Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | Wockhardt Ltd |
Strength | 0.5mg |
Shelf life | More than 2 years |
Composition | Dactinomycin |
Brand | Cosmegen |
Packaging Size | 1 ml in 1 vial |
Form | Injection |
Country of Origin | Made in India |
Uses: Cosmegen (Dactinomycin) is used primarily in the treatment of various cancers. Some of the specific uses include:
Wilms' Tumor: Dactinomycin is often used in combination with other drugs for the treatment of Wilms' tumor, a type of kidney cancer that primarily affects children.
Gestational Trophoblastic Neoplasia (GTN): This drug is used in the treatment of gestational trophoblastic neoplasia, which is a group of rare tumors that involve abnormal growth of cells inside a woman's uterus.
Rhabdomyosarcoma: Dactinomycin may be part of the treatment regimen for rhabdomyosarcoma, a type of cancer that forms in soft tissues, often in children.
Ewing's Sarcoma: It is used in the treatment of Ewing's sarcoma, a rare type of bone cancer that primarily affects children and young adults.
Side Effects: Cosmegen can cause various side effects, and their severity can vary from person to person. Common side effects may include:
Nausea and Vomiting: Dactinomycin may cause nausea and vomiting. Anti-nausea medications may be prescribed to manage these symptoms.
Bone Marrow Suppression: Dactinomycin can affect the bone marrow, leading to decreased production of blood cells. This may result in an increased risk of infections, anemia, and bleeding.
Hair Loss: Temporary hair loss is a common side effect of many chemotherapy drugs, including dactinomycin.
Mouth Sores: Dactinomycin may cause sores in the mouth and throat.
Liver and Kidney Problems: This drug may affect liver and kidney function, and blood tests are often performed to monitor these.
Allergic Reactions: Some individuals may experience allergic reactions to dactinomycin, which can be serious. Signs of an allergic reaction include rash, itching, swelling, severe dizziness, or difficulty breathing.
Precautions: Before using Cosmegen, healthcare providers consider several precautions:
Blood Counts: Regular monitoring of blood counts is essential to check for any signs of bone marrow suppression.
Liver and Kidney Function: Patients with pre-existing liver or kidney problems may require dose adjustments or close monitoring.
Pregnancy and Breastfeeding: Dactinomycin can cause harm to the developing fetus, so it is typically avoided during pregnancy. Breastfeeding is not recommended during treatment.
Hypersensitivity: Individuals with a history of severe hypersensitivity reactions to dactinomycin or other anthracyclines should not use this medication.
Infections: Since dactinomycin can suppress the immune system, patients should take precautions to avoid infections.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | Gufic Bioscience Ltd |
Minimum Order Quantity | 1 |
Strength | 3.75mg |
Manufactured By | Gufic Bioscience Ltd |
Composition | Leuprolide |
Brand | Luprocare Depot |
Packaging Size | 1 Injection in 1 vial |
Form | Injection |
Country of Origin | Made in India |
Hormone-Dependent Conditions:
Prostate Cancer:
Endometriosis:
Pregnancy and Breastfeeding:
Bone Health:
Liver Function:
Common side effects may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Strip |
Dose/Strength | 2.5 mg |
Manufacturer | Fourrts India Laboratories Pvt Ltd |
Brand | Letrofil |
Packaging Type | Blister |
Composition | Letrozole |
Packaging Size | 1/5 |
Oral Administration:
Treatment Duration:
Pregnancy:
Bone Health:
Liver Function:
Cardiovascular Health:
Other Medications:
Common side effects may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Dosage Form | 150mg |
Packaging | vial |
Brand | Fosaport 150mg injection |
Manufacturer | Biocon pharmaceutical |
Usage /Application | Personal. Hospital. Clinical |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | Fosaprepitant (150mg) |
Packaging Size | 1 INJECTION IN VAIL |
Deals in | PCD Pharma |
Common Side Effects:
Serious Side Effects (Rare):
Hypersensitivity:
Liver Function:
Drug Interactions:
Pregnancy and Breastfeeding:
Dizziness and Fatigue:
Alcohol Interaction:
Additional Information:
Product Details:
Dosage Form | 100mg |
Packaging | Box |
Brand | Xpreza 100mg Powder Injection |
Manufacturer | Natco Pharma Ltd |
Usage /Application | Personal. Hospital. Clinical |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | Azacitidine |
Packaging Size | 100 mg/vial |
Deals in | PCD Pharma |
Uses: Xpreza Azacitidine Injection is primarily used for the following conditions:
Myelodysplastic Syndromes (MDS): It is used to treat MDS, a group of disorders in which the bone marrow does not produce enough healthy blood cells.
Acute Myeloid Leukemia (AML): Azacitidine is also used to treat AML, a type of cancer that affects the bone marrow and blood.
Side Effects: Azacitidine may cause various side effects, which can vary from person to person. Common side effects may include:
Precautions: Here are some precautions to consider when using Xpreza Azacitidine Injection:
Medical Supervision: This medication should only be administered under the supervision of a qualified healthcare provider experienced in the use of chemotherapy drugs.
Blood Counts: Regular blood tests will be necessary to monitor your blood cell counts during treatment.
Pregnancy and Breastfeeding: Azacitidine can harm an unborn baby, so it's important to avoid becoming pregnant while receiving treatment. If you are pregnant or planning to become pregnant, discuss this with your healthcare provider. It is not recommended during breastfeeding.
Infections: Azacitidine may increase the risk of infections. Inform your healthcare provider if you develop signs of infection, such as fever, chills, or sore throat.
Liver and Kidney Function: Inform your healthcare provider of any liver or kidney problems you may have, as dosage adjustments may be necessary.
Other Medications: Inform your healthcare provider about all other medications and supplements you are taking, as they can interact with Azacitidine.
Skin Reactions: Be vigilant for skin reactions, and if they occur, inform your healthcare provider.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Usage/Application | Personal |
Packaging Size | 1/10 |
Brand | Evolve Biolabe |
Product Type | Finished Product |
Delivery | Average of 7 days anywhere in the World |
Strength | 100mg, 250mg |
Uses:
Anti-inflammatory Properties: Corticosteroids, such as prednisone and dexamethasone, are often prescribed to reduce inflammation and suppress the immune system. They are used to manage conditions like rheumatoid arthritis, asthma, and certain autoimmune diseases.
Hormone Replacement Therapy: Steroid hormones, such as estrogen and testosterone, can be used in hormone replacement therapy (HRT) for individuals with hormonal imbalances, including menopausal women and those with conditions like hypogonadism.
