Product Details:
Minimum Order Quantity | 1 Stripe |
Strength | 50mg |
Packaging Size | 1/10 |
Packaging Type | strips |
Dose | 1 tab / day |
Brand | Naltivia |
Composition | Naltrexone |
Also Gives | Third Party Manufacturing |
Manufactured By | Healing pharma |
Form | tablets |
Shelf Life | More than 2 years |
Country of Origin | Made in India |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Hydroxyurea (500mg) |
Brand | Myelostat |
Packaging Size | 1*10 |
Form | Tablet |
Deals in | Third Party Manufacturing |
Country of Origin | Made in India |
Uses:
Myeloproliferative Disorders: Hydroxyurea is often used in the treatment of myeloproliferative disorders, such as chronic myeloid leukemia (CML), polycythemia vera, essential thrombocythemia, and myeloid metaplasia.
Sickle Cell Anemia: It is also used for the management of sickle cell anemia to reduce the frequency of painful crises and the need for blood transfusions.
Side Effects:
Bone Marrow Suppression: Hydroxyurea can suppress bone marrow function, leading to decreased production of blood cells. Regular blood tests are typically performed to monitor blood cell counts.
Nausea and Vomiting: Gastrointestinal side effects, including nausea and vomiting, may occur.
Mucositis: Inflammation of the mucous membranes (mucositis) can occur.
Skin Changes: Some individuals may experience skin changes, such as darkening or thinning of the skin.
Anorexia: Loss of appetite or anorexia may occur.
Peripheral Neuropathy: Nerve damage affecting the extremities (peripheral neuropathy) is a potential side effect.
Fertility Issues: Hydroxyurea may cause temporary infertility. Discuss family planning with your healthcare provider.
Precautions:
Pregnancy and Breastfeeding: Hydroxyurea may harm the fetus, so it's crucial to avoid pregnancy during treatment. If you are pregnant, planning to become pregnant, or breastfeeding, discuss the risks and benefits with your healthcare provider.
Blood Cell Counts: Regular monitoring of blood cell counts is essential during treatment to detect and manage bone marrow suppression.
Kidney and Liver Function: Hydroxyurea is eliminated from the body through the kidneys. Monitoring kidney function is important, especially in individuals with pre-existing kidney conditions. Liver function should also be assessed.
Immunizations: Consult with your healthcare provider regarding vaccinations, as some live vaccines may need to be avoided during treatment.
Drug Interactions: Inform your healthcare provider about all medications, including over-the-counter drugs and supplements, to avoid potential interactions.
Pre-existing Conditions: Inform your healthcare provider about any pre-existing medical conditions, especially kidney or liver disease.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Brand | Mamaearth Retinol Night Cream |
Prescription/Non prescription | Prescription |
Manufacturer | Bellegirl Lifestyle Pvt Ltd |
Shelf Life | More than 2 years |
Country of Origin | Made in India |
Retinol Night Creams:
Uses:
Retinol, a form of vitamin A, is commonly used in skincare products due to its potential benefits, including promoting skin renewal, reducing the appearance of fine lines and wrinkles, and improving skin texture.
Side Effects:
Precautions:
Patch Test: Before using the Mamaearth Retinol Night Cream on your face, perform a patch test on a small area of skin to check for any adverse reactions or allergies.
Start Slowly: If you are new to retinol, start with a lower concentration and gradually increase as your skin builds tolerance. Sudden, high concentrations may lead to irritation.
Use Sunscreen: Always use a broad-spectrum sunscreen during the day, especially when using retinol at night. This helps protect the skin from sun damage and minimizes the risk of hyperpigmentation.
Moisturize: If you experience dryness or irritation, use a gentle and hydrating moisturizer to keep your skin moisturized.
Avoid Certain Ingredients: Some skincare ingredients, such as benzoyl peroxide, salicylic acid, and vitamin C, may interact with or enhance the effects of retinol. It's advisable to check for potential interactions and consult a dermatologist if you are using other active ingredients.
Pregnancy and Breastfeeding: If you are pregnant or breastfeeding, consult with a healthcare professional before using retinol products, as high doses of vitamin A derivatives may not be recommended during pregnancy.
Consult with a Dermatologist: If you have specific skin concerns or conditions, it's advisable to consult with a dermatologist before incorporating retinol into your skincare routine.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Strip |
Brand | Letroz |
Packaging Size | 1*5 |
Packaging Type | Box |
Prescription/Non prescription | Prescription |
Composition | Letrozole (2.5mg) |
Deals in | Third Party Manufacturing |
Country of Origin | Made in India |
Oral Administration:
Duration:
Pregnancy:
Liver and Kidney Function:
Bone Health:
Cardiovascular Health:
Other Medications:
Common side effects may include:
Serious side effects are rare but may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Brand | Ifex M |
Manufacturer | Biochem Pharmaceutical Industries |
Usage /Application | Hospital,Clinical,Personal |
Shelf life | More than 2 years |
Composition | Mesna (1gm) + Ifosfamide (NA) |
Packaging Size | 1 Injection in 1 vial |
Form | Injection |
Deals in | Third Party Manufacturing |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Storage | Store below 30 DegreeC |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Anastrozole (1mg) |
Brand | Arimidex |
Packaging Size | 2*14 Tablets |
Form | Tablet |
Deals in | Third Party Manufacturing |
Country of Origin | Made in India |
Common Side Effects:
Serious Side Effects (Rare):
Central Nervous System Effects:
Gastrointestinal Effects:
Musculoskeletal Effects:
Pregnancy and Breastfeeding:
Bone Health:
Liver Function:
Cardiovascular Health:
Hormone Replacement Therapy (HRT):
Routine Monitoring:
Interactions with Other Medications:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | Sun Pharmaceutical Industries Ltd |
Minimum Order Quantity | 1 |
Manufactured By | Sun Pharmaceutical Industries Ltd |
Strength | 3.75mg, 1.25mg, 22.5mg, 45mg |
Shelf life | More than 2 years |
Composition | Leuprolide |
Brand | Lupride Depot Injection |
Packaging Size | 1 Injection in 1 vial |
Application | Clinical, Hospital, Personal |
Country of Origin | Made in India |
Prostate Cancer: Lupride Depot is commonly used in the treatment of prostate cancer. It works by suppressing the production of testosterone, which can slow down the growth of prostate cancer cells.
Endometriosis: It may be prescribed for the management of endometriosis, a condition where tissue similar to the lining of the uterus grows outside the uterus.
