Leading Exporter of letroz tablet (letrozole), naltivia 50(naltrexone tablets 50mg ), lupride depot injection (leuprolide), myelostat 500mg capsule (hydroxyurea), octride depot injection (octreotide acetate) and trabec injection (trabectedin) from Bengaluru.
₹ 228.85/Stripe Get Latest Price
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 |
Minimum order quantity: 1 Stripe
Uses:
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:
₹ 847/Stripe Get Latest Price
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 |
Minimum order quantity: 1 Stripe
Naltivia 50mg (Naltrexone) is a medication primarily used to treat alcohol and opioid dependence. It is an opioid receptor antagonist, which means it blocks the effects of opioids and can help reduce cravings and prevent relapse in individuals recovering from addiction. Here is some information on its uses, side effects, and precautions:
Uses:
Alcohol dependence: Naltrexone can be prescribed as part of a comprehensive treatment program to help individuals with alcohol dependence reduce their alcohol consumption or maintain abstinence.Opioid dependence: Naltrexone can be used to prevent relapse in individuals who have already detoxified from opioids and are trying to stay drug-free.Opioid overdose: In some cases, emergency medical personnel may administer naltrexone to reverse the effects of an opioid overdose.Side Effects:
Common side effects: Nausea, vomiting, stomach pain, decreased appetite, headache, dizziness, fatigue, and trouble sleeping.Less common side effects: Joint or muscle pain, increased heart rate, nervousness, irritability, and difficulty concentrating.Rare but serious side effects: Liver damage, allergic reactions, mood changes (such as depression or hallucinations), and blurred vision.Precautions:
Allergies: Inform your healthcare provider if you have any known allergies to naltrexone or any other medications.Opioid withdrawal: Before starting naltrexone treatment, it is important to be opioid-free for a certain period to avoid precipitating withdrawal symptoms. Naltrexone can cause severe withdrawal symptoms if taken while opioids are still in the system.Liver problems: Individuals with liver disease or elevated liver enzymes should use naltrexone with caution, as it may worsen liver function.Pregnancy and breastfeeding: Naltrexone should be used during pregnancy only if the potential benefits outweigh the risks. It is not recommended for breastfeeding mothers.Other medications: Inform your healthcare provider about all the medications, including over-the-counter drugs and herbal supplements, that you are taking, as some medications may interact with naltrexone.It is important to consult a healthcare professional for personalized advice, as they can provide detailed information based on your specific medical history and circumstances.
₹ 4200/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
Uses:
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.
₹ 151/Stripe Get Latest Price
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 |
Minimum order quantity: 1 Stripe
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.
₹ 9995/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
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:
₹ 28600/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
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.
₹ 32250/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
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:
₹ 359/Strip Get Latest Price
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 |
Minimum order quantity: 1 Strip
Uses:
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:
₹ 366.81/Strip Get Latest Price
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 |
Minimum order quantity: 1 Strip
Uses:
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:
₹ 3434.5/Box Get Latest Price
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 |
Minimum order quantity: 1 Box
Uses:
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:
₹ 3471.91/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
Uses:
Common Side Effects:
Serious Side Effects:
Precautions:
₹ 155.91/Stripe Get Latest Price
Manufacturer | Cipla |
Shelf life | More than 2 years |
Composition | Flutamide |
Brand | Cytomid |
Packaging Size | 1/10 |
Form | Tablet |
Country of Origin | Made in India |
Minimum order quantity: 1 Stripe
Uses:
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.
₹ 13000/Bottle Get Latest Price
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 |
Minimum order quantity: 1 Bottle
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:
₹ 19500/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
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.
₹ 45000/Box Get Latest Price
Manufacturer | BDR Pharmaceuticals Internationals Pvt |
Minimum Order Quantity | 1 |
Strength | 200mg, 300mg |
Shelf life | More than 2 years |
Composition | Rucaparib |
Brand | Bdparib |
Packaging Size | 60 tablets in 1 bottle |
Form | Tablet |
Minimum order quantity: 1 Box
Uses: Rucaparib is often used in the treatment of advanced ovarian cancer. It is a poly (ADP-ribose) polymerase (PARP) inhibitor, and it works by interfering with the repair of damaged DNA in cancer cells, leading to their death.
Precautions:
Bone Marrow Suppression: Rucaparib can cause bone marrow suppression, leading to low blood cell counts. Regular blood tests are necessary to monitor for this.
Myelodysplastic Syndrome (MDS) and Acute Myeloid Leukemia (AML): There have been reports of the development of MDS and AML in patients treated with PARP inhibitors, including rucaparib.
Allergic Reactions: Patients should be monitored for signs of allergic reactions, and treatment should be discontinued if severe hypersensitivity reactions occur.
Pregnancy and Breastfeeding: Rucaparib may cause fetal harm, and its use is not recommended during pregnancy. Adequate contraception should be used during treatment, and breastfeeding is not recommended.
Side Effects: Common side effects of rucaparib may include:
Serious side effects may include:
₹ 117.9/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
Uses:
Acute Myeloid Leukemia (AML): Arasid Injection is frequently used as part of induction and consolidation therapy for AML, which is a type of cancer that affects the bone marrow and blood.Acute Lymphoblastic Leukemia (ALL): It may also be used in the treatment of ALL, a cancer that affects the white blood cells.Non-Hodgkin's Lymphoma: Arasid Injection can be utilized in combination with other chemotherapy drugs to treat certain types of non-Hodgkin's lymphoma.
Side Effects:
While Arasid Injection can be effective in treating cancer, it may also cause some side effects.
Nausea and vomitingDiarrhea or constipationLoss of appetiteMouth soresHair lossFatigue or weaknessFever or chillsEasy bruising or bleedingInfectionSkin rash or itchingPrecautions:Before starting Arasid Injection, it is important to inform your healthcare provider about any other medications you are taking, including over-the-counter drugs and herbal supplements.
Precautions:
Allergies: If you are allergic to cytarabine or any other ingredients in Arasid Injection, inform your healthcare provider before taking the medication.
Pregnancy and breastfeeding: Arasid Injection may harm an unborn baby, so it is important to discuss the risks and benefits with your healthcare provider if you are pregnant or planning to become pregnant. It is also not recommended to breastfeed while receiving Arasid Injection.
Blood disorders: Inform your healthcare provider if you have a history of blood disorders or if you have recently received radiation therapy or chemotherapy.
Liver or kidney problems: Arasid Injection may be processed by the liver and kidneys, so it is essential to let your healthcare provider know if you have any liver or kidney problems.
Vaccinations: Avoid getting live vaccines while receiving Arasid Injection, as it may weaken the immune system's response to the vaccine.
Always follow the instructions and dosage provided by your healthcare provider. If you experience severe or persistent side effects, contact your healthcare provider immediately.
₹ 5995/Box Get Latest Price
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 |
Minimum order quantity: 1 Box
Uses:
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.
₹ 5995/Bottle Get Latest Price
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 |
Minimum order quantity: 1 Bottle
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.
₹ 202391.48/Pack Get Latest Price
Manufacturer | AstraZeneca |
Strength | 40mg, 80mg |
Shelf life | More than 2 years |
Composition | Osimertinib |
Brand | Tagrisso |
Packaging Size | 1/10 |
Form | Tablet |
Country of Origin | Made in India |
Minimum order quantity: 1 Pack
Uses:
Tagrisso (Osimertinib) is a medication primarily used for the treatment of non-small cell lung cancer (NSCLC) that has specific mutations in the epidermal growth factor receptor (EGFR) gene. It falls under the category of targeted therapy.
Precautions:EGFR Mutation Testing: Tagrisso is generally prescribed for patients with NSCLC whose tumors have specific EGFR mutations. Proper testing is required to identify the presence of these mutations.
Pregnancy and Breastfeeding: It may cause harm to an unborn baby, so it is crucial to inform your healthcare provider if you are pregnant, planning to become pregnant, or breastfeeding.
Liver Function: Patients with pre-existing liver conditions may need careful monitoring while using Tagrisso.
Interactions with Other Medications: Inform your healthcare provider about all medications, including over-the-counter drugs and supplements, that you are taking to avoid potential interactions.
Lung Disease: Patients with pre-existing interstitial lung disease may require close monitoring as Tagrisso has been associated with lung-related side effects.
Common side effects of Tagrisso may include:
₹ 1339.88/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
Uses:
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.
₹ 1059.96/Box Get Latest Price
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 |
Minimum order quantity: 1 Box
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.
₹ 690/Box Get Latest Price
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 |
Minimum order quantity: 1 Box
Uses:
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:
₹ 354/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
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.
₹ 16800/Bottle Get Latest Price
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 |
Minimum order quantity: 1 Bottle
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:
₹ 9754/Piece Get Latest Price
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 |
Minimum order quantity: 1 Piece
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:
₹ 28000/Bottle Get Latest Price
Manufacturer | Glenmark Pharmaceuticals Ltd |
Strength | 250mg, 500mg |
Product Name | Abirapro |
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 |
Minimum order quantity: 1 Bottle
Abirapro Tablet, also known as Abiraterone Acetate, is a medication used in the treatment of prostate cancer. Here is some information about its uses, side effects, and precautions:
Uses:
Prostate Cancer: Abirapro Tablet is primarily prescribed for the treatment of metastatic castration-resistant prostate cancer (mCRPC). It is used in combination with prednisone or prednisolone.How it works:Abiraterone Acetate is an androgen biosynthesis inhibitor. It works by blocking the production of androgens (male hormones) in the body, including testosterone. Prostate cancer cells rely on androgens to grow and spread, and by inhibiting their production, Abiraterone helps slow down the progression of the disease.
Side Effects:Like any medication, Abirapro Tablet can cause side effects. Some common side effects include:
Fatigue or weaknessJoint swelling or painHot flashesHigh blood pressureFluid retention (edema)DiarrheaNausea or vomitingUrinary tract infectionCough or shortness of breathAbnormal liver function testsIt's important to note that not all individuals will experience these side effects, and some may experience different or more severe side effects. If you experience any persistent or concerning side effects, it is important to consult your doctor.
Precautions:Before starting Abirapro Tablet, it is important to inform your doctor about any existing medical conditions, allergies, or medications you are taking. Here are some precautions to consider:
Hormone Levels: Abiraterone affects hormone levels in the body. Inform your doctor if you have any hormone-related conditions such as adrenal insufficiency or mineralocorticoid excess.
Liver Problems: Abirapro Tablet can cause liver toxicity. Regular monitoring of liver function is necessary during treatment. Inform your doctor if you have a history of liver disease or any liver-related issues.
Cardiovascular Problems: Abiraterone may cause an increase in blood pressure, fluid retention, and cardiovascular events. Inform your doctor if you have a history of heart disease or any other cardiovascular conditions.
Pregnancy and Breastfeeding: Abiraterone should not be used by women, especially during pregnancy or breastfeeding, as it may harm the fetus or the nursing baby.
Interactions: Abirapro Tablet may interact with other medications, including prescription drugs, over-the-counter medications, and herbal supplements. Inform your doctor about all the medications you are taking to avoid potential interactions.
Always follow your doctor's instructions regarding the dosage, duration of treatment, and any additional precautions specific to your case. It is important to attend regular check-ups and monitoring while on Abirapro Tablet to ensure the medication's effectiveness and manage any potential side effects.
₹ 17983.91/Box Get Latest Price
Manufacturer | Prakash Biopharma |
Shelf life | More than 2 years |
Composition | Enzalutamide |
Brand | Bdenza |
Packaging Size | 28 capsules in 1 strip |
Form | Tablet |
Minimum order quantity: 1 Box
Bdenza 40mg Capsule is a medication that contains the active ingredient enzalutamide. It is primarily used in the treatment of prostate cancer. Here is some information about the uses, side effects, and precautions associated with Bdenza:
Uses:
Prostate Cancer: Bdenza (Enzalutamide) is prescribed for the treatment of metastatic castration-resistant prostate cancer (mCRPC). It is used in adult men whose cancer has spread to other parts of the body and is resistant to medical or surgical treatments that lower testosterone levels.Side Effects:Bdenza may cause various side effects. Some common side effects include:
FatigueHot flashesHeadacheHigh blood pressureDiarrheaNauseaConstipationJoint painMuscle painDecreased appetiteWeight lossPrecautions:Before taking Bdenza, it is important to consider the following precautions:
Allergies: Inform your doctor if you are allergic to enzalutamide or any other medications.
Other Medications: Let your doctor know about all the medications you are currently taking, including prescription, over-the-counter, and herbal supplements, as some drugs may interact with enzalutamide.
Medical Conditions: Inform your doctor about any existing medical conditions you have, especially liver problems or seizures, as Bdenza may not be suitable in such cases.
Pregnancy and Breastfeeding: Bdenza is not intended for use in women and should not be used during pregnancy or breastfeeding. It may cause harm to the fetus or nursing infant.
Driving and Operating Machinery: Bdenza may cause fatigue and dizziness, which can affect your ability to drive or operate machinery. Be cautious until you know how this medication affects you.
Regular Monitoring: Your doctor may order regular blood tests to monitor your liver function, as Bdenza can cause liver problems.
It's important to note that this information is not exhaustive, and it is essential to consult with a healthcare professional or your prescribing doctor for personalized advice and guidance regarding the use of Bdenza (Enzalutamide). They can provide you with detailed information based on your specific medical condition and history
₹ 30000/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
Uses:
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.
₹ 21500/Vial Get Latest Price
Strength | 40 mg |
composition | Nivolumab(40mg) |
packaging size | 40mg/4ml |
Manufacturer | BMS India Pvt Ltd |
packaging type | vial |
Minimum order quantity: 1 Vial
Opdyta 40mg Injection is used in the treatment of non-small cell lung cancer, kidney cancer, head and neck cancer, melanoma, Hodgkin's disease, and liver cancer.
₹ 50/Box Get Latest Price
Strength | 50 mg |
Packaging Type | Strip |
Packaging Size | 10*10 Tablets |
Brand | Zydus |
Manufacturer | Zydus celexa Ltd |
Also gives | Pharma Third party manufacturing |
Usage | Hospital, Clinical, Personal |
Shelf life | More than 2 years |
Minimum order quantity: 1 Box
Captomer 50mg Tablet is used in the treatment of blood cancer. It works by decreasing the number of red blood cells, which is produced by the body. Thereby prevents the cancer cells from growing and multiplying.
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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:
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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.
₹ 960/Box Get Latest Price
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 |
Minimum order quantity: 1 Box
Uses:
Chronic Lymphocytic Leukemia (CLL): Clokeran Tablet is commonly prescribed for the treatment of CLL, a type of cancer affecting the white blood cells.
Hodgkin's Lymphoma: It may be used as part of the treatment regimen for Hodgkin's lymphoma, a cancer that originates in the lymphatic system.
Non-Hodgkin's Lymphoma: Clokeran Tablet may also be used in the treatment of certain types of non-Hodgkin's lymphoma, which is a group of cancers affecting the lymphatic system.
Side Effects:While taking Clokeran Tablet, individuals may experience various side effects, which can vary in severity and frequency.
Side effects :
Nausea and vomitingDiarrhea or constipationLoss of appetiteHair loss or thinningFatigue or weaknessIncreased susceptibility to infectionsEasy bruising or bleedingAnemiaChanges in skin pigmentationLiver toxicity.
Precautions:
It is important to follow certain precautions while taking Clokeran Tablet:
Pregnancy and breastfeeding: Clokeran Tablet may harm the developing fetus or pass into breast milk, so it is generally not recommended during pregnancy or breastfeeding. Consult a healthcare professional for guidance.
Blood disorders: Clokeran Tablet can affect blood cell production and may worsen existing blood disorders. Regular blood tests are usually conducted to monitor blood cell counts.
Infections: This medication may suppress the immune system, increasing the risk of infections. Take precautions to avoid exposure to infectious agents and promptly report any signs of infection to your healthcare provider.
Liver and kidney function: Clokeran Tablet can affect liver and kidney function. Regular monitoring of liver and kidney function is usually performed during treatment.
Allergies: Inform your healthcare provider about any known allergies or hypersensitivity reactions to medications, including chlorambucil.
Other medical conditions: Inform your doctor about any pre-existing medical conditions, such as a history of seizures, kidney or liver problems, or any other significant health conditions.
It is crucial to follow the prescribed dosage and duration of treatment as directed by your healthcare provider. Always consult a healthcare professional for personalized advice and information about your specific medical condition and treatment.
₹ 1259.64/Strip Get Latest Price
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 |
Minimum order quantity: 1 Strip
Uses:
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:
₹ 5980/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
Uses:
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.
₹ 916.8/Vial Get Latest Price
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 |
Minimum order quantity: 10 Vial
Uses:
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:
₹ 2398/Bottle Get Latest Price
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 |
Minimum order quantity: 1 Bottle
Uses:
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.
₹ 19.46/Stripe Get Latest Price
Manufacturer | Cipla |
Minimum Order Quantity | 1 |
Strength | 10mg, 20mg |
Usage Application | Hospital |
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 |
Minimum order quantity: 1 Stripe
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:
₹ 6229.39/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
Uses:
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.
₹ 4425/Vial Get Latest Price
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 |
Minimum order quantity: 1 Vial
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:
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Avella International
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