Allergic Reactions: Corticosteroids can be used to manage severe allergic reactions, including anaphylaxis.
Side Effects:
Immunosuppression: Long-term use of corticosteroids can suppress the immune system, increasing the risk of infections.
Osteoporosis: Prolonged use of corticosteroids can lead to bone loss and an increased risk of fractures.
Weight Gain: Steroid hormones, especially corticosteroids, can cause fluid retention and increased appetite, leading to weight gain.
Mood Changes: Some individuals may experience mood swings, anxiety, or even depression with steroid use.
Gastrointestinal Effects: Steroids can cause stomach irritation and may increase the risk of gastrointestinal ulcers.
Fluid Retention: Corticosteroids can cause fluid retention, leading to swelling (edema) in various parts of the body.
Precautions:
Short-Term Use: Whenever possible, corticosteroids are usually prescribed for short-term use to minimize the risk of side effects.
Gradual Tapering: Abruptly stopping corticosteroids after prolonged use can lead to withdrawal symptoms. Dosages are often tapered gradually under medical supervision.
Monitoring: Regular monitoring of blood pressure, blood glucose levels, bone density, and other relevant parameters is important during steroid therapy.
Alternate-Day Therapy: In certain situations, physicians may prescribe steroids on an alternate-day schedule to reduce the risk of side effects.
Bone Health: Adequate calcium and vitamin D intake and weight-bearing exercises are recommended to support bone health.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Strength | 0.5 mg |
Packaging Size | 4 Tablets |
Packaging Type | Strips |
Brand Name | Dostinex |
Brand | Dostinex |
Dose | 0.25 mg q4Weeks (or longer) up to 1 mg 2x/week |
Manufacturer | pfizer |
Composition | Cabergoline |
Usage/Application | Hospital, Clinical, Personal |
Shelf Life | More than 2 years |
Deals in | Third Party Manufacturing |
Type Of Medicines | Allopathic |
Country of Origin | Made in India |
Cabergoline is used to treat different types of medical problems that occur when too much of the hormone prolactin is produced. It can be used to treat certain menstrual problems, fertility problems in men and women, and pituitary prolactinomas (tumors of the pituitary gland).
It works by stopping the brain from making and releasing the prolactin hormone from the pituitary gland. Cabergoline use is usually stopped when prolactin levels are normal for 6 months. It may be given again if symptoms of too much prolactin occur again.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Manufacturer | Sun Pharmaceutical Industries Ltd |
Minimum Order Quantity | 1 |
Strength | 4mg, 10mg |
Shelf life | More than 2 years |
Composition | Lenvatinib |
Brand | Lenvenib |
Packaging Size | 1/7 |
Form | Tablet |
Uses:
Potential Side Effects: Lenvatinib, like many cancer medications, may cause various side effects. Common side effects may include:
Hypertension (High Blood Pressure): Lenvatinib can lead to an increase in blood pressure.
Fatigue: Tiredness or weakness may occur.
Diarrhea: Gastrointestinal symptoms such as diarrhea.
Nausea and Vomiting: Some patients may experience nausea and vomiting.
Decreased Appetite: Loss of appetite may occur.
Proteinuria: Presence of excess protein in the urine.
Stomatitis (Mouth Sores): Inflammation of the mucous membranes in the mouth.
Palmar-Plantar Erythrodysesthesia (Hand-Foot Syndrome): Skin reaction that may cause redness, swelling, and pain on the palms of the hands and soles of the feet.
Headache: Some patients may experience headaches.
Problems with Voice: Changes in voice or hoarseness.
Hypothyroidism: Decreased thyroid function.
Increased Liver Enzymes: Elevated levels of liver enzymes may occur.
Blood Clotting Disorders: Lenvatinib may affect blood clotting.
Precautions:
Blood Pressure Monitoring: Regular monitoring of blood pressure is crucial during treatment.
Thyroid Function Monitoring: Regular monitoring of thyroid function is important.
Liver Function Monitoring: Monitoring of liver function is recommended.
Renal Function Monitoring: Regular monitoring of kidney function is advised.
Cardiac Function Monitoring: Due to the risk of cardiac disorders, including QT interval prolongation, cardiac function should be monitored.
Hand-Foot Syndrome Monitoring: Patients should be monitored for signs of hand-foot syndrome, and preventive measures may be taken.
Pregnancy and Contraception: Lenvatinib can cause harm to the fetus. Effective contraception is essential during treatment, and pregnancy should be avoided.
Bleeding Risk: Patients should be cautious to avoid activities that may increase the risk of bleeding.
Voice Changes: Patients should report any changes in voice promptly.
Interactions with Other Medications: Inform the healthcare provider about all medications, including prescription and over-the-counter drugs, as well as supplements, being taken.
Dental Care: Good oral hygiene is important, and patients should promptly report any signs of mouth sores.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Strip |
Strength | 0.5 mg |
Manufacturer | Healing Pharma India Pvt Lt |
Minimum Order Quantity | 1 |
Brand | Anaridex |
Shelf Life | More than 2 years |
Composition | Anastrozole |
Packaging Size | 1/10 |
Form Of Medicines | Blister |
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 Box |
Manufacturer | Eli Lilly and Company India Pvt Ltd |
Minimum Order Quantity | 1 |
Strength | 100mg,150mg,200mg |
Shelf life | More than 2 years |
Composition | Abemaciclib) |
Brand | Ramiven |
Packaging Size | 1/7 |
Form | Tablet |
Country of Origin | Made in India |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Manufacturer | Natco Pharma |
Dosage | Capsules |
Strength | 150mg |
Usage/Application | Personal. Hospital. Clinical |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Brand | Noxalk 150 mg |
Packaging Size | 1 x 30 |
Form | Capsule |
Deals in | PCD Pharma |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Packaging Type | Vial |
Composition | Itolizumab (100mg) |
Packaging Size | 250ml |
Brand | Biocon Biologics |
Injectable Form | Liquid |
Also Gives | Third Party Manufacturing |
Product Type | Finished Product |
Storage | Store below 30 DegreeC |
Form Of Medicine | Liquid |
Manufactured By | Biocon |
Uses: Itolizumab is primarily used in the treatment of moderate to severe plaque psoriasis and rheumatoid arthritis.
Side Effects: Common side effects may include injection site reactions (redness, swelling, itching), upper respiratory tract infections, and headache. Serious side effects are less common but may include hypersensitivity reactions.
Precautions:
Allergies: Inform your healthcare provider if you are allergic to itolizumab or any other medications.