Uterine Fibroids: Lupride Depot is sometimes used to treat symptoms associated with uterine fibroids.
Central Precocious Puberty: In some cases, it may be used to delay puberty in children with central precocious puberty.
Pregnancy: Lupride Depot should not be used during pregnancy, as it may harm the unborn baby.
Breastfeeding: It is advisable to avoid breastfeeding while receiving Lupride Depot treatment.
Bone Density: Prolonged use of Lupride Depot may lead to a decrease in bone density. This is more of a concern in individuals who have additional risk factors for osteoporosis.
Cardiovascular Risk: In patients with a history of cardiovascular disease, caution is needed as there might be an increased risk of certain cardiovascular events.
Hot Flashes: Flushing or feelings of warmth, particularly in the face, neck, or chest.
Decreased Libido: Some individuals may experience a decrease in sexual desire.
Injection Site Reactions: Pain, redness, or swelling at the injection site.
Mood Changes: Mood swings, including feelings of depression or irritability, have been reported.
Bone Pain: Some individuals may experience bone pain.
Reduced Bone Density: Long-term use of leuprolide may lead to decreased bone density.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | Sun Pharmaceutical Industries Ltd |
Brand | Octride |
Packaging Size | 1 Injection in 1 vial |
Composition | Octreotide acetate |
Shelf life | More than 2 years |
Form | Injection |
Strength | 10mg,20mg,30mg |
Country of Origin | Made in India |
Uses:
Potential Side Effects: Octride Depot Injection may cause side effects, and their intensity can vary. Common side effects may include:
Severe side effects are uncommon but may include hyperglycemia (elevated blood sugar levels) and gallstone formation.
Precautions:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Manufacturer | Cipla |
Shelf life | More than 2 years |
Composition | Flutamide |
Brand | Cytomid |
Packaging Size | 1/10 |
Form | Tablet |
Country of Origin | Made in India |
Liver Function: Flutamide is metabolized in the liver, and there have been reports of liver toxicity. Regular monitoring of liver function is necessary during treatment.
Allergic Reactions: Individuals with known allergies to flutamide or any of its components should avoid its use.
Pregnancy: Flutamide can cause harm to the developing fetus and should not be used during pregnancy. Adequate contraception is recommended during treatment.
Breastfeeding: Flutamide may pass into breast milk, and breastfeeding is not recommended during treatment.
Gastrointestinal Issues: Common side effects include nausea, vomiting, and diarrhea.
Liver Toxicity: Flutamide has been associated with liver toxicity. Signs of liver problems include jaundice (yellowing of the skin or eyes) and abdominal pain.
Hot Flashes: Some individuals may experience hot flashes.
Breast Changes: Enlargement or tenderness of the breasts may occur.
Sexual Dysfunction: Flutamide may cause sexual dysfunction, including impotence.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | Natco Pharma Ltd |
Minimum Order Quantity | 1 |
Strength | 1mg Solution for Infusion |
Shelf life | More than 2 years |
Composition | Trabectedin |
Brand | Trabec |
Packaging Size | 1 Solution for Infusion in 1 vial |
Form | Injection |
More Information | 1mg Solution for Infusion |
Country of Origin | Made in India |
Uses: Trabec Injection is primarily used for the treatment of:
Precautions:
Liver Function: Trabectedin can affect liver function, and patients should undergo regular liver function tests during treatment. The drug may be associated with hepatotoxicity, and dose adjustments or discontinuation may be necessary in case of liver function abnormalities.
Myelosuppression: Trabectedin may cause myelosuppression, leading to low blood cell counts. Regular blood tests are necessary to monitor for changes in white blood cells, red blood cells, and platelets.
Renal Impairment: Patients with renal impairment may require dose adjustments, and close monitoring of renal function is recommended.
Pregnancy and Breastfeeding: Trabectedin may cause fetal harm, and women of childbearing potential should use effective contraception during treatment and for a period after discontinuation. It is not recommended during pregnancy or breastfeeding.
Infections: Patients receiving trabectedin may be at an increased risk of infections. Caution and monitoring for signs of infection are important.
Side Effects:
Common side effects of Trabec Injection may include:
Serious side effects may include:
Myelosuppression: Trabectedin may lead to low blood cell counts, including neutropenia, anemia, and thrombocytopenia.
Hepatotoxicity: Liver function abnormalities, including elevated liver enzymes and hepatotoxicity, have been reported.
Rhabdomyolysis: Severe muscle toxicity, including rhabdomyolysis, has been reported in some cases.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Piece |
Manufacturer | AstraZeneca |
Minimum Order Quantity | 1 |
Strength | 3.6mg, 10.8mg |
Shelf life | More than 2 years |
Composition | Goserelin acetate |
Brand | Zoladex La Injection |
Packaging Size | 1/1 |
Form | Injection |
Country of Origin | Made in India |
Uses:
Prostate Cancer: Zoladex LA is commonly used in the treatment of advanced prostate cancer. It works by suppressing the production of certain hormones that can stimulate the growth of prostate cancer cells.
Breast Cancer: In some cases, Zoladex LA may be used in the treatment of premenopausal women with certain types of breast cancer.
Endometriosis: Zoladex LA is also used in the management of endometriosis, a condition where tissue similar to the lining of the uterus grows outside the uterus.
Uterine Fibroids: It may be used in the treatment of uterine fibroids in certain situations.
Precautions:
Pregnancy and Breastfeeding: Zoladex LA should not be used during pregnancy. It may harm an unborn baby. It is also not recommended for use while breastfeeding.
Allergies: Inform your healthcare provider if you are allergic to goserelin acetate or any other ingredients in Zoladex LA.
Bone Density: Zoladex LA may cause a decrease in bone density. Regular monitoring of bone density and appropriate measures to maintain bone health may be necessary.
Liver Function: Inform your healthcare provider about any liver problems, as the metabolism of Zoladex LA involves the liver.
Cardiovascular Risk: Individuals with a history of cardiovascular disease may need careful monitoring during treatment with Zoladex LA.
Blood Sugar Levels: Zoladex LA may affect blood sugar levels, and individuals with diabetes should monitor their blood sugar levels closely.
Side Effects:
Common side effects of Zoladex LA may include:
Serious side effects are less common but may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Dosage | 12.5 mg |
Packing | Box |
Dose | 12.5mg |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Brand | Nitnib Capsule |
Packaging Size | 1*7 tablets |
Form | Tablet |
Deals in | Third Party Manufacturing |
Country of Origin | Made in India |
Uses:
Sunitinib is primarily used for the treatment of:
Renal Cell Carcinoma (RCC): Sunitinib is approved for the treatment of advanced renal cell carcinoma, a type of kidney cancer.
