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Our offered Product range includes MEGESTROL ACETATE TABLETS USP 40 MG, ANASTROZOLE TABLETS 1 MG, BARACLUDE 1 MG TABLET, CYCLOPHOSPHAMIDE TABLETS USP 50 MG and Flutamide Tablets 250 mg.
Megestrol Acetate Tablets USP 40 mg Megestrol Acetate Tablets USP is a synthetic, antineoplastic and progestational drug.
Megestrol Acetate Tablets USP are indicated for the palliative treatment of advanced carcinoma of the breast or endometrium (i.e., recurrent, inoperable, or metastatic disease). It should not be used in lieu of currently accepted procedures such as surgery, radiation, or chemotherapy.
3s corporation is Supplier, Exporter , Wholesaler for Megestrol Acetate Tablets USP 40 mg in India.
India has many manufacturers who manufacture Megestrol Acetate Tablets USP 40 mg .
ADDITIONAL INFORMATION
Dose for breast Cancer: 160 mg/day (40 mg qid).
Dose for Endometrial Carcinoma: 40 to 320 mg/day in divided doses.
At least 2 months of continuous treatment is considered an adequate period for determining the efficacy of Megestrol Acetate Tablets USP.
SIDE EFFECTS
Weight gain is a frequent side effect of megestrol acetate. This gain has been associated with increased appetite and is not necessarily associated with fluid retention.
Thromboembolic phenomena including thrombophlebitis and pulmonary embolism (in some cases fatal) have been reported.
Heart failure, nausea and vomiting, edema, breakthrough menstrual bleeding, dyspnea, tumor flare (with or without hypercalcemia), hyperglycemia, glucose intolerance, alopecia, hypertension, carpal tunnel syndrome, mood changes, hot flashes, malaise, asthenia, lethargy, sweating and rash.
Anastrozole tablets for oral administration contain 1 mg of anastrozole, a non-steroidal aromatase inhibitor.Anastrozole is used to treat breast cancer in postmenopausal women. It is often given to women whose cancer has progressed even after taking tamoxifen (Nolvadex, Soltamox). It is a non-steroidal aromatase inhibitor. This medication is available in generic form.
BARACLUDE® (entecavir) is a chronic hepatitis B treatment that works to fight the hepatitis B virus (HBV) and may help to improve the condition of your liver.
BARACLUDE is a prescription medicine used to treat chronic hepatitis B virus (HBV) in adults who have active virus and liver damage.
Currently there is no cure for HBV. BARACLUDE will not cure HBV
BARACLUDE MAY :
This chronic hepatitis B treatment works to help fight HBV and may reduce the amount of the virus in your blood. BARACLUDE is taken once a day by mouth. BARACLUDE does not stop you from spreading the hepatitis B virus (HBV) to others by sex, sharing needles, or being exposed to your blood. Talk with your healthcare provider about safe sexual practices that protect your partner. Never share needles. Do not share personal items that can have blood or body fluids on them, like toothbrushes or razor blades. A shot (vaccine) is available to protect people at risk from becoming infected with HBV.
Read the sections below to learn more about choosing a chronic hepatitis B treatment, and to see how BARACLUDE may help to improve the condition of your liver. Ask your doctor if BARACLUDE is right for you. Remember, not all people who have HBV need treatment.
How BARACLUDE Works:
HBV attacks your healthy liver cells where it multiplies and infects more liver cells. As a chronic hepatitis B treatment, BARACLUDE works to fight HBV and may lower the amount of HBV in the body.
SIDE-EFFECTS:All medicines have benefits and risks. BARACLUDE® (entecavir) may cause the following serious side effects:
Your hepatitis B virus infection may get worse if you stop taking BARACLUDE. This usually happens within 6 months after stopping BARACLUDE.
If you have or get HIV that is not being treated with medicines while taking BARACLUDE, the HIV virus may develop resistance to certain HIV medicines and become harder to treat. You should get an HIV test before you start taking BARACLUDE and anytime after that when there is a chance you were exposed to HIV.
BARACLUDE can cause serious side effects including:
Lactic acidosis (buildup of acid in the blood). Some people who have taken BARACLUDE or medicines like BARACLUDE (a nucleoside analogue) have developed a serious condition called lactic acidosis. Lactic acidosis is a serious medical emergency that can cause death. Lactic acidosis must be treated in the hospital. Reports of lactic acidosis with BARACLUDE generally involved patients who were seriously ill due to their liver disease or other medical condition.
Call your healthcare provider right away if you get any of the following signs or symptoms of lactic acidosis:
Call your healthcare provider right away if you get any of the following signs or symptoms of liver problems:
The most common side effects of BARACLUDE include:
Tell your healthcare provider if you have any side effect that bothers you or that does not go away.
These are not all the possible side effects of BARACLUDE. For more information, ask your healthcare provider or pharmacist
Cyclophosphamide Tablets USP 50 mg is effective alone in susceptible malignancies, are more frequently used concurrently or sequentially with other antineoplastic drugs.It is used in treatment of Malignant lymphomas (Stages III and IV of the Ann Arbor staging system), Hodgkin’s disease, lymphocytic lymphoma (nodular or diffuse), mixed-cell type lymphoma, histiocytic lymphoma, Burkitt’s lymphoma, Multiple myeloma, Leukemias( Chronic lymphocytic leukemia, chronic granulocytic leukemia) (it is usually ineffective in acute blastic crisis), acute myelogenous and monocytic leukemia, acute lymphoblastic (stem-cell) leukemia in children (cyclophosphamide given during remission is effective in prolonging its duration), Mycosis fungoides (advanced disease), Neuroblastoma (disseminated disease), Adenocarcinoma of the ovary, Retinoblastoma, Carcinoma of the breast.
India has many manufacturers who manufacture Cyclophosphamide Tablets USP 50 mg .To know more contact us.
3s corporation is supplier, Exporter and Wholesaler for Cyclophosphamide Tablets USP 50 mg in India.
ADDITIONAL INFORMATION
Oral cyclophosphamide dosing is usually in the range of 1 to 5 mg/kg/day for both initial and maintenance dosing.
It ‘s storage should be at or below 25°C (77°F) is recommended; this product will withstand brief exposure to temperatures up to 30°C (86°F) but should be protected from temperatures above 30°C (86°F).
SIDE EFFECTS
Nausea and vomiting commonly occur with cyclophosphamide therapy. Anorexia and, less frequently, abdominal discomfort or pain and diarrhea may occur. There are isolated reports of hemorrhagic colitis, oral mucosal ulceration and jaundice occurring during therapy. These adverse drug effects generally remit when cyclophosphamide treatment is stopped.
SKIN AND ITS STRUCTURESAlopecia occurs commonly in patients treated with cyclophosphamide. The hair can be expected to grow back after treatment with the drug or even during continued drug treatment, though it may be different in texture or color. Skin rash occurs occasionally in patients receiving the drug. Pigmentation of the skin and changes in nails can occur. Very rare reports of Stevens-Johnson syndrome and toxic epidermal necrolysis have been received during postmarketing surveillance; due to the nature of spontaneous adverse event reporting, a definitive causal relationship to cyclophosphamide has not been established.
HEMATOPOIETIC SYSTEMLeukopenia occurs in patients treated with cyclophosphamide, is related to the dose of drug, and can be used as a dosage guide. Leukopenia of less than 2000 cells/mm3 develops commonly in patients treated with an initial loading dose of the drug, and less frequently in patients maintained on smaller doses. The degree of neutropenia is particularly important because it correlates with a reduction in resistance to infections. Fever without documented infection has been reported in neutropenic patients.
Thrombocytopenia or anemia develop occasionally in patients treated with cyclophosphamide. These hematologic effects usually can be reversed by reducing the drug dose or by interrupting treatment. Recovery from leukopenia usually begins in 7 to 10 days after cessation of therapy.
URINARY SYSTEMSee WARNINGS: Urinary System for information on cystitis and urinary bladder fibrosis.
Hemorrhagic ureteritis and renal tubular necrosis have been reported to occur in patients treated with cyclophosphamide. Such lesions usually resolve following cessation of therapy.
INFECTIONSSee WARNINGS: Infections for information on reduced host resistance to infections.
CARCINOGENESISSee WARNINGS: Carcinogenesis, Mutagenesis, and Impairment of Fertility.
RESPIRATORY SYSTEMInterstitial pneumonitis has been reported as part of the postmarketing experience. Interstitial pulmonary fibrosis has been reported in patients receiving high doses of cyclophosphamide over a prolonged period.
Flutamide Tablets 250 mg belongs to a group of medications known as nonsteroidal antiandrogens. Prostate cancer cells require testosterone in order to grow and reproduce. Flutamide is used in combination with a hormone therapy that reduces the amount of testosterone in the body (e.g., goserelin) for the treatment of prostate cancer.
India has many manufacturers who manufacture Flutamide Tablets 250 mg.To know more contact us.
3s corporation is Supplier, Exporter , Wholesaler for Flutamide Tablets 250 mg in India.
ADDITIONAL INFORMATION
The recommended dose is 250 mg 3 times daily at 8 hour intervals. This treatment should be started at the same time as treatment with an LHRH analogue (e.g., goserelin) or after surgical removal of the testicles.
SIDE EFFECTS
Like all medicines, Flutamide 250 mg Tablets can cause unwanted side effects, particularly when you first start taking them, although not everybody gets them.
Contact your doctor immediately if you experience any of the following as your Flutamide dose may need to be reduced or stopped:
· an allergic reaction to any of the ingredients of Flutamide Tablets (such as itching and/or rash, swelling of the face, lips, tongue and/or throat with difficulty in swallowing or breathing);
· problems with liver (such as itching of the skin, dark urine, lack of appetite, yellow eyes or skin, flu-like symptoms, irritability, changes in the level of consciousness);
· swelling of legs or any other parts of the body;
· breathing problems.
Gefitinib Tablets 250 mg is indicated as monotherapy for the continued treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of both platinum-based and docetaxel chemotherapies who are benefiting or have benefited from Gefitinib .
It is manufactured by many Indian manufacturers including Brands like Natco Pharma Ltd.
3S corporation is Supplier, Exporter, Wholesaler for Gefitinib Tablets 250 mg in India.
ADDITIONAL INFORMATION
The recommended daily dose of Gefitinib is one 250 mg tablet with or without food. Higher doses do not give a better response and cause increased toxicity.
Gefitinib Tablets 250 mg tablets can also be dispersed in half a glass of drinking water (noncarbonated). No other liquids should be used
SIDE EFFECTS
Letrozole Tablets USP 2.5 mg is an oral non-steroidal Aromatase inhibitor for the treatment of hormonally-responsive breast cancer after surgery.Letrozole is approved by the United States Food and Drug Administration (FDA) for the treatment of local or metastatic breast cancer that is hormone receptor positive or has an unknown receptor status in postmenopausal women.
3s corporation is Supplier, Exporter , Wholesaler for Letrozole Tablets USP 2.5 mg in India.
We even offer contract manufacturing services from WHO GMP approved factories.
ADDITIONAL INFORMATION
Letrozole is contraindicated in women having a pre-menopausal hormonal status, during pregnancy and lactation.
SIDE EFFECTS
The most common side effects are sweating, hot flashes, arthralgia (joint pain), and fatigue.
Generally, side effects include signs and symptoms of hypoestrogenism. There is concern that long term use may lead to osteoporosis, which is in certain patient populations such as post-menopausal women or osteoporotics.
LYNPARZA (Olaparib) is a prescription medicine used to treat adults with ovarian cancer, fallopian tube cancer, or primary peritoneal cancer.
Strengths available : 50mg & 150mg
Storage : Store at temperature between 15ºC to 25ºC
It is Approved by US FDA
Dosage :
SIDE EFFECTS
Common Side effects are Nausea or vomiting , low number of red or white blood cells, tiredness or weakness, sore throat or runny nose, diarrhea, joint, muscle, and back pain, headache, constipation, changes in the way food tastes, loss of appetite, mouth sores, respiratory infections, changes in kidney function blood test, low number of platelets, indigestion or heartburn
DESCRIPTION
Melphalan Tablet 2mg & 5mg is a chemotherapy drug that is used to treat certain types of cancer such as multiple myeloma, melanoma, ovarian cancer, breast cancer, Neuroblastoma, Rhabdomyosarcoma. It is also used in some conditioning regimens prior to bone marrow transplant. Melphalan Tablet 2mg & 5mg is a Alkeran which belongs to a class of drugs known as alkylating agents. It works by slowing or stopping the growth of cancer cells.
3s corporation is Supplier, Exporter , Wholesaler for Melphalan Tablet 2mg & 5mg in India.
We even offer contract manufacturing services from WHO GMP approved factories.
ADDITIONAL INFORMATION
The dosing of this medication is different for everyone. The amount of Alkeran that patient will receive depends on many factors, including his height and weight, his general health or other health problems, and the type of cancer or condition being treated. Also the dosage is based on patient’s medical condition, response to treatment, and blood counts. Doctor will determine patient’s dose and schedule.
patient should drink plenty of fluids while taking this medication. This helps kidneys to remove the drug from body and avoid some of the side effects.
Patient should contact doctor or pharmacist immediately for advice if he or she misses a dose.
SIDE EFFECTS
serious side effects are:
Less serious side effects may include:
DESCRIPTION
Procarbazine tablet 50 mg is a cancer (antineoplastic) medication. Procarbazine interferes with the growth of cancer cells and slows their growth and spread in the body.Procarbazine is used to treat Hodgkin’s Disease (a type of blood cancer).
We even offer contract manufacturing services from WHO GMP approved factories.
ADDITIONAL INFORMATION
Procarbazine can lower the activity of immune system making person susceptible to infections. Avoid contact with people who have colds, the flu, or other contagious illnesses and do not receive vaccines that contain live strains of a virus (e.g., live oral polio vaccine) during treatment with procarbazine.
SIDE EFFECTS
Serious side effects have been reported with the use of procarbazine including:
allergic reactions (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives);
decreased bone marrow function and blood problems (extreme fatigue);
easy bruising or bleeding;
black, bloody or tarry stools;
fever or chills;
signs of infection such as fever; chills, or sore throat;
nervous system side effects (numbness, tingling, or confusion);
sore in or around the mouth;
diarrhea.
Talk to doctor about the possible side effects from treatment with procarbazine.
Soranib contains sorafenib, which is a small molecular inhibitor of several tyrosine protein kinases.
Used For:
Soranib is used for the treatment of primary kidney cancer (advanced renal cell carcinoma) and advanced primary liver cancer. Soranib (sorafenib 200mg) is a cancer (chemotherapeutic) medication. Soranib (sorafenib 200mg) interferes with the growth of cancer cells and slows their growth and spread in the body.
Manufactured By : CIPLA
Specification:
Suninat from Natco is a prescription drug also popularly known as Sunitinib Malate or Sutent. It is used for treating GIST gastrointestinal stromal tumors in patients with tumors that were not treated successfully with imatinib (also known as Glivec) or patients who cannot take imatinib. Sunitinib is also used to treat advanced RCC (renal cell carcinoma) a type of cancer that begins in the cells of the kidneys. Sunitinib is also used for treating Pnet (pancreatic neuroendocrine tumors a type of tumor that begins in certain cells of the pancreas in patients with tumors that have worsened and cannot be treated with surgery.
It comes in dosage of 12.5 mg, 25 mg & 50 mg tablet. Pack size of 28 tabs. Natco is a generic and cheaper version of Pfizer’s patented drug Sutent.
SIDE EFFECTS
Common side effects of SUTENT include:
Veenat is a prescription drug manufactured by Natco India , used for the treatment of a type of leukemia (chronic myeloid leukemia or cml), gastrointestinal stromal tumors (gists – a type of tumor that grows in the walls of the digestive passages and may spread to other parts of the body). Veenat may also be used to prevent cancer from growing in patients after surgical removal of gist.
Mechanism of Action
Veenat works by blocking the action of an abnormal protein that promotes the multiplication of cancer cells. This helps slow or stop the spread of cancer cells.
Dosage:Veenat is usually taken once a day. Overdose:symptoms of overdose associated with veenat may include diarrhea, yellowing eyes and skin, stomach pain, fever, swelling, dark urine, change in amount of urine (severe increase or decrease), headache, loss of appetite, unusual bruising or bleeding, unusual tiredness or weakness, vomiting.
Precautions & WarningsVeenat should not be taken without consulting your doctor if you have ever had pulmonary fibrosis (scarring of the lungs), or liver or kidney disease, bone marrow problems, low white blood cell levels, or low blood platelet levels or if you have had your thyroid gland removed and if you have a history of swelling (edema) or fluid retention.
Drug Interactions The following drugs may interact with veenat: The side effects including the risk of bleeding may be increased by warfarin The risk of veenat’s side effects may be increased by azole antifungals (itraconazole, ketoconazole), ketolide antibiotics (telithromycin), macrolide antibiotics (clarithromycin, erythromycin), nefazodone, or protease inhibitors (ritonavir) Other cancer drugs (tamoxifen), corticosteroids (prednisone), cyclosporine, tacrolimus, cisapride, calcium channel blockers (diltiazem, verapamil), heart rhythm drugs (amiodarone, quinidine), certain diabetes medications (glipizide, pioglitazone, troglitazone), rifampin, st. John’s wort, nsaids (ibuprofen), antidepressants (desipramine, fluoxetine, paroxetine), beta-blockers (propranolol).
Vfend (Voriconazole) manufactured by Pfizer is a prescription drug, triazole antifungal medication that is generally used to treat serious, invasive fungal infections. These are generally seen in patients who are immunocompromised, and include invasive candidiasis, invasive aspergillosis, and certain emerging fungal infections. It is available in tablet & injection form both in 50 mg & 200 mg dosage.
nstructions for Use in All Patients
VFEND Tablets or Oral Suspension should be taken at least one hour before or after a meal.
VFEND I.V. for Injection requires reconstitution to 10 mg/mL and subsequent dilution to 5 mg/mL or less prior to administration as an infusion, at a maximum rate of 3 mg/kg per hour over 1 to 2 hours.
Do not administer as an IV bolus injection.
Use of VFEND I.V. With Other Parenteral Drug Products
Blood products and concentrated electrolytes
VFEND I.V. must not be infused concomitantly with any blood product or short-term infusion of concentrated electrolytes, even if the two infusions are running in separate intravenous lines (or cannulas). Electrolyte disturbances such as hypokalemia, hypomagnesemia and hypocalcemia should be corrected prior to initiation of VFEND therapy .
Intravenous solutions containing (non-concentrated) electrolytes
VFEND I.V. can be infused at the same time as other intravenous solutions containing (non-concentrated) electrolytes, but must be infused through a separate line.
Total parenteral nutrition (TPN)
VFEND I.V. can be infused at the same time as total parenteral nutrition, but must be infused in a separate line. If infused through a multiple-lumen catheter, TPN needs to be administered using a different port from the one used for VFEND I.V.
Recommended Dosing in Adults:
Invasive aspergillosis and serious fungal infections due to Fusarium spp. and Scedosporium apiospermum
See Table 1. Therapy must be initiated with the specified loading dose regimen of intravenous VFEND on Day 1 followed by the recommended maintenance dose regimen. Intravenous treatment should be continued for at least 7 days. Once the patient has clinically improved and can tolerate medication given by mouth, the oral tablet form or oral suspension form of VFEND may be utilized. The recommended oral maintenance dose of 200 mg achieves a voriconazole exposure similar to 3 mg/kg IV; a 300 mg oral dose achieves an exposure similar to 4 mg/kg IV.
Switching between the intravenous and oral formulations is appropriate because of the high bioavailability of the oral formulation in adults [see CLINICAL PHARMACOLOGY].
Candidemia in non-neutropenic patients and other deep tissue Candida infections
SIDE EFFECTS
Xefta (Gefitinib) 250mg is a prescription drug used to treat patients who had gone through cancer treatments previously and in whom cancer has spread to other parts of the body.
Dosage : The recommended dose of Xefta is one 250 mg tablet once a day, taken with or without food. If a dose of Xefta is missed, it should be taken as soon as the patient remembers. If it is less than 12 hours to the next dose, the patient should not take the missed dose. Patients should not take a double dose (two doses at the same time) to make up for a forgotten dose.
Where dosing of whole tablets is not possible, such as patients who are only able to swallow liquids, tablets may be administered as a dispersion in water. The tablet should be dropped into half a glass of drinking water (non-carbonated), without crushing, and the glass stirred until the tablet has dispersed (approximately 15 minutes) and the contents subsequently drunk immediately. The glass should be rinsed with a further half glass of water and the contents drunk. The liquid can also be administered via a nasogastric tube.
Xefta is not recommended for use in children or adolescents as safety and effectiveness in these patient populations has not been studied.
Most common side effects Nausea, Rash, Vomiting, Weakness, Loss of appetite, Dry skin, Diarrhoea, Stomatitis (Inflammation of the mouth).
Ondansetron Tablets 8 mg is a medicine which is used in nausea and vomiting after surgery, nausea and vomiting caused by cytotoxic medicinesand nausea and vomiting caused by radiotherapy.
3s corporation is Supplier, Exporter , Wholesaler for Ondansetron Tablets 8 mg in India.
We even offer contract manufacturing services from WHO GMP approved factories.
SIDE EFFECTS
Pirfenidome Tablet 200 mg is an anti-fibrotic drug for the treatment of idiopathic pulmonary fibrosis (IPF). It works by reducing lung fibrosis through downregulation of the production of growth factors and procollagens I and II Pirfenidone has well-established antifibrotic and anti-inflammatory properties in various in vitro systems and animal models of fibrosis.A number of cell-based studies have shown that pirfenidone reduces fibroblastproliferation, inhibits TGF-β stimulated collagen production and reduces the production of fibrogenic mediators such as TGF-β.Other research shows that pirfenidone may be an effective anti-fibrotic treatment for chronic liver fibrosis.
There are many generic manufacturers in India who manufacture Pirfenidome Tablet 200 mg including Cipla etc.
3s corporation is Supplier, Exporter , Wholesaler for Pirfenidome Tablet 200 mg in India.
SIDE EFFECTS
Pirfenidone is frequently associated with gastrointestinal side effects such as dyspepsia, nausea, gastritis, gastroesophageal reflux disease(GERD) and vomiting.To reduce the severity of these reactions, pirfenidone is to be taken after meals.
SKINPirfenidone is known to cause photosensitivity reactions, rash, pruritus and dry skin. Patients are usually advised to avoid direct exposure to sunlight, including sun lamps, and to use protective clothing and sunscreen agents. Continuing photosensitivity reactions are usually managed by dose adjustment and temporary discontinuation of treatment if required, along with local symptomatic treatment.
HEPATIC DYSFUNCTIONPirfenidone can increase hepatic enzyme levels, especially those of aspartate transaminase (AST), alanine transaminase (ALT) and gamma-glutamyl transpeptidase (GGT); periodic monitoring of hepatic enzyme levels is required during therapy: once before the initiation of therapy, monthly monitoring until 6 months after initiation of therapy, and 3 monthly thereafter. Extra precaution is required while prescribing the drug in patients with hepatic impairment and in patients who are concomitantly taking a CYP1A2 inhibitor. The drug is contraindicated in patients who have severe hepatic impairment.
DIZZINESS AND FATIGUEDizziness and fatigue have been reported in patients undergoing pirfenidone treatment. Dizziness typically resolves, although patients should know how they react to pirfenidone before undertaking activities that need mental alertness or coordination. If severe, dose adjustment or treatment discontinuation may be required.
WEIGHT LOSSWeight loss has been reported in patients treated with pirfenidone. Doctors should monitor patients’ weight and encourage increased calorific intake if necessary.
Voriconazole Tablet 50 & 200 mg is used as antifungal agent .It is indicated for use in patients 12 years of age and older in the treatment of infections such as Invasive Aspergillosis, Esophageal Candidiasis andis also used in disseminated Infections In Skin and infections in Abdomen, Kidney, Bladder Wall, And Wounds.
India has many manufacturers who manufacture Voriconazole Tablet 50 & 200 mg.To know more contact us.
3s corporation is Supplier, Exporter , Wholesaler for Voriconazole Tablet 50 & 200 mg in India.
ADDITIONAL INFORMATION
Voriconazole Tablet 50 & 200 mg should be taken at least one hour before or after a meal.
SIDE EFFECTS
Abacavir sulphate is an anti-HIV medicine that is used in the treatment of infection with human immunodeficiency virus ( HIV). It is used in combination with other anti-HIV medicines.HIV weakens the body’s immune system and reduces the body’s ability to fight infections. Anti-HIV medicines do not kill thevirus but they slow down or stop the HIV virus from making copies of itself. This allows the body’s immune system to keep working and gives the body a chance to fight other infections. Anti-HIV medicines do not cure HIV infections or prevent you from getting other infections.For HIV therapy to be effective and to reduce the chances of developing resistance to your medicine, it is important you take the full daily dose and take your medicines exactly as prescribed by your doctor.
Adults Dose : 600 mg daily, administered as either 300 mg twice daily or 600 mg once daily.
Pediatric Patients Aged 3 Months and Older: Dose should be calculated on body weight (kg) and should not exceed 300 mg twice daily.
Patients With Hepatic Impairment: Mild hepatic impairment – 200 mg twice daily; moderate/severe hepatic impairment – contraindicated.
General Common: Fever, lethargy, malaise Also reported: edema, lymphadenopathy, hypotension, conjunctivitis, anaphylaxis
Skin Common: rash
Gastrointestinal Common: nausea, vomiting, diarrhea, abdominal pain, elevated liver enzymes Also reported: mouth ulceration, hepatitis, liver failure
Respiratory Common: dyspnea, cough Also reported: sore throat, adult respiratory distress syndrome, respiratory failure
Neurological/Psychiatric Common: headache
paresthesias Musculoskeletal Common: myalgia , myolysis (rare), arthralgia, elevated creatine phosphokinase (CPK) Other Also reported: leukopenia, elevated creatinine levels, renal failure Rash and gastrointestinal manifestations (70% vs 54% respectively).
Tenofovir disoproxil fumarate (a prodrug of tenofovir) which is a fumaric acid salt of bis-isopropoxycarbonyloxymethyl ester derivative of tenofovir. In vivo tenofovir disoproxil fumarate is converted to tenofovir, an acyclic nucleoside phosphonate (nucleotide) analog of adenosine 5′-monophosphate. Tenofovir exhibits activity against HIV-1 reverse transcriptase. It is indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection in adults and pediatric patients 2 years of age and older. It is also indicated for the treatment of chronic hepatitis B in adults and pediatric patients 12 years of age and older.
India has many manufacturers who manufacture Tenofovir disoproxil.To know more contact us.
3s corporation is Supplier, Exporter , Wholesaler for Tenofovir disoproxil in India.
ADDITIONAL INFORMATION
For the treatment of HIV-1 or chronic hepatitis B: The dose is one 300 mg once daily taken orally, without regard to food.
For patients unable to swallow tablets, the oral powder formulation (7.5 scoops) may be used.
In the treatment of chronic hepatitis B, the optimal duration of treatment is unknown. Safety and efficacy in pediatric patients with chronic hepatitis B weighing less than 35 kg have not been established.
SIDE EFFECTS
Get emergency medical help if patient have any of these signs of an allergic reaction:
hives;
difficulty breathing;
swelling of your face, lips, tongue, or throat.
This medication may cause lactic acidosis (a build-up of lactic acid in the body, which can be fatal). Lactic acidosis can start slowly and get worse over time.Get emergency medical help if even mild symptoms of lactic acidosis occures, such as: muscle pain or weakness, numb or cold feeling in your arms and legs, trouble breathing, stomach pain, nausea with vomiting, fast or uneven heart rate, dizziness.
Ibandronic Acid Tablets is used in Treatment of osteoporosis in postmenopausal women at increased risk of fracture.A reduction in the risk of vertebral fractures has been demonstrated, efficacy on femoral neck fractures has not been established.Ibandronic acid is a highly potent bisphosphonate belonging to the nitrogen-containing group of bisphosphonates, which act selectively on bone tissue and specifically inhibit osteoclast activity without directly affecting bone formation. It does not interfere with osteoclast recruitment. Ibandronic acid leads to progressive net gains in bone mass and a decreased incidence of fractures through the reduction of elevated bone turnover towards premenopausal levels in postmenopausal women.
India has many manufacturers who manufacture Ibandronic Acid Tablets .To know more contact us.
3s corporation is Supplier, Exporter , Wholesaler for Ibandronic Acid Tablets in India.
ADDITIONAL INFORMATION
The recommended dose is one 150 mg film-coated tablet once a month. The tablet should preferably be taken on the same date each month.
Ibandronic acid should be taken after an overnight fast (at least 6 hours) and 1 hour before the first food or drink (other than water) of the day or any other oral medicinal products or supplementation (including calcium).
In case a dose is missed, patients should be instructed to take one ibandronic acid 150 mg tablet the morning after the tablet is remembered, unless the time to the next scheduled dose is within 7 days. Patients should then return to taking their dose once a month on their originally scheduled date.
Tablets should be swallowed whole with a glass of plain water (180 to 240 ml) while the patient is sitting or standing in an upright position. Patients should not lie down for 1 hour after taking ibandronic acid.
Plain water is the only drink that should be taken with ibandronic acid. Please note that some mineral waters may have a higher concentration of calcium and therefore, should not be used.
SIDE EFFECTS
Amaryl 1 mg tablet (Glimepiride) is an oral medication manufactured by Sanofi Aventis used to lower blood glucose levels in type 2 diabetes (non-insulin-dependent diabetes) patients. This medication is prescribed when high levels of blood sugar cannot be controlled by diet and exercise alone. It belongs to sulfonylurea class of diabetic drugs, which works by stimulating the pancreas to produce more insulin. Available in 1 mg, 2 mg & 3 mg dosage.
ADDITIONAL INFORMATION
Recommended Dosage :
The dosage of Amaryl prescribed to each patient will vary. Always follow your physician’s instructions and/or the directions on the prescription drug label.
Amaryl is usually taken once a day along with breakfast. Take the medication with a full glass of water.
Missed Dose:
If your physician has instructed or directed you to take Amaryl medication in a regular schedule and you have missed a dose of this medicine, take it as soon as you remember. However, if it is almost time for your next dose, then skip the missed dose and go back to your regular dosing schedule. Do not double the doses unless otherwise directed.
Overdose:
Any medication taken in excess can have serious consequences. If you suspect an overdose of Amaryl, seek medical attention immediately. Some of the overdose symptoms of this drug are cold sweats, loss of consciousness, anxiety, hunger, nausea, and drowsiness.
Drug Interaction:
Usually drug interactions occur when it is taken with another drug or with food. Before you take a medication for a particular ailment, you should inform the health expert about intake of any other medications including non-prescription medications, over-the-counter medicines that may increase the effect of Amaryl, and dietary supplements like vitamins, minerals and herbal, so that the doctor can warn you of any possible drug interactions.
Amaryl can interact with heart and blood pressure medications, diuretics, corticosteroids, oral contraceptives, estrogens, thyroid medications, sulfa drugs, MAO inhibitors, and nonsteroidal anti-inflammatory drugs.
Also, tell your prescriber or health care professional if you are a frequent user of drinks containing caffeine or alcohol, if you smoke, or if you use illegal drugs. These may affect the way your medicine works. Check with your health care professional before stopping or starting any of your medicines.
SIDE EFFECTS
Side Effects of Amaryl:
Like other medicines, Amaryl can cause some side effects. If they do occur, the side effects of Amaryl are most likely to be minor and temporary. However, some may be serious and may require the individual to inform the doctor or visit the nearest hospital immediately.
It is pertinent to note that side effects of Amaryl cannot be anticipated. If any side effects of Amaryl develop or change in intensity, the doctor should be informed as soon as possible.
Amaryl can cause side effects such as blurred vision, vomiting, diarrhea, dizziness, headache, nausea, sensitivity to light, and stomach pain. Some of the serious side effects of this drug include shortness of breath, dark urine, convulsions, rapid weight gain, difficulty breathing, chest tightness, jaundice, and swelling of the mouth, face, lips, or tongue. This is not a complete list of all side effects. Do concur with your doctor and follow his directions completely when you are taking Amaryl.
Gliclazide 80 mg:
Indication:Diabetes mellitus type-ii, Maturity onset diabetes, Softening and dilatation of cervix before mechanical cervical dilatation.
Metformin 500 mg:
Indication: Diabetes mellitus, Hyperlipoproteinaemia, Insulin dependent diabetes mellitus, Insulin resistance, Non-insulin dependent diabetes mellitus, Obesity.
Hepcinat 400 mg tablet from Natco (India) is a generic version of Sovaldi from Gilead. Sofosbuvir 400 mg is a prescription medicine used with other antiviral medicines to treat chronic (lasting a long time) hepatitis C genotype 1, 2, 3, and 4 infection in adults. It comes in bottle pack of 28 tabs.It is also safe and effective in children under 18 years of age. Its price is at 1% of the cost of original Sovaldi.
To buy generic Sovaldi, contact us on our email.
ADDITIONAL INFORMATION
If you or your sexual partner is pregnant or plans to become pregnant, do not take these medicines.You and your sexual partner must use 2 effective forms of birth control and should not become pregnant while being treated with SOVALDI combination therapy and for 6 months after your treatment is over. Talk to your doctor about forms of birth control.If you or your partner can become pregnant you must have a pregnancy test before starting treatment with SOVALDI combination therapy, every month while being treated, and for 6 months after your treatment ends.Tell your healthcare provider right away if a pregnancy occurs while taking or within 6 months after you stop taking SOVALDI combination therapy. You or your healthcare provider should contact the Ribavirin Pregnancy Registry. If you are also infected with HIV and taking medicines to treat your HIV infection, an Antiretroviral Pregnancy Registry is also available.
If you have: liver problems other than hepatitis C infection; had a liver transplant; severe kidney problems or are on dialysis; HIV; any other medical condition; or if you are breastfeeding or plan to breastfeed. You and your healthcare provider should decide if you will take SOVALDI or breastfeed. You should not do both.If you take rifampin (Rifadin®, Rifamate®, Rifater®), St. John’s wort or a product that contains St. John’s wort. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Other medicines may affect how SOVALDI works
SIDE EFFECTS
For Hepcinat used in combination with ribavirin they include tiredness and headache and for hepcinat used in combination with peginterferon alfa and ribavirin they include the additional side effects of nausea, difficulty sleeping, and low red blood cell count.
Sofosbuvir is used for treating chronic hepatitis C virus (HCV) infection in certain patients. It must be used with ribavirin or in combination with peginterferon alfa and ribavirin.Sofosbuvir is an HCV nucleotide analog polymerase inhibitor. It reduces the amount of HCV in the body by preventing the spread of the HCV within the body.
India has many manufacturers who manufacture Sofosbuvir.To know more contact us.
3s corporation is Supplier, Exporter , Wholesaler for Sofosbuvir in India.
ADDITIONAL INFORMATION
Store sofosbuvir at room temperature below 86 degrees F (30 degrees C). Keep sofosbuvir in the original container. Store away from heat, moisture, and light. Do not store in the bathroom.
SIDE EFFECTS
COMMON side effects persist or become bothersome:
Headache;
nausea;
tiredness;
trouble sleeping.
Seek medical attention right away if any of these SEVERE side effects occur:
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).
Dosage :
The recommended Velasof dosage is 1 tablet (Velpatasvir 100mg and sofosbuvir 400mg) taken orally daily without or with food.
The dosage level is prescribed by your doctor as per your age, current health condition and medical history.
Every treatment regimen is designed for 12 to 24 weeks.
SIDE EFFECTS
Most common side effects are Fatigue, Nausea, Headache, Insomnia (difficulty in sleeping), Anemia.
Mofilet (Mycophenolate mofetil) is an immunosuppressant used in organ transplantation. It suppresses body’s immune system and thereby prevents rejection of the transplanted organ. Mofilet can be obtained only with prescription.
Dosage :
Usual Adult Dose for Organ Transplant ( Rejection Prophylaxis)
RENAL TRANSPLANTATION : 1 g orally or IV 2 times a day (2 gm per day); [in clinical trials, 1.5 g orally or IV 2 times a day (3 gm per day) was used effectively, however, the safety profile for 3 gm a day was lower]
CARDIAC TRANSPLANTATION: 1.5 g orally or IV 2 times a day (3 gm per day)
HEPATIC TRANSPLANTATION: 1.5 gm orally or 1 gm IV 2 times a day (3 gm per day orally or 2 gm per day IV)
SIDE EFFECTS
Most common side effects are Nausea, Vomiting, Diarrhoea, Abdominal pain, Headache, Increased blood pressure, Decreased white blood cell count (neutrophils).
Sirolimus Tablet 1 & 2g is indicated for the prophylaxis of organ rejection in patients aged 13 years or older receiving renal transplants. Therapeutic drug monitoring is recommended for all patients receiving Rapamune.In patients at low- to moderate-immunologic risk, it is recommended that Rapamune be used initially in a regimen with cyclosporine and corticosteroids; cyclosporine should be withdrawn 2 to 4 months after transplantation.In patients at high-immunologic risk (defined as Black recipients and/or repeat renal transplant recipients who lost a previous allograft for immunologic reason and/or patients with high panel-reactive antibodies [PRA; peak PRA level > 80%]), it is recommended that Rapamune be used in combination with cyclosporine and corticosteroids for the first year following transplantation .
There are many generic manufacturers in India who manufacture Sirolimus Tablet 1 & 2g including Cadila Healthcare Ltd etc.
3s corporation is Supplier, Exporter , Wholesaler for Sirolimus Tablet 1 & 2g in India.
ADDITIONAL INFORMATION
Sirolimus Tablet 1 & 2g should be stored at 20° to 25°C . Use cartons to protect blister cards and strips from light. Dispense in a tight, light-resistant container.
SIDE EFFECTS
Kamagra 100 mg Tablet also known as Viagra is a medication used for erectile dysfunction. To buy it in bulk quantities contact us. We are registered wholesalers & distributors for sex enhancement medicines in India. It is manufactured by Ajanta Pharmaceuticals.
DESCRIPTION
Tadalafil is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5).Tadafil Tablet 20 mg is an oral drug called a phosphodiesterase inhibitor used for treating impotence (erectile dysfunction, or ED) and Benign Prostatic Hyperplasia .
There are many generic manufacturers in India who manufacture Tadafil Tablet 20 mg including Cipla Limited, Cadila Pharmaceuticals Ltd and Macleods etc.
3s corporation is Supplier, Exporter , Wholesaler for Tadafil Tablet 20 mg in India.
ADDITIONAL INFORMATION
The recommended starting dose of Tadafil Tablet for use as needed in most patients is 10 mg, taken prior to anticipated sexual activity.This dose may be increased to 20 mg or decreased to 5 mg, based on individual efficacy and tolerability. The maximum recommended dosing frequency is once per day in most patients.
SIDE EFFECTS
Stop using tadalafil and call your doctor at once if you have any of these serious side effects:
Less serious side effects may include:
Fycompa (perampanel) is a prescription drug used to treat people with epilepsy aged 12 and older, either alone or with other medicines to treat. partial-onset seizures with or without secondarily generalized seizures and with other medicines to treat primary generalized tonic-clonic seizures.
Dosage For Partial-Onset Seizures : The recommended starting dosage of FYCOMPA is 2 mg once daily taken orally at bedtime. Increase dosage by increments of 2 mg once daily no more frequently than at weekly intervals.
Dosage For Primary Generalized Tonic-Clonic Seizures : The recommended starting dosage of FYCOMPA is 2 mg once daily taken orally at bedtime. Increase dosage by increments of 2 mg once daily no more frequently than at weekly intervals.
In patients not taking enzyme-inducing AEDs, the recommended maintenance dose is 8 mg once daily taken at bedtime.
SIDE EFFECTS
Side effects of Fycompa are dizziness, sleepiness, drowsiness, tiredness, fatigue, headache, irritability, nausea, weight gain, joint pain, changes in mood, back pain, behavior, or personality, aggression, hostility, irritability, anger, anxiety, unusual thoughts, paranoid behavior, panic attacks, thoughts about hurting someone else, and suicidal or homicidal ideation and threats, problems maintaining balance.
Immutil-S (Mycophenolate sodium) is an immunosuppressant used in organ transplantation. It suppresses body’s own immunity and prevents rejection of the transplanted organ.
SIDE EFFECTS
Most common side effects are Nausea, Vomiting, Diarrhoea, Abdominal pain, Headache, Increased blood pressure, Decreased white blood cell count (neutrophils).
CAPRELSA (vandetanib) is a kinase inhibitor used for the treatment of symptomatic or progressive medullary thyroid cancer in patients with unresectable locally advanced or metastatic disease. CAPRELSA can also be used to treat a patients with indolent, asymptomatic or slowly progressing disease only after careful consideration of the treatment related risks of CAPRELSA. It is approved by the Food and Drug Administration (FDA).
SIDE EFFECTS
Most Common side effects may be Diarrhea, Rash, Elevated Liver Enzymes (ALT), Low calcium levels, Acne, High blood pressure, Nausea, Headache, Fatigue, Low blood sugar, Abdominal pain, Poor appetite, Low white blood cell count, Kidney problems, Dry skin, Vomiting, Weakness, Irregular, heart beat, Insomnia (difficulty sleeping), Photosensitivity (sensitivity to sunlight), Bleeding, Anemia, Liver tests increased (bilirubin), Itching, Heartburn, Cough, Upper respiratory infection, Depression, Weight loss.
NUBLEXA (Regorafenib) 40mg is a prescription drug used in the treatment of colorectal cancer. It blocks the action of abnormal protein that causes cancer and thereby This helps to stop or slow the spread of cancer cells. It is also used to treat certain type of stomach, bowel, or esophagus cancer called gastrointestinal stromal tumors (GIST).
Dosage :
SIDE EFFECTS
Most common side effects are – Rash, Weakness, Reduced blood platelets, Difficulty in speaking, Haemorrhage, Vomiting, Pain, Nausea, Infection, Hair loss, Fever, Anemia, Diarrhoea, Increased blood pressure, Decreased appetite, Mucosal inflammation, Stomatitis (Inflammation of the mouth).
Nododsis – DS (Sodium Bicarbonate) is used for alkalization, Acidity in the blood, Heartburn, intestinal ulcers and stomach ulcers. Nodosis works by neutralizing excess acid in the stomach.
Dosage :
Dosage for Metabolic Acidosis :
Oral: Moderate metabolic acidosis: 325 to 2000 mg orally 1 to 4 times a day. One gram provides 11.9 mEq (mmoL) for Urinary Alkalinizationeach of sodium and bicarbonate.
Dosage for Diabetic Ketoacidosis :
Parenteral: 50 to 150 mEq sodium bicarbonate diluted in 1 L of D5W to be intravenously infused at a rate of 1 to 1.5 L/hour.
Oral: 325 to 2000 mg orally 1 to 4 times a day. One gram provides 11.9 mEq (mmoL) each of sodium and bicarbonate.
Dosage for Dyspepsia :
325 to 2000 mg orally 1 to 4 times a day.
Dosage for Asystole :
1 mEq/kg slow IV initially, may repeat with 0.5 mEq/kg 10 minutes later one time, or as indicated by the patient’s acid-base status.
SIDE EFFECTS
Common side effects are Constipation, Swelling of feet or lower legs, Unpleasant taste, Loss of appetite, Unusual , tiredness or weakness, Frequent urge to urinate, Muscle pain or twitching
Tafero EM 200mg/25mg Tablet is a combination of two anti-HIV medicines that is Emtricitabine and Tenofovir. Tafero EM prevents HIV (virus) from multiplying, thereby reduces the amount of virus in the patient’s body. They also increase the count of CD4 cell (white blood cells that protect against infection) in the patient’s blood.
Dosage : The prescribed dose of Tafero EM in the condition of HIV-1 infection in adults is, one tablet should be taken once daily with or without food. In Pre-exposure Prophylaxis: uninfected adults should take one tablet orally as a single dose.
SIDE EFFECTS
The most common side effects are Nausea, Vomiting, Diarrhoea, Flatulence, Insomnia (difficulty in sleeping), Headache, Depression, Rash.
GEFTINAT 250mg (Gefitinib) is a prescription drug used in the treatment of non-small cell lung cancer. It is used in patients in which it has spread to other parts of the body, who have abnormal epidermal growth factor receptor (EGFR) genes, and who have not had previous treatment for cancer. It interferes with the growth and spread of cancer cells in the body.
Dosage :
Most common side effects are Nausea, Rash, Vomiting, Weakness, Loss of appetite, Dry skin, Diarrhoea, Stomatitis (Inflammation of the mouth).
We are second to none in offering Lanvis Tablets. The tablets offered by us are known for their high efficacy, long shelf life and precise composition. One can obtain these at competitive rates from us.
Description :
Additional Information : Store Tioguanine 40 mg Capsules at 15° to 25°C (59° to 77°F) in a dry place.
Side Effects :
Stop using thioguanine and call doctor at once if patient has any of these serious side effects:
Nexavar 200 mg Tablets are clinically approved for the treatment of primary kidney cancer (advanced renal cell carcinoma) and advanced primary liver cancer (hepatocellular carcinoma). Nexavar 200 mg Tablets (generic name : Sorafenib) has both US FDA & European Commision approval to be used in the treatment of advanced renal cancer & liver cancer. Nexavar 200 mg Tablets are available in 200 mg dosage & 60 tablets or bottle packing.
Baraclude 1mg Tablet is a chronic hepatitis B treatment that works to fight the hepatitis B virus (HBV) and may help to improve the condition of the liver. Our company shares glorious credentials with the leading Suppliers and Exporters of Baraclude 1mg Tablets from Maharashtra. The offered Baraclude 1mg Tablets is used to treat chronic hepatitis B virus (HBV) in adults who have active virus and liver damage. Customers can buy the Tablet in good quality packaging and at nominal rates.
BARACLUDE MAY :
This chronic hepatitis B treatment works to help fight HBV and may reduce the amount of the virus in your blood. BARACLUDE is taken once a day by mouth. BARACLUDE does not stop you from spreading the hepatitis B virus (HBV) to others by sex, sharing needles, or being exposed to your blood. Talk with your healthcare provider about safe sexual practices that protect your partner. Never share needles. Do not share personal items that can have blood or body fluids on them, like toothbrushes or razor blades. A shot (vaccine) is available to protect people at risk from becoming infected with HBV.
Read the sections below to learn more about choosing a chronic hepatitis B treatment, and to see how BARACLUDE may help to improve the condition of your liver. Ask your doctor if BARACLUDE is right for you. Remember, not all people who have HBV need treatment.
How BARACLUDE Works :
HBV attacks your healthy liver cells where it multiplies and infects more liver cells. As a chronic hepatitis B treatment, BARACLUDE works to fight HBV and may lower the amount of HBV in the body.
Side-Effects :
All medicines have benefits and risks. BARACLUDE® (entecavir) may cause the following serious side effects :
Your hepatitis B virus infection may get worse if you stop taking BARACLUDE. This usually happens within 6 months after stopping BARACLUDE.
If you have or get HIV that is not being treated with medicines while taking BARACLUDE, the HIV virus may develop resistance to certain HIV medicines and become harder to treat. You should get an HIV test before you start taking BARACLUDE and anytime after that when there is a chance you were exposed to HIV.
BARACLUDE can cause serious side effects including :
Lactic acidosis (buildup of acid in the blood). Some people who have taken BARACLUDE or medicines like BARACLUDE (a nucleoside analogue) have developed a serious condition called lactic acidosis. Lactic acidosis is a serious medical emergency that can cause death. Lactic acidosis must be treated in the hospital. Reports of lactic acidosis with BARACLUDE generally involved patients who were seriously ill due to their liver disease or other medical condition.
Call your healthcare provider right away if you get any of the following signs or symptoms of lactic acidosis :
Serious liver problems. Some people who have taken medicines like BARACLUDE have developed serious liver problems called hepatotoxicity, with liver enlargement (hepatomegaly) and fat in the liver (steatosis). Hepatomegaly with steatosis is a serious medical emergency that can cause death.
Call your healthcare provider right away if you get any of the following signs or symptoms of liver problems :
The most common side effects of BARACLUDE include :
Tell your healthcare provider if you have any side effect that bothers you or that does not go away.
Note : These are not all the possible side effects of BARACLUDE. For more information, ask your healthcare provider or pharmacist.
We are involved in making available Capegard-500 Tablets. The tablets we make available are acclaimed for their accurate composition, long shelf life and high efficacy. One can obtain these at reasonable rates.
Description :
Additional Information :
Call your doctor at once if you have a serious side effect such as :
We are a trusted name, engaged in making available a high-class range of Celkeran Tablets in different packaging options. Renowned for their qualitative attributes, our Celkeran Tablets are obtainable at feasible prices, from us.
Description :
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.
LediHep (Ledipasvir & Sofosbuvir) is a prescription drug used as an antiviral medication. It lowers the rate of hepatitis C virus in the body and eventually removes the virus from the blood.
Dosage :
Common side effects are Fatigue, Headache, Nausea, Insomnia (difficulty in sleeping), Anemia.
Imatinib 400 mg Tablets are used for treating certain types of leukemia other cancers of the blood cells. These tablets are also used to treat gastrointestinal stromal tumors (GIST) and dermatofibrosarcoma protuberans (a tumor that forms under the top layer of skin). Imatinib 400 Mg Tablets falls under the class of medications called protein-tyrosine kinase inhibitors. Manufactured by Natco, these Imatinib 400 Mg Tablets are available in 100 mg & 400 mg tablet pack. Imatinib 400 Mg Tablets help in stopping the spread of cancer cells.
Dosage : If doctor has prescribed to take 800 mg of imatinib, then the patient should take 2 of the 400-mg tablets. Do not take 8 of the 100-mg tablets as the coating contains iron. If the patient is unable to swallow these tablets, then these tablets can be diluted into a glass of water or apple juice. Use 50 milliliters (a little less than 2 ounces) of liquid for each 100-mg tablet and 100 milliliters (a little less than 4 ounces) of liquid for each 400-mg tablet. Stir with a spoon until the tablets crumble completely and drink the mixture immediately.
Other Information :
Our company is engaged in offering Bucelon Tablets. The tablets offered by us are sourced from known vendors of the market. One can obtain these at best possible rates from us.
Description :
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 :
Tenvir Tablets contains tenofovir and belongs to a class of antiviral medications called reverse transcriptase inhibitors.It is used to treat HIV infection. The company is a reliable Supplier and Exporter of Tenvir Tablets from Maharashtra. These Tenvir Tablets are used in combination with other antiviral medications medicines. These Tenvir Tablets have accurate composition and high effectiveness. We offer the Tenvir Tablets in excellent quality packages and at market leading rates.
We are a one-stop destination to get qualitative and effective Casodex 50 Tablets at reasonable prices. Buyers can approach us for acquiring Casodex 50 Tablets in retail or bulk as per their requirements.
Description :
Before taking Casodex :
Viread HIV Tablets are the tablets used for treating chronic hepatitis B virus in 18+ Person. The name of our company surfaces prominently among the trusted Suppliers and Exporters of Viread HIV Tablets from Maharashtra, India. The Viread HIV Tablets that we offer are sourced from the reliable vendors of the market. To cater to the extensive demands of the customers, we are providing Viread HIV Tablets in bulk quantities.
Sovaldi 400 mg Tablets is a prescription drug for Hepatitis C, with a high cure rate. Our company is counted among the best Suppliers and Exporters of Sovaldi 400 mg Tablets from Maharashtra. It is a once-a-day prescription medicine that is used with other antiviral medicines to treat chronic (lasting a long time) hepatitis C (Hep C) infection in adults. Sovaldi 400 mg Tablets offered should be taken as per the doctor’s advice.
Tenvir EM Tablets are used in combination with other medicines to treat Human Immunodeficiency Virus (HIV) infection in adults over age 18. We are proficient Suppliers and Exporters of Tenvir EM Tablets from Maharashtra. These Tenvir EM Tablets are used to treat patients with HIV infection who have already received treatment with other medications for HIV infection. The offered Tenvir EM Tablets have accurate composition and high effectiveness. Customers can purchase the Tablet at competitive rates.
Kandivali East, Mumbai, Maharashtra