Bull Pharmachem
Bull Pharmachem
Kalbadevi, Mumbai, Maharashtra
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Anticancer Capsule

Providing you the best range of lenangio (lenalidomide 5mg, 10mg , 25mg), pomalid (pomalidomide 1mg,2mg,4mg), syprine (trientine hydrochloride 250mg) and pomahope (pomalidomide 1mg, 2mg, 4mg ) with effective & timely delivery.

Lenangio (Lenalidomide 5mg, 10mg , 25mg)

Lenangio (Lenalidomide 5mg, 10mg , 25mg)
  • Lenangio (Lenalidomide 5mg, 10mg , 25mg)
  • Lenangio (Lenalidomide 5mg, 10mg , 25mg)
  • Lenangio (Lenalidomide 5mg, 10mg , 25mg)
  • Lenangio (Lenalidomide 5mg, 10mg , 25mg)
  • Lenangio (Lenalidomide 5mg, 10mg , 25mg)
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Product Details:

Packaging Size10 Capsule
BrandLenangio
ManufacturerDr Reddy's
Composition5mg ,10mg , 25mg
TreatmentBlood Cancer
Prescription/Non prescriptionPrescription
Deals inThird Party Manufacturing
Shelf Life2 Years
FormCapsule

Lenangio (Lenalidomide 5mg, 10mg , 25mg)is a prescription medicine, used to treat adults with multiple myeloma (MM) in combination with the medicine dexamethasone, or as maintenance treatment after autologous hematopoietic stem cell transplantation (a type of stem cell transplant that uses your own stem cells). Lenangio should not be used to treat people who have chronic lymphocytic leukemia (CLL) unless they are participants in a controlled clinical trial. It is not known if Lenangio is safe and effective in children.What is the most important information I should know about Lenangio ?Before you begin takingLenangio , you must read and agree to all of the instructions in the Lenangio REMS program. Before prescribingLenangio , your healthcare provider will explain the Lenangio REMS program to you and have you sign the Patient-Physician Agreement Form.
Lenangio may cause serious side effects, including:
Possible birth defects (deformed babies) or death of an unborn baby. Females who are pregnant or who plan to become pregnant must not takeLenangio .
Lenangio is similar to the medicine thalidomide which is known to cause severe life-threatening birth defects. Lenangio has not been tested in pregnant females. Lenangio has harmed unborn animals in animal testing.Females must not get pregnant:For at least 4 weeks before startingLenangio While takingLenangio During any breaks (interruptions) in your treatment withLenangio For at least 4 weeks after stoppingLenangio Females who can become pregnant:
Must have pregnancy tests weekly for 4 weeks, then every 4 weeks if your menstrual cycle is regular, or every 2 weeks if your menstrual cycle is irregular.If you miss your period or have unusual bleeding, you will need to have a pregnancy test and receive counseling.Must agree to use 2 different forms of effective birth control at the same time, for at least 4 weeks before, while taking, during any breaks (interruptions) in your treatment, and for at least 4 weeks after stoppingLenangio .Talk with your healthcare provider to find out about options for effective forms of birth control that you may use to prevent pregnancy before, during, and after treatment withLenangio .If you had unprotected sex or if you think your birth control has failed, stop taking Lenangio immediately and call your healthcare provider right away.If you become pregnant while takingLenangio , stop taking it right away and call your healthcare provider. If your healthcare provider is not available, you can call Celgene Customer Care Center at 1-888-423-5436. Healthcare providers and patients should report all cases of pregnancy to:
FDA MedWatch at 1-800-FDA-1088, andCelgene Corporation, a Bristol Myers Squibb company, at 1-888-423-5436.There is a pregnancy exposure registry that monitors the outcomes of females who take Lenangio during pregnancy, or if their male partner takes Lenangio and they are exposed during pregnancy. You can enroll in this registry by calling Celgene Corporation, a Bristol Myers Squibb company, at the phone number listed above.
Lenangio can pass into human semen:
Males, including those who have had a vasectomy, must always use a latex or synthetic condom during any sexual contact with a pregnant female or a female that can become pregnant while takingLenangio , during any breaks (interruptions) in your treatment withLenangio , and for up to 4 weeks after stoppingLenangio .Do not have unprotected sexual contact with a female who is or could become pregnant. Tell your healthcare provider if you do have unprotected sexual contact with a female who is or could become pregnant.Do not donate sperm while takingLenangio , during any breaks (interruptions) in your treatment, and for 4 weeks after stoppingLenangio . If a female becomes pregnant with your sperm, the baby may be exposed to Lenangio and may be born with birth defects.

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  • Delivery Time: Immediate
  • Packaging Details: Trademark shown are property of their respective owners and we do not lay any claim on them. Parallel trade if any is conducted under WTO¿¿¿s TRIPS agreement to which India is a Signatory. On this page we have made an ¿¿¿Honest Reference¿¿¿ of this product under the Trademark Act of India and applicable rules in the Territory of India. We do not claim ownership of displayed Trade mark.
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Pomalid (Pomalidomide 1mg,2mg,4mg)

Pomalid (Pomalidomide 1mg,2mg,4mg)
  • Pomalid (Pomalidomide 1mg,2mg,4mg)
  • Pomalid (Pomalidomide 1mg,2mg,4mg)
  • Pomalid (Pomalidomide 1mg,2mg,4mg)
  • Pomalid (Pomalidomide 1mg,2mg,4mg)
  • Pomalid (Pomalidomide 1mg,2mg,4mg)
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Product Details:

Minimum Order Quantity1 Box
BrandNatco
TreatmentBlood Cancer
Country of OriginMade in India
Pack Size21 Capsule
Dosage FormCapsule
Storage20 Degree to 25 DegreeC

Pomalid (Pomalidomide 1mg,2mg,4mg) is a prescription medicine used to treat adults with:
Multiple myeloma. Pomalid is taken along with the medicine dexamethasone, in people who:have received at least 2 prior medicines to treat multiple myeloma, including a type of medicine known as a proteasome inhibitor and lenalidomide, andtheir disease has become worse during treatment or within 60 days of finishing the last treatmentAIDS-related Kaposi sarcoma (KS). Pomalid is taken when highly active antiretroviral therapy (HAART) has not worked well enough or stopped working (failed)KS who do not have HIV infection (HIV negative).It is not known if Pomalid is safe and effective in children.
Who should not take Pomalid?
Do not take Pomalid if you:
are pregnant, plan to become pregnant, or become pregnant during treatment with Pomalid. See “What is the most important information I should know about Pomalid?”are allergic to pomalidomide or any of the ingredients in Pomalid. See the end of this Medication Guide for a complete list of ingredients in Pomalid.What are the possible side effects of Pomalid?
Pomalid can cause serious side effects, including:
Low white blood cells (neutropenia), low platelets (thrombocytopenia), and low red blood cells (anemia) arecommon with Pomalid, but can also be serious. You may need a blood transfusion or certain medicines if your blood counts drop too low. Your blood counts should be checked weekly for the first 8 weeks of treatment and monthly after that.Severe liver problems, including liver failure and death. Your healthcare provider should do blood tests to check your liver function during your treatment with Pomalid. Tell your healthcare provider right away if you develop any of the following symptoms of liver problems:Yellowing of your skin or the white part of your eyes (jaundice)Dark or brown (tea-colored) urinePain on the upper right side of your stomach area (abdomen)Bleeding or bruising more easily than normalFeeling very tiredSevere allergic reactions and severe skin reactions can happen with Pomalid and may cause death.Call your healthcare provider if you develop any of the following signs or symptoms during treatment with Pomalid:
a red, itchy, skin rashpeeling of your skin or blisterssevere itchingfeverGet emergency medical help right away if you develop any of the following signs or symptoms during treatment with Pomalid:
swelling of your lips, mouth, tongue, or throattrouble breathing or swallowingraised red areas on your skin (hives)a very fast heartbeatyou feel dizzy or faintDizziness and confusion. See “What should I avoid while taking Pomalid?Nerve damage. Stop taking Pomalid and call your healthcare provider if you develop symptoms of nerve damage including: numbness, tingling, pain, burning sensation in your hands, legs, or feet.Risk of new cancers (malignancies). New cancers, including certain blood cancers (acute myelogenous leukemia or AML) have been seen in people who received Pomalid. Talk with your healthcare provider about your risk of developing new cancers if you take Pomalid.Tumor lysis syndrome (TLS). TLS is caused by the fast breakdown of cancer cells. TLS can cause kidney failure and the need for dialysis treatment, abnormal heart rhythm, seizure, and sometimes death. Your healthcare provider may do blood tests to check you for TLS.Your healthcare provider may tell you to stop taking Pomalid if you develop certain serious side effects during treatment.
The most common side effects of Pomalid in people with Multiple Myeloma include:
tiredness and weaknessconstipationnauseadiarrheashortness of breathupper respiratory tract infectionback painfeverThe most common side effects of Pomalid in people with KS include:
tirednessdiarrheaabnormal kidney function testsdecreased phosphate and calcium in the bloodrash. See “Severe allergic reactions and severe skin reactions” above.
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  • Production Capacity: NA
  • Delivery Time: Immediate
  • Packaging Details: Trademark shown are property of their respective owners and we do not lay any claim on them. Parallel trade if any is conducted under WTO¿¿¿s TRIPS agreement to Trademark shown are property of their respective owners and we do not lay any claim on them. Parallel trade if any is conducted under WTO¿¿¿s TRIPS agreement to which India is a Signatory. On this page we have made an ¿¿¿Honest Reference¿¿¿ of this product under the Trademark Act of India and applicable rules in the Territory of India. We do not claim ownership of displayed Trade mark.
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Syprine (Trientine Hydrochloride 250mg)

Syprine (Trientine Hydrochloride 250mg)
  • Syprine (Trientine Hydrochloride 250mg)
  • Syprine (Trientine Hydrochloride 250mg)
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Product Details:

ManufacturerValeant
Prescription/Non prescriptionPrescription
Packaging Size100 Capsule
BrandSYPRINE
Strength250mg
Pack typeBottle
Storage25 Degree C (77 Degree F)
Minimum Order Quantity100 Capsule
DISCLAIMERTrademark shown are property of their respective owners and we do not lay any claim on them. Parall
TreatmentWilson's Disease

SYPRINE (Trientine Hydrochloride 250mg) is used to treat Wilson''s disease in patients who cannot take the medication known as penicillamine. Wilson''s disease is a condition where the body stores too much copper. SYPRINE is not recommended to treat cystinuria (a condition where a protein known as cystine is excreted into the urine), rheumatoid arthritis, or a disease affecting the bile ducts in the liver known as biliary cirrhosis. IMPORTANT SAFETY INFORMATION Do not take SYPRINE if you are allergic to it or any parts of the formulation. You should remain under regular medical supervision the entire time you are taking SYPRINE. Your doctor should regularly check to see if you have iron deficiency anemia. This is particularly important for women. Take SYPRINE® on an empty stomach, at least one hour before a meal or two hours after a meal and at least one hour apart from any other drug, food, or milk. The capsules should be swallowed whole with water and should not be opened or chewed. For the first month of treatment, take your temperature every night, and report any symptom such as fever or skin rash to your doctor. Tell your doctor if you are pregnant, plan to become pregnant, or are nursing. The following adverse reactions have been reported from a clinical study: iron deficiency and a condition affecting the immune system known as systemic lupus erythematosus. In addition, the following adverse reactions have been reported in marketed use: abnormal or uncontrolled muscle contractions, muscle spasm and an immune disease affecting muscles known as myasthenia gravis. Do not take mineral supplements because they may block the absorption of SYPRINE.
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Pomahope (Pomalidomide 1mg, 2mg, 4mg )

Pomahope (Pomalidomide 1mg, 2mg, 4mg )
  • Pomahope (Pomalidomide 1mg, 2mg, 4mg )
  • Pomahope (Pomalidomide 1mg, 2mg, 4mg )
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Approx. Price: Rs 1,000 / BottleGet Latest Price

Product Details:

Minimum Order Quantity1 Bottle
BrandAbbott
TreatmentBlood Cancer
Country of OriginMade in India

Pomahope (Pomalidomide 1mg, 2mg, 4mg )is a prescription medicine used to treat adults with:
Multiple myeloma. Pomahope is taken along with the medicine dexamethasone, in people who:have received at least 2 prior medicines to treat multiple myeloma, including a type of medicine known as a proteasome inhibitor and lenalidomide, andtheir disease has become worse during treatment or within 60 days of finishing the last treatmentAIDS-related Kaposi sarcoma (KS). Pomahope is taken when highly active antiretroviral therapy (HAART) has not worked well enough or stopped working (failed)KS who do not have HIV infection (HIV negative).It is not known if Pomahope is safe and effective in children.
Who should not take Pomahope?
Do not take Pomahope if you:
are pregnant, plan to become pregnant, or become pregnant during treatment with Pomahope. See “What is the most important information I should know about Pomahope?”are allergic to pomalidomide or any of the ingredients in Pomahope. See the end of this Medication Guide for a complete list of ingredients in Pomahope.What are the possible side effects of Pomahope?
Pomahope can cause serious side effects, including:
Low white blood cells (neutropenia), low platelets (thrombocytopenia), and low red blood cells (anemia) arecommon with Pomahope, but can also be serious. You may need a blood transfusion or certain medicines if your blood counts drop too low. Your blood counts should be checked weekly for the first 8 weeks of treatment and monthly after that.Severe liver problems, including liver failure and death. Your healthcare provider should do blood tests to check your liver function during your treatment with Pomahope. Tell your healthcare provider right away if you develop any of the following symptoms of liver problems:Yellowing of your skin or the white part of your eyes (jaundice)Dark or brown (tea-colored) urinePain on the upper right side of your stomach area (abdomen)Bleeding or bruising more easily than normalFeeling very tiredSevere allergic reactions and severe skin reactions can happen with Pomahope and may cause death.Call your healthcare provider if you develop any of the following signs or symptoms during treatment with Pomahope:
a red, itchy, skin rashpeeling of your skin or blisterssevere itchingfeverGet emergency medical help right away if you develop any of the following signs or symptoms during treatment with Pomahope:
swelling of your lips, mouth, tongue, or throattrouble breathing or swallowingraised red areas on your skin (hives)a very fast heartbeatyou feel dizzy or faintDizziness and confusion. See “What should I avoid while taking Pomahope?Nerve damage. Stop taking Pomahope and call your healthcare provider if you develop symptoms of nerve damage including: numbness, tingling, pain, burning sensation in your hands, legs, or feet.Risk of new cancers (malignancies). New cancers, including certain blood cancers (acute myelogenous leukemia or AML) have been seen in people who received Pomahope. Talk with your healthcare provider about your risk of developing new cancers if you take Pomahope.Tumor lysis syndrome (TLS). TLS is caused by the fast breakdown of cancer cells. TLS can cause kidney failure and the need for dialysis treatment, abnormal heart rhythm, seizure, and sometimes death. Your healthcare provider may do blood tests to check you for TLS.Your healthcare provider may tell you to stop taking Pomahope if you develop certain serious side effects during treatment.
The most common side effects of Pomahope in people with Multiple Myeloma include:
tiredness and weaknessconstipationnauseadiarrheashortness of breathupper respiratory tract infectionback painfever.
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Additional Information:

  • Production Capacity: NA
  • Delivery Time: Immediate
  • Packaging Details: Trademark shown are property of their respective owners and we do not lay any claim on them. Parallel trade if any is conducted under WTO¿¿¿s TRIPS agreement to Trademark shown are property of their respective owners and we do not lay any claim on them. Parallel trade if any is conducted under WTO¿¿¿s TRIPS agreement to which India is a Signatory. On this page we have made an ¿¿¿Honest Reference¿¿¿ of this product under the Trademark Act of India and applicable rules in the Territory of India. We do not claim ownership of displayed Trade mark.
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Bull Pharmachem
No. 64C, Dhan Sadan Co Operative Housing Society, 2nd Floor
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