Gastrointestinal Stromal Tumor (GIST): It is also used for the treatment of gastrointestinal stromal tumors that cannot be surgically removed or have spread to other parts of the body.
Pancreatic Neuroendocrine Tumor (pNET): Sunitinib is indicated for the treatment of progressive, well-differentiated pancreatic neuroendocrine tumors in patients with unresectable, locally advanced, or metastatic disease.
Precautions:
Cardiovascular Events: Sunitinib may be associated with an increased risk of cardiovascular events, including heart failure, myocardial infarction, and hypertension. Monitoring of blood pressure and cardiac function is important during treatment.
Hepatic Impairment: Caution is needed in patients with hepatic impairment, as sunitinib is metabolized in the liver. Liver function should be monitored during treatment.
Thyroid Dysfunction: Hypothyroidism or hyperthyroidism may occur during sunitinib treatment. Regular monitoring of thyroid function is recommended.
Renal Impairment: Sunitinib is excreted through the kidneys, and its dosage may need adjustment in patients with renal impairment.
Wound Healing: Sunitinib may impair wound healing. It is recommended to interrupt treatment for at least one week before elective surgery and until the wound is fully healed.
Hematologic Effects: Sunitinib can cause myelosuppression, leading to decreased blood cell counts. Regular monitoring of blood counts is essential.
Side Effects:
Common side effects of sunitinib may include:
Serious side effects can include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Shelf life | More than 2 years |
Composition | Cytarabine |
Brand | Arasid |
Packaging Size | 1 Injection in 1 vial |
Form | Injection |
Country of Origin | Made in India |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Strip |
Manufacturer | Prakash Biopharma |
Shelf life | More than 2 years |
Composition | Enzalutamide |
Brand | Bdenza |
Packaging Size | 28 capsules in 1 strip |
Form | Tablet |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | Sun Pharmaceutical Industries Ltd |
Minimum Order Quantity | 1 |
Strength | 100mg, 500mg |
Shelf life | More than 2 years |
Composition | Pemetrexed |
Drug Name | Pexitaz Injection |
Brand | Pexitaz |
Packaging Size | 1 Injection in 1 vial |
Available Dose | 1 Injection in 1 vial |
Form | Injection |
Manufactured By | Sun Pharmaceutical Industries Ltd |
Country of Origin | Made in India |
Non-Small Cell Lung Cancer (NSCLC): Pemetrexed is often used in combination with other chemotherapy drugs for the treatment of advanced NSCLC.
Mesothelioma: Pemetrexed, in combination with cisplatin, is approved for the treatment of malignant pleural mesothelioma.
Kidney Function: Pemetrexed may affect kidney function. Kidney function should be monitored, and dosage adjustments may be necessary in individuals with impaired renal function.
Bone Marrow Suppression: Pemetrexed can suppress bone marrow function, leading to decreased blood cell counts. Regular blood tests are typically performed to monitor for this effect.
Liver Function: Liver function should be monitored, and dosage adjustments may be needed in individuals with impaired liver function.
Pregnancy and Breastfeeding: Pemetrexed can cause harm to the fetus, and its use is generally not recommended during pregnancy. It is also not recommended during breastfeeding.
Common side effects of pemetrexed may include:
Serious side effects can include kidney problems, liver problems, and severe skin reactions. It's important to report any unusual or severe symptoms to a healthcare provider.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Manufacturer | Cipla |
Manufactured By | Cipla Ltd |
Strength | 200mg, 400mg |
Shelf life | More than 2 years |
Composition | Pazopanib |
Brand | Pazoci |
Packaging Size | 30 tablets in 1 bottle |
Form | Tablet |
Country of Origin | Made in India |
Uses:
Renal Cell Carcinoma (Kidney Cancer): Pazopanib is indicated for the treatment of advanced renal cell carcinoma, a type of kidney cancer.
Soft Tissue Sarcoma: It is also used to treat advanced soft tissue sarcoma in patients who have received prior chemotherapy.
Potential Side Effects: Pazopanib, like any medication, may cause side effects. Common side effects may include:
Hypertension (High Blood Pressure): Regular monitoring of blood pressure is recommended during treatment.
Fatigue: Tiredness or weakness may occur.
Diarrhea: Some patients may experience diarrhea.
Nausea and Vomiting: Gastrointestinal symptoms, including nausea and vomiting, may occur.
Changes in Liver Function: Elevated liver enzymes may occur. Liver function should be monitored.
Hair Color Changes: Some patients may experience changes in hair color.
Skin Reactions: Skin problems such as rash, dry skin, or hair depigmentation may occur.
Hematological Effects: Pazopanib may affect blood cell counts, leading to anemia, thrombocytopenia, or neutropenia.
Cardiovascular Effects: QT interval prolongation and cardiac dysfunction have been reported.
Thyroid Function: Changes in thyroid function may occur.
These are not exhaustive lists, and other side effects may occur. Patients should report any unusual or severe symptoms to their healthcare provider.
Precautions:
Blood Pressure Monitoring: Regular monitoring of blood pressure is essential during treatment with Pazopanib.
Liver Function Monitoring: Liver function tests should be performed before starting treatment and regularly during treatment.
Thyroid Function Monitoring: Thyroid function should be monitored regularly.
Cardiac Monitoring: ECG monitoring may be considered, especially in patients with a history of cardiac conditions.
Pregnancy and Breastfeeding: Pazopanib can cause harm to the fetus, and it is not recommended during pregnancy. Effective contraception should be used during treatment, and breastfeeding should be avoided.
Hematological Monitoring: Regular monitoring of blood cell counts is important.
Interactions with Other Medications: Inform the healthcare provider about all medications, including prescription and over-the-counter drugs, as well as supplements, being taken.
Pre-existing Conditions: Caution is advised in patients with pre-existing hypertension, liver impairment, thyroid dysfunction, or cardiac conditions.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | Sun Pharmaceutical Industries Ltd |
Minimum Order Quantity | 1 |
Strength | 10mg |
Shelf life | More than 2 years |
Composition | Doxorubicin (Liposomal) (2mg/ml) |
Brand | Lipodox |
Packaging Size | 5 ml in 1 vial |
Manufactured By | Sun Pharmaceutical Industries Ltd |
Application | Clinical |
Country of Origin | Made in India |
Uses:
Precautions:
Cardiac Function: Doxorubicin can have cardiotoxic effects, and patients with pre-existing heart conditions or those who have received previous anthracycline therapy may be at an increased risk. Cardiac function should be monitored before and during treatment.