Infections: Itolizumab may increase the risk of infections, and it is important to notify your healthcare provider if you develop signs of infection, such as fever or persistent cough.
Pre-existing Conditions: Inform your healthcare provider about any pre-existing medical conditions, especially if you have a history of infections or immunosuppression.
Pregnancy and Breastfeeding: Discuss the risks and benefits of Itolizumab if you are pregnant, planning to become pregnant, or breastfeeding.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Manufacturer | Cipla |
Strength | 200mg |
Shelf life | More than 2 years |
Composition | Sorafenib |
Brand | Soranib |
Packaging Size | 1/30 |
Form | Tablet |
Country of Origin | Made in India |
Uses:
Renal Cell Carcinoma (RCC): Sorafenib is used for the treatment of advanced renal cell carcinoma, a type of kidney cancer.
Hepatocellular Carcinoma (HCC): It is indicated for the treatment of advanced hepatocellular carcinoma, a form of liver cancer.
Thyroid Carcinoma: Sorafenib may be used for the treatment of radioactive iodine-resistant advanced thyroid carcinoma.
Precautions:
Hypertension: Sorafenib can cause an increase in blood pressure. Regular monitoring of blood pressure is essential, and antihypertensive medications may be required.
Hand-Foot Skin Reaction: Some individuals may experience skin reactions on the palms of the hands and soles of the feet (palmar-plantar erythrodysesthesia). Proper skin care and management of symptoms are important to prevent severe skin issues.
Cardiac Events: Sorafenib has been associated with cardiac events. Caution is advised in patients with a history of cardiovascular disease.
Bleeding: Sorafenib can increase the risk of bleeding. It should be used with caution in patients with a history of bleeding disorders.
Wound Healing: Sorafenib may impair wound healing. It is advisable to interrupt treatment for at least 4 weeks before elective surgery.
Liver Function: Sorafenib is metabolized in the liver, and liver function should be monitored during treatment.
Side Effects:
Common side effects of sorafenib may include:
Serious side effects can include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Manufacturer | AstraZeneca |
Strength | 3.6mg, 10.8mg |
Shelf life | More than 2 years |
Composition | Goserelin acetate |
Brand | Zoladex Injection |
Packaging Size | 1/1 |
Form | Injection |
Country of Origin | Made in India |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Dose/Strength | 15 mcg |
Brand | Actorise |
Drug | Actorise |
Usage/Application | Clinical, Personal, Hospital |
Packaging Size | 1/0.4ml, 1/0.42ml, 1/0.3ml, 1/0.5ml |
Form | Injection |
Anemia in Chronic Kidney Disease (CKD): Actorise Injection is used to treat anemia in patients with chronic kidney disease, including those on dialysis and those not on dialysis.
Anemia in Cancer Patients: It may be used to manage anemia in patients with non-myeloid malignancies receiving chemotherapy that can cause myelosuppression.
Hypersensitivity: Individuals with a known hypersensitivity or allergic reaction to darbepoetin alfa or any component of the formulation should avoid its use.
Blood Pressure Monitoring: Darbepoetin alfa can increase blood pressure. Regular monitoring of blood pressure is essential, and adjustments to antihypertensive medications may be necessary.
Thrombotic Events: There is an increased risk of thrombotic events (blood clots). Caution is advised in patients with a history of thrombotic events.
Pure Red Cell Aplasia (PRCA): Rare cases of pure red cell aplasia have been reported. Monitoring for this condition is important.
Hypertension: An increase in blood pressure may occur.
Thromboembolic Events: There may be an increased risk of blood clots, leading to conditions such as deep vein thrombosis or pulmonary embolism.
Pure Red Cell Aplasia: Though uncommon, it is a serious condition where the body stops producing red blood cells.
Hypersensitivity Reactions: Allergic reactions, including rash, itching, and swelling, may occur.
Injection Site Reactions: Pain, redness, or swelling at the injection site may occur.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Manufacturer | Cipla |
Minimum Order Quantity | 1 |
Strength | 200mg |
Shelf life | More than 2 years |
Composition | Sorafenib (200mg) |
Brand | Soranib |
Packaging Size | 1/30 |
Form | Tablet |
Country of Origin | Made in India |
Uses:
Renal Cell Carcinoma (RCC): Sorafenib is used for the treatment of advanced renal cell carcinoma, which is a type of kidney cancer.
Hepatocellular Carcinoma (HCC): It is also indicated for the treatment of advanced hepatocellular carcinoma, a form of liver cancer.
Thyroid Carcinoma: Sorafenib may be used for the treatment of radioactive iodine-resistant advanced thyroid carcinoma.
Precautions:
Hypertension: Sorafenib can cause an increase in blood pressure. Regular monitoring of blood pressure is important, and antihypertensive medications may be needed.
Hand-Foot Skin Reaction: Some individuals may experience skin reactions on the palms of the hands and soles of the feet. Proper skin care and management of symptoms are important to prevent severe skin issues.
Cardiac Events: Sorafenib has been associated with cardiac events. Caution is advised in patients with a history of cardiovascular disease.
Bleeding: Sorafenib can increase the risk of bleeding. It should be used with caution in patients with a history of bleeding disorders.
Wound Healing: Sorafenib may impair wound healing. It is advisable to interrupt treatment for at least 4 weeks before elective surgery.
Liver Function: Sorafenib is metabolized in the liver, and liver function should be monitored during treatment.
Side Effects:
Common side effects of sorafenib may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Manufacturer | Cipla |
Minimum Order Quantity | 1 |
Strength | 4mg, 10mg |
Shelf life | More than 2 years |
Composition | Lenvatinib |
Brand | Lenvatol |
Packaging Size | 1/10 |
Form | Tablet |
Uses:
Potential Side Effects: Lenvatinib, like many cancer medications, may cause various side effects. Common side effects may include:
Hypertension (High Blood Pressure): Lenvatinib can lead to an increase in blood pressure.
Fatigue: Tiredness or weakness may occur.
Diarrhea: Gastrointestinal symptoms such as diarrhea.
Nausea and Vomiting: Some patients may experience nausea and vomiting.
Decreased Appetite: Loss of appetite may occur.
Proteinuria: Presence of excess protein in the urine.
Stomatitis (Mouth Sores): Inflammation of the mucous membranes in the mouth.
Palmar-Plantar Erythrodysesthesia (Hand-Foot Syndrome): Skin reaction that may cause redness, swelling, and pain on the palms of the hands and soles of the feet.
Headache: Some patients may experience headaches.
Problems with Voice: Changes in voice or hoarseness.
