac 100 mg Injection.  

Driving  

The alcohol present in Nabpac 100 mg Injection may affect your ability to drive. Avoid driving if you feel unwell.

Side Effects

• Serious allergic reactions (rash, swelling of face, lips, throat, or tongue, trouble breathing, and swallowing)
• Severe diarrhea
• Severe stomach pain

• Anemia, feeling tired
• Hair loss
• Burning, tingling, or numbness in your feet or hands
• Muscle and joint pain
• Vomiting, nausea
• Mouth or lip sores
• Infections
• Swelling of hands, feet, and face
• Bleeding
• Irritation at the injection site
• Low blood pressure

Thiother 15mg Injection belongs to the class of medication known as Antineoplastics. It contains the active ingredient Thiotepa. It is prescribed in combination with other anti-cancer drugs before stem cell transplantation for adult patients with cancer in the lymph nodes of the central nervous system. It is used as a Preparation before stem cell transplant to reduce the risk of graft rejection. It controls the outflow within the cavity due to cancer in serous membranes. It is also indicated for treating breast, ovarian, and bladder cancer.

The common side effects that are likely to be associated with Thiother 15mg Injection are diarrhea, rashes, bleeding, blood in urine, and cytomegalovirus infection. Inform your doctor if these side effects disturb or persist in you. 

Inform your healthcare provider if you are allergic (hypersensitive) to Thiother 15mg injection and its ingredients. It is contraindicated in patients using a live virus or bacterial vaccine, including the yellow fever vaccine. If you have a history of cardiac, liver, kidney, and pulmonary disease and profound myelosuppression (anemia, neutropenia, and thrombocytopenia), report to your doctor. Liver and cardiac function must be monitored regularly, and caution is advised in patients with cardiac disease and liver impairment. It is not recommended to use in pregnant and breastfeeding women.

Uses of Thiother 15mg Injection

• Preparation for allogeneic hematopoietic stem cell transplantation in pediatric patients with class 3 beta-thalassemia
• Treatment of adenocarcinoma of breast and ovary.
• Treatment of superficial papillary cancer of the urinary bladder.

Therapeutic Effects of Thiother 15mg Injection

Thiother 15mg Injection acts by damaging the genetic material (DNA and RNA) of the cancer cells. It stops the growth and multiplication of cancer by directly attacking DNA. This causes the breakage of DNA strands. The process of cross-linking is crucial in exhibiting toxicity in cancer cells. This leads to the exertion of cytotoxic effect and death of tumor cells.

More Information

• Store between 2° to 8°C.
• Protect from light.
• Keep out of reach of children.

Safety Advices  Pregnancy  

Thiother 15mg Injection is unsafe to use during pregnancy as it may cause fetal harm. Hence, Consult your doctor for advice.   

Breast Feeding  

Breastfeeding while on treatment with Thiother 15mg Injection is not recommended. Consult your physician for advice before breastfeeding.  

Lungs  

It is unknown whether Thiother 15 mg Injection can be administered in lung failure patients. Please consult the doctor for more advice.  

Liver  

Inform your physician before taking Thiother 15mg Injection if you have liver problems. Ensure that your physician monitors your liver functions regularly.  

Alcohol  

It is unknown whether it is safe to consume alcohol while taking Thiother 15mg Injection. Consult your doctor for advice.   

Driving  

Thiother 15mg Injection is used with caution while driving as it may cause convulsion, hallucination, delirium, dizziness, headache, and blurred vision. 

Side Effects

• Severe drop in blood cell count
• Heart problem
• Kidney damage
• Nerve damage
• Lung toxicity
• Liver toxicity

• Cytomegalovirus infection
• Hemorrhage
• Diarrhea
• Blood in urine
• Rashes

NAB Celtax 100 mg Injection is an anticancer medicine. It treats breast cancer, non-small cell lung cancer, ovarian cancer, and AIDS (Acquired Immuno-Deficiency Syndrome). Cancer is a condition in which cells are dividing and growing fast and in an uncontrolled manner. This Injection may be given alone or in combination with other anticancer medicines. It should not be used for severe liver problems, uncontrolled infection, and low white blood cell or platelet count.

This injection is not recommended for adolescents and children under the age of 18. Talk to your doctor if you have heart disorders before taking this medicine. Administration of this medicine can cause serious allergic reactions. Use effective birth control during the treatment and for at least six months after the last dose. This Injection may harm patients suffering from alcoholism as this medicine contains alcohol.

Uses of NAB Celtax 100mg Injection

• Ovarian cancer
• Breast cancer
• Non-small cell lung cancer
• AIDS-related Kaposi’s sarcoma

Therapeutic Effects of NAB Celtax 100mg Injection

NAB Celtax 100 mg Injection binds to β-tubulin subunits of microtubules, interferes with interphase (a process involving cell growth) and mitotic functions (a process of cell division), and prevents the growth of cancer cells.

Interaction of NAB Celtax 100mg Injection with other drugs

Inform your doctor about any prescribed medicines, over-the-counter medications, nutritional and vitamin supplements, or herbal products that you are taking or have taken before the treatment. Certain medications may interact with NAB Celtax 100 mg injection and cause undesirable side effects.

More Information about NAB Celtax 100mg Injection

• Keep NAB Celtax 100 mg Injection out of sight and reach of children.
• Do not store above 25°C.

How to consume NAB Celtax 100mg Injection

It will be given to you by a doctor or nurse. Do not self-administer. Your doctor will decide the dose and dosage of the NAB Celtax 100 mg injection.

Safety Advices   Pregnancy  

NAB Celtax 100 mg Injection can harm your unborn baby. Tell your doctor if you are pregnant or planning to get pregnant before taking this Injection.   

Breast Feeding  

Stop breastfeeding during the treatment with NAB Celtax 100 mg Injection. Consult your doctor for potential risks.  

Lungs

It is unknown whether NAB Celtax 100 mg injection can be given to patients with lung disorders. Please consult your physician for more advice.  

Liver  

It is contraindicated in patients with severe liver disorders. Inform your doctor if you have any liver disorders before taking NAB Celtax 100 mg Injection.  

Alcohol  

It is unsafe to consume alcohol with NAB Celtax 100 mg Injection.  

Driving  

The alcohol present in NAB Celtax 100 mg Injection may affect your ability to drive. Avoid driving if you feel unwell.

Side Effects

• Serious allergic reactions (rash, swelling of face, lips, throat, or tongue, trouble breathing, and swallowing)
• Severe diarrhea
• Severe stomach pain

• Anemia, feeling tired
• Hair loss
• Burning, tingling, or numbness in your feet or hands
• Muscle and joint pain
• Vomiting, nausea
• Mouth or lip sores
• Infections
• Swelling of hands, feet, and face
• Bleeding
• Irritation at the injection site
• Low blood pressure

Bavencio 200mg/10ml injection contains the active ingredient avelumab. It is an antineoplastic drug that belongs to the class of medications called PD-1/PD-L1 (programmed death ligand-1) inhibitors. It is used to treat Merkel cell carcinoma, a rare type of skin cancer that has spread to other body parts in adults and children 12 years and older. It is also indicated to treat urothelial carcinoma, cancer that originates in the urinary tract that has spread to nearby tissues or other body parts of the body in people whose cancer worsened during or within 12 months after it was treated with other anticancer medications.  

It is also used in combination with other anticancer medicines to treat renal cell carcinoma, a type of kidney cancer that has spread to other body parts. PD-L1 is found on the surface of certain cancer cells and helps protect them from the immune system. It works by slowing or stopping the growth and spread of the cancer cells.  Do not take Bavencio 200mg/10ml injection if you are allergic to avelumab or any other ingredients of this medicine. Inform your physician if you have liver diseases, hepatitis B, HIV/AIDS, or other immune diseases before initiating the therapy. 

Uses

• Merkel cell carcinoma
• Urothelial carcinoma
• Renal cell carcinoma

 

More Information

• Store in a refrigerator (2°C to 8°C).
• Do not freeze. Store in the original package to protect from light.
• keep the injection away from the reach of children and pets.
• If you have missed any dosing appointments, inform your doctor and schedule immediately.

Safety Advices Pregnancy  

Bavencio 200mg/10ml injection is unsafe to administer in pregnant women because it may affect the fetus. Inform your physician if you are pregnant, suspect pregnancy, or planning to become pregnant. Using an effective birth control method during the treatment and for 1 months after your last dose is necessary.    

Breast Feeding  

Breastfeeding is not recommended in patients taking Bavencio 200mg/10ml injection because the medicine passes into the breast milk in small amounts and may harm your baby.   

Lungs  

It is unknown whether Bavencio 200mg/10ml injection can be used in patients with lung disorders. Consult your doctor if you have any lung diseases before starting the treatment.  

Liver  

Bavencio 200mg/10ml injection is safe to administer in patients with liver problems. Dose adjustments are not necessary. However, inform your physician if you have any liver diseases or problems before initiating the therapy.   

Alcohol  

It is unknown whether consuming alcohol is safe during the treatment with Bavencio 200mg/10ml injection. Inform your doctor if you are a chronic drinker.   

Driving  

Bavencio 200mg/10ml injection may make you feel tired, dizzy, or sleepy. It is unsafe to drive or operate heavy machinery after taking this medicine. 

Side Effects

• Increased blood pressure
• Swelling in the legs and feet
• Skin rash
• Abdominal pain
• Decrease in appetite
• Diarrhea
• Nausea
• Decreased RBC counts
• Muscle pain
• Cough, shortness of breath
• Difficulty in talking
• Tiredness

• Heart problems
• Severe skin reactions
• Thyroid problems
• Liver injury
• Visual impairment
• Infusion reactions

Thioplan 15mg Injection belongs to the class of medication known as Antineoplastics. It contains the active ingredient Thiotepa. It is prescribed in combination with other anti-cancer drugs before stem cell transplantation for adult patients with cancer in the lymph nodes of the central nervous system. It is used as a Preparation before stem cell transplant to reduce the risk of graft rejection. It controls the outflow within the cavity due to cancer in serous membranes. It is also indicated for treating breast, ovarian, and bladder cancer.

The common side effects that are likely to be associated with Thioplan 15mg Injection are diarrhea, rashes, bleeding, blood in urine, and cytomegalovirus infection. Inform your doctor if these side effects disturb or persist in you. 

Inform your healthcare provider if you are allergic (hypersensitive) to Thioplan 15mg injection and its ingredients. It is contraindicated in patients using a live virus or bacterial vaccine, including the yellow fever vaccine. If you have a history of cardiac, liver, kidney, and pulmonary disease and profound myelosuppression (anemia, neutropenia, and thrombocytopenia), report to your doctor. Liver and cardiac function must be monitored regularly, and caution is advised in patients with cardiac disease and liver impairment. It is not recommended to use in pregnant and breastfeeding women.

Uses of Thioplan 15mg Injection

• Preparation for allogeneic hematopoietic stem cell transplantation in pediatric patients with class 3 beta-thalassemia
• Treatment of adenocarcinoma of breast and ovary.
• Treatment of superficial papillary cancer of the urinary bladder.

Therapeutic Effects of Thioplan 15mg Injection

Thioplan 15mg Injection acts by damaging the genetic material (DNA and RNA) of the cancer cells. It stops the growth and multiplication of cancer by directly attacking DNA. This causes the breakage of DNA strands. The process of cross-linking is crucial in exhibiting toxicity in cancer cells. This leads to the exertion of cytotoxic effect and death of tumor cells.

More Information

• Store between 2° to 8°C.
• Protect from light.
• Keep out of reach of children.