Bone Marrow Suppression: Doxorubicin can suppress bone marrow function, leading to decreased production of blood cells. Regular blood cell counts are necessary during treatment.
Liver Function: Liver function should be monitored, and caution is needed in patients with pre-existing liver conditions.
Pregnancy and Breastfeeding: Lipodox may cause harm to the fetus, and effective contraception is recommended during treatment. It is not recommended for use during breastfeeding.
Extravasation: Doxorubicin is an irritant, and if it leaks outside the vein during administration (extravasation), it can cause tissue damage. Proper administration techniques and monitoring are crucial.
Immunizations: Live vaccines should be avoided during treatment with doxorubicin.
Side Effects: Common side effects of Lipodox may include:
Serious side effects that require prompt medical attention may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Packaging Type | Vial |
Brand | Oncotrex |
Manufacturer | Sun Pharmaceutical Industries Ltd |
Storage | Store below 30 DegreeC |
Shelf Life | More than 2 years |
Prescription/Non prescription | Prescription |
Composition | Methotrexate (50mg) |
Packaging Size | 50mg |
Form | Injection |
Deals in | Third Party Manufacturing |
Uses:
Cancer Treatment: Methotrexate is commonly used in the treatment of certain types of cancer, such as leukemia, lymphoma, and breast cancer.
Rheumatoid Arthritis: Methotrexate is used to manage rheumatoid arthritis, helping to reduce inflammation and slow the progression of the disease.
Psoriasis: It may be prescribed for severe cases of psoriasis that do not respond to other treatments.
Side Effects: Methotrexate can cause a range of side effects, and their severity can vary from person to person. Common side effects may include:
Serious side effects can also occur, and they may include:
It's important to note that methotrexate can have toxic effects on various organs, and regular monitoring of blood counts and liver function is typically required during treatment.
Precautions:
Pregnancy: Methotrexate is contraindicated during pregnancy due to its potential to cause harm to the developing fetus. Adequate contraception is essential for individuals of childbearing potential.
Breastfeeding: Methotrexate is not recommended during breastfeeding.
Liver and Kidney Function: Regular monitoring of liver and kidney function is important during methotrexate treatment.
Infections: Methotrexate can increase the risk of infections. Inform your healthcare provider if you experience signs of infection, such as fever or persistent sore throat.
Alcohol: Limit or avoid alcohol consumption during methotrexate treatment, as alcohol can enhance the risk of liver toxicity.
Folic Acid Supplementation: Some patients may be prescribed folic acid supplements to mitigate certain side effects of methotrexate.
Other Medications: Inform your healthcare provider about all medications, including prescription and over-the-counter drugs, as interactions with methotrexate are possible.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Composition | Enzalutamide |
Category | prostate gland Cancer |
Dose Strength | 40mg |
Brand | Zydus Cadila |
Manufacturer | Zydus Cadila |
Dosage Form | Oral |
Type | Allopathic |
Packaging Size | 28 capsules in 1 box |
Seizures: Enzalutamide has been associated with an increased risk of seizures. Caution is advised in individuals with a history of seizures or other predisposing factors.
Cardiovascular Risk: There may be an increased risk of certain cardiovascular events. Monitoring cardiovascular health is important.
Liver Function: Regular monitoring of liver function is recommended during treatment.
Fertility: Enzalutamide may impair fertility. Men who wish to father a child should discuss fertility preservation options before starting treatment.
Pregnancy: Enzalutamide can cause fetal harm and is not indicated for use in women. Women of reproductive potential should use effective contraception during treatment.
Fatigue: Fatigue is a common side effect.
Hypertension: Elevated blood pressure may occur.
Seizures: Seizures have been reported as a rare side effect.
Hot Flashes: Flushing or feelings of warmth, particularly in the face, neck, or chest.
Gastrointestinal Issues: Nausea, diarrhea, and constipation may occur.
Muscle Weakness: Weakness and muscle discomfort have been reported.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Storage | Store at 25 DegreeC (77 DegreeF); |
Dosage Form | 3.75mg |
Packaging | box |
Brand | LUPROCARE INJECTION |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | Leuprolide 3.75 MG |
Packaging Size | 1 Injection in 1 vial |
Deals in | PCD Pharma |
Uses:
Prostate Cancer: Luprocare Depot is commonly used in the treatment of advanced prostate cancer. It works by suppressing the production of testosterone, which can slow the growth of prostate cancer cells.
Endometriosis: In women, Luprocare Depot may be used to treat endometriosis, a condition where tissue similar to the lining of the uterus grows outside the uterus.
Uterine Fibroids: It may also be prescribed for the management of uterine fibroids.
Central Precocious Puberty: Luprocare Depot is sometimes used to treat central precocious puberty in children.
Side Effects: As with any medication, Luprocare Depot may cause side effects. Common side effects may include:
More serious side effects can occur, and these may include:
It's important to note that the side effects can vary among individuals, and the severity may depend on factors such as the specific condition being treated and the patient's overall health.
Precautions:
Pregnancy and Breastfeeding: Luprocare Depot is not intended for use during pregnancy. It may cause harm to a developing fetus. It is important to use effective contraception during treatment. It is not recommended during breastfeeding.
Allergies: Individuals with known allergies to leuprolide acetate or similar drugs should avoid Luprocare Depot.
Bone Health: Due to the potential for bone density loss, especially with long-term use, healthcare providers may monitor bone health during treatment.
Cardiovascular Health: Luprocare Depot may be associated with an increased risk of cardiovascular events. Inform your healthcare provider of any pre-existing cardiovascular conditions.
Liver Function: The drug may affect liver function, and periodic monitoring may be recommended.
Interactions with Other Medications: Inform your healthcare provider about all medications, including over-the-counter drugs and supplements, as leuprolide can interact with certain medications.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Manufacturer | Eli Lilly and Company |
Strength | 500 mg |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | 500 mg pemetrexed and 500 mg mannitol |
Brand | Alimta 500mg |
Packaging Size | 1 Vial |
Deals in | PCD Pharma |
Malignant Pleural Mesothelioma: Alimta, in combination with cisplatin, is used for the initial treatment of malignant pleural mesothelioma, a type of cancer affecting the lining of the lungs.
Non-Small Cell Lung Cancer (NSCLC): Alimta is used as a single agent or in combination with other chemotherapy drugs for the treatment of locally advanced or metastatic non-small cell lung cancer.
Kidney Function: Prior to initiating treatment with Alimta, kidney function should be assessed. Monitoring of kidney function during treatment is essential.
Blood Cell Counts: Regular monitoring of blood cell counts, including white blood cells, red blood cells, and platelets, is necessary during treatment.
Liver Function: Liver function should be assessed, and individuals with abnormal liver function may require dose adjustments.
Pregnancy and Breastfeeding: Alimta can cause fetal harm, and its use during pregnancy is not recommended. Adequate contraception should be used during treatment, and breastfeeding is not advised.
Pulmonary Toxicity: Alimta may cause interstitial lung disease, pneumonitis, or acute respiratory distress syndrome. Patients experiencing new or worsening respiratory symptoms should seek medical attention.
Hypersensitivity Reactions: Hypersensitivity reactions, including rash and anaphylaxis, have been reported. Premedication with corticosteroids may be recommended to prevent these reactions.
Hematologic Effects: Alimta can cause bone marrow suppression, leading to low blood cell counts, which may increase the risk of infection, anemia, and bleeding.
Gastrointestinal Effects: Nausea, vomiting, diarrhea, and stomatitis (inflammation of the mouth) are common gastrointestinal side effects.
Fatigue: Fatigue is a frequent side effect.
Liver Enzyme Elevations: Elevated liver enzymes may occur.
Rash: Skin rash is a possible side effect.
Renal Effects: Alimta may affect kidney function, leading to renal impairment.
Neurologic Effects: Neurologic side effects, such as neuropathy, have been reported.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Manufacturer | Natco Pharma Ltd |
Minimum Order Quantity | 1 |
Strength | 2mg, 5mg |
Shelf life | More than 2 years |
Composition | Chlorambucil |
Brand | Clokeran |
Packaging Size | 1/30 |
Country of Origin | Made in India |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Strip |
Manufacturer | Reliance Life Sciences |
Minimum Order Quantity | 1 |
Strength | 500mg |
Shelf life | More than 2 years |
Composition | Capecitabine |
Brand | Relicitabine |
Packaging Size | 1/10 |
Form | Tablet |
Country of Origin | Made in India |
Capecitabine is commonly used in the treatment of various cancers, including:
Hypersensitivity: Patients with known hypersensitivity to capecitabine or any of its components should avoid its use.
Liver and Kidney Function: Capecitabine is metabolized in the liver, and its dosage may need adjustment in patients with impaired liver function. Monitoring liver function is important during treatment.
Blood Counts: Regular monitoring of blood counts, including white blood cells, platelets, and hemoglobin, is essential due to the potential for bone marrow suppression.
Hand-Foot Syndrome: Capecitabine can cause hand-foot syndrome, characterized by redness, swelling, and pain on the palms of the hands and soles of the feet. Patients should be educated on managing and reporting symptoms.
Gastrointestinal Effects: Gastrointestinal side effects, including diarrhea and nausea, are common. Adequate hydration and antiemetic medications may be prescribed to manage these symptoms.
Common side effects of Capecitabine may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Brand | Syndyma |
Manufacturer | Cipla Ltd |
Company Name | Syndyma |
Usage /Application | Hospital, Clinical, Personal |
Strength | 100mg, 400mg |
Pack Size | 4 ml in 1 vial, 16 ml in 1 vial |
Country of Origin | Made in India |
ses:
Cancer Treatment: Bevacizumab is often used in combination with chemotherapy to treat various types of cancer, including colorectal cancer, lung cancer, breast cancer, kidney cancer, and certain types of brain tumors.
Eye Conditions: In ophthalmology, bevacizumab is sometimes used off-label to treat certain eye conditions, such as macular degeneration.
Precautions:
Allergies: Inform your healthcare provider if you are allergic to bevacizumab or any other medications.
Recent Surgery: Bevacizumab should be used with caution in individuals who have had recent surgery or have wounds that haven't healed.
High Blood Pressure: Bevacizumab may cause or exacerbate high blood pressure, so blood pressure should be monitored regularly during treatment.
Pregnancy and Breastfeeding: Bevacizumab can harm an unborn baby, and it is not recommended during pregnancy. Women should avoid becoming pregnant while on this medication, and men should avoid fathering a child during treatment. It is not known if bevacizumab passes into breast milk.
Side Effects: Common side effects of bevacizumab may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Strip |
Strength | 0.5 mg |
Manufacturer | Natco Pharma Ltd |
Minimum Order Quantity | 1 |
Brand | Anastronat |
Shelf Life | More than 2 years |
Composition | Anastrozole |
Packaging Size | 1/10, 1/30 |
Form | Tablet |
Form Of Medicines | Blister |
Drug Name | Anastronat |
Country of Origin | Made in India |
Common Side Effects:
Serious Side Effects (Rare):
Central Nervous System Effects:
Gastrointestinal Effects:
Musculoskeletal Effects:
Pregnancy and Breastfeeding:
Bone Health:
Liver Function:
Cardiovascular Health:
Hormone Replacement Therapy (HRT):
Routine Monitoring:
Interactions with Other Medications:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Strip |
Manufacturer | Zydus Cadila |
Brand | Femistra |
Shelf Life | More than 2 years |
Composition | Anastrozole (1mg) |
Packaging Size | 10 tablets in 1 strip |
Number Of Tablets | 10 tablets in 1 strip |
Common Side Effects:
Serious Side Effects (Rare):
Central Nervous System Effects:
Gastrointestinal Effects:
Musculoskeletal Effects:
Pregnancy and Breastfeeding:
Bone Health:
Liver Function:
Cardiovascular Health:
Hormone Replacement Therapy (HRT):
Routine Monitoring:
Interactions with Other Medications:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Strength | 2mg, 2.5mg, 3.5mg |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Bortezomib |
Brand | Borviz 2 |
Usage Application | Parsonal, Hospital, Clinical |
Packaging Size | vial Single Use Only |
Uses:
Common Side Effects:
Serious Side Effects:
Precautions:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Prescription/Non prescription | Prescription |
Composition | Abiraterone Acetate (250mg) |
Brand | Zelgor |
Packaging Size | 120 Tablets |
Form | Tablet |
Deals in | Third Party Manufacturing |
Country of Origin | Made in India |
Uses:
Precautions:
Liver Function: Zelgor can affect liver function, so regular monitoring of liver enzymes is essential. It may be necessary to adjust the dosage or discontinue treatment if there are significant liver function abnormalities.