Hypothyroidism: Decreased thyroid function.
Increased Liver Enzymes: Elevated levels of liver enzymes may occur.
Blood Clotting Disorders: Lenvatinib may affect blood clotting.
Precautions:
Blood Pressure Monitoring: Regular monitoring of blood pressure is crucial during treatment.
Thyroid Function Monitoring: Regular monitoring of thyroid function is important.
Liver Function Monitoring: Monitoring of liver function is recommended.
Renal Function Monitoring: Regular monitoring of kidney function is advised.
Cardiac Function Monitoring: Due to the risk of cardiac disorders, including QT interval prolongation, cardiac function should be monitored.
Hand-Foot Syndrome Monitoring: Patients should be monitored for signs of hand-foot syndrome, and preventive measures may be taken.
Pregnancy and Contraception: Lenvatinib can cause harm to the fetus. Effective contraception is essential during treatment, and pregnancy should be avoided.
Bleeding Risk: Patients should be cautious to avoid activities that may increase the risk of bleeding.
Voice Changes: Patients should report any changes in voice promptly.
Interactions with Other Medications: Inform the healthcare provider about all medications, including prescription and over-the-counter drugs, as well as supplements, being taken.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Manufacturer | Shilpa Medicare Ltd |
Shelf life | More than 2 yearsAverage |
Composition | Lenvatinib |
Brand | Lenshil |
Packaging Size | 1/10 |
Form | Tablet |
Uses: Lenvatinib is commonly used as a targeted therapy in the treatment of certain types of cancer, including:
Potential Side Effects: Lenvatinib, like many cancer medications, may cause various side effects. Common side effects may include:
Precautions:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Brand | Leuprolide Acetate |
Manufacturer | Lupin Ltd |
Composition | Leuprolide |
Packaging Size | 1 Injection in 1 vial |
Shelf life | More than 2 years |
Form | Injection |
Country of Origin | Made in India |
Uses:
Prostate Cancer: Leuprolide is often used in the management of prostate cancer. It reduces the production of testosterone, a hormone that fuels the growth of prostate cancer cells.
Breast Cancer: In some cases, leuprolide may be used in the treatment of hormone receptor-positive breast cancer.
Endometriosis: It is used to manage endometriosis, a condition where tissue similar to the lining of the uterus grows outside the uterus.
Uterine Fibroids: Leuprolide may be prescribed to shrink uterine fibroids before surgery.
Central Precocious Puberty: In children, leuprolide may be used to treat central precocious puberty, a condition where puberty begins too early.
Side Effects:
Common side effects of leuprolide acetate injection may include:
Serious side effects are rare but can include allergic reactions, bone thinning (osteoporosis), and potential cardiovascular effects.
Precautions:
Pregnancy and Breastfeeding: Leuprolide is not typically used during pregnancy, and it is important to avoid pregnancy during treatment. It is also not recommended during breastfeeding.
Bone Density: Long-term use of leuprolide may lead to a decrease in bone density. Your healthcare provider may monitor your bone health and recommend calcium and vitamin D supplements.
Cardiovascular Health: Leuprolide may have cardiovascular effects, and individuals with a history of heart disease should be closely monitored during treatment.
Liver Function: Leuprolide is metabolized by the liver, so individuals with liver problems may require dosage adjustments.
Diabetes: Leuprolide can affect blood sugar levels, and individuals with diabetes may need adjustments in their diabetes medications.
Hormone Replacement Therapy (HRT): In women, leuprolide induces a temporary menopause-like state. If hormone replacement therapy is considered, it should be carefully discussed with the healthcare provider.
Allergies: Inform your healthcare provider about any known allergies to leuprolide or similar medications.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Manufacturer | Dr Reddy's Laboratories Ltd |
Shelf life | More than 2 years |
Composition | Lomustine |
Brand | Lomtin Capsules |
Packaging Size | 1/5 |
Form | Tablet |
Country of Origin | Made in India |
Uses: Lomustine is commonly used in the treatment of:
Side Effects: Chemotherapy drugs like lomustine can have various side effects. Common side effects may include:
Serious side effects can also occur, and these may include:
It's important to note that the side effects can vary from person to person, and the severity depends on factors such as the dosage, treatment duration, and individual patient characteristics.
Precautions:
Blood Cell Counts: Regular blood tests are necessary during treatment to monitor blood cell counts. This is important to detect and manage potential bone marrow suppression.
Liver Function: Lomustine can affect liver function, so regular liver function tests are often performed.
Kidney Function: Monitoring kidney function is important as lomustine may impact the kidneys.
Pregnancy and Breastfeeding: Lomustine can harm the developing fetus, so it should be avoided during pregnancy. It is also advised to avoid breastfeeding while receiving lomustine.
Infections: Since lomustine can suppress the immune system, there is an increased risk of infections. Patients should take precautions to avoid infections and seek medical attention if signs of infection occur.
Other Medications: Inform your healthcare provider about all medications, including over-the-counter drugs and supplements, as interactions with lomustine are possible.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Manufacturer | Bruck |
Minimum Order Quantity | 1 |
Directions for Use | For oral use only Cytotoxic. |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | Sorafenib 200 mg |
Brand | Soravar |
Packaging Size | 1*30 Tablets. |
Form | Tablet |
Deals in | PCD Pharma |
Treatment | Cancer |
Country of Origin | Made in India |
Uses:
Renal Cell Carcinoma (RCC): Sorafenib is used for the treatment of advanced renal cell carcinoma, a type of kidney cancer.
Hepatocellular Carcinoma (HCC): It is also indicated for the treatment of advanced hepatocellular carcinoma, a form of liver cancer.
Thyroid Carcinoma: Sorafenib may be used for the treatment of radioactive iodine-resistant advanced thyroid carcinoma.
Precautions:
Hypertension: Sorafenib can cause an increase in blood pressure. Blood pressure should be monitored regularly, and antihypertensive medications may be required.
Hand-Foot Skin Reaction: Some individuals may experience skin reactions on the palms of the hands and soles of the feet. It's important to manage these symptoms to prevent severe skin issues.
Cardiac Events: Sorafenib has been associated with cardiac events. It should be used with caution in patients with a history of cardiovascular disease.
Bleeding: Sorafenib can increase the risk of bleeding. Caution is needed in patients with a history of bleeding disorders.
Wound Healing: Sorafenib may impair wound healing. It is advisable to interrupt treatment for at least 4 weeks before elective surgery.
Liver Function: Sorafenib is metabolized in the liver, and liver function should be monitored during treatment.
Side Effects:
Common side effects of sorafenib may include:
Serious side effects can include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Manufacturer | Glenmark Pharmaceuticals Ltd |
Dose | 150mg |
Form | Capsules |
Packaging Type | box |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Uses | Personal. Hospital. Clinical |
Composition | NINTEDANIB-150MG |
Brand | Nindanib |
Packaging Size | 30 tablets |
Deals in | PCD Pharma |
Idiopathic Pulmonary Fibrosis (IPF): Nintedanib is indicated for the treatment of idiopathic pulmonary fibrosis, a condition characterized by the scarring of lung tissue.
Systemic Sclerosis-Associated Interstitial Lung Disease (SSc-ILD): In some regions, nintedanib is also approved for use in certain cases of systemic sclerosis-associated interstitial lung disease.
Liver Function: Before starting nintedanib, healthcare providers often assess liver function, as the medication can affect the liver. Monitoring liver enzymes during treatment is essential.
GI Disorders: Nintedanib may cause gastrointestinal (GI) side effects, such as diarrhea, nausea, and vomiting. It's important to report severe or persistent GI symptoms to your healthcare provider.
Cardiac Conditions: Individuals with a history of cardiovascular conditions should use nintedanib with caution. Consult your healthcare provider if you have a history of heart problems.
Pregnancy and Breastfeeding: Inform your healthcare provider if you are pregnant, planning to become pregnant, or breastfeeding, as the safety of nintedanib during pregnancy and lactation is not well-established.
Gastrointestinal Disturbances: Diarrhea, nausea, vomiting, and abdominal pain are common side effects. Managing these symptoms with your healthcare provider is important.
Liver Enzyme Elevations: Nintedanib may cause elevated liver enzymes. Regular monitoring is typically recommended.
Fatigue: Some individuals may experience fatigue while taking nintedanib.
Dermatological Reactions: Skin rashes and photosensitivity reactions have been reported.
Cardiovascular Effects: Hypertension (high blood pressure) may occur in some individuals.
Bleeding Risk: There may be an increased risk of bleeding, especially in individuals with a history of bleeding disorders.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Litre |
Manufacturer | Akumentis Healthcare Ltd |
Strength | 100mg |
Side Effect | Diarrhoea, vomiting, nausea |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | Irinotecan 100mg |
Brand | Irnocel 100 injecion |
Packaging Size | 1 INJECTION IN VAIL |
Form | Injection |
Deals in | PCD Pharma |
Country of Origin | Made in India |
Colorectal Cancer: Irinotecan is commonly used in the treatment of colorectal cancer.
Other Cancers: It may also be used in the treatment of other cancers, such as lung cancer and pancreatic cancer.
Allergic Reactions: Individuals with known allergies to irinotecan or any of its components should avoid its use.
Severe Diarrhea: Irinotecan is associated with the risk of severe diarrhea, which can be life-threatening. Close monitoring and prompt management are essential.
Bone Marrow Suppression: Irinotecan can cause myelosuppression, leading to low blood cell counts. Regular blood tests are necessary to monitor for this.
Liver Dysfunction: Caution is advised in individuals with preexisting liver dysfunction, as irinotecan is metabolized in the liver.
Pregnancy: Irinotecan can cause fetal harm, and its use during pregnancy should be avoided. Adequate contraception is recommended during treatment.
Diarrhea: Diarrhea is a common side effect, and it can be severe.
Nausea and Vomiting: Gastrointestinal symptoms such as nausea and vomiting may occur.
Myelosuppression: Low blood cell counts, including white blood cells, red blood cells, and platelets, can occur.
Fatigue: Patients may experience fatigue.
Hair Loss: Temporary hair loss (alopecia) is a possible side effect.
Injection Site Reactions: Reactions at the injection site, such as redness or swelling, may occur.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Form | capsule |
Composition | Lenalidomide |
Manufacturer | Natco |
Prescription/Non prescription | Prescription |
Also Gives | PCD Pharma Franchise |
Brand | Lenalid 10 Mg |
Deals in | PCD Pharma |
Country of Origin | Made in India |
Uses: Lenalidomide, the active ingredient in Lenalid, is a medication used for various medical conditions, with its primary use in the treatment of certain cancers. Common uses include:
Multiple Myeloma: Lenalidomide is commonly used in combination with other medications for the treatment of multiple myeloma, a type of cancer affecting plasma cells in the bone marrow.
Myelodysplastic Syndromes (MDS): It may be prescribed for certain cases of myelodysplastic syndromes, a group of disorders characterized by abnormal blood cell development.
Mantle Cell Lymphoma: Lenalidomide is indicated for the treatment of mantle cell lymphoma in patients who have received at least one prior therapy.
Potential Side Effects: Lenalidomide may cause various side effects. Common side effects include:
Hematological Effects:
Gastrointestinal Issues:
Fatigue: Tiredness or weakness.
Rash: Skin reactions such as rash.
Peripheral Edema: Swelling of the extremities.
Dizziness: Feeling lightheaded or dizzy.
Musculoskeletal Issues:
Infections: Increased susceptibility to infections.
Cardiac Issues: Lenalidomide may affect the heart, including arrhythmias.
Hepatotoxicity: Changes in liver function.
Precautions:
Pregnancy Prevention: Lenalidomide poses a significant risk of birth defects. Women of childbearing age must use effective contraception during treatment and for a specific period after discontinuation.
Hematological Monitoring: Regular monitoring of blood counts, especially neutrophil, platelet, and red blood cell levels.
Thromboembolism Risk: Lenalidomide may increase the risk of blood clots, and preventive measures may be taken.
Dizziness: Patients should avoid activities that require mental alertness while experiencing dizziness.
Renal Function Monitoring: Regular monitoring of kidney function is recommended.
Infection Prevention: Patients should be vigilant in preventing infections, and healthcare providers may recommend prophylactic antibiotics.
Interactions with Other Medications: Inform the healthcare provider about all medications, including prescription and over-the-counter drugs, as well as supplements, being taken.