Safety Advices Pregnancy  

Thioplan 15mg Injection is unsafe to use during pregnancy as it may cause fetal harm. Hence, Consult your doctor for advice.   

Breast Feeding  

Breastfeeding while on treatment with Thioplan 15mg Injection is not recommended. Consult your physician for advice before breastfeeding.  

Lungs  

It is unknown whether Thioplan 15 mg Injection can be administered in lung failure patients. Please consult the doctor for more advice.  

Liver  

Inform your physician before taking Thioplan 15mg Injection if you have liver problems. Ensure that your physician monitors your liver functions regularly.  

Alcohol  

It is unknown whether it is safe to consume alcohol while taking Thioplan 15mg Injection. Consult your doctor for advice.   

Driving  

Thioplan 15mg Injection is used with caution while driving as it may cause convulsion, hallucination, delirium, dizziness, headache, and blurred vision. 

Side Effects

• Severe drop in blood cell count
• Heart problem
• Kidney damage
• Nerve damage
• Lung toxicity
• Liver toxicity

• Cytomegalovirus infection
• Hemorrhage
• Diarrhea
• Blood in urine
• Rashes

Hamsyl 3750IU Injection is a chemotherapy drug containing the active constituent Pegaspargase. It is used to treat a type of blood cancer called Acute Lymphoblastic Leukemia (ALL).  This is a white blood cell cancer in which the immature white cells start growing out of control, thus preventing the production of functional blood cells. Combined with other chemotherapy drugs, this medication can help increase the chances of remission and long-term survival for people with ALL. It is particularly effective in treating children with ALL, who have a higher remission rate and overall survival when included in their treatment plan. 

Uses

• Acute Lymphoblastic Leukemia
• Non-Hodgkin's Lymphoma

More Information

• Store in a refrigerator at 2-8°C.
• Do not freeze.
• Protected from light.
• Keep it in its original packaging until it is ready to be used.
• Keep out of the reach of children and pets.
• Should be disposed of properly.

Safety Advices  Pregnancy  

There are no established adverse effects of Hamsyl 3750IU Injection in pregnant women. Consult your doctor if you are pregnant or planning to get pregnant before taking this medicine.  

Breast Feeding  

It is unclear whether Hamsyl 3750IU Injection is excreted in human milk. So you should consult a doctor before taking this medication if you are a breastfeeding mother.  

Lungs  

There is no evidence to suggest that Hamsyl 3750IU Injection harms the lungs. However, as with any medication, there is a risk of side effects that could affect the respiratory system. So patients should consult their doctor if they have any pre-existing lung disease before taking this medication.  

Liver  

Hamsyl 3750IU Injection is primarily metabolized in the liver, so inform your healthcare provider if you have any liver problems or diseases. This medication may also increase liver enzymes, which can be a sign of liver damage or inflammation. Patients taking this medication require regular blood tests to monitor liver function.  

Alcohol  

It is recommended to avoid consuming alcohol while taking Hamsyl 3750IU Injection, as alcohol can increase the risk of certain side effects associated with the medication, such as stomach ulcers or gastrointestinal bleeding.  

Driving  

Patients receiving Hamsyl 3750IU Injection should be advised to avoid driving or operating machinery if they experience side effects such as fatigue, dizziness, or blurred vision, impairing a patient's ability to drive or operate machinery safely.

Side Effects

• Anaphylaxis (severe allergic reaction)
• Thrombosis (blood clots)
• Hemorrhage (bleeding)
• Tumor Lysis Syndrome (a potentially life-threatening condition due to breakdown of cancer cells)
• Acute pancreatitis (inflammation of the pancreas)
• Hepatotoxicity (liver damage or failure)
• Neurotoxicity (damage to the nervous system)
• Hypersensitivity reactions (allergic reactions, including anaphylaxis)
• Renal failure (kidney damage or failure)

• Nausea
• Vomiting
• Diarrhea
• Fatigue
• Loss of appetite
• Headache
• Fever or chills
• Muscle or joint pain
• Rash or itching
• Swelling or redness at the injection site

Bufatas IV 60mg injection is an anti-cancer (antineoplastic/cytotoxic) chemotherapy drug. It is an alkyl sulfonate belonging to the class alkylating agent. It is indicated for treating blood cancers, such as chronic myelogenous leukemia (A type of cancer that causes an increase in white blood cells). It is given as a treatment to prepare the bone marrow to receive healthy blood-forming cells (stem cells) from a donor to replace their stem cells that have been destroyed by treatment with radiation or high doses of chemotherapy). 

Chronic myelogenous leukemia is an uncommon type of cancer that affects bone marrow (soft, spongy tissue that produces blood cells for your body). It causes an increase in white blood cell count. Common side effects of Bufatas IV 60 mg injections are decreased white blood cells count, dizziness, shortness of breath, mouth inflammation, nausea, diarrhea, difficulty sleeping, skin rashes, and fever. Drink plenty of fluids while you are taking this medicine.    

Bufatas IV 60 mg injection can cause a severe decrease in bone marrow activity. If you are taking any other prescribed or non-prescribed medications that decrease the blood cell count, talk to your healthcare professional before taking the medications. It affects your immune system. You may get infections more easily, even serious or fatal infections. Call your doctor if you have a fever, chills, cough, mouth sores, or unusual bleeding or bruising.

 

Uses of Bufatas Iv 60mg Injection

• Hematopoietic progenitor cell transplantation
• Chronic myelogenous leukemia
• Polycythaemia vera (a type of cancer that causes an increase in red blood cells)
• Thrombocythemia (increased number of platelets in the blood)
• Myelofibrosis (type of blood cancer where scar tissues are formed in bone marrow)
• Hemoglobinopathies (a genetic disorder that produces abnormal hemoglobin)
• Brain Malignancies

Therapeutic Effects of Bufatas Iv 60mg Injection:

Bufatas IV 60 mg injection works by interfering with the DNA replication process, which is necessary for the cells to divide. It stops tumor growth by inhibiting cell division.  It causes cytotoxicity by reversibly binding to nucleophilic groups on different cell components. Alkylation of DNA is most likely the crucial cytotoxic reaction that kills tumor cells. It damages the DNA and RNA of the cancer cells by stopping their growth and multiplication. They are combined with other medications to treat various lymphatic and solid cancers.

Temodal 250mg Capsule contains the active ingredient temozolomide. It belongs to the class of medications known as Antitumor agents. It is prescribed to treat brain cancer, such as glioblastoma multiforme in adults and malignant glioma, including glioblastoma multiforme or anaplastic astrocytoma in patients older than three years. Glioblastoma and anaplastic astrocytoma are the most common and aggressive brain cancers with low chances of survival. Anaplastic astrocytoma is treated with Temodal 250mg Capsule or radiotherapy after biopsy, whereas Glioblastoma multiforme is treated with a combination of radiotherapy and Temodal 250mg Capsule, and it is continued as maintenance therapy.

The common side effects that are likely to associate with Temodal 250mg Capsule are nausea, vomiting, dizziness, diarrhea, constipation, hair loss, rashes, tiredness, frequent urination, vision and hearing problems, high blood sugar levels, muscle damage, pain in muscles and joints, memory loss, coordination problems, infections, sleep problems and loss of weight. Inform your doctor if any of these symptoms disturb you or persist.

Uses

•  Treatment of newly diagnosed glioblastoma multiforme.
• Treatment of refractory anaplastic astrocytoma

More Information

• Keep Temodal 250mg Capsule out of sight and reach of children.
• Store protected from light and moisture.
• Do not store above 25°C. 

Pregnancy  

Temodal 250mg Capsule is unsafe to use during pregnancy as it may cause fetal harm. It should not be used unless prescribed by your physician. Women with childbearing potential should use effective contraceptive precautions for at least 6 months following the completion of treatment.   

Breast Feeding  

Temodal 250mg Capsule is unsafe to use during breastfeeding as it passes through breast milk and harm the baby. Consult your physician for advice before breastfeeding.  

Lungs  

Inform your physician before taking Temodal 250mg Capsule if you have if you have any lung conditions.   

Liver  

Inform your physician before taking Temodal 250mg Capsule if you have severe liver problems. Dose adjustment is required based on the condition.   

Alcohol  

Avoid consuming alcohol while taking Temodal 250mg Capsule as it may cause unpleasant side effects. Consult our doctor for advice.  

Driving  

Do not drive or operate heavy machines while being treated with Temodal 250mg Capsule as it may decrease alertness, affect your vision and make you dizzy and sleepy. 

Side Effects

• Secondary cancer like myelodysplastic syndrome and myeloid leukemia.
• Severe Allergic reactions
• Inflammation and fluid buildup in lungs
• Blood clot in lungs or legs
• Liver toxicity
• Convulsions
• Fever and chills
• Severe headache
• Uncontrolled bleeding

• Hair loss
• Rashes
• Tiredness
• Nausea, vomiting and diarrhea
• Constipation
• High blood sugar levels
• Dizziness, impaired sensation, tingling sensation, abnormal taste
• Vision and Hearing problem
• Frequent urination
• Muscle damage, pain in muscles and joints
• Weight changes
• Infections and wounds
• Amnesia
• Abnormal blood cell counts
• Loss of appetite
• Sleep problems
• Memory loss
• Difficulty concentrating, changes in mental status and alertness
• Coordination problems

Introduction to Bucelon 60mg Injection

Bucelon 60mg injection is an anti-cancer (antineoplastic/cytotoxic) chemotherapy drug. It is an alkyl sulfonate belonging to the class alkylating agent. It is indicated for treating blood cancers, such as chronic myelogenous leukemia (A type of cancer that causes an increase in white blood cells). It is given as a treatment to prepare the bone marrow to receive healthy blood-forming cells (stem cells) from a donor to replace their stem cells that have been destroyed by treatment with radiation or high doses of chemotherapy). 

Chronic myelogenous leukemia is an uncommon type of cancer that affects bone marrow (soft, spongy tissue that produces blood cells for your body). It causes an increase in white blood cell count. Common side effects of Bucelon 60 mg injections are decreased white blood cells count, dizziness, shortness of breath, mouth inflammation, nausea, diarrhea, difficulty sleeping, skin rashes, and fever. Drink plenty of fluids while you are taking this medicine.    

Bucelon 60 mg injection can cause a severe decrease in bone marrow activity. If you are taking any other prescribed or non-prescribed medications that decrease the blood cell count, talk to your healthcare professional before taking the medications. It affects your immune system. You may get infections more easily, even serious or fatal infections. Call your doctor if you have a fever, chills, cough, mouth sores, or unusual bleeding or bruising.

Uses of Bucelon 60mg Injection

• Hematopoietic progenitor cell transplantation
• Chronic myelogenous leukemia
• Polycythaemia vera (a type of cancer that causes an increase in red blood cells)
• Thrombocythemia (increased number of platelets in the blood)
• Myelofibrosis (type of blood cancer where scar tissues are formed in bone marrow)
• Hemoglobinopathies (a genetic disorder that produces abnormal hemoglobin)
• Brain Malignancies

Therapeutic Effects of Bucelon 60mg Injection

Bucelon 60 mg injection works by interfering with the DNA replication process, which is necessary for the cells to divide. It stops tumor growth by inhibiting cell division.  It causes cytotoxicity by reversibly binding to nucleophilic groups on different cell components. Alkylation of DNA is most likely the crucial cytotoxic reaction that kills tumor cells. It damages the DNA and RNA of the cancer cells by stopping their growth and multiplication. They are combined with other medications to treat various lymphatic and solid cancers.

More Information about Bucelon 60mg Injection

Unopened vials of bucelon 60 mg injection should be stored under refrigerated conditions between 2°C to 8°C (36°F to 46°F). Unused medications should be disposed of properly. Keep it out of sight and reach of children.

Side Effects of Bucelon 60mg Injection

Side effects are unwanted symptoms caused by medicines. Even though all medications cause side effects, not everyone gets them. Bucelon 60 mg injection causes the following side effects 

Severe

Myelosuppression (decreased bone marrow activity) 

Common side effects 

• Thalassemia
• Skin rashes
• Hair loss
• Patches of dark skin
• Blood in urine
• Decrease in the number of blood cells and platelets
• Nausea and vomiting
• Jaundice
• Infertility and sterility
• Pneumonia Syndrome
• Itching

Temodal 100mg Capsule contains the active ingredient temozolomide. It belongs to the class of medications known as Antitumor agents. It is prescribed to treat brain cancer, such as glioblastoma multiforme in adults and malignant glioma, including glioblastoma multiforme or anaplastic astrocytoma in patients older than three years. Glioblastoma and anaplastic astrocytoma are the most common and aggressive brain cancers with low chances of survival. Anaplastic astrocytoma is treated with Temodal 100mg Capsule or radiotherapy after biopsy, whereas Glioblastoma multiforme is treated with a combination of radiotherapy and Temodal 100mg Capsule, and it is continued as maintenance therapy.

The common side effects that are likely to associate with Temodal 100mg Capsule are nausea, vomiting, dizziness, diarrhea, constipation, hair loss, rashes, tiredness, frequent urination, vision and hearing problems, high blood sugar levels, muscle damage, pain in muscles and joints, memory loss, coordination problems, infections, sleep problems and loss of weight. Inform your doctor if any of these symptoms disturb you or persist.

Uses

•  Treatment of newly diagnosed glioblastoma multiforme.
• Treatment of refractory anaplastic astrocytoma

More Information

• Keep Temodal 100mg Capsule out of sight and reach of children.
• Store protected from light and moisture.
• Do not store above 25°C.

Safety Advices  Pregnancy  

Temodal 100mg Capsule is unsafe to use during pregnancy as it may cause fetal harm. It should not be used unless prescribed by your physician. Women with childbearing potential should use effective contraceptive precautions for at least 6 months following the completion of treatment.   

Breast Feeding  

Temodal 100mg Capsule is unsafe to use during breastfeeding as it passes through breast milk and harm the baby. Consult your physician for advice before breastfeeding.  

Lungs  

Inform your physician before taking Temodal 100mg Capsule if you have if you have any lung conditions.   

Liver  

Inform your physician before taking Temodal 100mg Capsule if you have severe liver problems. Dose adjustment is required based on the condition.   

Alcohol  

Avoid consuming alcohol while taking Temodal 100mg Capsule as it may cause unpleasant side effects. Consult our doctor for advice.  

Driving  

Do not drive or operate heavy machines while being treated with Temodal 100mg Capsule as it may decrease alertness, affect your vision and make you dizzy and sleepy. 

Side Effects

• Secondary cancer like myelodysplastic syndrome and myeloid leukemia.
• Severe Allergic reactions
• Inflammation and fluid buildup in lungs
• Blood clot in lungs or legs
• Liver toxicity
• Convulsions
• Fever and chills
• Severe headache
• Uncontrolled bleeding

• Hair loss
• Rashes
• Tiredness
• Nausea, vomiting and diarrhea
• Constipation
• High blood sugar levels
• Dizziness, impaired sensation, tingling sensation, abnormal taste
• Vision and Hearing problem
• Frequent urination
• Muscle damage, pain in muscles and joints
• Weight changes
• Infections and wounds
• Amnesia
• Abnormal blood cell counts
• Loss of appetite
• Sleep problems
• Memory loss
• Difficulty concentrating, changes in mental status and alertness
• Coordination problems