Cardiovascular Effects: Zelgor may cause hypertension (high blood pressure), so blood pressure should be monitored regularly. Controlling blood pressure is important during treatment.
Mineralocorticoid Excess: Abiraterone can lead to mineralocorticoid excess, resulting in low potassium levels and high blood pressure. Therefore, patients should be monitored for signs of mineralocorticoid excess, such as fluid retention and edema.
Adrenal Insufficiency: Zelgor can cause adrenal insufficiency, so patients may need to take low-dose glucocorticoids (such as prednisone or prednisolone) in combination with Abiraterone to reduce the risk of side effects.
Fertility: Zelgor may impair male fertility, and patients should be advised to use effective contraception during and for a few weeks after stopping treatment.
Pregnancy and Breastfeeding: Zelgor is not indicated for use in women, especially pregnant or breastfeeding women, as it can harm the developing fetus or nursing infant.
Side Effects: Common side effects of Zelgor may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | Mylan Pharmaceuticals Pvt LtdMylan Pharmaceuticals Pvt Ltd |
Manufactured By | Mylan Pharmaceuticals Pvt Ltd |
Composition | Trastuzumab |
Brand | Hertraz |
Packaging Size | 1 Injection in 1 vial |
Product Name | Hertraz |
Marketed By | Mylan Pharmaceuticals Pvt Ltd |
Uses: Hertraz (Trastuzumab) is primarily used for the treatment of:
Breast Cancer: Trastuzumab is commonly used in the treatment of HER2-positive breast cancer. It may be used alone or in combination with other chemotherapy agents.
Gastric Cancer: Trastuzumab is also used for the treatment of HER2-positive metastatic gastric or gastroesophageal junction adenocarcinoma in combination with other chemotherapy drugs.
Precautions:
Cardiotoxicity: Trastuzumab can cause heart problems, including heart failure. Cardiac function should be evaluated before and during treatment, and caution is advised in patients with pre-existing heart conditions.
Infusion Reactions: Infusion reactions, including fever, chills, and allergic reactions, may occur during or after administration. Patients are usually premedicated to minimize these reactions.
Pregnancy and Breastfeeding: Trastuzumab may cause harm to the fetus, and its use during pregnancy should be avoided. Women of childbearing potential should use effective contraception during treatment. It is not recommended during breastfeeding.
Pulmonary Toxicity: Pulmonary events, including interstitial pneumonitis and pulmonary infiltrates, have been reported. Close monitoring is necessary, and treatment may need to be interrupted in case of severe respiratory symptoms.
Side Effects:
Common side effects of Hertraz may include:
Serious side effects may include:
Cardiotoxicity: Trastuzumab can affect the heart, leading to heart failure. Cardiac function should be closely monitored during treatment.
Infusion Reactions: Severe infusion reactions may occur in some cases.
Pulmonary Toxicity: Interstitial pneumonitis and pulmonary infiltrates have been reported.
Hematologic Effects: Thrombocytopenia (low platelet count) and neutropenia (low neutrophil count) may occur.
Additional Information:
Product Details:
Minimum Order Quantity | 10 Vial |
Manufacturer | Natco Pharma Ltd |
Minimum Order Quantity | 1 |
Strength | 100mg, 500mg |
Shelf life | More than 2 years |
Composition | Pemetrexed |
Brand | Pemnat |
Packaging Size | 1 Injection in 1 vial |
Form | Injection |
Application | Clinical, Hospital, Personal |
Country of Origin | Made in India |
Pemnat (Pemetrexed) is a chemotherapy medication used for the treatment of certain types of cancer, including:
Non-Small Cell Lung Cancer (NSCLC): Pemetrexed is often used in combination with other chemotherapy drugs for the treatment of advanced NSCLC.
Malignant Pleural Mesothelioma: Pemetrexed, in combination with cisplatin, is approved for the treatment of malignant pleural mesothelioma.
Kidney Function: Pemetrexed may affect kidney function. Regular monitoring of kidney function is important, and dosage adjustments may be required in individuals with impaired renal function.
Bone Marrow Suppression: Pemetrexed can lead to decreased blood cell counts (anemia, leukopenia, thrombocytopenia). Regular blood tests are typically conducted to monitor for this effect.
Liver Function: Monitoring liver function is important, and dosage adjustments may be needed in individuals with impaired liver function.
Pregnancy and Breastfeeding: Pemetrexed can cause harm to the fetus, and its use is generally not recommended during pregnancy. It is also not recommended during breastfeeding.
Common side effects of Pemnat (Pemetrexed) may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | Sun Pharmaceutical Industries Ltd |
Application | Hospital, Clinical, Personal |
Manufactured By | Sun Pharmaceutical Industries Ltd |
Composition | Decitabine |
Brand | Decitax |
Packaging Size | 1 Injection in 1 vial |
Country of Origin | Made in India |
Myelodysplastic Syndromes (MDS): Decitabine is used for the treatment of myelodysplastic syndromes, a group of disorders characterized by ineffective production of blood cells.
Acute Myeloid Leukemia (AML): It is also used in the treatment of acute myeloid leukemia.
Hypersensitivity: Individuals with a known hypersensitivity or allergic reaction to decitabine or any component of the formulation should avoid its use.
Renal Impairment: Caution is advised in patients with renal impairment. Dose adjustments may be necessary.
Hepatic Impairment: Patients with hepatic impairment may require dose adjustments.
Myelosuppression: Decitabine can cause myelosuppression, leading to low blood cell counts. Regular blood tests are necessary to monitor for this.
Myelosuppression: This is a common side effect and may manifest as low white blood cell counts, low platelet counts, and anemia.
Nausea and Vomiting: Gastrointestinal symptoms such as nausea and vomiting may occur.
Fatigue: Patients may experience fatigue.
Fever: Fever is a reported side effect.
Injection Site Reactions: Pain, redness, or swelling at the injection site may occur.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Manufacturer | Glenmark Pharmaceuticals Ltd |
Product Name | Abirapro |
Strength | 250mg, 500mg |
Manufactured By | Glenmark Pharmaceuticals Ltd |
Shelf life | More than 2 years |
Composition | Abiraterone Acetate |
Brand | Abirapro |
Packaging Size | 120 tablets in 1 bottle |
Form | Tablet |
Application | Hospital, Clinical, Personal |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Strength | 100mg/224mg |
Storage | Store below 30 DegreeC |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Tegafur (100mg) + Uracil (224mg) |
Brand | Tegafi |
Packaging Size | 10*14 Capsule |
Form | Tablet |
Deals in | Third Party Manufacturing |
Country of Origin | Made in India |
Uses:
Precautions:
Bone Marrow Suppression: Chemotherapy, including Tegafi, can suppress bone marrow function, leading to decreased production of blood cells. Regular blood tests are often performed to monitor for this effect.
Liver Function: Tegafi can affect liver function, and liver enzymes are usually monitored during treatment.
Pregnancy and Breastfeeding: Tegafi may cause harm to the developing fetus, and its use is generally avoided during pregnancy. Adequate contraception should be used during treatment, and breastfeeding is not recommended.
Renal Impairment: Adjustments in dosage may be necessary in individuals with impaired kidney function.
Cardiotoxicity: Some chemotherapy medications may have cardiotoxic effects. If you have a history of heart problems, inform your healthcare provider.
Neurological Effects: Chemotherapy can sometimes cause neurological side effects. Report any signs of neuropathy, confusion, or other neurological symptoms to your healthcare provider.
Side Effects:
Common side effects of Tegafi 100mg/224mg Capsule may include:
Gastrointestinal Effects: Nausea, vomiting, diarrhea, and loss of appetite are common gastrointestinal side effects.
Bone Marrow Suppression: Decreased blood cell counts, leading to anemia, leukopenia, and thrombocytopenia.
Hepatotoxicity: Changes in liver function, which are usually reversible after discontinuation of the medication.
Skin Reactions: Rash or skin discoloration.
Fatigue: Chemotherapy can cause fatigue, and adequate rest is important during treatment.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Manufacturer | Cipla |
Minimum Order Quantity | 1 |
Usage Application | Hospital |
Strength | 10mg, 20mg |
Manufactured By | Cipla Ltd |
Shelf life | More than 2 years |
Composition | Tamoxifen Citrate |
Brand | Cytotam |
Packaging Size | 1/10 |
Form | Tablet |
Country of Origin | Made in India |
Uses:
Breast Cancer Treatment: Tamoxifen is primarily used in the treatment of breast cancer. It is often prescribed for both premenopausal and postmenopausal women with certain types of breast cancer that are estrogen receptor-positive.
Breast Cancer Prevention: In some cases, tamoxifen may be used to reduce the risk of developing breast cancer in women at high risk.
Male Breast Cancer: Tamoxifen may also be prescribed for the treatment of breast cancer in men.
Precautions:
Pregnancy and Breastfeeding: Tamoxifen should not be used during pregnancy, as it may harm the unborn baby. Women of childbearing age should use effective contraception during tamoxifen treatment. It is also not recommended for use while breastfeeding.
Liver Disease: Patients with a history of liver disease may require special monitoring or adjusted dosages.
Blood Clotting Disorders: Tamoxifen has been associated with an increased risk of blood clots, so caution is advised in patients with a history of blood clotting disorders.
Cataracts: There is some evidence to suggest that tamoxifen use may be associated with an increased risk of developing cataracts.
Endometrial Cancer: Tamoxifen has been linked to an increased risk of developing endometrial cancer. Regular gynecological check-ups are recommended.
Drug Interactions: Tamoxifen can interact with certain medications, so it's important to inform your healthcare provider about all the medications you are taking.
Side Effects: Common side effects of tamoxifen may include:
Serious side effects are less common but may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Packaging Size | 43.4 ml |
Packaging Type | Vial |
Brand | Intaxel |
Manufacturer | Fresenius Kabi India Pvt Ltd |
Shelf Life | More than 2 years |
Prescription/Non prescription | Prescription |
Composition | Paclitaxel (260mg) |
Deals in | Third Party Manufacturing |
Uses:
COPD (Chronic Obstructive Pulmonary Disease): Ipravent Respules are often used as a maintenance treatment to alleviate symptoms in patients with COPD, including chronic bronchitis and emphysema.
Asthma: It may be used as part of the treatment plan for asthma to help control and prevent bronchospasms.
Side Effects:
Dry Mouth: Ipravent may cause dry mouth, which can be managed by maintaining adequate hydration.
Throat Irritation: Some individuals may experience irritation or dryness in the throat.
Coughing: Coughing may occur as a side effect.
Headache: Headaches are a possible side effect.
Nausea: Nausea may occur in some cases.
Dizziness: Some people may experience dizziness.
Blurred Vision: Blurred vision is a rare side effect but should be reported if it occurs.
Precautions:
Allergies: Inform your healthcare provider about any allergies to atropine or similar substances, as well as any other allergies you may have.
Medical Conditions: Inform your healthcare provider about any pre-existing medical conditions, especially narrow-angle glaucoma, enlarged prostate, or bladder issues.
Pregnancy and Breastfeeding: If you are pregnant, planning to become pregnant, or breastfeeding, consult your healthcare provider before using Ipravent Respules.
Medication Interactions: Inform your healthcare provider about all medications you are taking, including prescription and over-the-counter drugs, as well as herbal supplements.
Cautions in Specific Populations: Use Ipravent Respules with caution in elderly individuals and those with certain health conditions. Dosage adjustments may be necessary.
Proper Use: Ensure proper inhalation technique and understanding of how to use the nebulizer or inhalation device correctly.
Regular Monitoring: Regularly monitor your respiratory condition, and report any changes or worsening symptoms to your healthcare provider.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Minimum Order Quantity | 1 |
Strength | 250mg, 500mg |
Manufactured By | Glenmark Pharmaceuticals Ltd |
Shelf life | More than 2 years |
Composition | Abiraterone Acetate |
Brand | Abirapro |
Packaging Size | 120 tablets in 1 bottle |
Country of Origin | Made in India |
Uses:
Precautions:
Liver Function: Regular monitoring of liver function is essential during treatment, as Abiraterone Acetate can cause an increase in liver enzymes. Dose adjustments or discontinuation may be required in case of significant liver function abnormalities.
Cardiovascular Effects: Abiraterone Acetate may lead to an increase in blood pressure. Blood pressure should be monitored regularly, and appropriate management is important.
Mineralocorticoid Excess: Abiraterone Acetate can cause mineralocorticoid excess, leading to low potassium levels and high blood pressure. Monitoring for signs of fluid retention, edema, and electrolyte imbalances is crucial.
Adrenal Insufficiency: Adrenal insufficiency may occur during treatment, and patients may need to take low-dose glucocorticoids (such as prednisone or prednisolone) to manage potential side effects.
Fertility: Abirapro may affect male fertility, and patients should use effective contraception during and for some time after discontinuation of treatment.
Pregnancy and Breastfeeding: Abirapro is not indicated for use in women, especially pregnant or breastfeeding women, due to potential harm to the fetus or nursing infant.
Side Effects: Common side effects associated with Abirapro Tablet may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Manufacturer | Natco Pharma Ltd |
Minimum Order Quantity | 1 |
Strength | 25mg |
Shelf life | More than 2 years |
Composition | Exemestane |
Brand | Xtane |
Packaging Size | 30 tablets in 1 bottle |
Form | Tablet |
Application | Clinical, Personal, Hospital |
Country of Origin | Made in India |
Uses:
Side Effects:
Hot Flashes: A common side effect is hot flashes, which can cause a sudden feeling of warmth, sometimes with sweating.
Fatigue: Some individuals may experience increased tiredness or fatigue.
Joint Pain: Exemestane can cause joint pain or stiffness.
Nausea: Nausea is a possible side effect.
Insomnia: Difficulty sleeping or insomnia may occur.
Bone Loss: Long-term use may lead to bone loss, increasing the risk of fractures. Monitoring bone health is important.
Mood Changes: Some people may experience mood changes or depression.
Precautions:
Menopausal Status: Xtane is generally prescribed to postmenopausal women. It is not intended for use in premenopausal women.
Pregnancy: Xtane is contraindicated during pregnancy, as it may cause harm to the developing fetus. Effective contraception is recommended during treatment.
Liver Function: Individuals with pre-existing liver conditions should be monitored, as Exemestane is metabolized in the liver.
Bone Health: Regular monitoring of bone health is advisable, and supplementation with calcium and vitamin D may be recommended to counteract potential bone loss.
Hormonal Effects: Exemestane decreases estrogen levels, which may impact bone density, cholesterol levels, and mood. Regular monitoring is necessary.
Interactions: Inform your healthcare provider about all medications, including over-the-counter drugs and supplements, to avoid potential interactions.
Allergies: Inform your healthcare provider of any allergies or adverse reactions to medications.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Pack |
Manufacturer | Sun Pharmaceutical Industries Ltd |
Minimum Order Quantity | 1 |
Strength | 50mg |
Shelf life | More than 2 years |
Composition | Dasatinib |
Brand | Dastila |
Packaging Size | 1/12 |
Form | Tablet |
Application | Hospital, Personal, Clinical |
Country of Origin | Made in India |
Chronic Myeloid Leukemia (CML): Dasatinib is used to treat adults with newly diagnosed chronic phase CML as well as those who are resistant or intolerant to previous treatments.
Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia (Ph+ ALL): It is also indicated for the treatment of adults with Ph+ ALL.
Cardiovascular Events: Dasatinib may be associated with cardiovascular events, so patients with preexisting cardiovascular conditions should be closely monitored.
Myelosuppression: Dasatinib can cause myelosuppression, leading to low blood cell counts. Regular blood tests are necessary to monitor for this.
Fluid Retention: Patients may experience fluid retention. Monitoring for signs of pleural effusion or other fluid retention is important.
QT Prolongation: Dasatinib can cause QT prolongation. Caution is advised in patients with a history of QT prolongation or those taking medications that can prolong the QT interval.
Myelosuppression: This can manifest as low white blood cell counts, low platelet counts, and anemia.
Fluid Retention: Edema and pleural effusion may occur.
Bleeding: Dasatinib may increase the risk of bleeding.
Gastrointestinal Symptoms: Nausea, diarrhea, and abdominal pain are common.
Fatigue: Patients may experience fatigue.
Headache: Headache is a reported side effect.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | Sun Pharmaceutical Industries Ltd |
Minimum Order Quantity | 1 |
Strength | 50mg |
Application | Hospital, Clinical, Personal |
Manufactured By | Sun Pharmaceutical Industries Ltd |
Shelf life | More than 2 years |
Composition | Decitabine |
Brand | Decitex |
Packaging Size | 1 Injection in 1 vial |
Country of Origin | Made in India |
Myelodysplastic Syndromes (MDS): Decitabine is used for the treatment of myelodysplastic syndromes, a group of disorders characterized by ineffective production of blood cells.
Acute Myeloid Leukemia (AML): It is also used in the treatment of acute myeloid leukemia.
Hypersensitivity: Individuals with a known hypersensitivity or allergic reaction to decitabine or any component of the formulation should avoid its use.
Renal Impairment: Caution is advised in patients with renal impairment. Dose adjustments may be necessary.
Hepatic Impairment: Patients with hepatic impairment may require dose adjustments.
Myelosuppression: Decitabine can cause myelosuppression, leading to low blood cell counts. Regular blood tests are necessary to monitor for this.
Myelosuppression: This is a common side effect and may manifest as low white blood cell counts, low platelet counts, and anemia.
Nausea and Vomiting: Gastrointestinal symptoms such as nausea and vomiting may occur.
Fatigue: Patients may experience fatigue.
Fever: Fever is a reported side effect.
Injection Site Reactions: Pain, redness, or swelling at the injection site may occur.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Manufacturer | Cipla |
Minimum Order Quantity | 1 |
Strength | 100mg, 150mg |
Shelf life | More than 2 years |
Composition | Nintedanib |
Brand | Nintib |
Country of Origin | Made in India |
Idiopathic Pulmonary Fibrosis (IPF): Nintedanib is approved for the treatment of idiopathic pulmonary fibrosis, a progressive lung disease that leads to scarring of the lung tissue.
Systemic Sclerosis-Associated Interstitial Lung Disease (SSc-ILD): In some regions, Nintedanib is also approved for the treatment of systemic sclerosis-associated interstitial lung disease.
Liver Function: Nintedanib can affect liver function, so regular monitoring of liver enzymes is often recommended during treatment.
Gastrointestinal Issues: Nintedanib may cause gastrointestinal side effects such as diarrhea, nausea, and abdominal pain. If these symptoms are severe or persistent, inform your healthcare provider.
Bleeding Risk: There may be an increased risk of bleeding while on Nintedanib. Inform your healthcare provider if you have a history of bleeding disorders or are taking anticoagulants.
Pregnancy and Breastfeeding: Nintedanib may harm an unborn baby, so it is crucial to discuss the potential risks and benefits with your healthcare provider if you are pregnant or planning to become pregnant. It is not recommended during breastfeeding.
Common side effects of Nintedanib may include:
Additional Information: