Product Details:
Minimum Order Quantity | 1 Bottle |
Manufacturer | Samarth Life Sciences Pvt. Ltd. |
Strength | 500 mg/1 ml |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Alprostadil |
Brand | Alpostin 500 MCG Injection |
Packaging Size | Bottle |
Deals in | PCD Pharma |
Uses:
Side Effects:
Common side effects of Alprostadil for erectile dysfunction can include:
Precautions:
Prescription: Alpostin Injection is a prescription medication, and its use should be supervised by a healthcare provider who will determine the appropriate dosage and administration technique for each patient.
Priapism: Patients should be educated about the risk of priapism (prolonged erection) and instructed to seek immediate medical attention if an erection lasts longer than four hours.
Injection Technique: Proper injection technique should be taught by a healthcare professional to ensure the safe and effective administration of the medication.
Allergies: Patients with known allergies to Alprostadil or any of the injection components should not use Alpostin Injection.
Underlying Medical Conditions: Alprostadil may not be suitable for individuals with certain medical conditions, so a thorough medical evaluation is essential.
Interaction with Other Medications: Patients should inform their healthcare provider of all medications they are taking, as Alprostadil can interact with some medications.
Partner Safety: It's important to discuss safety measures with a sexual partner, as the medication can transfer to the partner and cause side effects.
Storage: Store Alpostin Injection as directed by the manufacturer and healthcare provider. Keep it out of reach of children.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Dosage Form | 10mg & 40mg |
Packaging | piece |
Brand | MITOMYCIN 10/40 MG INJECTION |
Manufacturer | Biochem Pharmaceutical Industries |
Usage /Application | Personal. Hospital. Clinical |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | Mitomycin (10mg)/ (40mg) |
Packaging Size | 1 Vial |
Deals in | PCD Pharma |
Treatment | Pancreatic cancer, Breast cancer, Non-small cell lung cancer & Stomach cancer |
Precautions:
Medical History:
Pregnancy and Breastfeeding:
Blood Cell Counts:
Kidney Function:
Immunizations:
Side Effects: Mitomycin can cause various side effects, and their severity can vary. Common side effects may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Manufacturer | Novartis India Ltd |
Usage/Application | Personal,Clinical,Hospital |
Storage | Store below 30 DegreeC |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Ruxolitinib (15mg) |
Brand | Jakavi 15mg Tablet |
Packaging Size | 14 tablets in 1 strip |
Form | Tablet |
Deals in | PCD Pharma |
Treatment | Polycythemia vera Chronic idiopathic myelofibrosis |
Country of Origin | Made in India |
Uses:
Jakavi 15 mg is prescribed for the treatment of the following conditions:
Myelofibrosis: Jakavi is approved for the treatment of myelofibrosis, a disorder characterized by abnormal bone marrow function, leading to symptoms such as an enlarged spleen, anemia, fatigue, and bone pain. Ruxolitinib can help alleviate these symptoms and improve the overall quality of life for individuals with myelofibrosis.
Polycythemia Vera: In some cases, Jakavi may also be prescribed for the treatment of polycythemia vera, another type of blood disorder characterized by an overproduction of red blood cells. It can help manage the disease and reduce symptoms like itching, headaches, and fatigue.
Precautions:
Prescription Requirement: Jakavi 15 mg is available by prescription and should only be used under the guidance of a healthcare provider experienced in the management of myeloproliferative neoplasms.
Monitoring: Regular monitoring, including blood tests and imaging, may be necessary while taking Jakavi to assess the medication's effectiveness and check for any potential side effects or changes in your condition.
Infections: Jakavi may increase the risk of certain infections. Inform your healthcare provider if you develop any signs of infection, such as fever, chills, or persistent cough.
Liver Function: Jakavi can affect liver function, so your healthcare provider may monitor your liver enzymes during treatment.