Liver Function Monitoring: Regular monitoring of liver function is recommended.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Packaging Size | 4 x 28 Capsules |
Composition | Enzalutamide 40mg |
Manufacturer | BDR Pharmaceuticals Int'l Pvt. Ltd |
Prescription/Non prescription | Prescription |
Also Gives | PCD Pharma Franchise |
Strength | 40mg |
Brand | Bdenza |
Shelf life | more than 2 years |
Deals in | PCD Pharma |
Country of Origin | Made in India |
Seizures: Enzalutamide has been associated with an increased risk of seizures. It is important to use caution 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 Bottle |
Packaging Size | 120 TABLETS |
Form | Tablet |
Composition | ABIRATERONE ACETATE 250 MG |
Manufacturer | BDR PHARMACEUTICALS PVT LTD |
Prescription/Non prescription | Prescription |
Also Gives | PCD Pharma Franchise |
Strength | 250 MG |
Brand | APRAZER HEALTHCARE PVT LTD |
Shelf life | more than 2 years |
Deals in | PCD Pharma |
Country of Origin | Made in India |
Uses: Abiraterone Acetate is primarily used in the treatment of metastatic castration-resistant prostate cancer (mCRPC) in adult men. It is often prescribed in combination with prednisone or prednisolone.
Precautions:
Liver Function: Regular monitoring of liver function is crucial during treatment, as Abiraterone Acetate may lead to an increase in liver enzymes. Dose adjustments or discontinuation may be required if significant liver function abnormalities occur.
Cardiovascular Effects: Abiraterone Acetate can cause an increase in blood pressure. Regular monitoring of blood pressure is important, and appropriate management should be initiated if hypertension occurs.
Mineralocorticoid Excess: This medication may lead to mineralocorticoid excess, resulting in low potassium levels and high blood pressure. Monitoring for signs of fluid retention, edema, and electrolyte imbalances is essential.
Adrenal Insufficiency: Abiraterone Acetate can cause adrenal insufficiency. Patients may need to take low-dose glucocorticoids (such as prednisone or prednisolone) in conjunction with Abiraterone to manage potential side effects.
Fertility: Abiraterone Acetate may affect male fertility. Patients should use effective contraception during and for some time after discontinuation of treatment.
Pregnancy and Breastfeeding: This medication 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 Abiraterone Acetate may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Packaging Size | 10 CAPSULES IN 1 STRIP |
Form | Tablet |
Composition | Lenalidomide (5mg,10mg,25mg) |
Manufacturer | Cipla Ltd |
Prescription/Non prescription | Prescription |
Treatment | Multiple myeloma Lepra reaction |
Also Gives | PCD Pharma Franchise |
Strength | 5MG,10MG & 25MG |
Brand | LENMID CAPSULE |
Shelf life | more than 2 years |
Deals in | PCD Pharma |
Country of Origin | Made in India |
Uses: Lenalidomide, often sold under the brand name Lenmid, is a medication used for various medical conditions, with its primary use in the treatment of certain cancers. Common uses include:
Multiple Myeloma: Lenalidomide is commonly used in combination with other medications for the treatment of multiple myeloma, a type of cancer affecting plasma cells in the bone marrow.
Myelodysplastic Syndromes (MDS): It may be prescribed for certain cases of myelodysplastic syndromes, a group of disorders characterized by abnormal blood cell development.
Mantle Cell Lymphoma: Lenalidomide is indicated for the treatment of mantle cell lymphoma in patients who have received at least one prior therapy.
Potential Side Effects: Lenalidomide may cause various side effects. Common side effects include:
Hematological Effects:
Gastrointestinal Issues:
Fatigue: Tiredness or weakness.
Rash: Skin reactions such as rash.
Peripheral Edema: Swelling of the extremities.
Dizziness: Feeling lightheaded or dizzy.
Musculoskeletal Issues:
Infections: Increased susceptibility to infections.
Cardiac Issues: Lenalidomide may affect the heart, including arrhythmias.
Hepatotoxicity: Changes in liver function.
Precautions:
Pregnancy Prevention: Lenalidomide poses a significant risk of birth defects. Women of childbearing age must use effective contraception during treatment and for a specific period after discontinuation.
Hematological Monitoring: Regular monitoring of blood counts, especially neutrophil, platelet, and red blood cell levels.
Thromboembolism Risk: Lenalidomide may increase the risk of blood clots, and preventive measures may be taken.
Dizziness: Patients should avoid activities that require mental alertness while experiencing dizziness.
Renal Function Monitoring: Regular monitoring of kidney function is recommended.
Infection Prevention: Patients should be vigilant in preventing infections, and healthcare providers may recommend prophylactic antibiotics.
Interactions with Other Medications: Inform the healthcare provider about all medications, including prescription and over-the-counter drugs, as well as supplements, being taken.
Liver Function Monitoring: Regular monitoring of liver function is recommended.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Storage | Cold chain |
Dosage Form | 10000IU |
Packaging | VIAL |
Brand | CELGINASE 10000 INJECTION |
Manufacturer | Celon Laboratories Ltd |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | Asparaginase (10000IU) |
Packaging Size | VIAL |
Deals in | PCD Pharma |
Country of Origin | Made in India |
Uses: Celginase Injection contains Asparaginase as its active ingredient. Asparaginase is an enzyme that is used in the treatment of certain types of cancer, particularly acute lymphoblastic leukemia (ALL) in both children and adults.
Potential Side Effects: Asparaginase, like many medications, may cause side effects. Common side effects may include:
Hypersensitivity Reactions: Allergic reactions, including rash, itching, swelling, and, rarely, severe allergic reactions (anaphylaxis).
Pancreatitis: Inflammation of the pancreas, which may present with abdominal pain, nausea, and vomiting.
Liver Dysfunction: Changes in liver function, including elevated liver enzymes.
Coagulation Disorders: Asparaginase may affect blood clotting, leading to bleeding or clotting disorders.
Gastrointestinal Issues: Nausea, vomiting, diarrhea.
Fatigue: Tiredness or weakness.
Allergic Skin Reactions: Skin reactions such as rash.
Fever: Elevated body temperature.
Metabolic Abnormalities: Changes in blood glucose levels and other metabolic abnormalities.
Precautions:
Hypersensitivity Reactions: Due to the risk of hypersensitivity reactions, Celginase Injection is often administered under the supervision of healthcare professionals who are prepared to manage allergic reactions.
Pancreatitis Risk: Patients should be monitored for signs and symptoms of pancreatitis, and treatment may need to be adjusted if pancreatitis occurs.
Liver Function Monitoring: Regular monitoring of liver function is important during treatment.
Blood Clotting Monitoring: Asparaginase may affect blood clotting, leading to bleeding or clotting disorders. Regular monitoring is necessary.
Pre-existing Conditions: Caution is advised in patients with pre-existing liver or pancreas conditions.
Pregnancy and Breastfeeding: The safety of Celginase Injection during pregnancy is not well-established. Adequate contraception is recommended during treatment, and breastfeeding should be avoided.
Immune System Monitoring: Regular monitoring of immune function may be recommended.
Interactions with Other Medications: Inform the healthcare provider about all medications, including prescription and over-the-counter drugs, as well as supplements, being taken.
Bone Marrow Suppression: Celginase may suppress bone marrow function, and caution is needed in patients with pre-existing bone marrow disorders.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Dosage Form | 100mg |
Packaging | vial |
Brand | CADILA |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | Etoposide 100mg |
Deals in | PCD Pharma |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Strength | 300 mg |
Pack Size | 5 ml |
Pack Type | Vial |
Storage | Store below 30 DegreeC |
Dosage Form | Liquid |
Packaging | Vial |
Brand | Nanoxel |
Manufacturer | Fresenius Kabi India Pvt Ltd |
Country of Origin | Made in India |
Uses:
Potential Side Effects: Chemotherapy medications like Paclitaxel can cause a range of side effects. The severity and occurrence of these side effects can vary from person to person. Common side effects may include:
Hematological Effects:
Gastrointestinal Effects:
Neurological Effects:
Hypersensitivity Reactions:
Musculoskeletal Effects:
Cardiovascular Effects:
Respiratory Effects:
Dermatological Effects:
Precautions:
Administered by Healthcare Professionals: Nanoxel Injection should be administered by qualified healthcare professionals experienced in the use of chemotherapy agents.
Hypersensitivity: Individuals with a known hypersensitivity to Paclitaxel or any of the components of the formulation should not receive Nanoxel Injection.
Blood Cell Counts: Regular monitoring of blood cell counts is essential during treatment to assess for bone marrow suppression.
Liver and Kidney Function: Monitoring of liver and kidney function is important, and dosage adjustments may be necessary in individuals with impaired liver or kidney function.
Peripheral Neuropathy: Monitoring for symptoms of peripheral neuropathy is crucial, and dosage adjustments may be considered if neuropathy becomes severe.
Pregnancy and Breastfeeding: Paclitaxel may harm the fetus, and its use during pregnancy is generally avoided. Adequate contraception is recommended during treatment, and breastfeeding should be avoided.
Cardiovascular Conditions: Caution is advised in individuals with pre-existing cardiovascular conditions, and monitoring of heart function is recommended.
Infections: Chemotherapy can suppress the immune system, increasing the risk of infections. Close monitoring for signs of infection is important.
Dermatological Care: Proper care of the skin and hair is recommended, as chemotherapy can cause hair loss and skin reactions.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Piece |
Strength | 100 mg |
Pack Size | 43.4 ml |
Pack Type | Vial |
Storage | Store below 30 DegreeC |
Dosage Form | Liquid |
Packaging | Vial |
Brand | Celtax |
Manufacturer | Celon Laboratories Ltd |
Country of Origin | Made in India |
Uses:
Potential Side Effects: Chemotherapy medications like Paclitaxel can cause a range of side effects. The severity and occurrence of these side effects can vary from person to person. Common side effects may include:
Hematological Effects:
Gastrointestinal Effects:
Neurological Effects:
Hypersensitivity Reactions:
Musculoskeletal Effects:
Cardiovascular Effects:
Respiratory Effects:
Dermatological Effects:
Precautions:
Administered by Healthcare Professionals: Celtax Injection should be administered by qualified healthcare professionals experienced in the use of chemotherapy agents.
Hypersensitivity: Individuals with a known hypersensitivity to Paclitaxel or any of the components of the formulation should not receive Celtax Injection.
Blood Cell Counts: Regular monitoring of blood cell counts is essential during treatment to assess for bone marrow suppression.
Liver and Kidney Function: Monitoring of liver and kidney function is important, and dosage adjustments may be necessary in individuals with impaired liver or kidney function.
Peripheral Neuropathy: Monitoring for symptoms of peripheral neuropathy is crucial, and dosage adjustments may be considered if neuropathy becomes severe.
Pregnancy and Breastfeeding: Paclitaxel may harm the fetus, and its use during pregnancy is generally avoided. Adequate contraception is recommended during treatment, and breastfeeding should be avoided.
Cardiovascular Conditions: Caution is advised in individuals with pre-existing cardiovascular conditions, and monitoring of heart function is recommended.
Infections: Chemotherapy can suppress the immune system, increasing the risk of infections. Close monitoring for signs of infection is important.
Dermatological Care: Proper care of the skin and hair is recommended, as chemotherapy can cause hair loss and skin reactions.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Piece |
Storage | 3750 IU |
Dosage Form | Injection |
Packaging | Box |
Brand | Peg-Ginase |
Manufacturer | Celon Labs |
Usage /Application | Personal. Hospital. Clinical |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | PEG L-ASPARAGINASE. |
Form | Injection |
Uses:
Potential Side Effects: Peg-Ginase, like other medications, can cause side effects. Common side effects may include:
Allergic Reactions: Hypersensitivity reactions, including rash, itching, swelling, and anaphylaxis, can occur. Asparaginase is known to have a higher risk of allergic reactions.
Pancreatitis: Inflammation of the pancreas (pancreatitis) can occur. This may present with abdominal pain, nausea, and vomiting.
Abnormal Liver Function: Changes in liver function, including elevated liver enzymes, may occur.
Blood Clotting Disorders: Peg-Ginase may affect blood clotting, leading to bleeding or clotting disorders.
Gastrointestinal Issues: Nausea, vomiting, and diarrhea may occur.
Fatigue: Tiredness or weakness may be experienced.
Changes in Blood Cell Counts: Peg-Ginase can affect the production of blood cells, leading to anemia, neutropenia, or thrombocytopenia.
Metabolic Abnormalities: Changes in blood glucose levels and other metabolic abnormalities may occur.
Precautions:
Allergic Reactions: Due to the risk of hypersensitivity reactions, Peg-Ginase is often administered under the supervision of healthcare professionals who are prepared to manage allergic reactions.
Pancreatitis Risk: Patients should be monitored for signs and symptoms of pancreatitis, and treatment may need to be adjusted if pancreatitis occurs.
Liver Function Monitoring: Regular monitoring of liver function is important during treatment.
Blood Clotting Monitoring: Peg-Ginase may affect blood clotting, and patients should be monitored for signs of bleeding or clotting disorders.
Pre-existing Conditions: Caution is advised in patients with pre-existing liver or pancreas conditions.
Pregnancy and Breastfeeding: The use of Peg-Ginase during pregnancy may pose risks to the fetus. Adequate contraception is recommended during treatment, and breastfeeding should be avoided.
Interactions with Other Medications: Inform the healthcare provider about all medications, including prescription and over-the-counter drugs, as well as supplements, being taken.
Immune System Monitoring: Regular monitoring of immune function may be recommended.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Packaging Size | 120 TABLET IN 1BOTTLE |
Form | Tablet |
Composition | Abiraterone Acetate (250mg) |
Manufacturer | CELON LABORATARIES |
Prescription/Non prescription | Prescription |
Treatment | Prostate cancer |
Also Gives | PCD Pharma Franchise |
Brand | celbira 250mg tablet |
Shelf life | more than 2 years |
Country of Origin | Made in India |
Uses:
Precautions:
Liver Function: Regular monitoring of liver function is essential during treatment, as elevated liver enzymes may occur.
Cardiovascular Effects: Blood pressure should be monitored regularly, as Abiraterone Acetate can cause hypertension (high blood pressure).
Mineralocorticoid Excess: Monitoring for signs of mineralocorticoid excess (e.g., low potassium levels, fluid retention) is important.
Adrenal Insufficiency: Abiraterone Acetate can lead to adrenal insufficiency, and patients may need to take low-dose glucocorticoids in conjunction with the medication.
Fertility: It may affect male fertility, and patients are advised to use effective contraception during and after treatment.
Pregnancy and Breastfeeding: The medication is not indicated for use in women, especially in pregnant or breastfeeding women, due to potential harm to the fetus or nursing infant.
Side Effects: Common side effects may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Strength | 10 mg |
Prescription/Non prescription | Prescription |
Packaging Size | 10 Capsules |
Brand | Celomide |
Manfacturer | Celon Laboratories Ltd |
Composition | Lenalidomide (10mg) |
Deals in | Third Party Manufacturing |
Shelf Life | More than 2 years |
Country of Origin | Made in India |
Uses: Celomide Capsule contains Lenalidomide as its active ingredient. Lenalidomide is a medication used for various medical conditions, with its primary use in the treatment of certain cancers. Common uses include:
Multiple Myeloma: Lenalidomide is commonly used in combination with other medications for the treatment of multiple myeloma, a type of cancer affecting plasma cells in the bone marrow.
Myelodysplastic Syndromes (MDS): It may be prescribed for certain cases of myelodysplastic syndromes, a group of disorders characterized by abnormal blood cell development.
Mantle Cell Lymphoma: Lenalidomide is indicated for the treatment of mantle cell lymphoma in patients who have received at least one prior therapy.
Potential Side Effects: Lenalidomide may cause various side effects. Common side effects include:
Hematological Effects:
Gastrointestinal Issues:
Fatigue: Tiredness or weakness.
Rash: Skin reactions such as rash.
Peripheral Edema: Swelling of the extremities.
Dizziness: Feeling lightheaded or dizzy.
Musculoskeletal Issues:
Infections: Increased susceptibility to infections.
Cardiac Issues: Lenalidomide may affect the heart, including arrhythmias.
Hepatotoxicity: Changes in liver function.
Precautions:
Pregnancy Prevention: Lenalidomide poses a significant risk of birth defects. Women of childbearing age must use effective contraception during treatment and for a specific period after discontinuation.
Hematological Monitoring: Regular monitoring of blood counts, especially neutrophil, platelet, and red blood cell levels.
Thromboembolism Risk: Lenalidomide may increase the risk of blood clots, and preventive measures may be taken.
Dizziness: Patients should avoid activities that require mental alertness while experiencing dizziness.
Renal Function Monitoring: Regular monitoring of kidney function is recommended.
Infection Prevention: Patients should be vigilant in preventing infections, and healthcare providers may recommend prophylactic antibiotics.
Interactions with Other Medications: Inform the healthcare provider about all medications, including prescription and over-the-counter drugs, as well as supplements, being taken.
Liver Function Monitoring: Regular monitoring of liver function is recommended.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Packaging Size | 0.5 ml |
Form | Injection |
Composition | Darbepoetin alfa (100mcg) |
Manufacturer | Dr. Reddy's |
Dose | 100mcg |
Brand | Cresp |
Prescription/Non prescription | Prescription |
Treatment | For SC single use |
Strength | 100mcg |
Packaging Type | Box, Bottle |
Shelf life | more than 2 years |
Deals in | PCD Pharma |
Hypersensitivity: Individuals with a known hypersensitivity or allergic reaction to darbepoetin alfa or any component of the formulation should avoid its use.
Blood Pressure Monitoring: Cresp Injection may lead to an increase in blood pressure. Regular monitoring of blood pressure is crucial, and adjustments to antihypertensive medications may be necessary.
Thrombotic Events: There is an increased risk of thrombotic events (blood clots). Caution is advised in patients with a history of thrombotic events.
Pure Red Cell Aplasia (PRCA): Cases of pure red cell aplasia, though rare, have been reported. Monitoring for this condition is important.
Hypertension: An increase in blood pressure may occur.
Thromboembolic Events: There may be an increased risk of blood clots, leading to conditions such as deep vein thrombosis or pulmonary embolism.
Pure Red Cell Aplasia: Though uncommon, it is a serious condition where the body stops producing red blood cells.
Hypersensitivity Reactions: Allergic reactions, including rash, itching, and swelling, may occur.
Injection Site Reactions: Pain, redness, or swelling at the injection site may occur.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Strength | 2 mg |
Packaging Type | Box |
Brand | Dexona |
Manufacturer | Zydus |
Prescription/Non prescription | Prescription |
Shelf Life | 24 Months |
Also Gives | PCD Pharma Franchise |
Usage/Application | Pain relief |
Brand name | Dexamethasone Tablets |
Uses:
2. Precautions:
3. Side Effects:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box of 100 Pieces |
Strength | 40 mg |
Composition | Enzalutamide (40mg) |
shelf life | more than 2 years |
usage | hospital, clinical, |
Brand | Glenza Enzalutamide 40 Mg Capsules |
Packaging size | 28 TAB |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Strength | 140 mg |
composition | Ibrutinib (140mg) |
Packaging size | 140 mg |
Shelf life | More than 2 years |
Manufacturer | Laurus Labs Limited |
Brand | Natco Pharma Ltd |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Strength | 150 mg |
Shelf life | More than 2 years |
Composition | Ceritinib (150mg) |
Manufacturer | Novartis India Ltd |
Brand | Novartis |
packaging type | capsules |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Strength | 200 mg |
Composition | Ribociclib (200mg) |
Brand | Novaritis |
Manufacturer | Novartis India Ltd |
Usage | Hospital, Clinical, Personal |
Shelf life | More than 2 years |
Additional Information: