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Isum Pharma


Anti Cancer Medicines

Our product range includes a wide range of eligard depot 45mg injection, xtandi 40mg capsule, velcade 3.5mg injection, velcade 1mg injection, derise 200mcg pre filled syringe and grafeel 300mcg injection.

Eligard Depot 45mg Injection

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Eligard Depot 45mg Injection
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Product Details:
Form of MedicineInjection
Packaging Size10 ml
Dose45 mg
BrandEmcure
UsageClinical, Hospital, Personal
Packaging TypeInjection
CertificationFDA, GMP

Leuprolide overstimulates the body's own production of certain hormones, which causes that production to shut down temporarily. Leuprolide reduces the amount of in men or estrogen in women.

Leuprolide is used in men to treat the symptoms of prostate cancer (but does not treat the canceritself). Leuprolide is used in women to treat symptoms of endometriosis (overgrowth of uterine lining outside of the uterus) or uterine fibroids.

Leuprolide is also used to treat precocious (early-onset) puberty in both male and female children.

Certain brands or strengths of leuprolide are only for men.

Your symptoms may become temporarily worse when you first start using leuprolide. Tell your doctor if this continues for longer than 2 months.

Call your doctor at once if you have a seizure, or unusual changes in mood or behavior.

 

Do not use if you are pregnant.

You should not use this medicine if you are allergic to leuprolide or similar medicines such as buserelin, goserelin, histrelin, nafarelin, or if you have abnormal vaginal bleeding that has not been checked by a doctor.

Certain brands or strengths of leuprolide are used to treat only men and should not be used in women or children. Always check your medicine to make sure you have received the correct brand and strength.

Leuprolide can cause birth defects. Do not use if you are pregnant. Tell your doctor right away if you become pregnant during treatment.

To make sure leuprolide is safe for you, tell your doctor if you have ever had:

  • depression, mental illness or psychosis;

  • seizures or epilepsy;

  • a brain tumor or blood vessel disorder;

  • heart disease, congestive heart failure, long QT syndrome;

  • an electrolyte imbalance (such as low levels of potassium or magnesium in your blood); or

  • risk factors for bone loss (personal or family history of osteoporosis, smoking, alcohol use, taking steroid or seizure medicines long term).

Leuprolide usually causes women to stop ovulating or having menstrual periods. However, you may still be able to get pregnant. Use a barrier form of birth control. Hormonal contraception (birth control pills, injections, implants, skin patches, and vaginal rings) may not be effective enough to prevent pregnancy during your treatment.

Call your doctor if your periods continue while you are being treated with this medicine.

It is not known whether leuprolide passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Follow all directions on your prescription label. Do not use this medicine in larger or smaller amounts or for longer than recommended.

Because different brands or strengths of leuprolide are used to treat different conditions, it is very important that you receive exactly the brand and strength your doctor has prescribed. Always check your medication to make sure you have received the correct brand and type prescribed by your doctor.

Leuprolide is injected under the skin or into a muscle, once every month or once every 3 to 6 months. You may be shown how to use injections at home. Do not give yourself this medicine if you do not understand how to use the injection and properly dispose of used needles and syringes.

Your symptoms may become temporarily worse while your hormones are adjusting to leuprolide. Keep using the medicine as directed, and tell your doctor if your condition is still worse after 2 months of using this medicine.

 

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Xtandi 40mg Capsule

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Xtandi 40mg Capsule
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Product Details:
Packaging Size112 Cap
Packaging TypeBottle
BrandXtandi
Application-
Dose/Strength40mg
Color-
UsageCommercial,Clinical

Enzalutamide is an anti-androgen. It works in the body by preventing the actions of androgens (male hormones).

Enzalutamide is used to treat prostate cancer.

Enzalutamide can increase your risk of having a seizure. To make sure this medicine is safe for you, tell your doctor if you have:

  • epilepsy or other seizure disorder; or

  • a recent head injury, stroke, or brain tumor (in the past 12 months).

Although not for use by women, enzalutamide can cause birth defects if the mother or the father is taking this medicine. Do not use enzalutamide if you are pregnant.

If you are taking enzalutamide and your sexual partner could become pregnant, use a and one other form of birth control to prevent pregnancy during treatment. Keep using these birth control methods for at least 3 months after your treatment ends. Tell your doctor at once if a pregnancy occurs while either parent is being treated with enzalutamide.

 

Although this medicine is not for use by women, it is not known whether enzalutamide passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

You may take enzalutamide with or without food. Take the medicine at the same time each day.

Do not crush, break, or dissolve an enzalutamide capsule. Swallow it whole.

Prostate cancer is sometimes treated with a combination of drugs. Use all medications as directed by your doctor. Do not change your doses or medication schedule without your doctor's advice.

 

Store at room temperature away from moisture and heat. Keep the bottle tightly closed when not in use.

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Velcade 3.5mg Injection

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Velcade 3.5mg Injection
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Product Details:
UsageCommercial, Clinical
Dose3.5 mg
Dose/Strength (ex. 1 mg or 1 ml)3.5mg/ml
Packaging Size1 Vial
Packaging TypeInjection
BrandVelcade

Bortezomib interferes with the growth of some cancer cells and keeps them from spreading in your body.

Bortezomib is used to treat multiple myeloma and mantle cell lymphoma.

You should not be treated with this medicine if you are allergic to bortezomib, mannitol, or boron.

To make sure bortezomib is safe for you, tell your doctor if you have ever had:

  • nerve problems such as numbness, tingling, or burning pain;

  • diabetes;

  • liver disease;

  • kidney disease, or if you are on dialysis;

  • a low level of platelets or white or red blood cells;

  • heart disease, congestive heart failure;

  • lung disease or breathing problems;

  • herpes or shingles (herpes zoster);

  • high or low blood pressure; or

  • if you are dehydrated.

You may need to have a negative pregnancy test before starting this treatment.

Bortezomib can harm an unborn baby. Do not use this medicine if you are pregnant. Use effective birth control to prevent pregnancy, whether you are a man or a woman. The use of this medicine by either parent may cause birth defects.

Keep using birth control for at least 2 months after your last dose of bortezomib. Tell your doctor right away if a pregnancy occurs while either the mother or the father is using this medicine.

This medicine may affect fertility (ability to have children) in both men and women. However, it is important to use birth control to prevent pregnancy because bortezomib may harm the baby if a pregnancy does occur.

 

It is not known whether bortezomib passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine and for at least 2 months after your last dose.

Bortezomib is injected into a vein through an IV.

You will receive this injection in a clinic or hospital setting. A doctor, nurse, or other healthcare provider will give you this injection.

You may be given medication to prevent nausea or vomiting while you are receiving bortezomib.

 

Bortezomib can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

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Velcade 1mg Injection

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Velcade 1mg Injection
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Product Details:
UsageHospital, Clinical
Dose/Strength (ex. 1 mg or 1 ml)1mg/ml
Packaging Size1 Vial
Packaging TypeInjection
BrandVelcade

Bortezomib interferes with the growth of some cancer cells and keeps them from spreading in your body.

Bortezomib is used to treat multiple myeloma and mantle cell lymphoma.

You should not be treated with this medicine if you are allergic to bortezomib, mannitol, or boron.

To make sure bortezomib is safe for you, tell your doctor if you have ever had:

  • nerve problems such as numbness, tingling, or burning pain;

  • diabetes;

  • liver disease;

  • kidney disease, or if you are on dialysis;

  • a low level of platelets or white or red blood cells;

  • heart disease, congestive heart failure;

  • lung disease or breathing problems;

  • herpes or shingles (herpes zoster);

  • high or low blood pressure; or

  • if you are dehydrated.

You may need to have a negative pregnancy test before starting this treatment.

Bortezomib can harm an unborn baby. Do not use this medicine if you are pregnant. Use effective birth control to prevent pregnancy, whether you are a man or a woman. The use of this medicine by either parent may cause birth defects.

Keep using birth control for at least 2 months after your last dose of bortezomib. Tell your doctor right away if a pregnancy occurs while either the mother or the father is using this medicine.

This medicine may affect fertility (ability to have children) in both men and women. However, it is important to use birth control to prevent pregnancy because bortezomib may harm the baby if a pregnancy does occur.

 

It is not known whether bortezomib passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine and for at least 2 months after your last dose.

Bortezomib is injected into a vein through an IV.

You will receive this injection in a clinic or hospital setting. A doctor, nurse, or other healthcare provider will give you this injection.

You may be given medication to prevent nausea or vomiting while you are receiving bortezomib.

 

Bortezomib can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

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Derise 200mcg Pre Filled Syringe

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Derise 200mcg Pre Filled Syringe
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Product Details:
Product TypeFinished Product
Dose/Strength (ex. 1 mg or 1ml)200 mg
Dose200mg
UsageHospital, Clinical
Packaging Size1 vial
Packaging TypeInjection
BrandDerise

Darbepoetin alfa is a man-made form of a protein that helps your body produce red blood cells. This protein may be reduced when you have kidney failure or use certain medications. When fewer red blood cells are produced, you can develop a condition called anemia.

Darbepoetin alfa is used to treat anemia caused by chemotherapy or chronic kidney disease.

This medicine can increase your risk of life-threatening heart or circulation problems, including heart attack or stroke. Darbepoetin alfa may also shorten remission time or survival time in some people with certain types of cancer. Talk with your doctor about the risks and benefits of using darbepoetin alfa.

 

You should not use this medicine if you have uncontrolled high blood pressure, or if you have ever had pure red cell aplasia (PRCA, a type of anemia) caused by using darbepoetin alfa or epoetin alfa (Epogen or Procrit).

You should not use this medicine if you are allergic to darbepoetin alfa or epoetin alfa (Epogen or Procrit), or if you have:

  • untreated or uncontrolled high blood pressure; or

  • if you have ever had pure red cell aplasia (PRCA, a type of anemia) caused by using darbepoetin alfa or epoetin alfa.

Darbepoetin alfa may shorten remission time in some people with head and neck cancer who are also being treated with radiation. Darbepoetin alfa may also shorten survival time in certain people with breast cancer, non-small cell lung cancer, head and neck cancer, cervical cancer, or lymphoid cancer. Talk with your doctor about your individual risk.

To make sure darbepoetin alfa is safe for you, tell your doctor if you have ever had:

  • heart disease, high blood pressure;

  • kidney disease (or if you are on dialysis);

  • a stroke, heart attack, or blood clot;

  • a seizure disorder; or

  • a latex allergy.

It is not known whether this medicine will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant.

 

It is not known whether darbepoetin alfa passes into breast milk or if it could affect the nursing baby. Tell your doctor if you are breast-feeding.

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Grafeel 300mcg Injection

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Grafeel 300mcg Injection
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Product Details:
Dose/Strength (ex. 1 mg or 1ml)300mcg
Packaging TypeInjection
Brandgrafeel
UsageHospital, Clinical
Packaging Size1 Pre filled Syring

Filgrastim is a man-made form of a protein that stimulates the growth of white blood cells in your body. White blood cells help your body fight against infection.

Filgrastim is used to treat neutropenia, a lack of certain white blood cells caused by cancer, bone marrow transplant, receiving chemotherapy, or by other conditions.

You should not use this medicine if you are allergic to filgrastim or pegfilgrastim, or to other medicines that contain the E. coli bacteria.

To make sure filgrastim is safe for you, tell your doctor if you have:

  • a blood cell disorder, such as sickle cell anemia;

  • kidney disease;

  • latex allergy; or

  • if you are receiving chemotherapy or radiation treatment.

It is not known whether filgrastim will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant.

 

It is not known whether filgrastim passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

Filgrastim should not be given within 24 hours before or 24 hours after you receive chemotherapy.

Filgrastim is injected into a vein or under the skin. You may be shown how to use injections at home. Do not give yourself this medicine if you do not understand how to use the injection and properly dispose of needles, IV tubing, and other items used.

Follow all directions on your prescription label. Do not use filgrastim in larger or smaller amounts or for longer than recommended. Filgrastim vials and prefilled syringes do not contain the same concentrations of this medicine. Do not give an injection unless you are trained in properly measuring your dose from either the vial or the prefilled syringe.

Read all patient information, medication guides, and instruction sheets provided to you. Ask your doctor or pharmacist if you have any questions.

Do not shake the medicine. Prepare your dose only when you are ready to give an injection. Do not use if the medicine has changed colors or has particles in it. Call your pharmacist for new medicine.

Your care provider will show you the best places on your body to inject filgrastim. Use a different place each time you give an injection. Do not inject into the same place two times in a row.

 

Each single-use vial or prefilled syringe is for one use only. Throw away after one use, even if there is still some medicine left in it after injecting your dose. Do not use filgrastim if the expiration date on the label has passed. Call your pharmacist for a new prescription.

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Neukine 300mcg Injection

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Neukine 300mcg Injection
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Product Details:
UsageHospital, Clinical
Packaging Size1 ml
Dose300mcg
Product TypeFinished Product
Packaging TypeInjection
BrandNeukine

Filgrastim is a man-made form of a protein that stimulates the growth of white blood cells in your body. White blood cells help your body fight against infection.

Filgrastim is used to treat neutropenia, a lack of certain white blood cells caused by cancer, bone marrow transplant, receiving chemotherapy, or by other conditions.

Filgrastim can cause your spleen to become enlarged and it could rupture (tear). Call your doctor right away if you have sudden or severe pain in your left upper stomach spreading up to your shoulder.

You should not use this medicine if you are allergic to filgrastim or pegfilgrastim, or to other medicines that contain the E. coli bacteria.

To make sure filgrastim is safe for you, tell your doctor if you have:

  • a blood cell disorder, such as sickle cell anemia;

  • kidney disease;

  • latex allergy; or

  • if you are receiving chemotherapy or radiation treatment.

It is not known whether filgrastim will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant.

 

It is not known whether filgrastim passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

Filgrastim should not be given within 24 hours before or 24 hours after you receive chemotherapy.

Filgrastim is injected into a vein or under the skin. You may be shown how to use injections at home. Do not give yourself this medicine if you do not understand how to use the injection and properly dispose of needles, IV tubing, and other items used.

Follow all directions on your prescription label. Do not use filgrastim in larger or smaller amounts or for longer than recommended. Filgrastim vials and prefilled syringes do not contain the same concentrations of this medicine. Do not give an injection unless you are trained in properly measuring your dose from either the vial or the prefilled syringe.

Read all patient information, medication guides, and instruction sheets provided to you. Ask your doctor or pharmacist if you have any questions.

Do not shake the medicine. Prepare your dose only when you are ready to give an injection. Do not use if the medicine has changed colors or has particles in it. Call your pharmacist for new medicine.

 

Your care provider will show you the best places on your body to inject filgrastim. Use a different place each time you give an injection. Do not inject into the same place two times in a row.

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Arsenox 1mg Injection

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Product Details:
Physical StateLiquid
UsageIndustrial, Commerical, Domestic
Packaging Size1mg
Grade StandardTechnical Grade, Analytical Grade
Packaging TypeInjection
Color-

Arsenic trioxide is a cancer medication that interferes with the growth and spread of cancer cells in the body.

Arsenic trioxide can cause a serious and sometimes fatal complication by changing the way your immune system works. Call your doctor at once if you have any signs of this condition, including fever, swelling, weight gain, pain when you breathe, rapid heart rate, feeling short of breath, or feeling like you might pass out.

Arsenic trioxide can also have harmful effects on your heart rhythm. This effect is increased when you also use certain other drugs. Tell your doctor about all medicines you use, and those you start or stop using during your treatment with arsenic trioxide.

You should not use arsenic trioxide if you are allergic to it.

To make sure arsenic trioxide is safe for you, tell your doctor if you have:

  • a history of heart disease;

  • a heart rhythm disorder or history of Long QT syndrome;

  • an electrolyte imbalance (such as low levels of potassium or magnesium in your blood);

  • kidney disease; or

  • liver disease.

Do not use arsenic trioxide if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

 

Arsenic trioxide can pass into breast milk and may harm a nursing baby. You should not breast-feed while using this medicine.

Arsenic trioxide is injected into a vein through an IV. A healthcare provider will give you this injection.

While using arsenic trioxide, you may need frequent blood tests at your doctor's office. Your heart function may need to be checked using an electrocardiograph or ECG (sometimes called an EKG).

 

You must remain under the care of a doctor while you are using arsenic trioxide. Do not miss any follow-up appointments.

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Targocid 400mg Injection

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Targocid 400mg Injection
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Product Details:
Packaging Size1ml
Packaging TypeInjection
Product TypeFinished Product
Dose/Strength (ex. 1 mg or 1 ml)400mg
UsageHospital, Clinical
Brandtargocid

Talk to your doctor, pharmacist or nurse before you are given teicoplanin if you: • are allergic to an antibiotic called ‘vancomycin’ • have a flushing of your upper part of your body (red man syndrome) • have a decrease in platelet count (thrombocytopenia) • have kidney problems • are taking other medicines which may cause hearing problems and/or kidney problems. You may have regular tests to check if your blood, kidneys and/or liver are working properly (see ‘Other medicines and teicoplanin’). If any of the above apply to you (or you are not sure), talk to your doctor, pharmacist or nurse before you are given teicoplanin. Tests During treatment you may have tests to check your kidneys and/or your hearing. This is more likely if: • your treatment will last for a long time • you have a kidney problem • you are taking or may take other medicines that may affect your nervous system, kidneys or hearing. In people who are given teicoplanin for a long time, bacteria that are not affected by the antibiotic may grow more than normal - your doctor will check for this. Other medicines and teicoplanin Tell your doctor, pharmacist or nurse if you are taking, have recently taken or might take any other medicines. This is because teicoplanin can affect the way some other medicines work. Also, some medicines can affect the way teicoplanin works. In particular, tell your doctor, pharmacist or nurse if you are taking the following medicines: • Aminoglycosides as they must not be mixed together with teicoplanin in the same injection. They may also cause hearing problems and/or kidney problems. • amphotericin B – a medicine that treats fungal infections which may cause hearing problems and/or kidney problems • cyclosporine – a medicine that affects the immune system which may cause hearing problems and/or kidney problems • cisplatin – a medicine that treats malignant tumours which may cause hearing problems and/or kidney problems • water tablets (such as furosemide) – also called ‘diuretics’ which may cause hearing problems and/or kidney problems. If any of the above apply to you, (or you are not sure), talk to your doctor, pharmacist or nurse before being given teicoplanin. 
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Mircera 100mcg Injection

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Mircera 100mcg Injection
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Product Details:
Dose/Strength (ex. 1 mg or 1ml)100 mcg
Product TypeFinished Product
Packaging TypeInjection
BrandMircera
Packaging Size1ml
UsagePersonal, Hospital

Epoetin alfa is a man-made form of a protein that helps your body produce red blood cells. This protein may be reduced when you have kidney failure or use certain medications. When fewer red blood cells are produced, you can develop a condition called anemia.

Epoetin alfa is used to treat anemia caused by chemotherapy or chronic kidney disease, or anemia caused by taking zidovudine to treat HIV (human immunodeficiency virus).

Epoetin alfa is also used to reduce the need for red blood cell transfusions in people having certain types of surgery.

You should not use this medication if you are allergic to epoetin alfa or darbepoetin alfa or (Aranesp), or if:

  • you have untreated or uncontrolled high blood pressure;

  • you have had pure red cell aplasia (PRCA, a type of anemia) after using darbepoetin alfa or epoetin alfa; or

  • you use an epoetin alfa multi-dose vial and you are pregnant or breast-feeding.

Do not use epoetin alfa from a multi-dose vial when giving medicine to a baby. The multi-dose vial contains an ingredient that can cause serious side effects or death in very young infants or premature babies.

Epoetin alfa may shorten remission time in some people with head and neck cancer who are also being treated with radiation. Epoetin alfa may also shorten survival time in certain people with breast cancer, non-small cell lung cancer, head and neck cancer, cervical cancer, or lymphoid cancer. Talk with your doctor about your individual risk.

To make sure epoetin alfa is safe for you, tell your doctor if you have:

  • heart disease, high blood pressure;

  • kidney disease (or if you are on dialysis);

  • a seizure disorder; or

  • a history of stroke, heart attack, or blood clots.

Using epoetin alfa during pregnancy could harm the unborn baby. Tell your doctor if you are pregnant or if you become pregnant while using this medicine.

It is not known whether epoetin alfa passes into breast milk or if it could affect the nursing baby. Tell your doctor if you are breast-feeding.

Do not use epoetin alfa from a multi-dose vial if you are pregnant or breast-feeding.

 

Epoetin alfa is made from human plasma (part of the blood) which may contain viruses and other infectious agents. Donated plasma is tested and treated to reduce the risk of it containing infectious agents, but there is still a small possibility it could transmit disease. Talk with your doctor about the risks and benefits of using this medication.

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Decitas 50mg Injection

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Product Details:
BrandDecitas
UsageClinical, Hospital
Packaging Size50 mg
Dose/Strength (ex. 1 mg or 1 ml)50 mg / ml
Packaging TypeInjection

Decitabine is a cancer medication that interferes with the growth and spread of cancer cells in the body.

Decitabine is used to treat myelodysplastic syndromes (certain types of blood or bone marrow cancer).

To make sure you can safely take decitabine, tell your doctor if you have any of these other conditions:

  • kidney disease; or

  • liver disease.

Do not use decitabine if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

If a man fathers a child while using this medication, the baby may have birth defects. Use a to prevent pregnancy during your treatment. Continue using for at least 2 months after you stop receiving decitabine.

 

It is not known whether decitabine passes into breast milk or if it could harm a nursing baby. You should not breast-feed while you are receiving decitabine.

Decitabine is injected into a vein through an IV. A healthcare provider will give you this injection.

In most cases, a decitabine injection is given every 8 hours for 3 days. This 3-day treatment is usually repeated every 6 weeks. You will most likely receive at least 4 of these treatments.

You may be given other medications to prevent nausea or vomiting while you are receiving decitabine.

 

Decitabine can lower blood cells that help your body fight infections and help your blood to clot. This can make it easier for you to bleed from an injury or get sick from being around others who are ill. Your blood may need to be tested often. Your kidney or liver function may also need to be checked.

Avoid being near people who are sick or have infections. Tell your doctor at once if you develop signs of infection.

Avoid activities that may increase your risk of bleeding or injury. Use extra care to prevent bleeding while shaving or brushing your teeth.

 

This medicine can pass into body fluids (urine, feces, vomit). For at least 48 hours after you receive a dose, avoid allowing your body fluids to come into contact with your hands or other surfaces. Caregivers should wear rubber gloves while cleaning up a patient's body fluids, handling contaminated trash or laundry or changing diapers. Wash hands before and after removing gloves. Wash soiled clothing and linens separately from other laundry.

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Dacogen 50mg Injection

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Product Details:
Packaging Size5 ml
Packaging TypeInjection
BrandDacogen
UsageClinical
Dose/Strength50mg / 1 ml

Decitabine is a cancer medication that interferes with the growth and spread of cancer cells in the body.

Decitabine is used to treat myelodysplastic syndromes (certain types of blood or bone marrow cancer).

To make sure you can safely take decitabine, tell your doctor if you have any of these other conditions:

  • kidney disease; or

  • liver disease.

Do not use decitabine if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

If a man fathers a child while using this medication, the baby may have birth defects.

It is not known whether decitabine passes into breast milk or if it could harm a nursing baby. You should not breast-feed while you are receiving decitabine.

Decitabine is injected into a vein through an IV. A healthcare provider will give you this injection.

In most cases, a decitabine injection is given every 8 hours for 3 days. This 3-day treatment is usually repeated every 6 weeks. You will most likely receive at least 4 of these treatments.

You may be given other medications to prevent nausea or vomiting while you are receiving decitabine.

 

Decitabine can lower blood cells that help your body fight infections and help your blood to clot. This can make it easier for you to bleed from an injury or get sick from being around others who are ill. Your blood may need to be tested often. Your kidney or liver function may also need to be checked.

Avoid being near people who are sick or have infections. Tell your doctor at once if you develop signs of infection.

Avoid activities that may increase your risk of bleeding or injury. Use extra care to prevent bleeding while shaving or brushing your teeth.

 

This medicine can pass into body fluids (urine, feces, vomit). For at least 48 hours after you receive a dose, avoid allowing your body fluids to come into contact with your hands or other surfaces. Caregivers should wear rubber gloves while cleaning up a patient's body fluids, handling contaminated trash or laundry or changing diapers. Wash hands before and after removing gloves. Wash soiled clothing and linens separately from other laundry.

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MyMust 100mg Injection

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MyMust 100mg Injection
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Product Details:
Dose100mg
UsageClinical, Personal
Packaging Size1 Vial
Packaging Typeinjection
BrandMyMust

Bendamustine is a cancer medicine that interferes with the growth and spread of cancer cells in the body.

Bendamustine is used to treat chronic lymphocytic leukemia. Bendamustine is also used to treat indolent B-cell non-Hodgkin lymphoma after other medicines have been tried without successful treatment of this condition.

You should not be treated with this medicine if you are allergic to bendamustine or mannitol (Osmitrol).

To make sure bendamustine is safe for you, tell your doctor if you have:

  • a weak immune system;

  • fever or other signs of infection;

  • a metabolic disorder or electrolyte imbalance;

  • liver disease;

  • kidney disease; or

  • if you smoke.

Some people receiving bendamustine have developed certain types of cancers. It is not known whether this medication causes cancer. Talk with your doctor about the risks and benefits of using bendamustine.

Do not receive bendamustine if you are pregnant. It could harm the unborn baby. Use effective birth control while you are using this medicine and for at least 3 months after your treatment ends.

 

It is not known whether bendamustine passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

Bendamustine is injected into a vein through an IV. A healthcare provider will give you this injection.

Bendamustine is usually given for 2 days in a row every 21 to 28 days. You may receive up to 8 treatments total, depending on the condition being treated. Follow your doctor's instructions.

You may be given other medications to help prevent certain side effects of bendamustine.

Tell your caregivers if you feel any burning, pain, or swelling around the IV needle when the medicine is injected.

Bendamustine can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

 

If you have ever had hepatitis B, bendamustine can cause this condition to come back or get worse. You will need frequent blood tests to check your liver function during treatment and for several months after you stop using this medicine.

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Bucelon 60mg Injection

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Dose60 mg
Packaging Size1 Vial
Packaging TypeInjecetion
BrandBecelon

Busulfan is a cancer medicine that interferes with the growth and spread of cancer cells in the body.

Busulfan taken by mouth is used to treat the symptoms of chronic myelogenous leukemia (a type of blood cancer). Busulfan injection is used together with a medicine called cyclophosphamide, to prepare your body to receive a stem cell transplant from a donor's bone marrow.

Busulfan is not a cure for leukemia.

You should not use busulfan if you are allergic to it.

To make sure you can safely take busulfan, tell your doctor if you have:

  • a weak immune system (bone marrow depression) caused by other cancer medications or radiation treatment;

  • epilepsy or other seizure disorder;

  • history of head injury; or

  • a history of lung or breathing problems.

Some people treated with busulfan have developed new forms of cancer. Talk to your doctor about your specific risks and benefits of using this medicine.

Do not use busulfan if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

Busulfan may affect fertility (your ability to have children), whether you are a man or a woman.

 

It is not known whether busulfan passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Use exactly as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.

Take the busulfan tablet with a full glass of water.

Busulfan injection is given through a needle placed into a vein in your upper chest (central IV). You will receive this injection in a clinic or hospital setting. You will also receive other medicines to help prevent certain side effects of busulfan.

Busulfan can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

Busulfan can have long lasting effects on your body. You may need frequent medical tests for a short time after you stop using this medicine.

 

Store at room temperature away from moisture and heat

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Bortenat 3.5mg Injection

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Packaging Size3.5 mg
Packaging TypeInjection
Dose/Strength (ex. 1 mg or 1 ml)3.5mg/ml
UsageClinical, Hospital
BrandBortenat

Bortezomib interferes with the growth of some cancer cells and keeps them from spreading in your body.

Bortezomib is used to treat multiple myeloma and mantle cell lymphoma.

You should not be treated with this medicine if you are allergic to bortezomib, mannitol, or boron.

To make sure bortezomib is safe for you, tell your doctor if you have ever had:

  • nerve problems such as numbness, tingling, or burning pain;

  • diabetes;

  • liver disease;

  • kidney disease, or if you are on dialysis;

  • a low level of platelets or white or red blood cells;

  • heart disease, congestive heart failure;

  • lung disease or breathing problems;

  • herpes or shingles (herpes zoster);

  • high or low blood pressure; or

  • if you are dehydrated.

You may need to have a negative pregnancy test before starting this treatment.

Bortezomib can harm an unborn baby. Do not use this medicine if you are pregnant. Use effective birth control to prevent pregnancy, whether you are a man or a woman. The use of this medicine by either parent may cause birth defects.

Keep using birth control for at least 2 months after your last dose of bortezomib. Tell your doctor right away if a pregnancy occurs while either the mother or the father is using this medicine.

This medicine may affect fertility (ability to have children) in both men and women. However, it is important to use birth control to prevent pregnancy because bortezomib may harm the baby if a pregnancy does occur.

 

It is not known whether bortezomib passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine and for at least 2 months after your last dose.

Bortezomib is injected into a vein through an IV.

You will receive this injection in a clinic or hospital setting. A doctor, nurse, or other healthcare provider will give you this injection.

You may be given medication to prevent nausea or vomiting while you are receiving bortezomib.

 

Bortezomib can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

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Myezom 2mg Injection

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Packaging Size2mg
Packaging TypeInjection
Dose/Strength (ex. 1 mg or 1 ml)2 mg
UsageClinical, Hospital
BrandMyezom

Bortezomib interferes with the growth of some cancer cells and keeps them from spreading in your body.

Bortezomib is used to treat multiple myeloma and mantle cell lymphoma.

You should not be treated with this medicine if you are allergic to bortezomib, mannitol, or boron.

To make sure bortezomib is safe for you, tell your doctor if you have ever had:

  • nerve problems such as numbness, tingling, or burning pain;

  • diabetes;

  • liver disease;

  • kidney disease, or if you are on dialysis;

  • a low level of platelets or white or red blood cells;

  • heart disease, congestive heart failure;

  • lung disease or breathing problems;

  • herpes or shingles (herpes zoster);

  • high or low blood pressure; or

  • if you are dehydrated.

You may need to have a negative pregnancy test before starting this treatment.

Bortezomib can harm an unborn baby. Do not use this medicine if you are pregnant. Use effective birth control to prevent pregnancy, whether you are a man or a woman. The use of this medicine by either parent may cause birth defects.

Keep using birth control for at least 2 months after your last dose of bortezomib. Tell your doctor right away if a pregnancy occurs while either the mother or the father is using this medicine.

This medicine may affect fertility (ability to have children) in both men and women. However, it is important to use birth control to prevent pregnancy because bortezomib may harm the baby if a pregnancy does occur.

 

It is not known whether bortezomib passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine and for at least 2 months after your last dose.

Bortezomib is injected into a vein through an IV.

You will receive this injection in a clinic or hospital setting. A doctor, nurse, or other healthcare provider will give you this injection.

You may be given medication to prevent nausea or vomiting while you are receiving bortezomib.

 

Bortezomib can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

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Myezom 3.5mg Injection

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Packaging Size3.5mg
Packaging TypeInjection
Dose/Strength (ex. 1 mg or 1 ml)3.5mg
UsageHospital, Clinical
BrandMyezom

Bortezomib interferes with the growth of some cancer cells and keeps them from spreading in your body.

Bortezomib is used to treat multiple myeloma and mantle cell lymphoma.

You should not be treated with this medicine if you are allergic to bortezomib, mannitol, or boron.

To make sure bortezomib is safe for you, tell your doctor if you have ever had:

  • nerve problems such as numbness, tingling, or burning pain;

  • diabetes;

  • liver disease;

  • kidney disease, or if you are on dialysis;

  • a low level of platelets or white or red blood cells;

  • heart disease, congestive heart failure;

  • lung disease or breathing problems;

  • herpes or shingles (herpes zoster);

  • high or low blood pressure; or

  • if you are dehydrated.

You may need to have a negative pregnancy test before starting this treatment.

Bortezomib can harm an unborn baby. Do not use this medicine if you are pregnant. Use effective birth control to prevent pregnancy, whether you are a man or a woman. The use of this medicine by either parent may cause birth defects.

Keep using birth control for at least 2 months after your last dose of bortezomib. Tell your doctor right away if a pregnancy occurs while either the mother or the father is using this medicine.

This medicine may affect fertility (ability to have children) in both men and women. However, it is important to use birth control to prevent pregnancy because bortezomib may harm the baby if a pregnancy does occur.

 

It is not known whether bortezomib passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine and for at least 2 months after your last dose.

Bortezomib is injected into a vein through an IV.

You will receive this injection in a clinic or hospital setting. A doctor, nurse, or other healthcare provider will give you this injection.

You may be given medication to prevent nausea or vomiting while you are receiving bortezomib.

 

Bortezomib can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

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Dacotin 100mg Injection

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Dose100 mg
Packaging Size1 Vial
Product TypeFinished Product
BrandDacotin
UsageClinical

Oxaliplatin is a cancer medicine that interferes with the growth and spread of cancer cells in the body.

Oxaliplatin is used together with other cancer medications to treat colon and rectal cancer.

You should not be treated with this medicine if you have ever had an allergic reaction to oxaliplatin or similar medications such as carboplatin (Paraplatin) or cisplatin (Platinol).

To make sure oxaliplatin is safe for you, tell your doctor if you have:

  • kidney disease;

  • liver disease;

  • heart disease, heart rhythm disorder;

  • a personal or family history of long QT syndrome;

  • an electrolyte imbalance (such as low levels of potassium or magnesium in your blood);

  • high blood pressure;

  • asthma or other breathing disorder;

  • a nerve problem; or

  • if you are using a blood thinner such as (Coumadin, Jantoven).

Do not use oxaliplatin if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

 

It is not known whether oxaliplatin passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Oxaliplatin is injected into a vein through an IV. You will receive this injection in a clinic or hospital setting. Oxaliplatin must be given slowly, and the infusion can take at least 2 hours to complete.

Oxaliplatin is given once every 2 weeks. Your doctor will determine how long to treat you with this medicine.

You may be given medication to prevent nausea or vomiting while you are receiving oxaliplatin.

Receiving oxaliplatin can make you more sensitive to cold, which can cause numbness, tingling, and muscle spasms. This includes exposure to cold temperature and coming into contact with cold objects. To prevent discomfort, follow these steps:

  • do not inhale deeply when you are exposed to cold air;

  • cover your skin, head, and face when you are outside in cold temperatures;

  • wear gloves when handling cold objects or refrigerated foods;

  • do not run an air conditioner at very cool temperature in your home or car (even during hot weather);

  • do not drink cold drinks or use ice cubes in drinks;

  • do not put ice packs on your body.

Chemotherapy often causes nausea or mouth sores. Do not eat ice chips to ease these discomforts because you will be more sensitive to cold. Talk to your doctor about other ways to treat nausea or mouth sores. You may be given other medications to prevent nausea or vomiting while you are receiving oxaliplatin.

Oxaliplatin can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

 

Your heart function may need to be checked using an electrocardiograph or ECG (sometimes called an EKG).

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Dacotin 50mg Injection

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Dose50 mg
Packaging Size1 Vial
Product TypeFinished Product
BrandDacotin
UsageHospital

Oxaliplatin is a cancer medicine that interferes with the growth and spread of cancer cells in the body.

Oxaliplatin is used together with other cancer medications to treat colon and rectal cancer.

You should not be treated with this medicine if you have ever had an allergic reaction to oxaliplatin or similar medications such as carboplatin (Paraplatin) or cisplatin (Platinol).

To make sure oxaliplatin is safe for you, tell your doctor if you have:

  • kidney disease;

  • liver disease;

  • heart disease, heart rhythm disorder;

  • a personal or family history of long QT syndrome;

  • an electrolyte imbalance (such as low levels of potassium or magnesium in your blood);

  • high blood pressure;

  • asthma or other breathing disorder;

  • a nerve problem; or

  • if you are using a blood thinner such as  (Coumadin, Jantoven).

Do not use oxaliplatin if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

 

It is not known whether oxaliplatin passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Oxaliplatin is injected into a vein through an IV. You will receive this injection in a clinic or hospital setting. Oxaliplatin must be given slowly, and the infusion can take at least 2 hours to complete.

Oxaliplatin is given once every 2 weeks. Your doctor will determine how long to treat you with this medicine.

You may be given medication to prevent nausea or vomiting while you are receiving oxaliplatin.

Receiving oxaliplatin can make you more sensitive to cold, which can cause numbness, tingling, and muscle spasms. This includes exposure to cold temperature and coming into contact with cold objects. To prevent discomfort, follow these steps:

  • do not inhale deeply when you are exposed to cold air;

  • cover your skin, head, and face when you are outside in cold temperatures;

  • wear gloves when handling cold objects or refrigerated foods;

  • do not run an air conditioner at very cool temperature in your home or car (even during hot weather);

  • do not drink cold drinks or use ice cubes in drinks;

  • do not put ice packs on your body.

Chemotherapy often causes nausea or mouth sores. Do not eat ice chips to ease these discomforts because you will be more sensitive to cold. Talk to your doctor about other ways to treat nausea or mouth sores. You may be given other medications to prevent nausea or vomiting while you are receiving oxaliplatin.

Oxaliplatin can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

 

Your heart function may need to be checked using an electrocardiograph or ECG (sometimes called an EKG).

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Colstim 300mcg Injection

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UsageClinical, Hospital
Packaging Size1 Vial
Packaging TypeInjection
BrandColstim

Filgrastim is a man-made form of a protein that stimulates the growth of white blood cells in your body. White blood cells help your body fight against infection.

Filgrastim is used to treat neutropenia, a lack of certain white blood cells caused by cancer, bone marrow transplant, receiving chemotherapy, or by other conditions.

You should not use this medicine if you are allergic to filgrastim or pegfilgrastim, or to other medicines that contain the E. coli bacteria.

To make sure filgrastim is safe for you, tell your doctor if you have:

  • a blood cell disorder, such as sickle cell anemia;

  • kidney disease;

  • latex allergy; or

  • if you are receiving chemotherapy or radiation treatment.

It is not known whether filgrastim will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant.

 

It is not known whether filgrastim passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

Filgrastim should not be given within 24 hours before or 24 hours after you receive chemotherapy.

Filgrastim is injected into a vein or under the skin. You may be shown how to use injections at home. Do not give yourself this medicine if you do not understand how to use the injection and properly dispose of needles, IV tubing, and other items used.

Follow all directions on your prescription label. Do not use filgrastim in larger or smaller amounts or for longer than recommended. Filgrastim vials and prefilled syringes do not contain the same concentrations of this medicine. Do not give an injection unless you are trained in properly measuring your dose from either the vial or the prefilled syringe.

Read all patient information, medication guides, and instruction sheets provided to you. Ask your doctor or pharmacist if you have any questions.

Do not shake the medicine. Prepare your dose only when you are ready to give an injection. Do not use if the medicine has changed colors or has particles in it. Call your pharmacist for new medicine.

Your care provider will show you the best places on your body to inject filgrastim. Use a different place each time you give an injection. Do not inject into the same place two times in a row.

Each single-use vial or prefilled syringe is for one use only. Throw away after one use, even if there is still some medicine left in it after injecting your dose. Do not use filgrastim if the expiration date on the label has passed. Call your pharmacist for a new prescription.

Use a disposable needle and syringe only once. Follow any state or local laws about throwing away used needles and syringes. Use a puncture-proof "sharps" disposal container (ask your pharmacist where to get one and how to throw it away). Keep this container out of the reach of children and pets.

You may need frequent medical tests to help your doctor determine how long to treat you with filgrastim. Your liver function will also need to be tested, and you may need bone density scans.

Store filgrastim in the original container in a refrigerator. Do not freeze.

 

Take the medicine out of the refrigerator and allow it to reach room temperature for 30 minutes before injecting your dose. Do not leave the medicine at room temperature for longer than 24 hours.

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Biceltis 440mg Injection

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Dose440 mg
Product TypeFinished Product
Packaging Size1 Vial
BrandBiceltis

Trastuzumab is a cancer medication that interferes with the growth and spread of cancer cells in the body.

Trastuzumab is used to treat certain types of breast cancer or stomach cancer. Other cancer medicines are sometimes used in combination with trastuzumab.

Do not use trastuzumab if you are pregnant. It could harm the unborn baby. Avoid becoming pregnant for at least 7 months after your last dose of trastuzumab.

Trastuzumab can cause heart failure, especially if you have heart disease or if you are also receiving certain other cancer medicines.

 

Some side effects may occur during the injection. Tell your caregiver right away if you feel dizzy, nauseated, light-headed, weak, short of breath, or if you have a headache, fever, chills, sudden chest pain, wheezing, dry cough, hives, or swelling of your face, lips, tongue, or throat.

You should not use trastuzumab if you are allergic to it.

To make sure trastuzumab is safe for you, tell your doctor if you have ever had:

  • heart disease;

  • congestive heart failure;

  • a heart attack; or

  • any allergies or breathing problems.

Trastuzumab can cause heart failure, especially if you have heart disease or if you are also receiving certain other cancer medicines (such as daunorubicin, doxorubicin, epirubicin, or idarubicin)

Do not use trastuzumab if you are pregnant. It could harm the unborn baby. Tell your doctor if you become pregnant during treatment. Use effective birth control to prevent pregnancy while you are using this medicine and for at least 7 months after your treatment ends.

If you become pregnant while using this medicine or within 7 months after you stop, your name may need to be listed on a pregnancy registry. This is to track the outcome of the pregnancy and to evaluate any effects of trastuzumab on the baby.

 

It is not known whether trastuzumab passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

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Zelgor 250mg Tablet

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Dose250 mg
UsageHospital
BrandZelgor
Packaging TypeBottle
Packaging Size120 Tablet

Abiraterone works by reducing androgen production in the body. Androgens are male hormones that can promote tumor growth in the prostate gland.

Abiraterone is used together with prednisone to treat prostate cancer that has spread to other parts of the body. This medicine is used in men whose prostate cancer cannot be treated with surgery or other medicines.

You should not use abiraterone if you are allergic to it, or if you have ever had:

  • severe liver disease.

To make sure abiraterone is safe for you, tell your doctor if you have:

  • liver disease;

  • heart disease, high blood pressure;

  • problems with your adrenal gland or pituitary gland;

  • low levels of potassium in your blood;

  • fluid retention;

  • a heart attack; or

  • if you take medicine to treat seizures, tuberculosis, HIV or AIDS.

While you are taking abiraterone and for at least 1 week after your treatment ends:

  • If your sexual partner is pregnant--Use a condom to prevent transfer of this medication to her.

  • If your sexual partner could become pregnant--Use a condom plus another form of effective birth control to prevent pregnancy.

Although abiraterone is not for use by women, this medicine can harm an unborn baby or cause birth defects. Abiraterone tablets should not be handled by a woman who is pregnant or who may become pregnant. If this cannot be avoided, the woman should wear latex gloves.

It is not known whether abiraterone passes into breast milk or if it could harm a nursing baby. Abiraterone should not be used by a woman who is breast-feeding a baby.

 

Abiraterone is not approved for use by anyone younger than 18 years old.

Abiraterone is usually taken once per day while also taking prednisone two times per day. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Your prednisone dosage needs may change if you have surgery, are ill, or are under stress. Do not change your medication dose or schedule without your doctor's advice.

Take abiraterone on an empty stomach. Do not eat anything for at least 2 hours before you take abiraterone and for at least 1 hour after you have taken the medicine.

Do not crush, chew, or break an abiraterone tablet. Swallow it whole with a full glass of water.

Your blood pressure will need to be checked often, and you may need frequent blood tests at your doctor's office.

You should not stop using abiraterone or prednisone suddenly. Follow your doctor's instructions about tapering your prednisone dose.

Store at room temperature away from moisture and heat.

 

Read all patient information, medication guides, and instruction sheets provided to you. Ask your doctor or pharmacist if you have any questions.

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Abiron 250mg Tablet

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Packaging TypeTab
Packaging Size120 Tab
Dose250 mg
UsageHospital
BrandAbiron

Abiraterone works by reducing androgen production in the body. Androgens are male hormones that can promote tumor growth in the prostate gland.

Abiraterone is used together with prednisone to treat prostate cancer that has spread to other parts of the body. This medicine is used in men whose prostate cancer cannot be treated with surgery or other medicines.

You should not use abiraterone if you are allergic to it, or if you have ever had:

  • severe liver disease.

To make sure abiraterone is safe for you, tell your doctor if you have:

  • liver disease;

  • heart disease, high blood pressure;

  • problems with your adrenal gland or pituitary gland;

  • low levels of potassium in your blood;

  • fluid retention;

  • a heart attack; or

  • if you take medicine to treat seizures, tuberculosis, HIV or AIDS.

While you are taking abiraterone and for at least 1 week after your treatment ends:

  • If your sexual partner is pregnant--Use a condom to prevent transfer of this medication to her.

  • If your sexual partner could become pregnant--Use a condom plus another form of effective birth control to prevent pregnancy.

Although abiraterone is not for use by women, this medicine can harm an unborn baby or cause birth defects. Abiraterone tablets should not be handled by a woman who is pregnant or who may become pregnant. If this cannot be avoided, the woman should wear latex gloves.

It is not known whether abiraterone passes into breast milk or if it could harm a nursing baby. Abiraterone should not be used by a woman who is breast-feeding a baby.

 

Abiraterone is not approved for use by anyone younger than 18 years old.

Abiraterone is usually taken once per day while also taking prednisone two times per day. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Your prednisone dosage needs may change if you have surgery, are ill, or are under stress. Do not change your medication dose or schedule without your doctor's advice.

Take abiraterone on an empty stomach. Do not eat anything for at least 2 hours before you take abiraterone and for at least 1 hour after you have taken the medicine.

Do not crush, chew, or break an abiraterone tablet. Swallow it whole with a full glass of water.

Your blood pressure will need to be checked often, and you may need frequent blood tests at your doctor's office.

You should not stop using abiraterone or prednisone suddenly. Follow your doctor's instructions about tapering your prednisone dose.

Store at room temperature away from moisture and heat.

Read all patient information, medication guides, and instruction sheets provided to you. Ask your doctor or pharmacist if you have any questions.

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Revolade 50mg Tablet

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Dose/Strength (ex. 1 mg or 1ml)50 Mg
Packaging TypeTablet
BrandRevolade
Packaging Size7 tablet
UsageHospital, Clinical

Eltrombopag is a man-made form of a protein that increases production of platelets (blood-clotting cells) in your body. Eltrombopag can lower the risk of bleeding by increasing platelets in your blood.

Eltrombopag is used to prevent bleeding episodes in people with chronic immune thrombocytopenic purpura (ITP), a bleeding condition caused by a lack of platelets in the blood. This medicine is for use in adults and children who are at least 1 year old, after other medicines have been tried without success.

Eltrombopag is also used to prevent bleeding in adults with chronic hepatitis C who are treated with an interferon (such as Intron A, Infergen, , PegIntron, Rebetron, Redipen, or Sylatron).

Eltrombopag is also used to treat severe aplastic anemia in adults after other medicines have been tried without success.

Eltrombopag is not a cure for ITP and it will not make your platelet counts normal if you have this condition.

You should not use eltrombopag if you are allergic to it.

To make sure eltrombopag is safe for you, tell your doctor if you have ever had:

  • liver disease (unless you are being treated for hepatitis C);

  • kidney disease;

  • high levels of platelets in your blood;

  • a blood cancer or bone marrow disorder;

  • cataracts or a blood clot;

  • if your spleen has been removed; or

  • if you are of East Asian descent (Chinese, Japanese, Taiwanese, or Korean).

Taking eltrombopag may increase your risk of developing blood cancers, especially if you have myelodysplastic syndrome (also called "preleukemia"). Talk with your doctor if you have concerns about this risk.

It is not known whether this medicine will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant.

If you are pregnant, your name may be listed on a pregnancy registry. This is to track the outcome of the pregnancy and to evaluate any effects of eltrombopag on the baby.

 

It is not known whether eltrombopag passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

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Mabthera 500mg Infusion

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Packaging Size50ml

Rituximab is a cancer medicine that interferes with the growth and spread of cancer cells in the body.

Rituximab is used to treat non-Hodgkin's lymphoma or chronic lymphocytic leukemia. Rituximab is also used in combination with another drug called methotrexate to treat symptoms of adult rheumatoid arthritis.

Rituximab is also used in combination with steroid medicines to treat certain rare disorders that cause inflammation of blood vessels and other tissues in the body.

Rituximab may cause a serious brain infection that can lead to disability or death. Call your doctor right away if you have changes in your mental state, decreased vision, weakness, or problems with speech or walking. These symptoms may start gradually and get worse quickly.

Tell your doctor if you have ever had hepatitis B. Rituximab can cause this condition to come back or get worse.

Severe skin problems can also occur during treatment with rituximab. Call your doctor if you have painful skin or mouth sores, or a severe skin rash with blistering, peeling, or pus.

 

Some side effects may occur during the injection or within 24 hours afterward. Tell your caregiver right away if you feel dizzy, weak, light-headed, short of breath, or if you have chest pain, wheezing, sudden cough, or pounding heartbeats or fluttering in your chest.

Rituximab may cause a serious brain infection called progressive multifocal leukoencephalopathy (PML). This infection may be more likely if have used an immunosuppressant drug in the past, or if you have received rituximab with a stem cell transplant.

You should not be treated with rituximab if you are allergic to it.

To make sure rituximab is safe for you, tell your doctor if you have:

  • liver disease or hepatitis (or if you are a carrier of hepatitis B);

  • kidney disease;

  • lung disease or a breathing disorder;

  • a weak immune system (caused by disease or by using certain medicines);

  • a recent or active infection, including herpes, shingles, cytomegalovirus, chickenpox, parvovirus, West Nile virus, or hepatitis B or C;

  • a history of heart disease, angina (chest pain), or heart rhythm disorder; or

  • a history of using rituximab in the past.

Using rituximab during pregnancy could harm the unborn baby. Tell your doctor if you are pregnant or if you become pregnant. Use effective birth control to prevent pregnancy while you are using this medicine and for at least 12 months after your last dose.

 

It is not known whether rituximab passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

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Ristova 500mg Injection

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Dose/Strength (ex. 1 mg or 1 ml)500mg / 50ml
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BrandRistova

Rituximab is a cancer medicine that interferes with the growth and spread of cancer cells in the body.

Rituximab is used to treat non-Hodgkin's lymphoma or chronic lymphocytic leukemia. Rituximab is also used in combination with another drug called methotrexate to treat symptoms of adult rheumatoid arthritis.

Rituximab is also used in combination with steroid medicines to treat certain rare disorders that cause inflammation of blood vessels and other tissues in the body.

Rituximab may cause a serious brain infection that can lead to disability or death. Call your doctor right away if you have changes in your mental state, decreased vision, weakness, or problems with speech or walking. These symptoms may start gradually and get worse quickly.

Tell your doctor if you have ever had hepatitis B. Rituximab can cause this condition to come back or get worse.

Severe skin problems can also occur during treatment with rituximab. Call your doctor if you have painful skin or mouth sores, or a severe skin rash with blistering, peeling, or pus.

 

Some side effects may occur during the injection or within 24 hours afterward. Tell your caregiver right away if you feel dizzy, weak, light-headed, short of breath, or if you have chest pain, wheezing, sudden cough, or pounding heartbeats or fluttering in your chest.

Rituximab may cause a serious brain infection called progressive multifocal leukoencephalopathy (PML). This infection may be more likely if have used an immunosuppressant drug in the past, or if you have received rituximab with a stem cell transplant.

You should not be treated with rituximab if you are allergic to it.

To make sure rituximab is safe for you, tell your doctor if you have:

  • liver disease or hepatitis (or if you are a carrier of hepatitis B);

  • kidney disease;

  • lung disease or a breathing disorder;

  • a weak immune system (caused by disease or by using certain medicines);

  • a recent or active infection, including herpes, shingles, cytomegalovirus, chickenpox, parvovirus, West Nile virus, or hepatitis B or C;

  • a history of heart disease, angina (chest pain), or heart rhythm disorder; or

  • a history of using rituximab in the past.

Using rituximab during pregnancy could harm the unborn baby. Tell your doctor if you are pregnant or if you become pregnant. Use effective birth control to prevent pregnancy while you are using this medicine and for at least 12 months after your last dose.

 

It is not known whether rituximab passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

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Sandostatin 0.1mg Injection

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BrandSandostatin
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Packaging Size0.1mg/ml
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Octreotide is a man-made protein that is similar to a hormone in the body called somatostatin. Octreotide lowers many substances in the body such as insulin and glucagon (involved in regulating blood sugar), growth hormone, and chemicals that affect digestion.

Octreotide is used to treat acromegaly. Octreotide is also used to reduce flushing episodes and watery diarrhea caused by cancerous tumors (carcinoid syndrome) or tumors called vasoactive intestinal peptide tumors (VIP adenomas).

You should not use octreotide if you are allergic to it.

To make sure you can safely use octreotide, tell your doctor if you have any of these other conditions:

  • diabetes;

  • gallbladder disease;

  • heart disease, high blood pressure, or heart rhythm disorder;

  • thyroid problems;

  • pancreatitis;

  • liver disease; or

  • kidney disease (or if you are on dialysis).

Octreotide is not expected to be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment.

Using octreotide can affect certain hormones that may make it easier for you to get pregnant, even if you were unable to get pregnant before. Talk to your doctor about using birth control to avoid unwanted pregnancy.

 

It is not known whether octreotide passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

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Aromasin 25mg Tablet

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BrandAromasin

Exemestane lowers estrogen levels in postmenopausal women, which may slow the growth of certain types of breast tumors that need estrogen to grow in the body.

Exemestane is used to treat breast cancer in postmenopausal women. It is often given to women whose cancer has progressed even after surgery, radiation, or other cancer medications have been tried without success.

You should not use exemestane if you are allergic to it, or:

  • if you are pregnant or able to become pregnant; or

  • if you have not yet completed menopause, and are still having menstrual periods.

To make sure exemestane is safe for you, tell your doctor if you have:

  • liver disease; or

  • kidney disease.

Exemestane can decrease bone mineral density, which may increase your risk of developing osteoporosis. Talk to your doctor about your individual risk of bone loss.

Although it is not likely that a postmenopausal woman would be pregnant, exemestane can cause birth defects. Do not take this medicine if you are pregnant or may become pregnant. You may need to have a negative pregnancy test before starting this treatment.

If you are not past menopause, use effective birth control to prevent pregnancy while you are taking exemestane and for at least 1 month after your last dose. Tell your doctor right away if you become pregnant while taking exemestane.

 

It is not known whether exemestane passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Exemestane is usually taken once per day, after a meal. Try to take the medicine at the same time each day.

While using exemestane, you may need frequent blood tests.

Use exemestane regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely. You may need to keep taking take this medication for up to 5 years.

 

Store in the original container at room temperature away from moisture and heat.

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Rapact 5mg Tablet

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Packaging Size10 Tab
Dose5mg
Packaging TypeTablet
BrandRapact

Everolimus lowers your body's immune system. The immune system helps your body fight infections. The immune system can also fight or "reject" a transplanted organ such as a liver or kidney. This is because the immune system treats the new organ as an invader.

The Zortress brand of everolimus is used to prevent organ rejection after a kidney or liver transplant. Zortress is used together with cyclosporine, steroids, and other medications.

You should not use Zortress if you are allergic to everolimus or sirolimus.

Using Zortress can increase your risk of serious infections or getting certain cancers, such as lymphomaor skin cancer. Ask your doctor about your specific risk.

Tell your doctor if you have ever had:

  • problems digesting lactose or galactose (sugar);

  • high cholesterol or triglycerides;

  • liver disease;

  • a heart transplant; or

  • skin cancer in you or a family member.

Zortress may harm an unborn baby. Use effective birth control while you are using this medicine and for at least 8 weeks after your last dose. Tell your doctor if you become pregnant.

This medicine may affect fertility (ability to have children) in both men and women. However, it is important for women to use birth control because Zortress may harm the baby if a pregnancy does occur.

 

It is not known whether everolimus passes into breast milk or if it could harm a nursing baby. You should not breast-feed while you are taking Zortress.

Follow all directions on your prescription label and read all medication guides or instruction sheets. Your doctor may occasionally change your dose. Use the medicine exactly as directed.

Take Zortress at evenly spaced times with a full glass (8 ounces) of water.

Take the medicine with or without food, but the same way each time. If you also take cyclosporine or tacrolimus, take both medications at the same time.

Do not crush or chew an everolimus tablet. Swallow the pill whole.

You will need frequent medical tests.

Do not change doses or stop taking any of your medications without asking your doctor.

 

Store at room temperature away from moisture, heat, and light.

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Imalek 400mg Tablet

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Dose400mg
Packaging Size6 Tablet
Product TypeFinished Product
BrandImalek

Imatinib interferes with the growth of some cancer cells.

Imatinib is used to treat certain types of leukemia (blood cancer), bone marrow disorders, and skin cancer. Imatinib is also used to treat certain tumors of the stomach and digestive system.

You should not use imatinib if you are allergic to it.

To make sure imatinib is safe for you, tell your doctor if you have ever had:

  • liver disease (especially hepatitis B);

  • kidney disease;

  • underactive thyroid, recent or upcoming thyroid surgery;

  • heart disease, congestive heart failure;

  • a stomach ulcer or bleeding;

  • diabetes; or

  • chemotherapy.

Do not use imatinib if you are pregnant. It could harm the unborn baby or cause birth defects. Use effective birth control to prevent pregnancy while you are using this medicine and for at least 14 days after your last dose.

You may need to have a negative pregnancy test before starting this treatment.

 

Imatinib can pass into breast milk and may cause side effects in the nursing baby. You should not breast-feed while taking imatinib and for at least 1 month after your last dose.

Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Imatinib should be taken with a meal and a large glass of water. Do not take imatinib on an empty stomach.

You may dissolve an imatinib tablet in a glass of water or apple juice to make the pill easier to swallow. Be sure to use the correct number of tablets to get an entire dose. Use about 2 ounces of liquid for each 100-milligram tablet, or 7 ounces of liquid for each 400-milligram tablet. Stir the mixture and drink all of it right away.

Do not crush, chew, or break an imatinib tablet. The medicine from a crushed or broken pill can be dangerous if it gets in your eyes, mouth, or nose, or on your skin. If this occurs, wash your skin with soap and water or rinse your eyes with water. Ask your doctor or pharmacist how to safely handle and dispose of a crushed or broken tablet.

Imatinib can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

 

You will also need frequent tests to check your liver function.

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Adriamycin 10mg Injection

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Packaging Size1 vial
Packaging Typeinjection
Dose/Strength (ex. 1 mg or 1 ml)5mg/Vial
UsageClinical, Hospital
BrandAdriamycin

Doxorubicin is a cancer medication that interferes with the growth and spread of cancer cells in the body.

Doxorubicin is used to treat different types of cancers that affect the breast, bladder, ovary, thyroid, stomach, lungs, bones, nerve tissues, muscles, joints, and soft tissues. Doxorubicin is also used to treat Hodgkin's disease and certain types of leukemia.

You should not use this medicine if you are allergic to doxorubicin or similar medications (doxorubicin, daunorubicin, epirubicin, idarubicin, mitoxantrone), or if you have:

  • an untreated or uncontrolled infection (including mouth sores);

  • severe liver disease;

  • severe heart problems; or

  • if you have recently had a heart attack.

To make sure doxorubicin is safe for you, tell your doctor if you have:

  • liver or kidney disease;

  • bone marrow suppression;

  • heart disease or a history of heart failure; or

  • if you have been treated before with doxorubicin, daunorubicin, epirubicin, idarubicin, or mitoxantrone.

Tell your doctor about all other cancer medicines or radiation treatments you have received in the past.

Using doxorubicin may increase your risk of developing a bone marrow disease or other types of leukemia later in life. Ask your doctor about your specific risk.

Do not use doxorubicin if you are pregnant. It could harm the unborn baby or cause birth defects. Use birth control to prevent pregnancy while you are using this medicine, whether you are a man or a woman. Doxorubicin use by either parent may cause birth defects.

If you are a woman, you should avoid pregnancy while you are using this medicine and for at least 6 months after your last dose.

If you are a man, use effective birth control if your  partner is able to get pregnant. An unborn baby can be harmed if a man fathers the child while he is using doxorubicin. Keep using birth control for at least 6 months after your last dose.

Tell your doctor right away if a pregnancy occurs while either the mother or the father is using doxorubicin.

This medicine may affect fertility (your ability to have children), whether you are a man or a woman. Ask your doctor about your specific risk.

 

Doxorubicin can pass into breast milk and may harm a nursing baby. You should not breast-feed while you are using doxorubicin.

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Dacarex 200mg Injection

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Dose200 mg
Packaging Size20 ml
Packaging TypeInjection
BrandDacarex

Dacarbazine is a cancer medication that interferes with the growth and spread of cancer cells in the body.

Dacarbazine is used to treat skin cancer (malignant melanoma) and Hodgkin's disease.

Dacarbazine is used to treat skin cancer (malignant melanoma) and Hodgkin's disease.

Avoid eating anything for 4 to 6 hours before your injection. This may help prevent severe nausea or vomiting.

 

Dacarbazine can lower blood cells that help your body fight infections and help your blood to clot. You may get an infection or bleed more easily. Call your doctor if you have unusual bruising or bleeding, or signs of infection (fever, chills, body aches).

You should not use dacarbazine if you are allergic to it.

It is not known whether dacarbazine will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication.

 

It is not known whether dacarbazine passes into breast milk or if it could harm a nursing baby. You should not breast-feed while you are being treated with dacarbazine.

Dacarbazine is injected into a vein through an IV. You will receive this injection in a clinic or hospital setting.

Avoid eating anything for 4 to 6 hours before your injection. This may help prevent severe nausea or vomiting.

Tell your caregivers if you feel any burning, pain, or swelling around the IV needle when dacarbazine is injected.

Dacarbazine is sometimes given daily for 5 to 10 days in a row every 3 or 4 weeks. For Hodgkin's disease, you may only receive dacarbazine for 1 day every 15 days. Your doctor will determine how long to treat you with dacarbazine.

 

Dacarbazine can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

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Daunomycin 20mg Injection

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Dose20mg
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Packaging Size10ml
BrandDaunomycin

Daunorubicin is a cancer medication that interferes with the growth and spread of cancer cells in the body.

Daunorubicin is used in the treatment of leukemia (blood cancer).

Daunorubicin may cause dangerous effects on your heart. Call your doctor at once if you have chest pain, shortness of breath (even with mild exertion), swelling, or rapid weight gain.

 

Daunorubicin can lower blood cells that help your body fight infections and help your blood to clot. You may get an infection or bleed more easily. Call your doctor if you have unusual bruising or bleeding, or signs of infection (fever, chills, body aches).

To make sure daunorubicin is safe for you, tell your doctor if you have:

  • heart disease;

  • kidney disease;

  • liver disease;

  • a weak immune system (caused by disease or by using certain medicines); or

  • if you have ever been treated with doxorubicin, epirubicin, idarubicin, mitoxantrone, or liposomal daunorubicin (Daunoxome).

Using daunorubicin may increase your risk of developing other types of leukemia. Ask your doctor about your specific risk.

Do not use daunorubicin if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

 

It is not known whether daunorubicin passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Daunorubicin is injected into a vein through an IV. A healthcare provider will give you this injection.

Before you receive each dose of daunorubicin, your heart function may need to be checked with an electrocardiograph or ECG (sometimes called an EKG). Your kidney and liver function may also need to be checked.

Tell your caregivers if you feel any burning, pain, or swelling around the IV needle when daunorubicin is injected.

Skin accidentally exposed to daunorubicin should be rinsed thoroughly with soap and warm water.

 

Daunorubicin can lower blood cells that help your body fight infections and help your blood to clot. Your blood will need to be tested often. Your cancer treatments may be delayed based on the results of these tests.

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Glioz 250mg

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Dose250mg
Packaging Size5 Tablet
BrandGlioz
Strength (milligram)250 mg
Product TypeFinished Product

Temozolomide is a cancer medicine that interferes with the growth and spread of cancer cells in the body.

Temozolomide is used together with radiation therapy to treat certain types of brain tumor in adults.

Temozolomide is usually given after other cancer medicines have been tried without success.

You should not take this medicine if you are allergic to temozolomide or to another cancer medication called dacarbazine (DTIC).

To make sure temozolomide is safe for you, tell your doctor if you have:

  • liver disease; or

  • kidney disease.

Using temozolomide may increase your risk of developing certain types of bone marrow cancer. Ask your doctor about your specific risk.

Do not use temozolomide if you are pregnant. It could harm the unborn baby. Use effective birth control, and tell your doctor if you become pregnant during treatment.

This medicine may affect fertility in men. Talk to your doctor about your own risk.

 

It is not known whether temozolomide passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Temozolomide is given in a 28-day treatment cycle, and you may only need to take the medicine during the first few days of each cycle.

If you are also receiving radiation treatment, you may need to take temozolomide for 6 to 7 weeks in a row during your first treatment cycle. Then you may be switched to a 28-day maintenance treatment cycle.

Your doctor will determine how long to treat you with temozolomide. Follow your doctor's dosing instructions very carefully.

Your doctor may occasionally change your dose to make sure you get the best results. The size, color, and number of temozolomide capsules you take may sometimes be different from earlier treatment cycles. Be sure you know the correct number of capsules to take and on which days to take them. Ask your doctor or pharmacist if you have any questions.

 

Take all of your capsules for the day (one entire daily dose) at the same time on each dosing day of a treatment cycle. Swallow the capsules whole with a full glass of water.

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Tretizen 20mg Cap

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Strength10 mg

Isotretinoin is a form of vitamin A. It reduces the amount of oil released by oil glands in your skin, and helps your skin renew itself more quickly.

Isotretinoin is used to treat severe nodular acne that has not responded to other treatments, including antibiotics.

Isotretinoin is available only from a certified pharmacy under a special program called iPLEDGE. You must be registered in the program and understand the risks and benefits of taking this medicine.

Isotretinoin may also be used for purposes not listed in this medication guide.

You must have a negative pregnancy test before taking isotretinoin. You will also be required to use two forms of birth control to prevent pregnancy while taking this medicine. Stop using isotretinoin and call your doctor at once if you think you might be pregnant.

 

Isotretinoin is available only under a special program called iPLEDGE. It is dangerous to try and purchase isotretinoin on the Internet or from vendors outside of the United States.

Primary forms of birth control include:

  • tubal ligation (tubes tied);

  • vasectomy of the male sexual partner;

  • an IUD (intrauterine device);

  • estrogen-containing birth control pills (not mini-pills); and

  • hormonal birth control patches, implants, injections, or vaginal ring.

Secondary forms of birth control include:

  • a male latex with or without spermicide;

  • a diaphragm plus a spermicide;

  • a cervical cap plus a spermicide; and

  • a vaginal sponge containing a spermicide.

Not having sexual intercourse (abstinence) is the most effective method of preventing pregnancy.

Stop using isotretinoin and call your doctor at once if you have unprotected sex, if you quit using birth control, if your period is late, or if you think you might be pregnant. If you get pregnant while taking isotretinoin, call the iPLEDGE pregnancy registry at 1-866-495-0654.

You should not use isotretinoin if you are allergic to it.

To make sure isotretinoin is safe for you, tell your doctor if you have:

  • a history of depression or mental illness;

  • asthma;

  • liver disease;

  • diabetes;

  • heart disease or high cholesterol;

  • osteoporosis or low bone mineral density;

  • an eating disorder such as anorexia;

  • an intestinal disorder such as inflammatory bowel disease, ulcerative colitis, or Crohn's disease; or

  • a food or drug allergy.

It is dangerous to try and purchase isotretinoin on the Internet or from vendors outside of the United States. The sale and distribution of isotretinoin outside of the iPLEDGE program violates the regulations of the U.S. Food and Drug Administration for the safe use of this medication.

 

It is not known whether isotretinoin passes into breast milk or if it could harm a nursing baby. You should not breast-feed while using this medicine.

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