Side Effects:
Common side effects of Jakavi 15 mg may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Dose/Strength | 450 mg |
Packaging Size | 45 ml |
Packaging Type | Vial |
Strength | 450mg |
Brand | Kemocarb |
Storage | Store below 30 DegreeC |
Manufactured By | Fresenius Kabi India Pvt Ltd |
Shelf Life | More than 2 years |
Prescription/Non prescription | Prescription |
Composition | Carboplatin (450mg) |
Deals in | Third Party Manufacturing |
Country of Origin | Made in India |
Uses:
Side Effects: As with any chemotherapy medication, Kemocarb (carboplatin) can cause various side effects. It's important to note that not everyone will experience these side effects, and their severity can vary. Common side effects include:
Precautions:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Strength | 6 mg |
Packaging Size | 10 Tablets |
Packaging Type | Strips |
Brand Name | Defcort 6 Mg Tablet |
Manufacturer | Macleods Pharmaceuticals Pvt Ltd |
Dose | 0.9 mg/kg |
Composition | Deflazacort (6mg) |
Shelf Life | More than 2 years |
Storage | Store below 30 DegreeC |
Deals in | Third Party Manufacturing |
Form | Tablets |
Country of Origin | Made in India |
Uses:
Inflammatory Conditions: Defcort (Deflazacort) is used to treat various inflammatory conditions such as arthritis, dermatitis, asthma, and other inflammatory disorders.
Allergic Conditions: It may be prescribed for the management of allergic conditions like allergic rhinitis and asthma.
Autoimmune Disorders: Deflazacort can be used to suppress the immune response in certain autoimmune disorders.
Certain Respiratory Conditions: In some cases, it might be used to manage respiratory conditions with an inflammatory component.
Precautions:
Long-Term Use: Prolonged use of corticosteroids, including deflazacort, may lead to various side effects. The duration of treatment and the dosage should be determined by a healthcare professional, and regular follow-ups are essential.
Immunosuppression: Corticosteroids can suppress the immune system, increasing the risk of infections. It is important to take precautions to avoid exposure to infections and to seek medical attention if signs of infection develop.
Glucose Levels: Deflazacort can affect blood glucose levels, and diabetic patients may need adjustments in their antidiabetic medications. Regular monitoring of blood glucose is advisable.
Osteoporosis: Long-term use of corticosteroids can lead to bone loss and an increased risk of osteoporosis. Adequate calcium and vitamin D intake and bone density monitoring may be recommended.
Gastrointestinal Effects: Deflazacort may cause gastrointestinal side effects such as stomach ulcers. It is often recommended to take the medication with food to minimize these effects.
Psychiatric Effects: Corticosteroids can sometimes cause mood swings, anxiety, and insomnia. Patients with a history of psychiatric disorders should be monitored closely.
Side Effects:
Common side effects of Defcort 6 mg Tablet may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Strip |
Strength | 100mg |
Packaging Size | 1*10 |
Brand | Picasa |
Composition | Posaconazole (100mg) |
Prescription/Non prescription | Prescription |
Manufacturer | Intas |
Also Gives | Third Party Manufacturing |
Prescription Required | Yes |
Form | Tablet |
Shelf life | More than 2 years |
Country of Origin | Made in India |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Storage | 15IU |
Dosage Form | As directed by physician |
Packaging | vial |
Brand | Celon Laboratories Ltd |
Manufacturer | pharmaceutical |
Usage /Application | Personal. Hospital. Clinical |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Bleomycin. |
Packaging Size | Per Box 1 Vial |
Country of Origin | Made in India |
Uses:
Precautions:
Side Effects:
Additional Information:
Product Details:
Packaging Size | Box 1 vial |
Form | Injection |
Composition | Cabazitaxel 60mg |
Manufacturer | Panacea |
Prescription/Non prescription | Prescription |
Also Gives | PCD Pharma Franchise |
Strength | 60mg |
Brand | Panacea |
Shelf life | More than 2 years |
Country of Origin | Made in India |
Product Details:
Minimum Order Quantity | 1 Piece |
Storage | Store below 30 Degree |
Dosage Form | 60mg |
Packaging | vial |
Brand | Kabanat Injection |
Manufacturer | natco |
Usage /Application | Personal. Hospital. Clinical |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Cabazitaxel 60mg/1.5 ml |
Packaging Size | 60 mg / ml . 1.5 ml vial |
Form | Injection |
Deals in | PCD Pharma |
Usage:
Cabazitaxel is primarily used for the treatment of hormone-refractory prostate cancer that has spread to other parts of the body (metastatic prostate cancer). It is generally used in patients who have previously received treatment with docetaxel, another chemotherapy drug.
Precautions:
Side Effects:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Packaging Size | 30 Capsules |
Form | Tablet |
Composition | Lenalidomide 10 mg |
Manufacturer | Aprazer |
Dose | 10mg |
Brand | Lenakast |
Prescription/Non prescription | Prescription |
Treatment | treatment of multiple myeloma and lepra reaction. |
Also Gives | PCD Pharma Franchise |
Strength | 10mg |
Packaging Type | Bottle |
Shelf life | More than 2 years |
Uses: Lenalidomide, the active ingredient in Lenakast Capsules, is used for various medical conditions. The primary use of Lenalidomide is 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 Stripe |
Packaging Size | 30 Tablets per Strip |
Form | Tablet |
Composition | Geftinat 250mg |
Manufacturer | Natco Pharma Ltd |
Dose | 250mg |
Brand | Geftinat |
Prescription/Non prescription | Prescription |
Treatment | Non-small cell lung cancer |
Also Gives | PCD Pharma Franchise |
Strength | 250mg |
Packaging Type | Strip, Bottle |
Country of Origin | Made in India |
Uses: Gefitinib is primarily used for the treatment of:
Precautions:
Side Effects: Common side effects of Gefitinib may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Packaging Size | 120 Tablets |
Form | Tablet |
Composition | Abiraterone Acetate (250mg) |
Manufacturer | Janssen Pharmaceuticals |
Brand | OZytiga |
Prescription/Non prescription | Prescription |
Treatment | Prostate cancer |
Also Gives | PCD Pharma Franchise |
Packaging Type | Bottle |
Shelf life | More than 2 years |
Country of Origin | Made in India |
Zytiga (Abiraterone Acetate) is a medication primarily used in the treatment of advanced prostate cancer. It is often prescribed in combination with other medications. Abiraterone acetate works by inhibiting the production of androgens (male hormones), which are known to fuel the growth of prostate cancer cells.
Precautions:Liver Function: Zytiga can affect liver function, and regular monitoring of liver enzymes is typically recommended during treatment.
Blood Pressure: Abiraterone may lead to an increase in blood pressure. Blood pressure should be monitored regularly, and appropriate measures may be taken to manage elevated blood pressure.
Mineralocorticoid Excess: Abiraterone can cause an increase in mineralocorticoid levels, leading to side effects such as fluid retention and high blood pressure. Corticosteroids are often co-prescribed to counteract these effects.
Pregnancy and Breastfeeding: Zytiga should not be used in women who are pregnant, and it may harm a developing fetus. It is not indicated for use in breastfeeding women.
Adrenal Function: Abiraterone can impact adrenal function, and corticosteroids may be co-administered to maintain adrenal function.
Common side effects of Zytiga may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Packaging Size | 21 Capsules |
Form | capsules |
Composition | Pomalidomide 4 MG |
Manufacturer | Natco Pharma Ltd. |
Prescription/Non prescription | Prescription |
Also Gives | PCD Pharma Franchise |
Strength | 4mg |
Brand | Pomalid |
Packaging Type | box |
Shelf life | More than 2 years |
Country of Origin | Made in India |
Uses:
Potential Side Effects: Pomalidomide, like other medications, may cause side effects. Common side effects may include:
Hematological Effects:
Fatigue: Tiredness or weakness may occur.
Infections: Increased susceptibility to infections.
Nausea and Vomiting: Gastrointestinal symptoms such as nausea and vomiting.
Diarrhea: Some patients may experience diarrhea.
Peripheral Neuropathy: Numbness or tingling in the hands or feet.
Rash: Skin reactions such as rash.
Back Pain: Musculoskeletal symptoms, including back pain.
Fever: Elevated body temperature.
Respiratory Issues: Shortness of breath or cough.
Precautions:
Blood Cell Count Monitoring: Regular monitoring of blood cell counts is essential during treatment.
Infection Prevention: Patients should be vigilant in preventing infections, and healthcare providers may recommend prophylactic antibiotics.
Thromboembolism Risk: Pomalidomide may increase the risk of blood clots, and preventive measures may be taken.
Pregnancy and Contraception: Pomalidomide can cause severe birth defects. It should not be used during pregnancy, and effective contraception should be used by both males and females during treatment.
Liver Function: Monitoring of liver function is recommended.
Renal Function: Patients with impaired renal function may require dose adjustments.
Peripheral Neuropathy: Patients should be monitored for signs of peripheral neuropathy, and dose adjustments may be necessary.
Drug Interactions: Inform the healthcare provider about all medications, including prescription and over-the-counter drugs, as well as supplements, being taken.
Hypersensitivity: Patients with a known hypersensitivity to pomalidomide should not use this medication.
Bone Marrow Suppression: Pomalidomide may suppress bone marrow function, and caution is needed in patients with pre-existing bone marrow disorders.
Respiratory Conditions: Caution is needed in patients with pre-existing respiratory conditions.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Packaging Size | 120 TABLETS |
Form | Tablet |
Composition | Abiraterone Acetate (250mg) |
Manufacturer | Cipla |
Dose | 250mg |
Brand | Xbira |
Usage/Application | Commercial |
Prescription/Non prescription | Prescription |
Treatment | Anti- Cancer |
Strength | 250mg |
Packaging Type | Bottle |
Shelf life | More than 2 years |
Deals in | Third Party Manufacturing |
Uses:
Precautions:
Liver Function: Regular monitoring of liver function is crucial during treatment with Xbira. Elevated liver enzymes may occur, and appropriate action, such as dose adjustment or discontinuation, may be necessary if significant abnormalities are observed.
Cardiovascular Effects: Xbira can cause hypertension (high blood pressure), so blood pressure should be monitored regularly. Managing blood pressure is important during the course of treatment.
Mineralocorticoid Excess: Similar to other medications containing Abiraterone Acetate, Xbira may lead to mineralocorticoid excess, resulting in low potassium levels and high blood pressure. Monitoring for signs of fluid retention and edema is essential.
Adrenal Insufficiency: Abiraterone, the active ingredient in Xbira, can lead to adrenal insufficiency. Patients may need to take low-dose glucocorticoids (such as prednisone or prednisolone) in conjunction with Abiraterone to prevent side effects associated with adrenal insufficiency.
Fertility: Xbira may affect male fertility, and patients should use effective contraception during and for some time after discontinuing the treatment.
Pregnancy and Breastfeeding: Xbira 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 associated with Xbira may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Piece |
Dosage Form | Injection |
Packaging | Box |
Brand | Cytoblastin |
Manufacturer | Cipla Ltd |
Usage /Application | Personal. Hospital. Clinical |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Vinblastine (10mg) |
Packaging Size | 10 ml X 1 Vial |
Form | Injection |
Uses: Vinblastine is used in the treatment of various cancers, including:
Side Effects: Chemotherapy drugs like vinblastine can cause various side effects. Common side effects may include:
Serious side effects can also occur, including:
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, as vinblastine can cause bone marrow suppression.
Liver and Kidney Function: Monitoring liver and kidney function is important, as vinblastine may affect these organs.
Neurotoxicity: Vinblastine can cause peripheral neuropathy (nerve damage), so symptoms such as tingling or numbness in the hands and feet should be reported to the healthcare provider.
Pregnancy and Breastfeeding: Vinblastine can harm the developing fetus, so it should be avoided during pregnancy. Breastfeeding is not recommended during vinblastine treatment.
Infections: Since vinblastine 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 vinblastine are possible.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Manufacturer | Cipla Ltd |
Prescription/Non prescription | Prescription |
Shelf life | more than 2 years |
Composition | Abiraterone Acetate (250mg) |
Brand | Zecyte |
Packaging Size | 1 X 120 |
Form | Tablet |
Deals in | PCD Pharma |
Liver Function: Regular monitoring of liver function is important during treatment with Zecyte. Elevated liver enzymes may occur, and appropriate measures, such as dose adjustment or discontinuation, may be necessary if significant abnormalities are observed.
Cardiovascular Effects: Zecyte can cause hypertension (high blood pressure), so blood pressure should be monitored regularly. Managing blood pressure is crucial during the course of treatment.
Mineralocorticoid Excess: Similar to Zelgor, Zecyte may lead to mineralocorticoid excess, resulting in low potassium levels and high blood pressure. Monitoring for signs of fluid retention and edema is important.
Adrenal Insufficiency: Abiraterone, the active ingredient in Zecyte, can lead to adrenal insufficiency. Therefore, patients may need to take low-dose glucocorticoids (such as prednisone or prednisolone) in conjunction with Abiraterone to prevent side effects associated with adrenal insufficiency.
Fertility: Zecyte may affect male fertility, and patients should use effective contraception during and for some time after discontinuing the treatment.
Pregnancy and Breastfeeding: Zecyte is not indicated for use in women, especially in pregnant or breastfeeding women, due to potential harm to the fetus or nursing infant.
Uses:
Precautions:
Side Effects: Common side effects associated with Zecyte Tablet may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Packaging Size | 28 Tablet |
Composition | Regorafenib |
Manufacturer | BAYER |
Prescription/Non prescription | Prescription |
Strength | 40 mg |
Brand | Resihance |
Shelf life | more than 2 years |
Regorafenib is a medication that belongs to the class of kinase inhibitors and is used for the treatment of certain types of cancer. Specific uses may include:
Colorectal Cancer: Regorafenib is indicated for the treatment of metastatic colorectal cancer that has not responded to other treatments.
Gastrointestinal Stromal Tumors (GIST): It may also be used for the treatment of gastrointestinal stromal tumors that are not responding to other treatments.
Hepatocellular Carcinoma (Liver Cancer): Regorafenib is approved for the treatment of hepatocellular carcinoma (HCC) in patients who have been previously treated with sorafenib.
Blood Pressure Monitoring: Regular monitoring of blood pressure is important during regorafenib treatment.
Liver Function: Liver function should be assessed before starting treatment and regularly during therapy.
Hand-Foot Skin Reaction: This is a common side effect, and measures to manage it should be discussed with the healthcare provider.
Cardiac Function: Cardiac function should be assessed, and any pre-existing cardiac conditions should be managed.
Pregnancy and Breastfeeding: Regorafenib can harm an unborn baby, so it should be avoided during pregnancy. Breastfeeding is not recommended during treatment.
Common side effects of regorafenib may include:
Additional Information:
Product Details:
Packaging Size | 1 Syringe in 1 Box |
Form | Injection |
Composition | Darbepoetin alfa 40mcg |
Manufacturer | Zydus Healthcare Ltd |
Dose | 40MCG |
Brand | Zynesp |
Usage/Application | Commercial |
Prescription/Non prescription | Prescription |
Treatment | Treatment of Anemia due to chronic kidney disease |
Strength | 40mcg |
Product Details:
Minimum Order Quantity | 1 Box |
Manufacturer | Bayer Pharmaceuticals Pvt Ltd. |
Strength | 40mg |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Regorafenib 40 mg |
Brand | Nublexa |
Packaging Size | 28 Tablets |
Form | Tablet |
Deals in | PCD Pharma |
Colorectal Cancer: Regorafenib is used to treat metastatic colorectal cancer that has not responded to other treatments.
Gastrointestinal Stromal Tumors (GIST): It is also used for the treatment of advanced gastrointestinal stromal tumors that have not responded to other treatments.
Hepatocellular Carcinoma (HCC): Regorafenib is approved for the treatment of hepatocellular carcinoma (HCC) in patients who have been previously treated with sorafenib.
Liver Function: Prior to starting regorafenib, healthcare providers usually assess liver function, as the medication can affect the liver. Regular monitoring of liver function during treatment is important.
Hypertension (High Blood Pressure): Regorafenib can cause an increase in blood pressure. Blood pressure should be monitored regularly, and antihypertensive medications may be required.
Cardiac Effects: It may cause cardiac events. Patients with a history of cardiovascular conditions should use regorafenib with caution.
Gastrointestinal Perforations: There is a risk of gastrointestinal perforations, and patients with a history of these events may be at an increased risk.
Wound Healing: Regorafenib may impair wound healing, so precautions should be taken before and after surgical procedures.
Thyroid Dysfunction: Thyroid function should be monitored, as regorafenib can cause hypothyroidism.
Pregnancy and Contraception: Regorafenib can cause fetal harm, and effective contraception should be used during treatment. Pregnant women should avoid its use.
Fatigue: Fatigue is a common side effect of regorafenib.
Hypertension: An increase in blood pressure may occur.
Hand-Foot Skin Reaction: Skin reactions on the palms of the hands and soles of the feet, such as redness, swelling, and pain, may occur.
Diarrhea: Diarrhea is a common side effect and should be managed with your healthcare provider.
Decreased Appetite: Some individuals may experience a decrease in appetite.
Liver Enzyme Elevations: Elevated liver enzymes may occur, requiring regular monitoring.
Voice Changes: Hoarseness or voice changes may occur.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Box |
Strength | 40mg |
Storage | Store below 30 DegreeC |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Enzalutamide (40mg) |
Brand | Obnyx |
Packaging Size | 1*4 Cpasule |
Form | Tablet |
Deals in | Third Party Manufacturing |
Country of Origin | Made in India |
Enzalutamide (Xtandi) Uses:
Precautions:
Pregnancy and Contraception: Enzalutamide may cause harm to a developing fetus, and it is not recommended during pregnancy. Effective contraception is crucial for both men and their female partners during treatment and for a certain period afterward.
Liver Function: Liver function should be monitored during treatment, and caution is needed in patients with pre-existing liver conditions.
Seizures: Enzalutamide has been associated with an increased risk of seizures. Patients with a history of seizures or other predisposing factors should be closely monitored.
Side Effects: Common side effects of enzalutamide may include:
Serious side effects that require medical attention may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Manufacturer | Glenmark Pharmaceuticals Ltd. |
Strength | 250mg, 500mg |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Abiraterone Acetate (500mg) |
Brand | Abirapro |
Packaging Size | 120 Tablets |
Form | Tablet |
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Strength | 0.5 mg |
Prescription/Non prescription | Prescription |
Packaging Size | 1/6 |
Brand | ZYDUS |
Pack Type | Box |
Composition | SIROLIMUS 1 MG |
Dose | 1mg |
Deals in | PCD Pharma |
Shelf Life | More than 2 years |
Form | Tablet |
Country of Origin | Made in India |
Uses:
Precautions:
Side Effects:
Additional Information:
Product Details:
Dose/Strength | 300 mcg |
Manufacturer | WESTMONT |
Prescription/Non prescription | Prescription |
Composition | DEXAMETHASONE |
Packaging Size | 100 TABLETS IN BOX |
Strength | 500mg |
Deals in | PCD Pharma |
Dosage Form | 500mg |
Dacilon is a prescription medicine that is available as a Injection. It is typically used for the treatment of Testicular Cancer, Wilms Tumor. The alternative uses of Dacilon have also been explained below.
The right dosage of Dacilon depends on the age, gender, and medical history of the patient. Dosage also depends on the route of administration and your chief complaint for which the drug is prescribed. Refer to the dosage section for a detailed discussion.
The most common side effects of Dacilon are Nausea or vomiting, Diarrhoea, Hair Loss. While these are the most often observed Dacilon side effects, there are can be others also. These have been listed below. Usually, these side effects of Dacilon go away soon, and do not persist beyond the duration of the treatment. If, however, they worsen or do not go away, please speak with your physician.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Dosage | 2ml |
Dose | 2ml |
Composition | Methotrexate (2.5mg) |
Brand | Imutrex |
Packaging Size | 2 ml X 1 Vial |
Form | Injection |
Deals in | PCD Pharma |
Uses:
Cancer Treatment: Methotrexate is used in chemotherapy for certain types of cancer, including leukemia and lymphoma.
Rheumatoid Arthritis: It is a disease-modifying antirheumatic drug (DMARD) used to manage rheumatoid arthritis by reducing inflammation and slowing disease progression.
Psoriasis: Methotrexate 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. Common side effects may include:
Serious side effects can occur and may include serious infections, liver toxicity, lung problems, kidney problems, and gastrointestinal ulcers or bleeding.
Precautions:
Pregnancy: Methotrexate is contraindicated during pregnancy due to its potential to cause harm to the developing fetus. Adequate contraception is essential for individuals of childbearing potential.
Breastfeeding: Methotrexate is not recommended during breastfeeding.
Liver and Kidney Function: Regular monitoring of liver and kidney function is important during methotrexate treatment.
Infections: Methotrexate can increase the risk of infections. Inform your healthcare provider if you experience signs of infection, such as fever or persistent sore throat.
Alcohol: Limit or avoid alcohol consumption during methotrexate treatment, as alcohol can enhance the risk of liver toxicity.
Folic Acid Supplementation: Some patients may be prescribed folic acid supplements to mitigate certain side effects of methotrexate.
Other Medications: Inform your healthcare provider about all medications, including prescription and over-the-counter drugs, as interactions with methotrexate are possible.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Vial |
Dose | 1gm & 200mg |
Manufacturer | Dr. Reddys |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Packing | Bottle |
Dosage | 1gm & 200mg |
Composition | Gemcitabine |
Brand | CYTOGEM |
Packaging Size | 1gm &200mg |
Form | Injection |
Deals in | PCD Pharma |
Uses:
Pancreatic Cancer: Gemcitabine is commonly used in the treatment of pancreatic cancer, both in the adjuvant and palliative settings.
Non-Small Cell Lung Cancer: It is used as a part of combination therapy for non-small cell lung cancer.
Breast Cancer: Gemcitabine may be used in combination with other drugs for the treatment of breast cancer.
Bladder Cancer: It is indicated for the treatment of advanced bladder cancer.
Ovarian Cancer: Gemcitabine may be used in the treatment of ovarian cancer.
Other Cancers: Gemcitabine is also used in the treatment of various other cancers, including certain types of sarcoma.
Precautions:
Blood Cell Counts: Gemcitabine can suppress bone marrow function, leading to decreased production of blood cells. Regular blood cell counts are necessary during treatment.
Liver and Kidney Function: Liver and kidney function should be monitored during gemcitabine therapy.
Pregnancy and Breastfeeding: Gemcitabine may cause harm to the fetus, and it is not recommended during pregnancy. Effective contraception is crucial during treatment, and breastfeeding is generally not recommended.
Allergic Reactions: Inform your healthcare provider about any known allergies to gemcitabine or other components of the injection.
Infections: Gemcitabine may increase the risk of infections, and caution is needed, especially in the presence of existing infections.
Side Effects: Common side effects of gemcitabine may include:
Serious side effects may include severe allergic reactions, liver problems, and suppression of bone marrow function.
Additional Information:
Product Details:
Minimum Order Quantity | 1 Bottle |
Manufacturer | Natco Pharma Ltd |
Strength | 2mg, 5mg |
Storage | Store below 30 DegreeC |
Prescription/Non prescription | Prescription |
Shelf life | More than 2 years |
Composition | Melphalan |
Brand | Alphalan |
Packaging Size | 25 Tablets |
Form | Tablet |
Deals in | PCD Pharma |
Country of Origin | Made in India |
Uses:
Multiple Myeloma: Melphalan is often used in the treatment of multiple myeloma, a type of cancer that affects plasma cells in the bone marrow.
Ovarian Cancer: It may also be used in the treatment of ovarian cancer.
Breast Cancer: In some cases, melphalan is used for breast cancer, particularly in combination with other medications.
Conditioning Treatment for Stem Cell Transplant: Melphalan is sometimes used as a conditioning treatment before stem cell transplantation.
Precautions:
Bone Marrow Suppression: Melphalan can suppress bone marrow function, leading to decreased production of blood cells (white blood cells, red blood cells, and platelets). Regular blood tests are often required to monitor blood counts.
Pregnancy and Breastfeeding: Melphalan can harm the developing fetus, and its use is generally not recommended during pregnancy. It may also be excreted in breast milk, so breastfeeding is usually avoided during treatment.
Kidney Function: The dosage of melphalan may need adjustment in patients with impaired kidney function. Kidney function should be monitored during treatment.
Liver Function: Patients with liver problems may require careful monitoring, and dosage adjustments may be needed.
Infections: Melphalan can increase the risk of infections. Patients should take precautions to avoid exposure to infections, and any signs of infection should be reported to the healthcare provider.
Side Effects:
Common side effects of melphalan may include:
Additional Information:
Product Details:
Minimum Order Quantity | 1 Stripe |
Packaging Size | 1 x 10 |
Form | Tablet |
Composition | Imatinib 400 mg |
Manufacturer | Cipla Ltd |
Prescription/Non prescription | Prescription |
Also Gives | PCD Pharma Franchise |
Brand | Imatikast |
Shelf life | more than 2 years |
Country of Origin | Made in India |
Uses:
Chronic Myeloid Leukemia (CML): Imatib is commonly used for the treatment of CML, a type of cancer that affects the blood and bone marrow.
Gastrointestinal Stromal Tumors (GISTs): Imatib is also used in the treatment of GISTs, which are tumors that originate in the gastrointestinal tract.
Side Effects:
Nausea and Vomiting: Gastrointestinal side effects, including nausea and vomiting, are common.
Muscle Cramps: Some individuals may experience muscle cramps.
Edema (Fluid Retention): Edema or fluid retention can occur.
Fatigue: Imatib may cause fatigue or weakness.
Rash: Skin rash or other skin reactions may occur.
Diarrhea: Diarrhea is a possible side effect.
Headache: Some individuals may experience headaches.
Myelosuppression: Imatib can cause myelosuppression, leading to low blood cell counts. Regular blood tests are typically performed to monitor blood cell counts.
Precautions:
Pregnancy and Breastfeeding: Imatib may harm the developing 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.
Liver Function: Monitoring of liver function is important during treatment, as Imatib is metabolized in the liver.
Cardiac Function: Imatib may affect cardiac function, and regular cardiac monitoring may be recommended.
Fluid Retention: Individuals with a history of fluid retention or edema should be closely monitored.
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.
Regular Follow-up: Regular follow-up appointments with your healthcare provider are important for monitoring your response to the medication and managing potential side effects.
Additional Information: