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  4. Pharmaceutical Capsules 26 Products available
  5. Anti Cancer Medicine 17 Products available
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Anti Cancer Medicine

We offer the best product range of SUNITINIB MALATE CAPSULE, ERLOTINIB TABLET 100MG & 150 MG, Hydroxyurea Capsules 500 mg, methotrexate and ABIRAPRO ABIRATERONE ACETATE 250MG.

SUNITINIB MALATE CAPSULE

  • CATEGORY Anti Cancer Capsules
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder
  • Packaging Type Plastic Bottle
  • Usage Clinical, hospital etc.

Sunitinib Malate capsule is used in treatment of Gastrointestinal Stromal Tumor (GIST), Advanced Renal Cell Carcinoma (RCC) and Advanced Pancreatic Neuroendocrine Tumors (pNET).

India has many manufacturers who manufacture Sunitinib Malate capsule .To know more contact us.

3s corporation is Supplier, Exporter , Wholesaler  for Sunitinib Malate capsule in India.

 

ADDITIONAL INFORMATION

The recommended dose of Sunitinib Malate capsule for pancreatic neuroendocrine tumors (pNET) is 37.5 mg taken orally once daily continuously without a scheduled off-treatment period.Sunitinib Malate capsule may be taken with or without food.

Sunitinib Malate capsule is Stored at 25°C (77°F); excursions permitted to 15-30°C (59-86°F).

 

SIDE EFFECTS

Stop using sunitinib and call your doctor at once if you have a serious side effect such as:

  • headache with chest pain and severe dizziness, fainting, fast or pounding heartbeats;
  • feeling short of breath (even with mild exertion), swelling in your ankles or feet;
  • sudden numbness or weakness, problems with vision, speech, or balance;
  • numbness or tingly feeling around your mouth;
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ERLOTINIB TABLET 100MG & 150 MG

  • Packaging Type Plastic Bottle
  • Usage Clinical, hospital etc.
  • CATEGORY Anti Cancer Tablets
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder

Erlotinib Tablet is indicated for:

  • The first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor(EGFR) exon 19 deletions or exon 21 (L858R) substitution mutations as detected by an FDA-approved test.
  • The maintenance treatment of patients with locally advanced or metastatic non-small cell lung cancer,  whose disease has not progressed after four cycles of platinum-based first-line chemotherapy.
  • The treatment of patients with locally advanced or metastatic non- small cell lung cancer after failure of at least one prior chemotherapy regimen.

3s corporation is Supplier, Exporter , Wholesaler  for Erlotinib Tablet 100mg & 150 mg in India.

We even  offer contract manufacturing services from WHO GMP approved factories.

 

ADDITIONAL INFORMATION

Single oral doses of Erlotinib up to 1, 000 mg in healthy subjects and weekly doses up to 1, 600 mg in cancer patients have been tolerated. Repeated twice-daily doses of 200 mg single-agent Erlotinib in healthy subjects were poorly tolerated after only a few days of dosing. Based on the data from these studies, an unacceptable incidence of severe adverse reactions, such as diarrhea, rash, and liver transaminase elevation, may occur above the recommended dose.

 

SIDE EFFECTS-

MOST COMMON SIDE EFFECTS

  • Metastatic NSCLC – First-Line Treatment of Patients With EGFR Mutations:
    • Most frequent (≥30%) adverse reactions were diarrhea, asthenia, rash, cough, dyspnea, and decreased appetite.
  • Advanced NSCLC – Maintenance Treatment:
    • Rash and diarrhea.
    •  Rash (9%) and diarrhea (2%). Rash and diarrhea resulted in dose reductions or interruption (5% and 3%, respectively) and discontinuation (1% and 0.5%, respectively) of Erlotinib-treated patients.
  • Advanced NSCLC – Second/Third-Line Treatment:
    • Rash and diarrhea.
    • Rash (9%) and diarrhea (6%). Rash and diarrhea each resulted in dose reductions (6% and 1%, respectively) and discontinuation in 1% of Erlotinib-treated patients.
  • Advanced Pancreatic Cancer –Erlotinib Administered Concurrently with Gemcitabine:
    • Fatigue, rash, nausea, anorexia, and diarrhea.
    • Grade 3/4 (NCI-CTC Version 2.0) adverse reactions were rash (5%) and diarrhea (5%). Rash and diarrhea each resulted in dose reductions in 2% of patients and discontinuation in up to 1% of patients receiving Erlotinib plus gemcitabine.
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Hydroxyurea Capsules 500 Mg

  • Storage Cool and Dry Place
  • Dosage 50mg
  • Form Capsules
  • Packaging Type Stripes
  • Usage Clinical, hospital etc.
  • Grade Standard Medicine Grade

Hydroxyurea Capsules 500 mg that we offer is an antineoplastic agent that is taken orally. Our Hydroxyurea Capsules 500 mg is widely acknowledged by the medical practitioners owing to its accurate composition and effective results. We provide Hydroxyurea Capsules 500 mg in safe blister packing.


Inactive ingredients : citric acid, colorants (D&C Yellow No. 10, FD&;C Blue No. 1, FD&C Red 40, and D&;C Red 28), gelatin, lactose, magnesium stearate, sodium phosphate, and titanium dioxide.

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Methotrexate

  • Packaging Type Plastic Bottle
  • Usage Clinical, hospital etc.
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder
Methotrexate Tablet 2.5mg is a chemotherapy drug. This medicine affects cells that are rapidly growing, such as cancer cells and cells in mouth and stomach. It is used to treat many cancers and other medical conditions. It is used for leukemias, lymphomas, breast cancer, lung cancer, head and neck cancers, and other cancers. This medicine also works on the immune system and is commonly used to treat psoriasis and rheumatoid arthritis. Methotrexate interferes with the growth of certain cells of the body, especially cells that reproduce quickly, such as cancer cells, bone marrow cells, and skin cells.
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ABIRAPRO ABIRATERONE ACETATE 250MG

  • Grade Standard Medicine Grade
  • Form Tablets / Liquid / Capsules / Powder
  • Packaging Type Plastic Bottle
  • CATEGORY Anti Cancer Tablets
  • Strengths available : 250 mg tablets
  • Storage Store at temperature between 20°C -25°C
  • Dosage for Prostate Cancer (For Adult) 1, 000 mg orally once a day on an empty stomach (in combination with prednisone 5 mg orally 2 times
  • PACK SIZE Bottle of 120 tabs
  • Dosage 5mg
  • Storage Cool and Dry Place
  • Usage Clinical, hospital etc.

ABIRARO 250mg (Abiraterone Acetate) tablet is a prescription drug  used in the treatment of prostate cancer. Abirapro contains Abiraterone acetate which  belongs to a class drugs known as antiandrogens. It stops the body from making testosterone which can slow the growth of prostate cancer.

Precaution : No food should be consumed for at least 2 hours before the dose and for at least 1 hour after the dose of this drug.

 

SIDE EFFECTS

Common side effects are decreased potassium level in blood, Edema, Increased blood pressure, Urinary tract infection, Diarrhoea.

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Busulfan 2 Mg Tablet

  • Category Anti Cancer Tablets
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder
  • Packaging Type Plastic Bottle
  • Usage Clinical, hospital etc.

Busulfan tablets contain a medicine called busulfan. This belongs to a group of medicines called cytotoxics (also called chemotherapy). Busulfan is used for certain blood problems and cancers of the blood. It works by reducing the number of new blood cells your body makes. Busulfan is used for Chronic granulocytic leukaemia (also called chronic myeloid leukaemia) – a disease that increases the number of white blood cells.

3s corporation is supplier, Exporter  for Busulfan 2 mg tablets in India.

 

ADDITIONAL INFORMATION

The recommended dose of busulfan in adult patients is 1 mg/kg every 6 hours for four days, starting seven days prior to transplantation. 60 mg/kg per day of cyclophosphamide is usually given for two days commencing 24 h after the final dose of Busulfan.

 

 

SIDE EFFECTS

Toxicity may include interstitial pulmonary fibrosis (“Busulfan Lung”),  hyperpigmentation,  seizures,  hepatic (veno-occlusive disease) (VOD), emesis, and wasting syndrome. Busulfan also induces thrombocytopenia, a condition of lowered blood platelet count and activity. Seizures and VOD are serious concerns with busulfan therapy and prophylaxis is often utilized to avoid these effects. Hepatic VOD is a dose-limiting toxicity.

Antiemetics are often administered prior to busulfan to prevent emesis.

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CELKERAN(CHLORAMBUCIL)

  • Form Tablets / Liquid / Capsules / Powder
  • Packaging Type Plastic Bottle
  • CATEGORY Anti Cancer Tablets
  • Manufacturer Celon Labs
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Usage Clinical, hospital etc.
CELKERAN(CHLORAMBUCIL)

 

  • chemotherapy drug
  • nitrogen mustard alkylating agent
  • immunosuppressive drug

 

 

Chlorambucil is a chemotherapy drug that has been mainly used in the treatment of chronic lymphocytic leukemia. It is a nitrogen mustard alkylating agent . It also has been used as an immunosuppressive drug for various autoimmune and inflammatory conditions, such as nephrotic syndrome. In India, its manufactured by two companies Natco & Celon. Celon sells it on the brand name of Celkeran 2 mg tablet. Packing is for 30 tabs per pack.

 

SIDE EFFECTS INCLUDE:   GI DISTURBANCES; HEPATOTOXICITY; SKIN RASHES; PERIPHERAL NEUROPATHY; CENTRAL NEUROTOXICITY INCLUDING SEIZURES; INTERSTITIAL PNEUMONIA, PULMONARY FIBROSIS. HIGH DOSES MAY PRODUCE AZOOSPERMIA AND AMENORRHOEA. STERILITY WHEN GIVEN TO BOYS AT OR BEFORE PUBERTY. POTENTIALLY FATAL: SEVERE BONE MARROW SUPPRESSION, CARCINOGENIC AND HUMAN INFERTILITY.
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CHLORAMBUCIL TABLET

  • Form Tablets / Liquid / Capsules / Powder
  • Packaging Type Plastic Bottle
  • CATEGORY Anti Cancer Tablets
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Usage Clinical, hospital etc.
CHLORAMBUCIL TABLET

 

  • bifunctional alkylating agent

Chlorambucil  is a bifunctional alkylating agent of the nitrogen mustard type that has been found active against selected human neoplastic diseases. Chlorambucil is used to treat some cancers particularly cancer of white blood cells and cancers of the lymphatic system. In cancer, certain cells in the body grow and multiply too fast. Chemotherapy (anti-Cancer) medicines like chlorambucil work by preventing the growth and division of cells, and this reduces the number of cancer cells  body makes. It can be prescribed for both adults and children. Chlorambucil is available in tablet form for oral administration.

It  is manufatured in India by many brands like Divya Enterprises,  Natco India Limited  etc. 3s corporation offer contract manufacturing services from WHO GMP approved factories.

 

ADDITIONAL INFORMATION

 

Chlorambucil lowers the number of white cells in your blood, increasing the chance of you getting an infection. You should take certain precautions to reduce the risk of infection – if possible, avoid people with infections and let your doctor know if you think you are getting a sore throat or if you have a high temperature.

 

 

SIDE EFFECTS

Stop taking chlorambucil and call your doctor at once if you have a serious side effect such as:

  • seizure (convulsions);
  • fever, chills, body aches, flu symptoms, sores in your mouth and throat, ongoing cough;
  • pale skin, feeling light-headed or short of breath, rapid heart rate, trouble concentrating;
  • easy bruising, unusual bleeding (nose, mouth, vagina, or rectum).
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ERLONAT (ERLOTINIB) 150 MG TABLET

  • Packaging Type Plastic Bottle
  • Usage Clinical, hospital etc.
  • CATEGORY Anti Cancer Tablets
  • Manufacturer Natco
  • Packing 150 mg tablet 30 tablets
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder

Erlonat ( Erlotinib), Manufacturer: Natco

Erlonat (Erlotinib) is primarily used to treat cell lung cancer, or pancreatic cancer when combined with a certain other medicine. It works by inhibiting growth to adjacent tissues in the body so that the cancerous cells slow down, allowing the patient a better environment to recover and fight the cancer naturally.

Dosage and Administration

Typically, an adult patient will be instructed to take between 100mg and 150mg of Erlonat (Erlotinib), at least 1 hour before any meals or snacks and 2 hours after. Unless otherwise instructed, you should always swallow each tablet whole without chewing, crushing, splitting, or dissolving the tablet in liquid. Wash tablets down with full glass of water.

Side effects are Coughing , Fever , Weakness, Chest pains , Severe or persistent nausea, Vomiting, Diarrhea, , Eye discomfort, Irritated or dry skin, Inward growing eyelashes, Unusual bruising or bleeding, Loss of appetite

 

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EVEROLIMUS TABLET 5 & 10 MG

  • Packaging Type Plastic Bottle
  • Usage Clinical, hospital etc.
  • CATEGORY Anti Cancer Tablets
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder
EVEROLIMUS TABLET 5 & 10 MG

 

  • cancer medication

Everolimus Tablet 5 & 10 mg  is a cancer medication that interferes with the growth of cancer cells and slows their spread in the body.Everolimus is used to treat certain types of kidney cancer, breast cancer, or brain tumor. It is usually given after other cancer medications have been tried without successful treatment.Everolimus is also used to treat non-cancerous (benign) kidney tumors, and certain types of advanced or progressive tumors of the pancreas.

3s corporation is Supplier, Exporter , Wholesaler  for Everolimus Tablet 5 & 10 mg in India.

India has many manufacturers who manufacture Everolimus Tablet 5 & 10 mg. 

 

ADDITIONAL INFORMATION

 Everolimus tablet  should be taken at the same time each day. You may take Everolimus tablet with or without food, but take it the same way each time.

Do not take an Everolimus tablet  regular tablet together with the dispersible tablet. Use only one form of this medicine.

Do not crush, chew, or break an regular tablet. Swallow the pill whole.

 

SIDE EFFECTS

Stop using Everolimus and patient should call doctor at once if he has:

  • new or worsening cough, wheezing, feeling short of breath;
  • fever, swollen gums, painful mouth sores, pain when swallowing, tired feeling, cold or flu symptoms;
  • seizure (convulsions);
  • swelling, rapid weight gain, urinating less than usual or not at all;
  • pain or burning when you urinate;
  • pain or fullness in your ear, hearing problems;
  • pale skin, easy bruising, unusual bleeding;
  • a skin wound that is swollen, red, warm, bleeding, or oozing;
  • any wound that will not heal; or
  • nausea, pain in your upper stomach, itching, joint pain, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of your skin or eyes).

Common Afinitor side effects may include:

  • mild skin rash;
  • headache; or
  • diarrhea, mild stomach pain or nausea.
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LEUKERAN 2 MG & 5 MG

  • Application Clinical, hospital etc.
  • CATEGORY Anti Cancer Tablets
  • Manufacturer Glaxosmithkline
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder
  • Packaging Type Plastic Bottle
LEUKERAN 2 MG & 5 MG

 

  • chemotherapy prescription drug
DESCRIPTION

Leukeran tablet manufactured by GSK also known as Chlorambucil is a chemotherapy prescription drug given to patients to treat diseases like

1. Chronic lymphocytic leukaemia (CLL),

2. Low-grade non-Hodgkin lymphoma,

3. Hodgkin lymphoma

4. Waldenstrom’s macroglobulinaemia

 

 

ADDITIONAL INFORMATION

How to take Leukeran:

The tablets should be swallowed whole. You should take them as directed by your doctor, nurse or pharmacist.

Chemotherapy is usually given as a course of several sessions (cycles) of treatment over a few months. The length of your treatment and the number of cycles you have will depend on which type of cancer or leukaemia you’re being treated for. Your nurse or doctor will discuss your treatment plan with you.

Before you have your treatment your doctor will arrange for you to have blood tests. You’ll usually be given anti-sickness drugs before and/or during your treatment.

 

 

SIDE EFFECTS

Fever, chills, body aches, flu symptoms, sores in your mouth and throat, ongoing cough;

Pale skin, easy bruising, unusual bleeding, blood in your urine or stools;

feeling weak or tired, loss of appetite, rapid weight loss;

nausea, upper stomach pain, itching, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);

an unusual mass or lump;

chest discomfort, feeling short of breath on exertion, dry cough or hack;

severe vomiting or diarrhea;

seizure (convulsions); or

severe skin reaction — fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Common side effects may include:

mild nausea or diarrhea;

tremors or shaking; or

numbness, burning pain, or tingly feeling.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.

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METHOTREXATE TABLET 2.5MG

  • Packaging Type Plastic Bottle
  • CATEGORY Anti Cancer Tablets
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder
  • Usage Clinical, hospital etc.
METHOTREXATE TABLET 2.5MG

 

  • chemotherapy drug.

Methotrexate Tablet 2.5mg  is a chemotherapy drug. This medicine affects cells that are rapidly growing, such as cancer cells and cells in  mouth and stomach. It is used to treat many cancers and other medical conditions. It is used for leukemias, lymphomas, breast cancer, lung cancer, head and neck cancers, and other cancers. This medicine also works on the immune system and is commonly used to treat psoriasis and rheumatoid arthritis. Methotrexate interferes with the growth of certain cells of the body, especially cells that reproduce quickly, such as cancer cells, bone marrow cells, and skin cells.

3s corporation is Supplier, Exporter , Wholesaler  for Methotrexate Tablet 2.5mg in India.

India has many manufacturers who manufacture  Methotrexate Tablet 2.5mg .

 

ADDITIONAL INFORMATION

Methotrexate is usually taken once or twice per week and not every day.

 

SIDE EFFECTS

 

serious side effects are:

  • dry cough, shortness of breath;
  • diarrhea, vomiting, white patches or sores inside your mouth or on your lips;
  • blood in your urine or stools;
  • urinating less than usual or not at all;
  • fever, chills, body aches, flu symptoms;
  • sore throat and headache with a severe blistering, peeling, and red skin rash;
  • pale skin, easy bruising or bleeding, weakness; or
  • nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes).

Less serious side effects may include:

  • nausea, vomiting, upset stomach;
  • dizziness, tired feeling;
  • headache;
  • bleeding of your gums; or
  • blurred vision.
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NEXAVAR 200 MG

  • Packaging Type Plastic Bottle
  • CATEGORY Anti Cancer Tablets
  • Manufacturer: Bayer
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder
  • Usage Clinical, hospital etc.

Nexavar by Bayer is a medicine approved for the treatment of primary kidney cancer (advanced renal cell carcinoma) and advanced primary liver cancer (hepatocellular carcinoma). Its generic name is Sorafenib. It has both US FDA & European Commision approval for use in the treatment of advanced renal cancer & liver cancer. Sorafenib is a small molecular inhibitor of several Tyrosine protein kinases (VEGFR and PDGFR) and Raf kinases. It is available in 200 mg dosage & 60 tablets/bottle packing.

 

 

SIDE EFFECTS

Possible Side Effects:

While Nexavar is working to help treat your cancer, it may change some things in the rest of your body. This could lead to serious side effects, including:

Birth defects or death of an unborn baby. Women should not get pregnant during treatment with Nexavar and for at least 2 weeks after stopping treatment. Men and women should use effective birth control during treatment with Nexavar and for at least 2 weeks after stopping treatment. Talk with your doctor about effective birth control methods. Call your doctor right away if you become pregnant during treatment with Nexavar

Decreased blood flow to the heart and heart attack. Get emergency help right away and call your doctor if you have symptoms such as chest pain, palpitations, shortness of breath, feeling light-headed or faint, nausea, vomiting, or sweating a lotBleeding problems. Nexavar may cause bleeding, which can be serious and sometimes lead to death. Tell your doctor if you have any bleeding while taking Nexavar

High blood pressure. Your blood pressure should be checked weekly during the first 6 weeks of treatment with Nexavar, and regularly thereafter. Any high blood pressure should be treated while you are taking NexavarA skin problem called hand-foot skin reaction. This causes redness, pain, swelling, or blisters on the palms of your hands or soles of your feet. If you get this side effect, your doctor may change your dose or stop treatment for some timeSerious skin and mouth reactions. Nexavar may cause serious skin reactions, which can be life-threatening. Tell your doctor if you have skin rash, blistering and peeling of the skin, or blistering and peeling of the inside of your mouthAn opening in the wall of your stomach or intestines (perforation of the bowel). Tell your doctor right away if you get high fever, nausea, vomiting, or severe abdominal (stomach) painPossible wound healing problems. If you need to have a surgical or dental procedure, tell your doctor that you are taking Nexavar. Nexavar may need to be stopped until your wound heals after some types of surgeryChanges in the electrical activity of your heart called “QT prolongation.” QT prolongation can cause irregular heartbeats that can be life-threatening. Your doctor may do tests during your treatment with Nexavar to check the levels of potassium, magnesium, and calcium in your blood, and check the electrical activity of your heart with an ECG. Tell your doctor right away if you feel faint, lightheaded, dizzy, or feel your heart beating irregularly or fast while taking NexavarInflammation of your liver (drug-induced hepatitis). Nexavar may cause liver problems that may lead to liver failure and death. Your doctor may stop your treatment with Nexavar if you develop changes in certain liver function tests. Call your doctor right away if you develop any of the following symptoms: your skin or the white part of your eyes turns yellow (jaundice), dark “tea-colored” urine, light-colored bowel movements (stools), worsening nausea, worsening vomiting, abdominal pain, or confusionHere are some of the side effects many—but not all—people get when they take Nexavar:

  • Rash, redness, itching, or peeling skin
  • Hair thinning or patchy hair loss
  • Diarrhea (frequent and/or loose bowel movements)
  • Nausea or vomiting
  • Loss of appetite
  • Pain in stomach or abdomen area
  • Feeling tired
  • Losing weight

 

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SORAFENAT SORAFENIB 200MG TABLETS

  • Packaging Type Plastic Bottle
  • CATEGORY Anti Cancer Tablets
  • Manufactured Natco Pharma Ltd.
  • Strengths available 200mg tablets
  • Storage Store in a cool place, protected from light
  • PACK SIZE Bottle of 60 tabs & Bottle of 120 tabs
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder
  • Usage Clinical, hospital etc.

SORAFENAT 200mg (Sorafenib) is an anti-cancer medication prescribed for renal cell carcinoma (kidney cancer), hepatocellular carcinoma (liver cancer) and thyroid cancer. SORAFENAT works by blocking the action of the abnormal protein that signals cancer cells to multiply thereby  helps to stop or slow the spread of cancer cells. It decreases tumor growth and replication. SORAFENAT harms cancer cells causing their death. This drug can be obtained only with prescription.

 

 

Dosage :  

400 mg twice a day at least one hour before or two hours after eating

Treatment should continue until the patient is no longer clinically benefiting from therapy or until unacceptable toxicity occurs.

Consult your doctor for specific prescription

 

SIDE EFFECTS

Common side effects are Fatigue, Nausea, Loss of appetite, Diarrhoea, Abdominal pain, Hair loss, Weight loss, Rash, Hand-foot syndrome.

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XBIRA ABIRATERONE ACETATE 250MG

  • Grade Standard Medicine Grade
  • Form Tablets / Liquid / Capsules / Powder
  • Packaging Type Plastic Bottle
  • CATEGORY Anti Cancer Tablets
  • Manufactured Cipla Ltd
  • Strengths available 250mg tablets
  • Storage Store below 30°C
  • PACK SIZE 120 tablets per bottle
  • Dosage 5mg
  • Storage Cool and Dry Place
  • Usage Clinical, hospital etc.

XBIRA 250mg (Abiraterone Acetate) is a prescription drug used for treating a certain type of prostate cancer that has spread to other parts of the body. XBIRA contains Abiraterone acetate which belongs to a class drugs known as antiandrogens. It stops the body from making testosterone which can slow the growth of prostate cancer.

 

Dosage :  

The recommended dose of XBIRA tablets is 1000mg (four 250mg tablets) administered orally once daily in combination with Prednisone 5mg administered orally twice daily.

XBIRA tablets must be taken on an empty stomach. No food should be consumed for at least 2 hours before the dose of XBIRA tablets is taken and for at least 1 hour after the dose of XBIRA tablets is taken.

The tablets should be swallowed whole with water and not to be crushed or chewed. It is highly advisable to administer the drug under strict medical supervision and advice.

 

SIDE EFFECTS

Most common side effects are Decreased potassium level in blood, Edema, Increased blood pressure, Urinary tract infection, Diarrhoea

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EVERMIL EVEROLIMUS 5MG & 10MG TABLETS

  • Packaging Type Plastic Bottle
  • Usage Clinical, hospital etc.
  • CATEGORY Anti Cancer Tablets
  • Manufacturer Glenmark Pharmaceuticals Ltd
  • Strengths available 5mg & 10mg
  • Storage Store at temperature between 15°C – 25°C
  • PACK SIZE 1 x 10 tablets per pack
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder

Evermil (Everolimus) Tablet is prescription drug used in treatment of breast cancer, pancreatic cancer, lung cancer and kidney cancer. EVERMIL is an immunosuppressant , ie, It suppresses the activity of body’s immune system that may cause the body to reject the transplanted organ.

 

 

Dosage :

Patients receiving Evermil may require dose adjustments based on Evermil blood concentrations achieved, tolerability, individual response, change in concomitant medications and the clinical situation.

Dosage in Adult Kidney Transplant Patients

An initial Evermil dose of 0.75 mg orally twice daily (1.5 mg per day) is recommended for adult kidney transplant patients in combination with reduced dose cyclosporine, administered as soon as possible after transplantation. Oral prednisone should be initiated once oral medication is tolerated. Steroid doses may be further tapered on an individualized basis depending on the clinical status of patient and function of graft.

Dosage in Adult Liver Transplant Patients

Start Evermil at least 30 days post-transplant. An initial dose of 1.0 mg orally twice daily (2.0 mg per day) is recommended for adult liver transplant patients in combination with reduced dose tacrolimus. Steroid doses may be further tapered on an individualized basis depending on the clinical status of patient and function of graft.

 

 

SIDE EFFECTS

Side effects : Weakness, Sinus inflammation, Infection, Fever, Cough, Fatigue, Stomatitis (Inflammation of the mouth), Otitis media (infection of ear), Diarrhoea, Upper respiratory tract infection.

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ERLOCIP ERLOTINIB 100MG

  • Packaging Type Plastic Bottle
  • Usage Clinical, hospital etc.
  • CATEGORY Anti Cancer Tablets
  • Manufacturer Cipla Ltd.
  • Strengths available 100mg & 150mg
  • Storage Store in a cool dry place
  • Dosage ERLOCIP Tablets treatment should be supervised by a physician experienced in the use of anti-cancer
  • PACK SIZE Pack of 30 tablets
  • Dosage 5mg
  • Grade Standard Medicine Grade
  • Storage Cool and Dry Place
  • Form Tablets / Liquid / Capsules / Powder

Erlocip also known as Erlotinib is a prescription drug used in the treatment of non-small cell lung cancer and pancreatic cancer. It interfers with the protein epidermal growth factor, preventing it from activating enzymes which is required in certain cancer cells to grow and multiply.

Recommended Dose: NSCLC

EGFR mutation testing should be performed prior to initiation of ERLOCIP Tablets therapy in chemo-naïve patients with advanced or metastatic NSCLC.

The recommended daily dose of ERLOCIP Tablets for NSCLC is 150 mg taken on an empty stomach at least 1 hour before or 2 hours after the ingestion of food. Treatment should continue until disease progression or unacceptable toxicity occurs. There is no evidence that treatment beyond progression is beneficial.

Recommended Dose: Pancreatic Cancer

The recommended daily dose of ERLOCIP Tablets for pancreatic cancer is 100 mg taken on an empty stomach at least 1 hour before or 2 hours after the ingestion of food, in combination with gemcitabine. Treatment should continue until disease progression or unacceptable toxicity occurs.

In patients who do not develop rash within the first 4–8 weeks of treatment, further treatment with ERLOCIP Tablets should be re-assessed.

When dose adjustment is necessary, the dose should be reduced in steps of 50 mg. Concomitant use of CYP3A4 substrates and modulators may require dose adjustment.

 

IDE EFFECTS

Most common side effects are Nausea, Vomiting, Fatigue, Breathing difficulty, Abdominal pain, Edema, Weight loss, Loss of appetite, Anemia, Infection, Bone pain, Constipation, Diarrhea, Fever, Stomatitis (Inflammation of the mouth), Rash.

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