Criticalkare Pharma

Biomab EGFR 50mg Injection consists of the active Nimotuzumab. It is a monoclonal antibody used in cancer treatment.  It has been approved for the treatment of head and neck cancer, as well as for certain types of brain cancer. This medication is typically used with other cancer treatments, such as chemotherapy and radiation therapy. The drug effectively improves overall survival and disease-free survival in some cancer patients. However, like all cancer treatments, it can have side effects, including allergic reactions, skin rashes, and flu-like symptoms. transplant.

There are no absolute contraindications to Biomab EGFR 50mg Injection, but there are some precautions and potential contraindications to consider. For example, patients with a history of severe allergic reactions or hypersensitivity to it or its components should not receive the medication. Additionally, patients with certain medical conditions, such as severe liver or kidney disease, may need to be monitored closely or have their dosages adjusted.

• Head and neck cancer
• Certain types of brain cancer
• Esophageal cancer

Therapeutic Effects of Biomab Egfr 50mg Injection

The therapeutic effect of Biomab EGFR 50mg Injection is primarily focused on its ability to target and bind to the epidermal growth factor receptor (EGFR) found on many cancer cells. Doing so can block the growth and spread of cancer cells, ultimately leading to improved patient outcomes. One of the advantages is its targeted therapy approach, which allows it to target cancer cells while minimizing damage to healthy cells specifically. This can help to reduce side effects and improve the overall quality of life for cancer patients undergoing treatment.

• Biomab EGFR 50mg Injection should be stored in a refrigerator at a temperature between 2°C to 8°C (36°F to 46°F).
• Not need to be frozen, as this can damage its efficacy.
• Once a vial is opened, it should be used immediately.
• If the drug is not used immediately, it can be stored at room temperature for 4 hours. After 4 hours, any remaining drug should be discarded.
• Keep out of reach of children and pets.

Biomab EGFR 50mg Injection is an injectable medication that a healthcare professional administers. It is typically given as an intravenous injection. The dose and frequency will depend on the type of cancer being treated, the patient's overall health, and other medications the patient may be taking.  If you miss a dose, contact your healthcare provider as soon as possible. Your healthcare provider may recommend rescheduling your next dose or adjusting your dosing schedule. Do not double the dose to make a missed dose.

Like all medications, Biomab EGFR 50mg Injection can cause side effects, although not everyone who takes it will experience them. 

Serious:

• Allergic reactions
• Difficulty breathing
• Swelling of the face or throat, or hives
• Infusion reactions (fever, chills, or low blood pressure)
• Chest pain
• Irregular heartbeat
• Lung problems (cough or shortness of breath)
• Liver problems (jaundice or abdominal pain)

Common: 

• Skin rash
• Diarrhea
• Nausea and vomiting
• Fatigue
• Headache
• Fever
• Pain at the injection site

Esentra 120mg Injection consists of the active ingredient Denosumab. It is a medication used to treat osteoporosis, characterized by weakened bones. It is also prescribed to prevent bone complications in patients with certain types of cancer, such as multiple myeloma and bone metastases. Esentra 120mg Injection works by inhibiting a protein called RANK ligand, which plays a role in the breakdown of bone tissue. Studies proved it can significantly increase bone density, reducing fracture risk in postmenopausal women with osteoporosis and patients with cancer-related bone loss. Close monitoring of renal function may be necessary for patients with moderate renal impairment.

Esentra 120mg Injection should not be used in individuals with known hypersensitivity or allergic reactions to its components. Adequate calcium and vitamin D supplementation is required to ensure during the treatment. It is not approved for use in children and adolescents. Its safety and effectiveness in pediatric populations have not been established, so its use is contraindicated in individuals under 18. This medication should be used cautiously in individuals with pre-existing hypoparathyroidism, characterized by low parathyroid hormone levels.

Esentra 120mg Injection is used in the treatment of the following condition:

• Osteoporosis
• Bone loss due to hormonal therapy in breast or prostate cancer
• Multiple myeloma (cancer affects plasma cells in the bone marrow)
• Bone metastases (cancer that spreads to bone)

• Esentra 120mg Injection should be stored in the refrigerator at a temperature between 2°C to 8°C (36°F to 46°F).
• Do not freeze it.
• Keep in the original package.
• Keep away from light, moisture, and heat.
• Avoid taking double doses for missed doses. 

The safety of using Esentra 120mg Injection during pregnancy has not been established. Limited studies are available regarding the use of this medication in pregnant women, so it is recommended to use caution and consult a doctor before considering its use during pregnancy.  

Whether Esentra 120mg Injection is excreted in milk is unknown. So it is better to consult a healthcare provider if you are a breastfeeding mother before taking this medication.  

If you have a lung or respiratory disorders history, it is important to consult your healthcare provider before taking Esentra 120mg Injection.  

Esentra 120mg Injection is primarily metabolized in the liver, and its safety has not been extensively studied in individuals with severe liver impairment. It is crucial to communicate any pre-existing liver conditions or changes in liver function to your healthcare provider to ensure this medication's safe and effective use.  

It is generally recommended to avoid or limit alcohol consumption while taking Esentra 120mg Injection. Alcohol can interact with this medication, potentially increasing the risk of side effects.  

Patients receiving Esentra 120mg 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. 

• Osteonecrosis of the jaw (severe necrosis or death of jaw cells)
• Atypical femoral fractures
• Hypocalcemia (low blood calcium levels)

• Injection site reactions
• Back pain
• Musculoskeletal pain
• Infections
• Abdominal pain
• Headache
• Hypophosphatemia (low blood phosphate levels)

• Treatment of hemophilia B
• Prophylactic treatment
• Management of bleeding episodes
• Surgical procedures
• Trauma and injuries
• Alternative treatment for hemophilia A with inhibitors
• Other bleeding disorders

Alphanine 500IU Injection  contains active components such as factor IX. In some cases, individuals with hemophilia A (caused by a deficiency of factor VIII) may develop inhibitors (antibodies) against factor VIII, making standard treatment less effective. In such situations, it may be considered as an alternative. It can be used before, during, and after surgery to prevent excessive bleeding. Some people with hemophilia B may receive it  as a preventive measure to maintain a certain level of this in their bloodstream, reducing the risk of spontaneous bleeding episodes, particularly in joints and muscles. It may be administered following traumatic injuries or accidents to prevent or control bleeding. In rare cases, it may be considered for treating other bleeding disorders or conditions that involve a deficiency, such as acquired hemophilia.

If a person has a known allergy or hypersensitivity to Alphanine 500IU Injection or any components of  this product, it is a contraindication to its use.  It is inappropriate for individuals with DIC, a complex bleeding disorder characterized by abnormal clotting and bleeding. People with severe liver disease may not respond well to it, and the risks and benefits should be carefully weighed. While it is commonly used in pediatric patients with hemophilia B, the dosage and administration should be carefully adjusted based on age and weight, and the treatment should be closely monitored. Alphanine 500IU Injection replacement therapy can be safe and effective for older adults with hemophilia B. However, dosing and treatment plans may need to be adjusted based on individual health and medical history.

Alphanine 500IU Injection is used in the following:

• Treatment of hemophilia B
• Prophylactic treatment
• Management of bleeding episodes
• Surgical procedures
• Trauma and injuries
• Alternative treatment for hemophilia A with inhibitors
• Other bleeding disorders
• Pediatric hemophilia B

Therapeutic Effects of Alphanine 500iu Injection

Once administered, the infused form  Alphanine 500IU Injection, it mixes with the patient's blood, becoming available to participate in the coagulation cascade. In the event of an injury or bleeding episode, it helps initiate and accelerate the formation of a stable blood clot by activating other coagulation factors, ultimately leading to the cessation of bleeding. 

Inform the doctor about your medicines, including prescription, over-the-counter, nutritional or vitamin supplements, and herbal products. Certain medications may interact with Alphanine 500IU Injection , reducing effectiveness by causing undesirable side effects. 

• Stored at room temperature from 20°C to 25°C.
• Keep away from moisture, heat, and light.
• It should not be frozen.
• Keep away from children and pets.

Alphanine 500IU Injection replacement therapy can be administered through intravenous (IV) infusion or intravenous injection. The choice of administration route depends on the specific Alphanine 500IU Injection product, the patient's age, the severity of hemophilia B, and individual preferences.

Alphanine 500IU Injection  causes some side effects like all medications, although not everyone will experience them. 

Serious

• Allergic reactions
• Development of inhibitors
• Thrombosis (blood clots)
• Hepatitis transmission
• Liver complications

Common

• Localized reactions

Bleocel 15IU Injection consists of the active ingredient Bleomycin. It belongs to a group of drugs known as antineoplastic antibiotics. Commonly used in cancer treatment to slow or stop the growth of cancer cells. This medication used to treat lymph node cancers (Hodgkin’s and non-Hodgkin’s lymphoma), head and neck cancer, and cancer in external genitalia. It either be used alone or with radio therapy and chemotherapy treatment. This injection is also beneficial to prevent and treat the fluid accumulation in the lungs that occurs due to cancer. It works by interfering with the production of DNA and RNA in cancer cells. It can cause breaks in the DNA strands and prevent cancer cells from dividing and growing. 

Bleocel 15IU injection can have side effects, including lung problems, skin reactions, fever, and nausea. In some cases it can also affect kidneys, liver, and heart. Patients receiving it, need to be closely monitored for these side effects.  It is typically administered through injection or infusion, either alone or in combination with other chemotherapy drugs. The dosage and frequency of treatment depend on several factors, including the type and stage of cancer, the patient's age and overall health, and the specific treatment plan developed by the oncologist.

• Hodgkin's lymphoma
• Non-Hodgkin's lymphoma
• Testicular cancer
• Some types of lung cancer

Therapeutic Effects of Bleocel 15iu Injection

The therapeutic effect of Bleocel 15IU Injection is inhibiting cancer cell growth and proliferation. By interfering with DNA replication and transcription, it can slow or stop the growth of cancer cells, leading to their destruction. This effect is particularly important in the treatment of Hodgkin's lymphoma, non-Hodgkin's lymphoma, testicular cancer, and some types of lung cancer, where rapid cell growth and division are characteristic features of the disease. Overall, this medication can help to shrink tumours and improve symptoms in cancer patients.

• Bleocel 15IU Injection should be stored according to the manufacturer's instructions or as directed by a healthcare provider.
• Should be stored at room temperature, between 20°C and 25°C (68°F and 77°F), in a dry place, away from light and moisture.
• Keep in its original packaging until ready to use.
• Keep stored out of the reach of children and pets.
• Unused or expired medication should be properly disposed of in accordance with local regulations or guidelines.

Side effects are unwanted symptoms caused by medicines. Even though all drugs cause side effects, not everyone gets them. It  can cause a variety of side effects. following the most common side effects include

Serious

• Interstitial pneumonitis (inflammation of lung linings)
• Pulmonary fibrosis
• Liver toxicity
• Kidney toxicity
• Allergic reactions
• Increased risk of infections

Common

• Fever
• Chills
• Fatigue
• Loss of appetite
• Nausea and vomiting
• Mouth sores
• Skin rash or itching
• Hair loss
• Cough or shortness of breath
• Low blood cell counts

Epbriv 0.88mg Injection is a chemotherapy drug that contains the active substance eribulin, which belongs to the class of antineoplastic agents. Epbriv 0.88mg Injection is used in adults for advanced breast cancer or liposarcoma (a type of cancer originating from fat tissue) when other treatments have stopped working.

It is not recommended to take Epbriv 0.88mg Injection if you are allergic to Eribulin or any of its other ingredients. Consult your doctor if you believe this applies to you. It is not recommended for children and adolescents younger than 18 years since the effects of Epbriv 0.88mg Injection in this population are unknown. Before starting the treatment, you should inform your physician if you have fever, infections, liver, or heart problems. Before starting the treatment, give a detailed account of your medical history and medications.

• Advanced breast cancer
• Liposarcoma

Therapeutic Effects of Epbriv 0.88mg Injection

Epbriv 0.88mg Injection stops the growth and spread of cancer cells, specifically targeting the growth phase of microtubules, which are structures that help cells divide. It prevents them from growing without interfering with their shrinking phase. Additionally, it causes tubulin, a protein essential for cell division, to clump together in a way that disrupts cell division. This ultimately leads to the blockage of the cell cycle (G2/M phase), disrupting the formation of structures necessary for cell division (mitotic spindles) and triggering cell death through apoptosis.

Inform your doctor about all the medicines you take, including prescription, over-the-counter, nutritional or vitamin supplements, and herbal products. Certain medications may interact with Epbriv 0.88mg Injection and reduce effectiveness by causing undesirable side effects.

• Store Epbriv 0.88mg Injection in the refrigerator between 25°C.
• Keep it in its original packaging.
• Protect it from light and moisture.
• Keep it out of the reach of children and pets.

Side effects are unwanted symptoms that occur due to medicines. Even though all drugs cause side effects, not everyone gets them.

Serious

• Sepsis (severe infection)
• Severe allergic reaction
• Serious skin conditions (Stevens-Johnson syndrome)

Common

• Decrease in the number of white blood cells or red blood cells
• Tiredness or weakness
• Nausea, vomiting, constipation, diarrhea
• Numbness, tingling or prickling sensations
• Fever
• Loss of appetite, weight loss
• Difficulty breathing, cough
• Pain in the joints, muscles, and back
• Headache
• Hair loss

Intacept 25 Solution for Injection is a medicine used to treat a variety of conditions such as ankylosing spondylitis, rheumatoid arthritis, psoriasis, ulcerative colitis, and Crohn’s disease.

It provides relief from swelling, pain, and redness associated with various disorders and improves physical function.

Intacept 25 Solution for Injection is given by a healthcare professional and should not be self-administered. You should use it regularly and at the same time each day to get the maximum benefit from it. Continue using it as recommended by your doctor and complete the dose even if you feel better.

To make sure the medicine is safe for you, before taking it, let your doctor know of all the other medicines you are taking. Your doctor may also monitor your blood counts by taking regular blood tests to make sure the medicine is not affecting your blood counts. It is important for pregnant and breastfeeding women to ask the advice of their doctors before taking this medicine.

Uses Of Intacept Solution For Injection:

• Ankylosing spondylitis
• Rheumatoid arthritis
• Psoriasis
• Ulcerative colitis
• Crohn’s disease

Side Effects Of Intacept Solution For Injection:

Most side effects do not require any medical attention and disappear as your body adjusts to the medicine. Consult your doctor if they persist or if you’re worried about them

Common side effects of Intacept

• Allergic reaction
• Upper respiratory tract infection
• Itching
• Rash
• Injection site reaction

How To Use Intacept Solution For Injection

• Your doctor or nurse will guide you how to use this medicine.

Alcohol

• Consuming alcohol with Intacept 25 Solution for Injection does not cause any harmful side effects.

Pregnancy

• Intacept 25 Solution for Injection is generally considered safe to use during pregnancy.
• Animal studies have shown low or no adverse effects to the developing baby; however, there are limited human studies.

BreastFeeding

• Intacept 25 Solution for Injection is probably safe to use during breastfeeding. Limited human data suggests that the drug does not represent any significant risk to the baby.

Driving

• It is not known whether Intacept 25 Solution for Injection alters the ability to drive. Do not drive if you experience any symptoms that affect your ability to concentrate and react.

Kidney

• Intacept 25 Solution for Injection is probably safe to use in patients with kidney disease.
• Limited data available suggests that dose adjustment of Intacept 25 Solution for Injection may not be needed in these patients.

Liver

• Intacept 25 Solution for Injection is probably safe to use in patients with liver disease.
• Limited data available suggests that dose adjustment of Intacept 25
• Solution for Injection may not be needed in these patients.

Suviray 70 mg Injection contains an active component of Erenumab. It belongs to the class of medicines called monoclonal antibodies. This medication is used for the preventive treatment of migraines in abdults.  Migraine is a neurological disorder characterized by recurring and intense headaches, often accompanied by other symptoms such as nausea, sensitivity to light, and visual disturbances. For individuals who have not responded well to or have contraindications to other migraine preventive medications, Suviray 70 mg Injection provides an alternative treatment option. It is not recommended to use this medicine if you are allergic to the active compound Suviray 70 mg Injection and its compounds. If you have a history of hypersensitivity reactions to biologic agents or other injectable treatments, you should discuss this with your healthcare provider before starting Suviray 70 mg Injection. It is not recommended to use in children and adolescents under 18 years old. The use in elderly individuals needs close monitoring. 

Individuals with severe liver or kidney impairment may require dosage adjustments or careful monitoring when using this medication. It may have an effect on your blood pressure. Individuals with severe cardiovascular illnesses, such as uncontrolled hypertension or a history of heart attack, may need to monitor or change their treatment plan while using this medicine. If you develop serious constipation of new hypertension it is advised to see a healthcare professional. Pregnant women and nursing mothers are required to get their consultation prior to taking Suviray 70 mg Injection. It is advised to inform your healthcare provider about all the medicines you are taking including herbal, vitamin supplements and over the counter medicines before starting the treatment.

• Prevention of migraine in adults 

Therapeutic Effects of Suviray 70mg Injection:

• Suviray 70 mg Injection works by targeting and inhibiting the calcitonin gene-related peptide (CGRP) receptor. This affects the signaling pathway responsible for sending pain signals and dilation of blood vessels, both of which contribute to the development of migraines. This blockade seeks to minimize the frequency and intensity of migraine attacks, providing a preventive approach to migraine management in adults.

• Inform your healthcare provider about all the medicines you take, including prescription, over the counter, nutritional or vitamin supplements, and herbal products. Certain medications may interact with Suviray 70 mg Injection and reduce effectiveness by causing undesirable side effects. 

• Store Suviray 70 mg Injection Tablet in the original package at room temperature (20°C to 25°C).
• Keep it out of reach from children
• Keep away from moisture, heat, and light.
• It should not be frozen.

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

Common:

• Constipation
• Itching
• Vomiting
• Fatigue
• Nausea
• Muscle spasms
• Injection site reactions

Serious:

• Serious allergic reactions
• Chronic constipation

Bleocel 15IU Injection consists of the active ingredient Bleomycin. It belongs to a group of drugs known as antineoplastic antibiotics.  Commonly used in cancer treatment to slow or stop the growth of cancer cells. It treats lymph node cancers (Hodgkin’s and non-Hodgkin’s lymphoma), head and neck cancer, and cancer in external genitalia. Either be used alone or with radiotherapy and chemotherapy treatment. This injection is also beneficial to prevent and treat the fluid accumulation in the lungs due to cancer. It works by interfering with the production of DNA and RNA in cancer cells. This drug can cause breaks in the DNA strands and prevent cancer cells from dividing and growing. 

Bleocel 15IU injection can have side effects, including lung problems, skin reactions, fever, and nausea. In some cases, affect the kidneys, liver, and heart. Patients receiving it, need to be closely monitored for these side effects.  It is typically administered through injection or infusion, either alone or in combination with other chemotherapy drugs. The dosage and frequency of treatment depend on several factors, including the type and stage of cancer, the patient's age and overall health, and the specific treatment plan developed by the oncologist.

• Hodgkin's lymphoma
• Non-Hodgkin's lymphoma
• Testicular cancer
• Some types of lung cancer

Therapeutic Effects of Bleochem 15iu Injection

The therapeutic effect of Bleochem 15IU Injection is inhibiting cancer cell growth and proliferation. By interfering with DNA replication and transcription, it can slow or stop the growth of cancer cells, leading to their destruction. This effect is particularly important in the treatment of Hodgkin's lymphoma, non-Hodgkin's lymphoma, testicular cancer, and some types of lung cancer, where rapid cell growth and division are characteristic features of the disease. Overall, this medication can help to shrink tumours and improve symptoms in cancer patients.

Inform your healthcare provider about all your medicines, including prescription, over-the-counter, nutritional or vitamin supplements, and herbal products. Certain medications may interact with Bleochem 15IU Injection and reduce effectiveness by causing undesirable side effects.

• Bleochem 15IU Injection should be stored according to the manufacturer's instructions or as directed by a healthcare provider.
• In general, the medication should be stored at room temperature, between 20°C and 25°C (68°F and 77°F), in a dry place, away from light and moisture.
• It should be kept in its original packaging until ready to use.
• It should be stored out of the reach of children and pets.
• Unused or expired medication should be properly disposed of in accordance with local regulations or guidelines.

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

Serious

• Interstitial pneumonitis (inflammation of lung linings)
• Pulmonary fibrosis
• Liver toxicity
• Kidney toxicity
• Allergic reactions
• Increased risk of infections

Common

• Fever
• Chills
• Fatigue
• Loss of appetite
• Nausea and vomiting
• Mouth sores
• Skin rash or itching
• Hair loss
• Cough or shortness of breath
• Low blood cell counts

Novoseven 2mg injection contains active components such as Factor VII. It, also known as coagulation Factor VII or FVII, is a protein involved in the blood clotting (coagulation) cascade. This medication can treat bleeding episodes in hemophilia A or B individuals who have developed inhibitors (antibodies) against Factor VIII or Factor IX. In certain situations, healthcare providers may use it to manage bleeding in patients with coagulation disorders who are undergoing surgery or experiencing trauma. Acquired Novoseven 2mg injection deficiency can occur due to various medical conditions, such as liver disease, vitamin K deficiency, or certain medications. Treatment with this may be considered to address bleeding associated with these conditions. Novoseven 2mg injection has been used experimentally to manage intracranial hemorrhages, particularly in cases of traumatic brain injury or bleeding in the brain. 

Patients with a known allergy or hypersensitivity to Novoseven 2mg injection or any of their components should not receive this medication. It is generally not recommended for individuals with DIC, a condition characterized by widespread abnormal blood clotting and bleeding. Patients with a history of thromboembolic events or those at a high risk of developing them should use it cautiously and under close medical supervision.  In some cases of intracranial hemorrhage (bleeding within the brain), using It can be contraindicated when there is evidence of inappropriate clot formation, such as in cases of cerebral venous sinus thrombosis. Novoseven 2mg injection concentrates can be used in children with bleeding disorders, but a healthcare provider should closely monitor and prescribe their use. Novoseven 2mg injection concentrates can be used in older adults, but age-related factors, such as other medications, should be considered.

Novoseven 2mg injection  is used in the following:

• Hemophilia with inhibitors
• Congenital Novoseven 2mg injection deficiency
• Surgery and trauma
• Acquired Novoseven 2mg injection deficiency
• Intracranial hemorrhage

Therapeutic Effects of Novoseven 2mg Injection

Novoseven 2mg injection is a blood clotting protein that plays a pivotal role in coagulation. When tissue damage occurs, it interacts with tissue factor (TF) at the injury site, forming the FVIIa-TF complex. This complex acts as an enzyme, triggering a series of reactions that culminate in thrombin formation and the subsequent creation of a blood clot. This mechanism is essential for stopping bleeding after vascular injury.

Inform the doctor about your medicines, including prescription, over-the-counter, nutritional or vitamin supplements, and herbal products. Certain medications may interact with Novoseven 2mg injection, reducing effectiveness by causing undesirable side effects. 

• Stored at room temperature from 20°C to 25°C.
• Keep away from moisture, heat, and light.
• It should not be frozen.
• Keep away from children and pets

Novoseven 2mg injection causes some side effects like all medications, although not everyone will experience them. 

Serious:

• Thromboembolic events
• Hypersensitivity reactions
• Arterial thrombosis
• Disseminated intravascular coagulation (DIC)
• Hemorrhage
• Hepatic events
• Inhibitor development

Common:

• Fever
• Headache
• Nausea and vomiting
• Injection site reactions

Bevaro 100mg Injection is an anticancer medicine consisting of the active ingredient Bevacizumab. This medicine is developed to prevent the growth of tumors. It is indicated along with other chemotherapy drugs to treat metastatic breast cancer, brain cancer, cervical cancer, kidney cancer, lung cancer, and colorectal cancer. It is also used to treat cancers of the ovary, fallopian tube or primary peritoneal cancer. Use effective birth control during the treatment and for at least six months after the last dose. Bevaro 100mg Injection is not recommended for adolescents and children under the age of 18. Discuss with your doctor about the preservation of ovaries if you are planning for pregnancy in the near future as this medicine may cause fertility issues in women. It would be best to avoid breastfeeding your baby as this medicine may interfere with the growth and development.

Bevaro 100mg Injection is often administered as a combination with other chemotherapy agents. Constipation, appetite loss, runny nose, fever, skin problems, and weight loss are common side effects of Bevaro 100mg Injection. Before starting treatment with this medicine, let your doctor know if you have high blood pressure, high blood sugar, stomach disorders, or heart problems. This medicine should not be taken for 28 days before and after surgery as it is associated with poor wound healing and high bleeding complications. It is advised to report to your doctor if you have any dental issues that require surgery before taking this medicine. In case you develop any visual changes or confusion, report to your doctor to prevent complications.

• Glioblastoma multiforme (brain cancer)
• Persistent, recurrent, or metastatic breast cancer
• Metastatic cervical cancer
• Advanced kidney cancer
• Metastatic colorectal cancer
• Advanced non-small-cell lung cancer
• Liver Cancer- Hepatocellular carcinoma
• Cancers of the ovary, cervical, fallopian tube, or primary peritoneal cancer

• Store Bevaro 100mg Injection at 2˚C to 8˚C. Do not freeze or shake.

Inform your physician before starting your treatment with it in case, if you are pregnant or planning for pregnancy as this medicine may cause harm to the unborn baby and interrupt the formation of blood vessels.

It is recommended to avoid breastfeeding for a minimum of 6 months after your treatment with it as this medicine may interfere with the growth of your child.

Inform your doctor if you have any lung conditions before starting treatment with it.

Inform your physician before starting it if you have liver diseases to avoid any serious side effects.

Consult your doctor to know if it is safe to consume while you are on treatment with Bevaro 100mg Injection as only limited studies are available.

Avoid driving or using machinery while you are on your treatment with Bevaro 100mg Injection as it is related to cause dizziness or sleepiness. 

• Headache
• Vision changes
• Confusion
• Severe allergic reactions
• High Blood pressure
• Delayed wound healing following surgery
• Protein in urine
• Severe infections
• Blood clots in arteries and blood vessels of lungs
• Gut perforation
• Nosebleeds and bleeding risk
• Heart problems with an increase in heart rate
• Mouth sores, dryness
• Shortness of breath

• Numbness in hands or feet
• Weakness and lack of energy
• Diarrhoea, nausea, vomiting, abdominal pain
• Constipation
• Loss of appetite
• Weight loss
• Changes in taste and speech
• Decrease in counts of white blood cells
• Fever
• Dry skin
• Back pain

Bevazza 100mg Injection is an anticancer medicine consisting of the active ingredient Bevacizumab. This medicine is developed to prevent the growth of tumors. It is indicated along with other chemotherapy drugs to treat metastatic breast cancer, brain cancer, cervical cancer, kidney cancer, lung cancer, and colorectal cancer. It is also used to treat cancers of the ovary, fallopian tube or primary peritoneal cancer. Use effective birth control during the treatment and for at least six months after the last dose. Bevazza 100mg Injection is not recommended for adolescents and children under the age of 18. Discuss with your doctor about the preservation of ovaries if you are planning for pregnancy in the near future as this medicine may cause fertility issues in women. It would be best to avoid breastfeeding your baby as this medicine may interfere with the growth and development.

• Glioblastoma multiforme (brain cancer)
• Persistent, recurrent, or metastatic breast cancer
• Metastatic cervical cancer
• Advanced kidney cancer
• Metastatic colorectal cancer
• Advanced non-small-cell lung cancer
• Liver Cancer- Hepatocellular carcinoma
• Cancers of the ovary, cervical, fallopian tube, or primary peritoneal cancer

• Store Bevazza 100mg Injection at 2˚C to 8˚C. Do not freeze or shake.

Inform your physician before starting your treatment with Bevazza 100mg Injection in case, if you are pregnant or planning for pregnancy as this medicine may cause harm to the unborn baby and interrupt the formation of blood vessels.

It is recommended to avoid breastfeeding for a minimum of 6 months after your treatment with Bevazza 100mg Injection as this medicine may interfere with the growth of your child.

Inform your doctor if you have any lung conditions before starting treatment with Bevazza 100mg injection

Inform your physician before starting Bevazza 100mg Injection if you have liver diseases to avoid any serious side effects.

Consult your doctor to know if it is safe to consume while you are on treatment with Bevazza 100mg Injection as only limited studies are available.

Avoid driving or using machinery while you are on your treatment with Bevazza 100mg Injection as it is related to cause dizziness or sleepiness. 

• Headache
• Vision changes
• Confusion
• Severe allergic reactions
• High Blood pressure
• Delayed wound healing following surgery
• Protein in urine
• Severe infections
• Blood clots in arteries and blood vessels of lungs
• Gut perforation
• Nosebleeds and bleeding risk
• Heart problems with an increase in heart rate
• Mouth sores, dryness
• Shortness of breath

• Numbness in hands or feet
• Weakness and lack of energy
• Diarrhoea, nausea, vomiting, abdominal pain
• Constipation
• Loss of appetite
• Weight loss
• Changes in taste and speech
• Decrease in counts of white blood cells
• Fever
• Dry skin
• Back pain

Ceribulin 0.88mg Injection is a chemotherapy drug that contains the active substance eribulin, which belongs to the class of antineoplastic agents. Ceribulin 0.88mg Injection is used in adults for advanced breast cancer or liposarcoma (a type of cancer originating from fat tissue) when other treatments have stopped working.

It is not recommended to take Ceribulin 0.88mg Injection if you are allergic to Eribulin or any of its other ingredients. Consult your doctor if you believe this applies to you. It is not recommended for children and adolescents younger than 18 years since the effects of Ceribulin 0.88mg Injection in this population are unknown. Before starting the treatment, you should inform your physician if you have fever, infections, liver, or heart problems. Before starting the treatment, give a detailed account of your medical history and medications.

• Advanced breast cancer
• Liposarcoma

Therapeutic Effects of Ceribulin 0.88mg Injection

Ceribulin 0.88mg Injection stops the growth and spread of cancer cells, specifically targeting the growth phase of microtubules, which are structures that help cells divide. It prevents them from growing without interfering with their shrinking phase. Additionally, it causes tubulin, a protein essential for cell division, to clump together in a way that disrupts cell division. This ultimately leads to the blockage of the cell cycle (G2/M phase), disrupting the formation of structures necessary for cell division (mitotic spindles) and triggering cell death through apoptosis.

Inform your doctor about all the medicines you take, including prescription, over-the-counter, nutritional or vitamin supplements, and herbal products. Certain medications may interact with Ceribulin 0.88mg Injection and reduce effectiveness by causing undesirable side effects.

• Store Ceribulin 0.88mg Injection at 25°C.
• Keep it in its original packaging.
• Protect it from light and moisture.
• Keep it out of the reach of children and pets

• Side effects are unwanted symptoms that occur due to medicines. Even though all drugs cause side effects, not everyone gets them.

Serious:

• Sepsis (severe infection)
• Severe allergic reaction
• Serious skin conditions (Stevens-Johnson syndrome)

Common:

• Decrease in the number of white blood cells or red blood cells
• Tiredness or weakness
• Nausea, vomiting, constipation, diarrhea
• Numbness, tingling or prickling sensations
• Fever
• Loss of appetite, weight loss
• Difficulty breathing, cough
• Pain in the joints, muscles, and back
• Headache
• Hair loss

Somatorel 5mg Injection is a recombinant human growth hormone drug (hGH) containing an active ingredient called Somatropin. It is used to treats growth failure in kids or childrens with an deficiency of growth hormone, Turner's syndrome (chromosomal defect in girls that can affect growth), chronic renal (kidney) insufficiency, which affects growth, Prader-Willi syndrome (chromosomal disorder), and also gives children who are not able to grow until four years.

Inform your doctor if you are allergic to somatropin, sodium, or any of the ingredients present in them. Consult your doctor if you have a severe illness, prader-willi syndrome, a patient with severe obesity, upper airway obstruction, sleep apnea, cancer, diabetes, hypothyroidism, hypoadrenalism, scoliosis, and pancreatitis. During treatment with Somatorel 5mg Injection, your healthcare provider may monitor the blood count, blood sugar, thyroid, and other vital parameters to prevent serious complications. Consult your doctor if you are planning to get pregnant or think you may be pregnant or while you are breastfeeding.

• Growth failure due to growth hormone deficiency
• Children with retarded growth

Therapeutic Effects of Somatorel 5mg Injection

Somatorel 5mg Injection is equivalent to the human pituitary hormone that helps in growth. It regulates the amount of insulin-like growth factor I (IGF-I) and improves linear growth in patients with growth hormone deficiency.

Inform your healthcare provider about all the medicines you take, including prescription medications, over-the-counter medications, nutritional or vitamin supplements, and herbal products. Certain medications may interact with Somatorel 5mg Injection and reduce effectiveness by causing undesirable side effects.

• Store Somatorel 5mg Injection in a refrigerator (2°C-8°C).
• Do not freeze.
• Keep the injection away from children and pets' reach.
• Protect it from light.

It will be given to you by a doctor or nurse in a hospital or clinical setting. It is given as a subcutaneous (under the skin). Do not self-administer the injection. Your doctor will decide the dose and duration of the treatment based on your disease severity, body weight, and other factors.

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

Serious

• Critical illnesses
• Intracranial hypertension (strong headache, visual disturbances or vomiting)
• Severe abdominal pain
• High blood glucose level

Common

• Joint pain
• Injection site reaction (redness, itchiness, or pain)
• Numbness
• Swelling (puffy fingers or swollen ankles)
• Rash
• Itching
• Bumps on the skin (itchy)
• Pain or burning in the hand/ underarms
• Stiffness

Ivzumab 100mg Injection is an anticancer medicine consisting of the active ingredient Bevacizumab. This medicine is developed to prevent the growth of tumors. It is indicated along with other chemotherapy drugs to treat metastatic breast cancer, brain cancer, cervical cancer, kidney cancer, lung cancer, and colorectal cancer. It is also used to treat cancers of the ovary, fallopian tube or primary peritoneal cancer. Use effective birth control during the treatment and for at least six months after the last dose. Ivzumab 100mg Injection is not recommended for adolescents and children under the age of 18. Discuss with your doctor about the preservation of ovaries if you are planning for pregnancy in the near future as this medicine may cause fertility issues in women. It would be best to avoid breastfeeding your baby as this medicine may interfere with the growth and development.

• Glioblastoma multiforme (brain cancer)
• Persistent, recurrent, or metastatic breast cancer
• Metastatic cervical cancer
• Advanced kidney cancer
• Metastatic colorectal cancer
• Advanced non-small-cell lung cancer
• Liver Cancer- Hepatocellular carcinoma
• Cancers of the ovary, cervical, fallopian tube, or primary peritoneal cancer

• Store Ivzumab 100mg Injection at 2˚C to 8˚C. Do not freeze or shake.

Inform your physician before starting your treatment with Ivzumab 100mg Injection in case, if you are pregnant or planning for pregnancy as this medicine may cause harm to the unborn baby and interrupt the formation of blood vessels. 

It is recommended to avoid breastfeeding for a minimum of 6 months after your treatment with Ivzumab 100mg Injection as this medicine may interfere with the growth of your child.  

Inform your doctor if you have any lung conditions before starting treatment with Ivzumab 100mg injection 

Inform your physician before starting Ivzumab 100mg Injection if you have liver diseases to avoid any serious side effects. 

Consult your doctor to know if it is safe to consume while you are on treatment with Ivzumab 100mg Injection as only limited studies are available. 

Avoid driving or using machinery while you are on your treatment with Ivzumab 100mg Injection as it is related to cause dizziness or sleepiness. 

• Headache
• Vision changes
• Confusion
• Severe allergic reactions
• High Blood pressure
• Delayed wound healing following surgery
• Protein in urine
• Severe infections
• Blood clots in arteries and blood vessels of lungs
• Gut perforation
• Nosebleeds and bleeding risk
• Heart problems with an increase in heart rate
• Mouth sores, dryness
• Shortness of breath
• Numbness in hands or feet
• Weakness and lack of energy
• Diarrhoea, nausea, vomiting, abdominal pain
• Constipation
• Loss of appetite
• Weight loss
• Changes in taste and speech
• Decrease in counts of white blood cells
• Fever
• Dry skin
• Back pain

Zybev 100mg Injection is an anticancer medicine consisting of the active ingredient Bevacizumab. This medicine is developed to prevent the growth of tumors. It is indicated along with other chemotherapy drugs to treat metastatic breast cancer, brain cancer, cervical cancer, kidney cancer, lung cancer, and colorectal cancer. It is also used to treat cancers of the ovary, fallopian tube or primary peritoneal cancer. Use effective birth control during the treatment and for at least six months after the last dose. Zybev 100mg Injection is not recommended for adolescents and children under the age of 18. Discuss with your doctor about the preservation of ovaries if you are planning for pregnancy in the near future as this medicine may cause fertility issues in women. It would be best to avoid breastfeeding your baby as this medicine may interfere with the growth and development.

Zybev 100mg Injection is often administered as a combination with other chemotherapy agents. Constipation, appetite loss, runny nose, fever, skin problems, and weight loss are common side effects of Zybev 100mg Injection. Before starting treatment with this medicine, let your doctor know if you have high blood pressure, high blood sugar, stomach disorders, or heart problems. This medicine should not be taken for 28 days before and after surgery as it is associated with poor wound healing and high bleeding complications. It is advised to report to your doctor if you have any dental issues that require surgery before taking this medicine. In case you develop any visual changes or confusion, report to your doctor to prevent complications.

• Glioblastoma multiforme (brain cancer)
• Persistent, recurrent, or metastatic breast cancer
• Metastatic cervical cancer
• Advanced kidney cancer
• Metastatic colorectal cancer
• Advanced non-small-cell lung cancer
• Liver Cancer- Hepatocellular carcinoma
• Cancers of the ovary, cervical, fallopian tube, or primary peritoneal cancer

• Store Zybev 100mg Injection at 2˚C to 8˚C. Do not freeze or shake.
• Protect from light. Keep out of reach of children.

The infusion should be given immediately after the dilution. 

Inform your physician before starting your treatment with Zybev 100mg Injection in case, if you are pregnant or planning for pregnancy as this medicine may cause harm to the unborn baby and interrupt the formation of blood vessels.

It is recommended to avoid breastfeeding for a minimum of 6 months after your treatment with Zybev 100mg Injection as this medicine may interfere with the growth of your child. 

Inform your doctor if you have any lung conditions before starting treatment with Zybev 100mg injection 

Inform your physician before starting Zybev 100mg Injection if you have liver diseases to avoid any serious side effects. 

Consult your doctor to know if it is safe to consume alcohol while you are on treatment with Zybev 100mg Injection as only limited studies are available.  

Avoid driving or using machinery while you are on your treatment with Zybev 100mg Injection as it is related to cause dizziness or sleepiness. 

• Headache
• Vision changes
• Confusion
• Severe allergic reactions
• High Blood pressure
• Delayed wound healing following surgery
• Protein in urine
• Severe infections
• Blood clots in arteries and blood vessels of lungs
• Gut perforation
• Nosebleeds and bleeding risk
• Heart problems with an increase in heart rate
• Mouth sores, dryness
• Shortness of breath

Accentrix 2.3mg Injection contains the active ingredient Ranibizumab. It is an anti-neovascularisation agent in the class of medications called vascular endothelial growth factor A (VEGF-A) antagonists. It is used in adults to treat several eye diseases causing vision impairment. It is used to treat wet age-related macular degeneration (AMD, a persistent eye disease that causes loss of the ability to see straight ahead and may make it more difficult to read, drive, or perform other daily activities).

Accentrix 2.3mg Injection is also used to treat myopic choroidal neovascularization (mCNV; a complication in near-sighted people where new blood vessels can grow in the back of the eye), and to treat macular edema after retinal vein occlusion (an eye disease caused by blockage of blood flow from the eye that leads to blurry vision and vision loss). It is also used to treat diabetic macular edema (an eye disease caused by diabetes that can lead to vision loss) and diabetic retinopathy (damage to the eyes caused by diabetes).

Do not use Accentrix 2.3mg Injection if you are allergic to Ranibizumab or other ingredients of this medicine. Do not take this medicine if you have an infection in or around your eye and if you have pain or redness in your eye. Inform your doctor immediately if you develop symptoms such as eye pain or increased discomfort, worsening eye redness, blurred or decreased vision, an increased number of small particles in your vision, or increased sensitivity to light. Inform your doctor if you have a prior history of eye conditions or eye treatments or had a stroke before initiating the treatment.

Accentrix 2.3mg Injection is used to treat several eye diseases causing vision impairment, including,

• Age-related macular degeneration
• Macular edema
• Diabetic macular edema and retinopathy
• Myopic choroidal neovascularization
• Retinal vein occlusion

Therapeutic Effects of Accentrix 2.3mg Injection

Accentrix 2.3mg Injection specifically recognizes and binds to a protein called human vascular endothelial growth factor A (VEGF-A) present in the eye. In excess, VEGF-A causes abnormal blood vessel growth and swelling in the eye, leading to impairment of vision in certain eye diseases. This medicine can block its actions and prevent this abnormal growth and swelling. This injection can help to stabilize and improve your vision.

Inform your healthcare provider about all the medicines you take, including prescription, over-the-counter, nutritional or vitamin supplements, and herbal products. Certain medications interact with Accentrix 2.3mg Injection and reduce their effectiveness by causing undesirable side effects.

• Store in a refrigerator (2°C – 8°C)
• Do not freeze
• Protect the medicine from light and excessive moisture.
• Keep the medicine out of reach of children and pets.

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

Common:

• Pain and swelling in the eye
• Bleeding in the eye
• Blurred vision
• Urinary tract infection
• Skin rashes
• Discharge from the eye

Serious:

• Tear of the layer in the back of the eye
• Flashes of light in the eye
• Temporary loss of sight
• Clouding of lens
• Infection of the eyeball

• Side Effects of Berirab P 300iu InjectionBerirab P 300IU Injections cause some side effects like all medications, although noteveryone will experience them. Serious:
• Severe allergic reactions
• Respiratory distress
• Blood pressure changes
• Seizures or convulsions
• Chest pain
• Unusual warmth of limbCommon:
• Pain, swelling, or redness at the injection site Fever
• Headache
• Nausea
• Dizziness

Razumab 2.3mg Injection, contains the active ingredient Ranibizumab. It is an anti-neovascularisation agent in the class of medications called vascular endothelial growth factor A (VEGF-A) antagonists. It is used in adults to treat several eye diseases causing vision impairment. It is used to treat wet age-related macular degeneration (AMD, a persistent eye disease that causes loss of the ability to see straight ahead and may make it more difficult to read, drive, or perform other daily activities).

Razumab 2.3mg Injection is also used to treat myopic choroidal neovascularization (mCNV; a complication in near-sighted people where new blood vessels can grow in the back of the eye), and to treat macular edema after retinal vein occlusion (an eye disease caused by blockage of blood flow from the eye that leads to blurry vision and vision loss). It is also used to treat diabetic macular edema (an eye disease caused by diabetes that can lead to vision loss) and diabetic retinopathy (damage to the eyes caused by diabetes).

Do not use Razumab 2.3mg Injection if you are allergic to Ranibizumab or other ingredients of this medicine. Do not take this medicine if you have an infection in or around your eye and if you have pain or redness in your eye. Inform your doctor immediately if you develop symptoms such as eye pain or increased discomfort, worsening eye redness, blurred or decreased vision, an increased number of small particles in your vision, or increased sensitivity to light. Inform your doctor if you have a prior history of eye conditions or eye treatments or had a stroke before initiating the treatment.

Razumab 2.3mg Injection is used to treat several eye diseases causing vision impairment, including,

• Age-related macular degeneration
• Macular edema
• Diabetic macular edema and retinopathy
• Myopic choroidal neovascularization
• Retinal vein occlusion

Therapeutic Effects of Razumab 2.3mg Injection

Razumab 2.3mg Injection specifically recognizes and binds to a protein called human vascular endothelial growth factor A (VEGF-A) present in the eye. In excess, VEGF-A causes abnormal blood vessel growth and swelling in the eye, leading to impairment of vision in certain eye diseases. This medicine can block its actions and prevent this abnormal growth and swelling. This injection can help to stabilize and improve your vision.

Inform your healthcare provider about all the medicines you take, including prescription, over-the-counter, nutritional or vitamin supplements, and herbal products. Certain medications interact with Razumab 2.3mg Injection and reduce their effectiveness by causing undesirable side effects.

• Store in a refrigerator (2°C – 8°C)
• Do not freeze
• Protect the medicine from light and excessive moisture.
• Keep the medicine out of reach of children and pets.

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

Common

• Pain and swelling in the eye
• Bleeding in the eye
• Blurred vision
• Urinary tract infection
• Skin rashes
• Discharge from the eye

Serious

• Tear of the layer in the back of the eye
• Flashes of light in the eye
• Temporary loss of sight
• Clouding of lens
• Infection of the eyeball

Otide 50mcg injection contains the active substance octreotide. It is a synthetic compound derived from somatostatin, a substance naturally found in the human body that inhibits the effects of certain hormones, such as growth hormones. It is used to reduce the amount of growth hormone produced by people with acromegaly (a condition in which the body produces too much growth hormone, causing enlargement of the hands, feet, and facial features; joint pain; and other symptoms) who cannot be treated with surgery, radiation, or another medication. 

It is also used to control diarrhea and flushing caused by carcinoid tumors (slow-growing tumors that release natural substances that can cause symptoms) and vasoactive intestinal peptide-secreting adenomas (VIP-omas; tumors that form in the pancreas and release natural substances that can cause symptoms). It is used to prevent complications following surgery of the pancreas gland. . This medicine is used to treat people with pituitary tumors that produce too much thyroid-stimulating hormone (TSH) when other types of treatment (surgery or radiotherapy) are not suitable or have not worked and after radiotherapy, to cover the interim period until the radiotherapy becomes fully effective. 

Do not use this medicine if you are allergic to octreotide or any of the other ingredients of this medicine. Inform your physician if you have gallstones, high or low blood sugar levels, vitamin B12 deficiency, and liver diseases. Otide 50mcg injection may lower your heart rate, and very high doses can cause abnormal heart rhythm, so your doctor may monitor your heart function regularly during the treatment. Inform your physician if you are pregnant or breastfeeding before initiating the treatment.

• To treat acromegaly
• Relieve symptoms associated with some tumors of the GI tract
• To prevent complications following surgery of the pancreas gland
• To treat pituitary tumors that produce too much TSH

Therapeutic Effects of Otide 50mcg Injection

Otide 50mcg injection acetate, a cyclic octapeptide agent, inhibits growth hormone, glucagon, and insulin more effectively than the natural hormone somatostatin. The drug also reduces growth hormone and IGF-I (somatomedin C) in acromegaly, inhibits gallbladder contractions, reduces bile secretion, and suppresses thyroid stimulating hormone (TSH) secretion.

Inform your healthcare provider about all the medicines you take, including prescription, over-the-counter, nutritional or vitamin supplements, and herbal products. Certain medications interact with Otide 50mcg injection and reduce their effectiveness by causing undesirable side effects. 

• Store the Otide 50mcg injection in the refrigerator at 2°C to 8°C
• Do not freeze
• Protect the medicine from light and excessive moisture.
• Keep the medicine out of reach of children and pets
• If you forgot to take the injection, inform your healthcare professional immediately and reschedule the appointment.

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

Common

• Diarrhea, flatulence
• Abdominal pain
• Back pain
• Tiredness
• Headache, nausea

Serious 

• Increased heart rate
• Changes in heart rhythm
• Increased or decreased blood sugar levels
• Changes in thyroid levels
• Vitamin B12 deficiency
• Gall stones

Emzumab 150mg combikit injection contains an active component called Omalizumab 150mg combikit injection. This medicine belongs to monoclonal antibodies. This medication is used to treat allergic asthma, chronic rhinosinusitis (inflammation of the nose and sinuses) with nasal polyps, and chronic spontaneous urticaria (CSU). Inform your doctor if you are allergic to Emzumab 150mg combikit injection or any of the ingredients that are allergic to latex because the needle cap of the syringe may contain latex. Before using Emzumab 150mg combikit injection, it's crucial to consult your doctor if you have kidney or liver problems or suffer from an autoimmune disease.

Discussing these factors with your doctor ensures safe and informed use of Emzumab 150mg combikit injection for your specific medical condition. The safety and efficacy of the drug in children has not been established. So, it is recommended that you ask your doctor. Consult your doctor if you are planning to get pregnant or think you may be pregnant while breastfeeding.

• Allergic asthma
• Chronic rhinosinusitis (inflammation of the nose and sinuses) with nasal polyps
• Chronic spontaneous urticaria (CSU)

Therapeutic Effects of Emzumab 150mg Combikit Injection

Emzumab 150mg combikit injection works by blocking and targeting a substance called immunoglobulin E (IgE) in the body; in this way, it reduces allergic reactions like Chronic rhinosinusitis (inflammation of the nose and sinuses) with nasal polyps and chronic spontaneous urticaria (CSU).

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional or vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with Emzumab 150mg combikit injection and can cause undesirable side effects.

• Keep Emzumab 150mg combikit injection out of the sight and reach of children.
• Store in a refrigerator between 2°C to 8°C.
• Do not freeze

This medicine is given only in a hospital setup by a healthcare provider. Cernos Depot 1gm injection will be given to you by your doctor. It is given subcutaneous injection, either as a single injection or as a continuous infusion (a drip). Your physician will decide the dosage and frequency of this injection based on the severity of your disease and other factors.

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

Common:

• Fever (in children)
• Reactions at the injection site (pain, swelling, itching, and redness)
• Pain in stomach
• Headache (very common in children)
• Upper respiratory tract infection (inflammation of the pharynx and common cold)
• Feeling of pressure or pain in the cheeks and forehead (sinusitis, sinus headache)
• Joint pain (arthralgia)
• Feeling dizzy

Biocure 2mg Injection is a chemotherapy medication that belongs to the class of medicines called proteasome inhibitors. It consists of the active ingredient Bortezomib. It is indicated for the treatment of multiple myeloma and mantle cell lymphoma. Multiple myeloma refers to the cancerous progression of plasma cells that are predominant in the bone marrow. Mantle cell lymphoma is a less common cancer affecting the lymph nodes. This medication is concomitantly used with other chemotherapy medicines like pegylated liposomal doxorubicin, rituximab, cyclophosphamide, doxorubicin, dexamethasone, prednisolone or thalidomide for patients who have not started treatment and are ineligible for blood stem cell transplant. 

The common side effects likely associated with Biocure 2mg Injection are Pneumonia, loss of appetite, sensitivity, tingling and burning sensation of the skin, nausea, vomiting, diarrhea, mouth ulcers, constipation, muscle and bone pain, hair loss, fever, infections, itching, redness, dehydration, stomach problems, etc., Inform your physician if these side effects disturb or persist in you.  

Inform your doctor if you are allergic to Biocure 2mg Injection and its ingredients. Do not use this medication if you have severe lung or heart problems. Before starting treatment with this medication, let your physician know if you are suffering from neuropathy (nerves malfunction), cardiac disorders, severe lung problems, pulmonary disorders, posterior reversible encephalopathy syndrome disorders, gastrointestinal disorders, thrombocytopenia (a low platelet count), neutropenia (low white blood cell count), tumor lysis syndrome (metabolic abnormalities that can occur as a complication during the treatment of cancer), hepatic disorders. Inform your doctor of diabetes because this Injection can affect your blood glucose levels.

• Treatment of multiple myeloma and mantle cell lymphoma.

Therapeutic Effects of Biocure 2mg Injection

Biocure 2mg Injection Injection works by exerting a toxic effect on cancer cells. It inhibits the 26S proteasome and blocks a major cell signaling pathway. This inhibition of the signaling pathway makes the cancer cells sensitive to chemotherapy. This medicine also enhances the build-up of a protein and minimizes cancer cell growth and multiplication.

• Store unopened vials in the refrigerator (2 °C – 8 °C) and protect them from light.
• Keep this medicine out of sight and reach of children. 

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

Serious

• Muscle cramps
• Confusion, visual disturbances, seizures, and headache
• Breathlessness
• Swelling of feet
• Changes in heartbeat
• High blood pressure
• Fainting and tiredness
• Cough and chest tightness

Common

• Pneumonia
• Loss of appetite
• Sensitivity, tingling and burning sensation of the skin
• Nausea, vomiting, and diarrhea
• Mouth ulcers
• Constipation
• Muscle and bone pain
• Hair loss
• Fever
• Reduction in blood cell count
• Reduced kidney function
• Shivering
• Infections
• Itching and redness
• Dehydration
• Stomach problems
• Difficulty sleeping, anxiety, mood swings, depressed mood

Hemazide 100mg Injection for injection is used for treating adults with Myelodysplastic syndrome (MDS) 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.

• Treatment of Acute Myeloid Leukemia with 20-30% blasts in patients who are not eligible for Haemopoietic stem cell transplant
• Intermediate-2 and High-risk Myelodysplastic syndrome (MDS)

Therapeutic Effects of Hemazide 100mg Injection

In MDS and AML, the development of tumor cells is caused by the process of transcriptional repression of various genes, which is due to the hypermethylation of DNA. Transcriptional repression is a process where proteins bind directly or indirectly to DNA and control the activity of copying a specific gene or a set of genes. The active form of Hemazide 100mg Injection binds to RNA and DNA, interrupts their activity in actively multiplying cells, and exhibits a toxic effect on cancer cells.

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 100 mg injection and cause undesirable side effects. 

Store at room temperature (15-30°C). If the product is reconstituted, it must be used immediately; if not, store at 2-8°C for not more than 8 hours. Keep the injection out of sight and reach of children.

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

Serious:

• Unexpected bleeding, with blood in stool and urine
• Fever
• Pneumonia is characterized by chest pain or breathlessness.
• Allergic reaction with symptoms of swelling of lips, itching, or rashes.
• Seizures, loss of consciousness, severe headache, or bleeding in the brain
• Frequent urination with pain or burning sensation

Common:

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

Kyfil 60mg Injection is an anticancer medication containing the active constituent Carfilzomib. It is used to treat a type of cancer called multiple myeloma. Multiple myeloma is a cancer of a white blood cell called the plasma cell. These cells grow uncontrolled and accumulate in the bone marrow, damaging the bones and kidneys. The treatment with this medication reduces symptoms of multiple myelomas, such as bone pain, fatigue, and anemia, improving a patient's quality of life.

Combined with other medications, this medication can significantly increase survival rates in patients with multiple myeloma. It is often used in combination with other medications. Like all medications, it can have side effects. Common side effects include fatigue, nausea, vomiting, diarrhea, fever, and low blood cell counts. Patients need to stay hydrated while taking, as this medication causes dehydration, and dehydration can exacerbate some of the side effects of the medication. It effectively treats multiple myeloma, and the benefits may outweigh the risks for many patients.

Kyfil 60mg Injection is used to treat

• Multiple myeloma

Therapeutic Effects of Kyfil 60mg Injection

Kyfil 60mg Injection is a proteasome inhibitor, which means it works by blocking the action of proteasomes, the enzymes responsible for breaking down proteins in cells. By blocking proteasomes, this medication can prevent the growth and survival of cancer cells, ultimately leading to the death of cancer cells. This can help to slow or stop the progression of multiple myeloma and may improve survival rates for some patients.

Inform your healthcare provider about all your medicines, including prescription, over-the-counter, nutritional or vitamin supplements, and herbal products. Certain medications may interact with Kyfil 60mg Injection and reduce effectiveness by causing undesirable side effects.

• Kyfil 60mg Injection should be stored under refrigeration between 2°C to 8°C (36°F to 46°F).
• Keep it in the original package until it is ready to use.
• Should not be frozen.
• Discard any unused portion after 4 hours.
• Keep reaching out to children and pets.

Kyfil 60mg Injection is typically administered as an intravenous (IV) injection in a hospital or clinical setting by a healthcare provider. The exact dosing and frequency of administration will depend on the specific condition being treated and other individual factors, such as the patient's age, weight, and overall health

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

Serious:

• Cardiac events such as heart failure, heart attack, or arrhythmias
• Blood clotting disorders or bleeding
• Acute kidney injury
• Lung damage or inflammation
• Infections
• Tumor lysis syndrome (a condition that can occur when cancer cells break down rapidly)

Common Side:

• Fatigue
• Nausea and vomiting
• Diarrhea
• Low blood cell counts (anemia, low white blood cell count, low platelet count)
• Fever
• Headache
• Difficulty breathing or shortness of breath
• Cough
• Muscle weakness or pain
• Rash
• Back pain

This medication is used with a doctor-approved exercise, behavior change, and reduced-calorie diet program to help you lose weight. It is used by certain overweight people, such as those who are obese or have weight-related medical problems.

Losing weight and keeping it off can lessen the many health risks that come with obesity, including heart disease,diabetes,high blood pressure, and a shorter life.Liraglutide is similar to a natural hormone in your body (incretin). It works by controlling your appetite

.Saxenda® (liraglutide) injection 3 mg is an injectable prescription medicine used for adults with excess weight (BMI ≥27) who also have weight-related medical problems or obesity (BMI ≥30), and children aged 12-17 years with a body weight above 132 pounds (60 kg) and obesity to help them lose weight and keep the weight off.

Saxenda® should be used with a reduced calorie diet and increased physical activity.

Saxenda 6 Mg Ml Injection, injectable Victoza / Saxenda Solution for Injection is a medicine used to lower blood sugar levels in adults with type 2 diabetes mellitus

This helps to prevent serious complications of diabetes like kidney damage and blindness

Is Saxenda a good weight loss?

In a clinical study of people taking Saxenda® for 3 years

56% achieved significant weight loss at year 1, and. Approximately half of these patients maintained weight loss at 3 years when taking Saxenda® added to a reduced-calorie meal plan and increased physical activity, compared with people not on the drug.

Does Saxenda work immediately?

Yes, the medication does start working immediately

. However, most people won't see any kind of changes, until they get to the higher doses of their treatment.

What is the major side effect of Saxenda?

Nausea is the most common side effect when first starting Saxenda®

. If you (or your teen) experience nausea, speak with your respective health care providers about ways to manage it. They may suggest some of the following: Eat bland, low-fat foods, like crackers,toast, and rice.

What foods to avoid while on Saxenda?

·Alcohol

Alcohol isn't off-limits while taking Saxenda, but being mindful about your intake is super important because it's working to help lower your blood glucose levels in your body.

·Ultra-processed foods.

·Sugary foods and drinks.

·Fried foods.

Saxenda injection side effects

·Abdominal pain

·Dizziness

·Fatigue

·Nausea

·Hypoglycemia

·Belching

·Constipation

·Headache

·Heartburn

Ranizurel 0.5mg Injection, contains the active ingredient Ranibizumab. It is an anti-neovascularisation agent in the class of medications called vascular endothelial growth factor A (VEGF-A) antagonists. It is used in adults to treat several eye diseases causing vision impairment. It is used to treat wet age-related macular degeneration (AMD, a persistent eye disease that causes loss of the ability to see straight ahead and may make it more difficult to read, drive, or perform other daily activities).

Ranizurel 0.5mg Injection is also used to treat myopic choroidal neovascularization (mCNV; a complication in near-sighted people where new blood vessels can grow in the back of the eye), and to treat macular edema after retinal vein occlusion (an eye disease caused by blockage of blood flow from the eye that leads to blurry vision and vision loss). It is also used to treat diabetic macular edema (an eye disease caused by diabetes that can lead to vision loss) and diabetic retinopathy (damage to the eyes caused by diabetes).

Do not use Ranizurel 0.5mg Injection if you are allergic to Ranibizumab or other ingredients of this medicine. Do not take this medicine if you have an infection in or around your eye and if you have pain or redness in your eye. Inform your doctor immediately if you develop symptoms such as eye pain or increased discomfort, worsening eye redness, blurred or decreased vision, an increased number of small particles in your vision, or increased sensitivity to light. Inform your doctor if you have a prior history of eye conditions or eye treatments or had a stroke before initiating the treatment.

Ranizurel 0.5mg Injection is used to treat several eye diseases causing vision impairment, including,

• Age-related macular degeneration
• Macular edema
• Diabetic macular edema and retinopathy
• Myopic choroidal neovascularization
• Retinal vein occlusion

Therapeutic Effects of Ranizurel 0.5mg Injection

Ranizurel 0.5mg Injection specifically recognizes and binds to a protein called human vascular endothelial growth factor A (VEGF-A) present in the eye. In excess, VEGF-A causes abnormal blood vessel growth and swelling in the eye, leading to impairment of vision in certain eye diseases. This medicine can block its actions and prevent this abnormal growth and swelling. This injection can help to stabilize and improve your vision.

• Store in a refrigerator (2°C – 8°C)
• Do not freeze
• Protect the medicine from light and excessive moisture.
• Keep the medicine out of reach of children and pets.

Ranizurel 0.5mg Injection is administered as an injection into your eye by an eye doctor under a local anesthetic. Your doctor will decide the dose and frequency of the injection based on your disease condition. Do not self-administer the medicine. 

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

Common

• Pain and swelling in the eye
• Bleeding in the eye
• Blurred vision
• Urinary tract infection
• Skin rashes
• Discharge from the eye

Serious

• Tear of the layer in the back of the eye
• Flashes of light in the eye
• Temporary loss of sight
• Clouding of lens
• Infection of the eyeball

Preventeron sachet 5gm contains the active constituent Immunoglobulin G and Zinc citrate. It belongs to the medication class known as Immunizing agents. It is used to treat gastric problems induced by Escherichia coli infection, such as diarrhea. Infections with E.coli are common in children and travelers who visit high-risk areas. Exposure to E.coli strains also reduces the incidence of diarrhea and urinary tract infections.  

Before starting treatment with this medication, let your physician know if you have allergies to Immunoglobulin G +Zinc citrate and its ingredients. Inform your doctor if you have lactose intolerance. Before consuming Preventeron sachet 5gm, inform your doctor if you are a pregnant or breastfeeding woman.

• Prevents diarrhea and gastric infections
• Prevents urinary tract infection
• Improvement of metabolic conditions
• Treatment of inflammations

Therapeutic Effects of Preventeron Sachet 5gm

Preventeron sachet 5gm contains immune response components that help the body against infectious pathogens. The immunoglobulin in this sachet serves as a barrier to the microbe by neutralizing allergic and infectious substances that help in lowering gastrointestinal inflammation. It reduces E.coli activity in the intestine without affecting the normal composition of gut bacteria.

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional or vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with Preventeron sachet 5gm and can cause undesirable side effects. 

• Store below 25°C in a cool and dry place.
• Keep away from sunlight and out of reach of children.
• Keep the container tightly closed.

Use Preventeron sachet 5gm as recommended by your physician. Your doctor will decide the dose and frequency based on your disease condition and other factors. Do not take more than recommended.

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

Preventeron sachet 5gm is typically safe to take and has no known adverse effects. However, if you have any uncommon symptoms, seek medical advice from your doctor. 

Sandostatin Lar 10mg injection contains the active substance octreotide. It is a synthetic compound derived from somatostatin, a substance naturally found in the human body that inhibits the effects of certain hormones, such as growth hormones. It is used to reduce the amount of growth hormone produced by people with acromegaly (a condition in which the body produces too much growth hormone, causing enlargement of the hands, feet, and facial features; joint pain; and other symptoms) who cannot be treated with surgery, radiation, or another medication. It is also used to control diarrhea and flushing caused by carcinoid tumors (slow-growing tumors that release natural substances that can cause symptoms) and vasoactive intestinal peptide-secreting adenomas (VIP-omas; tumors that form in the pancreas and release natural substances that can cause symptoms). It is used to prevent complications following surgery of the pancreas gland.  It is also indicated to stop bleeding and to protect from re-bleeding from ruptured gastro-esophageal varices in patients suffering from chronic liver disease. This medicine is used to treat people with pituitary tumors that produce too much thyroid-stimulating hormone (TSH) when other types of treatment (surgery or radiotherapy) are not suitable or have not worked and after radiotherapy, to cover the interim period until the radiotherapy becomes fully effective. Do not use this medicine if you are allergic to octreotide or any of the other ingredients of this medicine. Inform your physician if you have gallstones, high or low blood sugar levels, vitamin B12 deficiency, and liver diseases. Sandostatin Lar 10mg injection may lower your heart rate, and very high doses can cause abnormal heart rhythm, so your doctor may monitor your heart function regularly during the treatment. Inform your physician if you are pregnant or breastfeeding before initiating the treatment.

Therapeutic Effects of Sandostatin Lar 10mg Injection

Sandostatin Lar 10mg injection acetate, a cyclic octapeptide agent, inhibits growth hormone, glucagon, and insulin more effectively than the natural hormone somatostatin. The drug also reduces growth hormone and IGF-I (somatomedin C) in acromegaly, inhibits gallbladder contractions, reduces bile secretion, and suppresses thyroid stimulating hormone (TSH) secretion.

• Store the Sandostatin Lar 10mg injection in the refrigerator at 2°C to 8°C
• Do not freeze
• Protect the medicine from light and excessive moisture.
• Keep the medicine out of reach of children and pets
• If you forgot to take the injection, inform your healthcare professional immediately and reschedule the appointment.

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

Common
Diarrhea, flatulence
Abdominal pain
Back pain
Tiredness
Headache, nausea

Serious 
Increased heart rate
Changes in heart rhythm
Increased or decreased blood sugar levels
Changes in thyroid levels
Vitamin B12 deficienc
Gall stones

Lirafit Solution for Injection is a medicine used to lower blood sugar levels in adults with type 2 diabetes mellitus. This helps to prevent serious complications of diabetes like kidney damage and blindness. Proper control of diabetes also helps to lower your chances of a heart attack or a stroke.

Lirafit Solution for Injection belongs to the GLP-1 (glucagon-like peptide) group of diabetes medicines. It works by helping your body produce insulin and by reducing appetite. It also helps to reduce weight in some people. This medicine should be stored in a refrigerator until you need it but do not freeze it.

It is normally injected under the skin once daily. The dose will depend on your condition and what other diabetes medicines you are taking. You can use it at any time of the day with or without food but try to use it at the same time each day to get the most benefit. Your doctor or nurse will show you how and where to inject the medicine. Follow the instructions carefully.

Do not stop taking this medicine without talking to your doctor. If you do, your blood sugar levels may increase and put you at risk of serious complications. Remember that it is only part of a treatment program that should also include a healthy diet and regular exercise as advised by your doctor. Your lifestyle plays a big part in controlling diabetes.

The most common side effects of this medicine include nausea, diarrhea, vomiting, decreased appetite, indigestion, and constipation. It can also lead to low blood sugar levels (hypoglycemia) especially if you are also taking other medicines like insulin or sulphonylureas for treatment of diabetes. To prevent this, it is important to have regular meals and always carry a fast-acting source of glucose such as sugary candy or glucose candy with you.

Before using it, let your doctor know if you have any pancreas or stomach problems or severe dehydration (loss of body water), or diabetic ketoacidosis (a complication of diabetes characterized by too much acid and ketones in your blood). This medicine may not be suitable. Pregnant or breastfeeding women should also consult their doctor before using this medicine. If you experience blurred vision, dizziness, or drowsiness due to extremely low or high blood sugar, do not drive, use machinery or do any activity that requires alertness or clear vision until you are sure you can do them safely.

• Treatment of Type 2 diabetes mellitus

Lirafit Solution for Injection helps lower blood sugar levels in the body, promotes weight loss, and reduces the risk of cardiovascular events. It also preserves beta-cell function in the pancreas, which is important for insulin production. It can improve blood sugar control throughout the day and helps people with type 2 diabetes to manage their condition effectively. Taking this medicine regularly along with a proper diet, exercises, and other lifestyle changes are important for overall diabetes management.

Most side effects do not require any medical attention and disappear as your body adjusts to the medicine. Consult your doctor if they persist or if you’re worried about them

• Constipation
• Decreased appetite
• Diarrhea
• Nausea
• Vomiting
• Abdominal pain
• Dyspepsia
• Flatulence
• Nasopharyngitis (inflammation of the throat and nasal passages)

Your doctor or nurse will guide you how to use this medicine.

Lirafit Solution for Injection is an anti-diabetic medication. It works by increasing the release of insulin from pancreas, decreases hormones that raise blood sugar levels, slows down digestion, and reduces appetite.

Victoza Solution for Injection is a medicine used to lower blood sugar levels in adults with type 2 diabetes mellitus. This helps to prevent serious complications of diabetes like kidney damage and blindness. Proper control of diabetes also helps to lower your chances of a heart attack or a stroke.

Victoza Solution for Injection belongs to the GLP-1 (glucagon-like peptide) group of diabetes medicines. It works by helping your body produce insulin and by reducing appetite. It also helps to reduce weight in some people. This medicine should be stored in a refrigerator until you need it but do not freeze it.

It is normally injected under the skin once daily. The dose will depend on your condition and what other diabetes medicines you are taking. You can use it at any time of the day with or without food but try to use it at the same time each day to get the most benefit. Your doctor or nurse will show you how and where to inject the medicine. Follow the instructions carefully.

Do not stop taking this medicine without talking to your doctor. If you do, your blood sugar levels may increase and put you at risk of serious complications. Remember that it is only part of a treatment program that should also include a healthy diet and regular exercise as advised by your doctor. Your lifestyle plays a big part in controlling diabetes.

The most common side effects of this medicine include nausea, diarrhea, vomiting, decreased appetite, indigestion, and constipation. It can also lead to low blood sugar levels (hypoglycemia) especially if you are also taking other medicines like insulin or sulphonylureas for treatment of diabetes. To prevent this, it is important to have regular meals and always carry a fast-acting source of glucose such as sugary candy or glucose candy with you.

Before using it, let your doctor know if you have any pancreas or stomach problems or severe dehydration (loss of body water), or diabetic ketoacidosis (a complication of diabetes characterized by too much acid and ketones in your blood). This medicine may not be suitable. Pregnant or breastfeeding women should also consult their doctor before using this medicine. If you experience blurred vision, dizziness, or drowsiness due to extremely low or high blood sugar, do not drive, use machinery or do any activity that requires alertness or clear vision until you are sure you can do them safely.

• Treatment of Type 2 diabetes mellitus

Victoza Solution for Injection helps lower blood sugar levels in the body, promotes weight loss, and reduces the risk of cardiovascular events. It also preserves beta-cell function in the pancreas, which is important for insulin production. It can improve blood sugar control throughout the day and helps people with type 2 diabetes to manage their condition effectively. Taking this medicine regularly along with a proper diet, exercises, and other lifestyle changes are important for overall diabetes management.

Most side effects do not require any medical attention and disappear as your body adjusts to the medicine. Consult your doctor if they persist or if you’re worried about them

• Constipation
• Decreased appetite
• Diarrhea
• Nausea
• Vomiting
• Abdominal pain
• Dyspepsia
• Flatulence
• Nasopharyngitis (inflammation of the throat and nasal passages)

Victoza Solution for Injection is an anti-diabetic medication. It works by increasing the release of insulin from pancreas, decreases hormones that raise blood sugar levels, slows down digestion, and reduces appetite.

Myzomib 2mg Injection is a chemotherapy medication that belongs to the class of medicines called proteasome inhibitors. It consists of the active ingredient Bortezomib. It is indicated for the treatment of multiple myeloma and mantle cell lymphoma. Multiple myeloma refers to the cancerous progression of plasma cells that are predominant in the bone marrow. Mantle cell lymphoma is a less common cancer affecting the lymph nodes. This medication is concomitantly used with other chemotherapy medicines like pegylated liposomal doxorubicin, rituximab, cyclophosphamide, doxorubicin, dexamethasone, prednisolone or thalidomide for patients who have not started treatment and are ineligible for blood stem cell transplant. 

The common side effects likely associated with Myzomib 2mg Injection are Pneumonia, loss of appetite, sensitivity, tingling and burning sensation of the skin, nausea, vomiting, diarrhea, mouth ulcers, constipation, muscle and bone pain, hair loss, fever, infections, itching, redness, dehydration, stomach problems, etc., Inform your physician if these side effects disturb or persist in you.  

Inform your doctor if you are allergic to Myzomib 2mg Injection and its ingredients. Do not use this medication if you have severe lung or heart problems. Before starting treatment with this medication, let your physician know if you are suffering from neuropathy (nerves malfunction), cardiac disorders, severe lung problems, pulmonary disorders, posterior reversible encephalopathy syndrome disorders, gastrointestinal disorders, thrombocytopenia (a low platelet count), neutropenia (low white blood cell count), tumor lysis syndrome (metabolic abnormalities that can occur as a complication during the treatment of cancer), hepatic disorders. Inform your doctor of diabetes because this Injection can affect your blood glucose levels.

• Treatment of multiple myeloma and mantle cell lymphoma.

Therapeutic Effects of Myzomib 2mg Injection

Myzomib 2mg Injection Injection works by exerting a toxic effect on cancer cells. It inhibits the 26S proteasome and blocks a major cell signaling pathway. This inhibition of the signaling pathway makes the cancer cells sensitive to chemotherapy. This medicine also enhances the build-up of a protein and minimizes cancer cell growth and multiplication.

• Store unopened vials in the refrigerator (2 °C – 8 °C) and protect them from light.
• Keep this medicine out of sight and reach of children. 

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

Serious

• Muscle cramps
• Confusion, visual disturbances, seizures, and headache
• Breathlessness
• Swelling of feet
• Changes in heartbeat
• High blood pressure
• Fainting and tiredness
• Cough and chest tightness

Common

• Pneumonia
• Loss of appetite
• Sensitivity, tingling and burning sensation of the skin
• Nausea, vomiting, and diarrhea
• Mouth ulcers
• Constipation
• Muscle and bone pain
• Hair loss
• Fever
• Reduction in blood cell count
• Reduced kidney function
• Shivering
• Infections
• Itching and redness
• Dehydration
• Stomach problems
• Difficulty sleeping, anxiety, mood swings, depressed mood

Myezom 2mg Injection is a chemotherapy medication that belongs to the class of medicines called proteasome inhibitors. It consists of the active ingredient Bortezomib. It is indicated for the treatment of multiple myeloma and mantle cell lymphoma. Multiple myeloma refers to the cancerous progression of plasma cells that are predominant in the bone marrow. Mantle cell lymphoma is a less common cancer affecting the lymph nodes. This medication is concomitantly used with other chemotherapy medicines like pegylated liposomal doxorubicin, rituximab, cyclophosphamide, doxorubicin, dexamethasone, prednisolone or thalidomide for patients who have not started treatment and are ineligible for blood stem cell transplant. 

The common side effects likely associated with Myezom 2mg Injection are Pneumonia, loss of appetite, sensitivity, tingling and burning sensation of the skin, nausea, vomiting, diarrhea, mouth ulcers, constipation, muscle and bone pain, hair loss, fever, infections, itching, redness, dehydration, stomach problems, etc., Inform your physician if these side effects disturb or persist in you.  

Inform your doctor if you are allergic to Myezom 2mg Injection and its ingredients. Do not use this medication if you have severe lung or heart problems. Before starting treatment with this medication, let your physician know if you are suffering from neuropathy (nerves malfunction), cardiac disorders, severe lung problems, pulmonary disorders, posterior reversible encephalopathy syndrome disorders, gastrointestinal disorders, thrombocytopenia (a low platelet count), neutropenia (low white blood cell count), tumor lysis syndrome (metabolic abnormalities that can occur as a complication during the treatment of cancer), hepatic disorders. Inform your doctor of diabetes because this Injection can affect your blood glucose levels.

• Treatment of multiple myeloma and mantle cell lymphoma.

Therapeutic Effects of Myezom 2mg Injection

Myezom 2mg Injection Injection works by exerting a toxic effect on cancer cells. It inhibits the 26S proteasome and blocks a major cell signaling pathway. This inhibition of the signaling pathway makes the cancer cells sensitive to chemotherapy. This medicine also enhances the build-up of a protein and minimizes cancer cell growth and multiplication.

• Store unopened vials in the refrigerator (2 °C – 8 °C) and protect them from light.
• Keep this medicine out of sight and reach of children.

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

Serious

• Muscle cramps
• Confusion, visual disturbances, seizures, and headache
• Breathlessness
• Swelling of feet
• Changes in heartbeat
• High blood pressure
• Fainting and tiredness
• Cough and chest tightness

Common

• Pneumonia
• Loss of appetite
• Sensitivity, tingling and burning sensation of the skin
• Nausea, vomiting, and diarrhea
• Mouth ulcers
• Constipation
• Muscle and bone pain
• Hair loss
• Fever
• Reduction in blood cell count
• Reduced kidney function
• Shivering
• Infections
• Itching and redness
• Dehydration
• Stomach problems
• Difficulty sleeping, anxiety, mood swings, depressed mood

Buselin 0.5mg Injection is an anticancer drug belonging to the category of gonadotropin releasing hormone analogues, containing the active ingredient Buserelin. It is used in the treatment of advanced prostatic carcinoma(a type of prostate cancer that has spread outside of the prostate gland). It is also used in the treatment of endometriosis (is a condition in which the tissue that normally lines the inside of the uterus (endometrium) grows outside of it). This drug is also treated for the adjunctive use in ovulation induction.

If you experience any pain, swelling, feeling of tension in your stomach, feel sick, gain weight, diarrhoea, difficulty breathing, or passing less urine. These could be signs of a serious side effect called “Ovarian Hyperstimulation Syndrome (OHSS)”, so it is advised to inform your doctor immediately if all these symptoms exist. Incase of ectopic pregnancies, miscarriages or multiple pregnancies this drug can be used as adjunctive therapy. This drug may reduce the effect of drugs used to treat high blood pressure, and diabetes. It is recommended to monitor the blood pressure and blood glucose levels regularly to prevent complications. In addition, changes in blood lipids, increase in bilirubin levels, increase in serum liver enzymes levels (e.g. transaminases), leucopenia, thrombopenia have been observed with the use of this medicine. Talk to your doctor if you take any other medications or before using over-the-counter medicines or herbal products. Your doctor will evaluate the risk of interaction with this medication.

Consult your doctor before using this medication if you are pregnant or plan to have a baby. This injection is unsafe to use during pregnancy as it causes harm to an unborn fetus. Your health care practitioner will conduct a pregnancy test before you start treatment with Buselin 0.5mg Injection. Discuss with your doctor effective birth control methods and utilise them for at least two weeks following the last dose. s.

• Advanced prostatic carcinoma
• Treatment of endometriosis
• Adjunctive use in ovulation induction

Therapeutic Effects of Buselin 0.5mg Injection

It works by reducing the production of certain hormones in the body. This drug specifically gets binding to and stimulating GnRH receptors in the pituitary gland, which is located at the base of the brain. This leads to a transient increase in the production and release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) from the pituitary gland. However, with continued use, this injection suppresses the production of LH and FSH, leading to a decrease in the production of testosterone in men and estrogen in women

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

Serious:

• Allergic reactions like difficulty swallowing, rashes and swelling
• Diarrhea
• Pain and stomach problems
• Breathlessness
• Weight gain
• Low urination
• Sickness
• High BP
• Unusual bruising
• Severe headache and eyesight problems
• Infections

Common:

• Menopause-like symptoms
• Increased sweating, dry vagina, hot flushes
• Shoulder pain and stiffness
• Constipation or diarrhea
• Low glucose tolerance
• Mood changes, depression, anxiety
• Tinnitus
• Heart palpitations
• Hair loss
• Vaginal discharge
• Changes in liver enzymes

Otide 100mcg injection contains the active substance octreotide. It is a synthetic compound derived from somatostatin, a substance naturally found in the human body that inhibits the effects of certain hormones, such as growth hormones. It is used to reduce the amount of growth hormone produced by people with acromegaly (a condition in which the body produces too much growth hormone, causing enlargement of the hands, feet, and facial features; joint pain; and other symptoms) who cannot be treated with surgery, radiation, or another medication. 

It is also used to control diarrhea and flushing caused by carcinoid tumors (slow-growing tumors that release natural substances that can cause symptoms) and vasoactive intestinal peptide-secreting adenomas (VIP-omas; tumors that form in the pancreas and release natural substances that can cause symptoms). It is used to prevent complications following surgery of the pancreas gland.  It is also indicated to stop bleeding and to protect from re-bleeding from ruptured gastro-esophageal varices in patients suffering from chronic liver disease. This medicine is used to treat people with pituitary tumors that produce too much thyroid-stimulating hormone (TSH) when other types of treatment (surgery or radiotherapy) are not suitable or have not worked and after radiotherapy, to cover the interim period until the radiotherapy becomes fully effective. 

Do not use this medicine if you are allergic to octreotide or any of the other ingredients of this medicine. Inform your physician if you have gallstones, high or low blood sugar levels, vitamin B12 deficiency, and liver diseases. Otide 100mcg injection may lower your heart rate, and very high doses can cause abnormal heart rhythm, so your doctor may monitor your heart function regularly during the treatment. Inform your physician if you are pregnant or breastfeeding before initiating the treatment.

• To treat acromegaly
• Relieve symptoms associated with some tumors of the GI tract
• To prevent complications following surgery of the pancreas gland
• To treat pituitary tumors that produce too much TSH

Therapeutic Effects of Otide 100mcg Injection

Otide 100mcg injection acetate, a cyclic octapeptide agent, inhibits growth hormone, glucagon, and insulin more effectively than the natural hormone somatostatin. The drug also reduces growth hormone and IGF-I (somatomedin C) in acromegaly, inhibits gallbladder contractions, reduces bile secretion, and suppresses thyroid stimulating hormone (TSH) secretion.

• Store the Otide 100mcg injection in the refrigerator at 2°C to 8°C
• Do not freeze
• Protect the medicine from light and excessive moisture.
• Keep the medicine out of reach of children and pets
• If you forgot to take the injection, inform your healthcare professional immediately and reschedule the appointment.

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

Common:

• Diarrhea, flatulence
• Abdominal pain
• Back pain
• Tiredness
• Headache, nausea

Serious:

• Increased heart rate
• Changes in heart rhythm
• Increased or decreased blood sugar levels
• Changes in thyroid levels
• Vitamin B12 deficiency
• Gall stones

Bortesam 2mg Injection is a chemotherapy medication that belongs to the class of medicines called proteasome inhibitors. It consists of the active ingredient Bortezomib. It is indicated for the treatment of multiple myeloma and mantle cell lymphoma. Multiple myeloma refers to the cancerous progression of plasma cells that are predominant in the bone marrow. Mantle cell lymphoma is a less common cancer affecting the lymph nodes. This medication is concomitantly used with other chemotherapy medicines like pegylated liposomal doxorubicin, rituximab, cyclophosphamide, doxorubicin, dexamethasone, prednisolone or thalidomide for patients who have not started treatment and are ineligible for blood stem cell transplant. 

The common side effects likely associated with Bortesam 2mg Injection are Pneumonia, loss of appetite, sensitivity, tingling and burning sensation of the skin, nausea, vomiting, diarrhea, mouth ulcers, constipation, muscle and bone pain, hair loss, fever, infections, itching, redness, dehydration, stomach problems, etc., Inform your physician if these side effects disturb or persist in you.  

Inform your doctor if you are allergic to Bortesam 2mg Injection and its ingredients. Do not use this medication if you have severe lung or heart problems. Before starting treatment with this medication, let your physician know if you are suffering from neuropathy (nerves malfunction), cardiac disorders, severe lung problems, pulmonary disorders, posterior reversible encephalopathy syndrome disorders, gastrointestinal disorders, thrombocytopenia (a low platelet count), neutropenia (low white blood cell count), tumor lysis syndrome (metabolic abnormalities that can occur as a complication during the treatment of cancer), hepatic disorders. Inform your doctor of diabetes because this Injection can affect your blood glucose levels.

• Treatment of multiple myeloma and mantle cell lymphoma.

Therapeutic Effects of Bortesam 2mg Injection

Bortesam 2mg Injection Injection works by exerting a toxic effect on cancer cells. It inhibits the 26S proteasome and blocks a major cell signaling pathway. This inhibition of the signaling pathway makes the cancer cells sensitive to chemotherapy. This medicine also enhances the build-up of a protein and minimizes cancer cell growth and multiplication.

• Store unopened vials in the refrigerator (2 °C – 8 °C) and protect them from light.
• Keep this medicine out of sight and reach of children.

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

Serious

• Muscle cramps
• Confusion, visual disturbances, seizures, and headache
• Breathlessness
• Swelling of feet
• Changes in heartbeat
• High blood pressure
• Fainting and tiredness
• Cough and chest tightness

Common

• Pneumonia
• Loss of appetite
• Sensitivity, tingling and burning sensation of the skin
• Nausea, vomiting, and diarrhea
• Mouth ulcers
• Constipation
• Muscle and bone pain
• Hair loss
• Fever
• Reduction in blood cell count
• Reduced kidney function
• Shivering
• Infections
• Itching and redness
• Dehydration
• Stomach problems
• Difficulty sleeping, anxiety, mood swings, depressed mood

Carboplatin 450mg injection belongs to the medication class known as an alkylating agent. It is an anti-cancer medicine that contains the active ingredient Carboplatin. It treats a certain type of ovarian and lung cancer as a single or combined with other medications. 

Consult your doctor if you have any symptoms of allergic reactions, abnormal bruises, kidney problems (haemolytic-uraemic syndrome), and a decrease in red blood cells (anemia). Report to your doctor if you experience any lung-related symptoms like; shortness of breath, lung tissue inflammation, or lung infection while taking a Carboplatin 450mg injection. 

Use effective contraception while receiving this medication and continue to use it for six months, even after receiving the final dose. Carboplatin 450mg injection may reduce fertility temporarily or permanently in both men and women. So it is advised to get suggestions about fertility concerns from your doctor. 

• Carboplatin 450mg injection treats ovarian and lung cancer.

Therapeutic Effects of Carboplatin 450mg Injection

Carboplatin 450mg injection acts as an alkylating agent. This medication reduces the proliferation of cells by inhibiting the formation of DNA, RNA, and proteins, which stops DNA replication and results in programmed cell death.

Inform your healthcare professional about all the medicines you take, including prescription medications, over-the-counter medications, nutritional and vitamin supplements, and herbal products. Certain medications, such as Cisplatin and other anticancer drugs, interacting with Carboplatin 450mg injection may reduce effectiveness by causing undesirable side effects.

• Keep away from the reach of children.
• Protect the tablets from light and metal; store them below 25°C.
• Do not refrigerate the injection.

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

Serious:

• Reduced number of red blood cells (anemia)
• Allergic reactions
• Abnormal bruises
• Kidney problems
• Hearing problems
• Fever, chills

Common:

• Loss of taste, diarrhea
• Constipation
• Hair loss
• Skin rashes
• Itchiness
• Extreme tiredness and weakness
• Inflammation in lung tissues
• Tingling or numbness in your hands, arms, or legs
• Prickling sensation
• Difficulties in breathing

Omalirel 150mg injection contains an active component called Omalizumab 150mg injection. This medicine belongs to monoclonal antibodies. This medication is used to treat allergic asthma, chronic rhinosinusitis (inflammation of the nose and sinuses) with nasal polyps, and chronic spontaneous urticaria (CSU). Inform your doctor if you are allergic to Omalirel 150mg injection or any of the ingredients that are allergic to latex because the needle cap of the syringe may contain latex. Before using Omalirel 150mg injection, it's crucial to consult your doctor if you have kidney or liver problems or suffer from an autoimmune disease.

Discussing these factors with your doctor ensures safe and informed use of Omalirel 150mg injection for your specific medical condition. The safety and efficacy of the drug in children has not been established. So, it is recommended that you ask your doctor. Consult your doctor if you are planning to get pregnant or think you may be pregnant while breastfeeding.

• Allergic asthma
• Chronic rhinosinusitis (inflammation of the nose and sinuses) with nasal polyps
• Chronic spontaneous urticaria (CSU)

Therapeutic Effects of Omalirel 150mg Injection

Omalirel 150mg injection works by blocking and targeting a substance called immunoglobulin E (IgE) in the body; in this way, it reduces allergic reactions like Chronic rhinosinusitis (inflammation of the nose and sinuses) with nasal polyps and chronic spontaneous urticaria (CSU).

Inform your doctor about any prescribed medications, over-the-counter medicines, nutritional or vitamin supplements, and herbal products you take or have taken before the treatment. Certain medications may interact with Omalirel 150mg  injection and can cause undesirable side effects.

• Keep Omalirel 150mg injection out of the sight and reach of children.
• Store in a refrigerator between 2°C to 8°C.
• Do not freeze

This medicine is given only in a hospital setup by a healthcare provider. Cernos Depot 1gm injection will be given to you by your doctor. It is given subcutaneous injection, either as a single injection or as a continuous infusion (a drip). Your physician will decide the dosage and frequency of this injection based on the severity of your disease and other factors.

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

Common

• Fever (in children)
• Reactions at the injection site (pain, swelling, itching, and redness)
• Pain in stomach
• Headache (very common in children)
• Upper respiratory tract infection (inflammation of the pharynx and common cold)
• Feeling of pressure or pain in the cheeks and forehead (sinusitis, sinus headache)
• Joint pain (arthralgia)
• Feeling dizzy.

Glenstim 6mg Injection consists of the active ingredient Peglylated granulocyte colony-stimulating factor. This is synthesized from the bacteria E.coli. It belongs to a category of proteins called cytokines and is similar to the natural protein produced by the body. It is a leukocyte growth factor indicated to reduce infections in patients receiving anti-cancer drugs with bone marrow suppressive properties. By reducing the risk of infections, Glenstim 6mg Injection can help cancer patients receive their full dose of chemotherapy on schedule, improving treatment outcomes. 

This medication is also prescribed to increase the survival of patients exposed to radiotherapy. Patients who receive Glenstim 6mg Injection may experience less fatigue, fewer days of fever and infection, and less time spent in the hospital. This can lead to an improved quality of life during cancer treatment. This can interfere with bone marrow function testing, such as aspiration and biopsy, and cause false-positive results. Patients should inform their healthcare provider that they receive Glenstim 6mg Injection before undergoing any bone marrow function testing.

• Chemotherapy-induced neutropenia
• Chemotherapy-induced fever
• Chemotherapy-induced infections

The therapeutic effect of the Glenstim 6mg Injection is to stimulate the production of neutrophils in the bone marrow. Neutrophils are a type of white blood cell that help to fight infections. Chemotherapy drugs can cause damage to the bone marrow, leading to a decrease in the number of neutrophils, which can increase the risk of infections. So this medication works by stimulating the bone marrow to produce more neutrophils, which can help prevent infections in cancer patients undergoing chemotherapy. This can reduce the risk of infections, hospitalizations, and other complications associated with chemotherapy-induced neutropenia.

• Store in a refrigerator between 2°C and 8°C (36°F and 46°F).
• It should not be frozen.
• It should not be shaken before use.
• Keep it in its original packaging until it is ready to be used.

Glenstim 6mg Injection may harm the developing fetus, so it is unsafe to use it during pregnancy. 

It is unknown whether Glenstim 6mg Injection is excreted in human milk. So breastfeeding women should consult their doctor before taking it.

Glenstim 6mg Injection may cause a side effect called interstitial lung disease (ILD), a serious lung condition that can cause symptoms such as shortness of breath, coughing, and fatigue. Patients with pre-existing lung disease may be at a higher risk of developing ILD while receiving this medicine.

If a patient with liver disease experiences symptoms such as yellowing of the skin or eyes, abdominal pain, or dark urine while receiving Glenstim 6mg Injection, they should notify their healthcare provider immediately.

Alcohol use can negatively affect the immune system, and patients receiving Glenstim 6mg Injection may already have compromised immune systems due to their medical condition or treatment. Therefore, it is generally recommended that patients limit their alcohol consumption or avoid alcohol entirely while receiving it.

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

• Allergic reactions
• Acute respiratory distress syndrome (ARDS)
• Splenic rupture
• Kidney damage
• Interstitial lung disease (ILD)

• Bone pain
• Headache
• Fatigue
• Muscle aches
• Nausea
• Vomiting
• Diarrhea
• Loss of appetite
• Injection site reactions

Cytarine 100mg injection contains the active substance Cytarabine. It is an antineoplastic drug that belongs to the class antimetabolite. It is used alone or with other chemotherapy medications to treat certain types of leukemias (a type of blood cancer with too many white blood cells), including acute myeloid leukemia (AML) and chronic myelogenous leukemia (CML). It is also indicated to use alone or with other chemotherapy drugs to treat and prevent meningeal leukemia (cancer in the membrane that covers and protects the spinal cord and brain). 

Do not take Cytarine 100mg injection if you are allergic to Cytarabine or any other ingredients of this medicine. Inform your physician if you have difficulties in body coordination, or taking any other anti-cancer medications, decreased bone marrow functioning, have liver problems, or have undergone dialysis immediately before or after treatment with this medicine.  

Cytarine 100mg injection may cause an increased uric acid level in your blood, your doctor will tell you if you need to take any medicine to control this. Notify your physician if you have sudden signs of allergy, such as rash, itching, or hives on the skin, swelling of the face, lips, mouth, or throat, shortness of breath, or wheezing. It is unknown whether this medicine can be administered in patients with kidney failure, inform your doctor if you have any kidney diseases. 

• Acute myeloid leukemia (AML)
• Chronic myelogenous leukemia (CML)
• Meningeal leukemia

Therapeutic Effects of Cytarine 100mg Injection

Cytarine 100mg injection is a cytotoxic drug that acts by primarily killing cells undergoing DNA synthesis. It works by slowing or stopping the growth of cancer cells in your body. 

Inform your healthcare provider about all the medicines you take, including prescription medications, over-the-counter medications, nutritional and vitamin supplements, vaccines, and herbal products. Certain medications may interact with the effects of Cytarine 100mg injection and reduce its effectiveness by causing undesirable side effects. Inform your physician if you are using digoxin. 

• Store Cytarine 100mg injection at room temperature (25°C)
• Do not refrigerate or freeze.
• Keep the injection away from the reach of children and pets.
• If you forgot to take a dose on the scheduled day, contact your physician and reschedule the dose.
• Do not take a double dose to make up for a forgotten dose.

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

 Common

• Fever
• Loss of appetite, abdominal pain
• Swallowing difficulties
• Nausea, vomiting
• Diarrhoea
• Inflammation or ulceration in the mouth or anus
• High blood uric acid levels
• Hair loss
• Skin rashes
• Speaking difficulties
• Inflammation in the vein

Serious 

• Swelling and irritation of the skin
• Increased blood uric acid levels
• Blisters of the skin
• Irregular heartbeat
• Lung diseases
• Anemia
• Infection
• Kidney problems