Oncology Medicine

Approx. Rs 2,000 / BoxGet Latest Price

Product BrochureProduct Details:

Nintedanib is used to treat idiopathic pulmonary fibrosis. It helps prevent changes to the lung tissue. It is also used to treat people with a chronic (long-lasting) interstitial lung disease in which lung fibrosis continues to progress or becomes worse.

Approx. Rs 2,000 / BoxGet Latest Price

Product BrochureProduct Details:

LONSURF (Trifluridine and Tipiracil 15mg)is a prescription medicine used to treat adults with colorectal cancer that has spread to other parts of the body and who have been previously treated or cannot receive certain chemotherapy medicines. a kind of stomach cancer called gastric cancer including cancer of the gastroesophageal junction that has spread to other parts of the body and who have been previously treated or cannot receive certain chemotherapy medications. It is not known if LONSURF is safe and effective in children IMPORTANT SAFETY INFORMATION LONSURF may cause serious side effects, including: Low blood counts. Low blood counts are common with LONSURF and can sometimes be severe and life-threatening. LONSURF can cause a decrease in your white blood cells, red blood cells, and platelets. Low white blood cells can make you more likely to get serious infections that could lead to death. Your healthcare provider should do blood tests before you receive LONSURF, at day 15 during treatment with LONSURF, and as needed to check your blood cell counts. Your healthcare provider may lower your dose of LONSURF or stop LONSURF if you have low white blood cell or platelet counts Tell your healthcare provider right away if you get any of the following signs and symptoms of infection during treatment with LONSURF: fever, chills, or body aches. Before taking LONSURF, tell your healthcare provider about all of your medical conditions, including if you: Have kidney or liver problems Are pregnant or plan to become pregnant. LONSURF can harm your unborn baby. Females who can become pregnant: Your healthcare provider will verify your pregnancy status before you start treatment with LONSURF. You should use effective birth control during and 6 months after the last dose of treatment with LONSURF. Tell your healthcare provider immediately if you become pregnant Males, while on treatment and for 3 months after your last dose of LONSURF, you should use a condom during sex with female partners who are able to become pregnant. Tell your healthcare provider right away if your partner becomes pregnant while you are taking LONSURF Are breast-feeding or plan to breast-feed. It is not known if LONSURF passes into your breast milk. Do not breast-feed during treatment with LONSURF and for 1 day after your last dose of LONSURF Tell your healthcare provider about all the prescription and over-the-counter medicines, vitamins, and herbal supplements you take. The most common side effects with LONSURF include tiredness (fatigue, weakness), nausea, decreased appetite, diarrhea, vomiting, abdominal pain, and fever. Tell your doctor if you have nausea, vomiting, or diarrhea that is severe or that does not go away. These are not all of the possible side effects of LONSURF. For more information, ask your healthcare provider. Call your doctor for medical advice about side effects.

Product Price :Get Latest Price

Product BrochureProduct Details:

Selinexor 80 Mg is a prescription medicine used: in combination with bortezomib and dexamethasone to treat adult patients with multiple myeloma who have received at least one prior therapy. It is not known if Selinexor 80 Mgis safe and effective in children less than 18 years of age. Your healthcare provider will do blood tests before you start taking Selinexor 80 Mg, and often during the first 3 months of treatment, and then as needed during treatment. Selinexor 80 Mgcan cause serious side effects, including: Low platelet counts. Low platelet counts are common with Selinexor 80 Mgand can lead to bleeding, which can be severe and can sometimes cause death. Your healthcare provider may prescribe platelet transfusions or other treatments for your low platelet counts. Tell your healthcare provider right away if you have any bleeding or easy bruising during treatment with Selinexor 80 Mg. Low white blood cell counts. Low white blood cell counts are common with Selinexor 80 Mgand can sometimes be severe. You may have an increased risk of getting bacterial infections during treatment with Selinexor 80 Mg. If needed, your healthcare provider may prescribe antibiotics if you have signs or symptoms of infection. Serious infections. Infections are common with Selinexor 80 Mgand can be serious and can sometimes cause death. This includes upper or lower respiratory tract infections, such as pneumonia, and an infection throughout your body (sepsis). Tell your healthcare provider right away if you have any signs or symptoms of an infection such as cough, chills, or fever during treatment with Selinexor 80 Mg. Neurologic side effects. Selinexor 80 Mgcan cause dizziness, fainting, decreased alertness, and changes in your mental status, including problems with thinking, seeing or hearing things that are not really there (hallucinations). These problems can sometimes be severe and life-threatening. Tell your healthcare provider right away if you get any of these symptoms. Do not drive or operate heavy or dangerous machinery until you know how Selinexor 80 Mgaffects you. Take precautions to prevent a fall. Nausea, vomiting, and/or diarrhea. Nausea, vomiting, and/or diarrhea can occur when you take Selinexor 80 Mgand can sometimes be severe. You may be at risk for becoming dehydrated. Your healthcare provider may prescribe anti-nausea or anti-diarrhea medicines. Loss of appetite and weight loss. Loss of appetite and weight loss are common with Selinexor 80 Mg. Tell your healthcare provider if you have a decrease or loss of appetite and if you are losing weight. Decreased sodium levels in your blood. Decreased sodium levels in your blood are common with Selinexor 80 Mg. Your healthcare provider may talk with you about your diet and prescribe IV fluids or salt tablets. New or worsening cataract, cloudiness, or loss of transparency of the lens in the eye. New or worsening cataract are common with Selinexor 80 Mg. If a cataract forms, your vision may decrease, and you may need eye surgery to remove the cataract and restore your vision. Tell your healthcare provider right away if you have symptoms of a cataract such as double vision, blurred vision, or sensitivity to light or glare. Common side effects of Selinexor 80 Mginclude: tiredness weakness low red blood cell count (anemia). Symptoms may include tiredness and shortness of breath constipation shortness of breath increased blood sugar changes in body salt and mineral levels in your blood changes in kidney and liver function blood tests These are not all of the possible side effects of Selinexor 80 Mg.

Product Price :Get Latest Price

Product BrochureProduct Details:

XPOVIO (Selinexor) is a prescription medicine used: in combination with bortezomib and dexamethasone to treat adult patients with multiple myeloma who have received at least one prior therapy. It is not known if XPOVIO is safe and effective in children less than 18 years of age. Your healthcare provider will do blood tests before you start taking XPOVIO, and often during the first 3 months of treatment, and then as needed during treatment. XPOVIO can cause serious side effects, including: Low platelet counts. Low platelet counts are common with XPOVIO and can lead to bleeding, which can be severe and can sometimes cause death. Your healthcare provider may prescribe platelet transfusions or other treatments for your low platelet counts. Tell your healthcare provider right away if you have any bleeding or easy bruising during treatment with XPOVIO. Low white blood cell counts. Low white blood cell counts are common with XPOVIO and can sometimes be severe. You may have an increased risk of getting bacterial infections during treatment with XPOVIO. If needed, your healthcare provider may prescribe antibiotics if you have signs or symptoms of infection. Serious infections. Infections are common with XPOVIO and can be serious and can sometimes cause death. This includes upper or lower respiratory tract infections, such as pneumonia, and an infection throughout your body (sepsis). Tell your healthcare provider right away if you have any signs or symptoms of an infection such as cough, chills, or fever during treatment with XPOVIO. Neurologic side effects. XPOVIO can cause dizziness, fainting, decreased alertness, and changes in your mental status, including problems with thinking, seeing or hearing things that are not really there (hallucinations). These problems can sometimes be severe and life-threatening. Tell your healthcare provider right away if you get any of these symptoms. Do not drive or operate heavy or dangerous machinery until you know how XPOVIO affects you. Take precautions to prevent a fall. Nausea, vomiting, and/or diarrhea. Nausea, vomiting, and/or diarrhea can occur when you take XPOVIO and can sometimes be severe. You may be at risk for becoming dehydrated. Your healthcare provider may prescribe anti-nausea or anti-diarrhea medicines. Loss of appetite and weight loss. Loss of appetite and weight loss are common with XPOVIO. Tell your healthcare provider if you have a decrease or loss of appetite and if you are losing weight. Decreased sodium levels in your blood. Decreased sodium levels in your blood are common with XPOVIO. Your healthcare provider may talk with you about your diet and prescribe IV fluids or salt tablets. New or worsening cataract, cloudiness, or loss of transparency of the lens in the eye. New or worsening cataract are common with XPOVIO. If a cataract forms, your vision may decrease, and you may need eye surgery to remove the cataract and restore your vision. Tell your healthcare provider right away if you have symptoms of a cataract such as double vision, blurred vision, or sensitivity to light or glare. Common side effects of XPOVIO include: tiredness weakness low red blood cell count (anemia). Symptoms may include tiredness and shortness of breath constipation shortness of breath increased blood sugar changes in body salt and mineral levels in your blood changes in kidney and liver function blood tests These are not all of the possible side effects of XPOVIO.

Approx. Rs 1,000 / VialGet Latest Price

Product BrochureProduct Details:

Bortezomib for Injection is used to treat certain types of cancer such as multiple myeloma (a cancer of the cells of the immune system in the bone marrow) and mantle cell lymphoma (a cancer of the cells of the immune system affecting the lymph nodes).
It works by stopping or slowing down the growth and spread of cancer cells in the body.

Approx. Rs 8,000 / BottleGet Latest Price

Product BrochureProduct Details:

We are offering Sorafenib Tablets  which are a cancer (chemotherapeutic) medication. Sorafenat Tablets interfere with the growth and spread of cancer cells in the body. Sorafenat Tablets is used to treat a type of kidney cancer called advanced renal cell carcinoma. It is also used to treat liver cancer. Sorafenat Tablets may also be used for purposes not listed in this medication guide.Do not use Sorafenat Tablets if you are pregnant. It could harm the unborn baby. Use effective birth control while you are using this medication and for at least 2 weeks after your treatment ends, whether you are a man or a woman.

Precautions & Warnings:

• Should not be taken without consulting the doctor if the patient ever had pulmonary fibrosis (scarring of the lungs), or liver or kidney disease
• Not recommended if the patient is allergic to the medicine or any of its constituents
• Kindly notify the doctor immediately, if allergic reactions (difficulty breathing, closing of the throat, swelling of the lips, tongue, or face; or hives), lung problems, liver problems, eye problems, severe nausea, vomiting, loss of appetite, or diarrhea during treatment are noticed
• Doctor consultation recommended for pregnant women or for those who are breast feeding their child

Overdose:

• Symptoms like diarrhea and rash

Side effects:

• Get emergency medical help if you have any of these signs of an allergic reaction to Sorafenat Tablets: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

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

• Rash, blisters, oozing, or severe pain in the palms of your hands or the soles of your feet;
• Mouth sores;
• Black or bloody stools, coughing up blood or vomit that looks like coffee grounds;
• Pale skin, feeling light-headed or short of breath, rapid heart rate, trouble concentrating;
• Easy bruising, unusual bleeding (nose, mouth, , or rectum), purple or red pinpoint spots under your skin;
• Chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;
• Dry cough, wheezing.

Approx. Rs 2,000 / BoxGet Latest Price

Product BrochureProduct Details:

RELUMINA (Relugolix 40 Mg) is a prescription medicine used for the treatment of advanced prostate cancer. It is the only androgen deprivation therapy (ADT) medicine that is not an injection. IMPORTANT SAFETY INFORMATION What should I tell my healthcare provider before taking RELUMINA? Tell your healthcare provider about all of your medical conditions, including if you: Have any heart problems, including a condition called long QT syndrome. Are pregnant or plan to become pregnant. RELUMINA can harm your unborn baby and cause loss of pregnancy (miscarriage). Have a partner who is pregnant or may become pregnant. Males who have female partners who are able to become pregnant should use effective birth control (contraception) during treatment with RELUMINA and for 2 weeks after the last dose of RELUMINA. Are breastfeeding or plan to breastfeed. It is not known if RELUMINA passes into your breast milk. Tell your healthcare provider about all the medicines or treatments you receive, including: prescription and over-the-counter medicines, vitamins, and herbal supplements. Taking RELUMINA with certain other medicines can affect how RELUMINA works or may cause side effects. You should not start or stop any medicine before you talk with your healthcare provider who prescribed RELUMINA. What are the possible side effects of RELUMINA? Serious side effects of RELUMINA include: Changes in the electrical activity of your heart (QT prolongation). Your healthcare provider may check your body salts (electrolytes) and the electrical activity of your heart during treatment with RELUMINA. Tell your healthcare provider right away if you get any signs or symptoms of QT prolongation, including: dizziness fainting feeling that your heart is pounding or racing (palpitations) chest pain Most common side effects of RELUMINA include: hot flushes increased blood sugar levels increased blood fat (triglyceride) levels muscle and joint pain decreased blood hemoglobin levels increased liver enzymes tiredness constipation diarrhea RELUMINA may cause other side effects including weight gain, decreased sex drive, and erectile function problems. RELUMINA may cause fertility problems in males, which may affect your ability to father children. Talk to your healthcare provider if this is a concern for you. These are not all the possible side effects of RELUMINA. Call your doctor for medical advice about side effects or if you have a side effect that bothers you or does not go away.  RELUMINA is a prescription medicine used in adults for the treatment of advanced prostate cancer. It is not known if RELUMINA is safe or effective in females or children.

Approx. Rs 2,000 / VialGet Latest Price

Product BrochureProduct Details:

Voriconazole 200 mg Injection belongs to a group of medicines called antifungals. It works by stopping the growth of fungus and is used to treat a wide range of fungal infections. It kills fungi by destroying the fungal cell membrane. Voriconazole 200mg200mg Injection is administered under the supervision of a doctor or a nurse. Do not self-administered the injection. To get the most benefit, get the injection at evenly spaced times and continue taking it until your prescription is finished, even if your symptoms disappear after a few days. If you stop treatment too early, the infection may return and if you miss doses you can increase your risk of infections that are resistant to further treatment. The most common side effects of this medicine include rash, vomiting, nausea, and headache. These are not usually serious, but you should call your doctor if you think you might have a severe allergic reaction. Signs of this include rash, swelling of the lips, throat, or face, swallowing or breathing problems, feeling dizzy or faint, and nausea. Get emergency help if this happens. Do not take it if you are pregnant or could become pregnant unless your doctor has told you to. Talk to your doctor before taking it if you have ever had heart failure, kidney problems, or liver problems such as yellow skin (jaundice). This medicine may not be suitable for you. If your course of treatment is for more than a month, your doctor may want to check your liver by testing your blood. The medicine may make you dizzy or have blurred vision so do not drive or operate machines until it is safe.

Approx. Rs 2,000 / BoxGet Latest Price

Product BrochureProduct Details:

Caprelsa (Vandetanib 300 mg) is a prescription medicine used to treat medullary thyroid cancer that cannot be removed by surgery or that has spread to other parts of the body. It takes a long time to get rid of Caprelsa from your body and you may be at risk for side effects related to Caprelsa after you have stopped your treatment. It is not known if Caprelsa is safe and effective in children. What are the possible side effects of Caprelsa? Caprelsa may cause serious side effects, including: Serious skin reactions. Caprelsa can cause serious skin reactions such as toxic epidermal necrolysis and Stevens-Johnson syndrome, or other serious skin reactions that may affect any part of your body. These serious skin reactions may be life threatening and you may need to be treated in a hospital. Call your healthcare provider right away if you experience any of these symptoms. Skin rash or acne Dry skin Itching Blisters on your skin Blisters or sores in your mouth Peeling of your skin Fever Muscle or joint aches Redness or swelling of your face, hands, or soles of your feet Breathing problems (interstitial lung disease). Caprelsa may cause a breathing problem called interstitial lung disease that can lead to death. Tell your healthcare provider right away if you experience sudden or worsening shortness of breath or cough. Stroke. Strokes have been reported in some people who have taken Caprelsa and in some cases have caused death. Stop taking Caprelsa and call your healthcare provider right away if you have symptoms of a stroke which may include: numbness or weakness of the face, arm or leg, especially on one side of the body sudden confusion, trouble speaking or understanding sudden trouble seeing in one or both eyes sudden trouble walking, dizziness, loss of balance or coordination sudden, severe headache Bleeding. Bleeding can happen during your treatment with Caprelsa. Tell your healthcare provider right away if you have severe bleeding while you are taking Caprelsa. Heart failure. Caprelsa can cause heart failure that can lead to death. You may have to stop taking Caprelsa if you have heart failure. Heart failure may not be reversible after stopping Caprelsa. Your healthcare provider should monitor you for signs and symptoms of heart failure. Diarrhea. Diarrhea is often a symptom of medullary thyroid cancer. Caprelsa can also cause diarrhea or make diarrhea worse. Your healthcare provider should check your blood levels to monitor your electrolytes more frequently if you have diarrhea. Thyroid hormones. You can have changes in your thyroid hormone when taking Caprelsa. Your healthcare provider should monitor your thyroid hormone levels while taking Caprelsa. High blood pressure (hypertension). If you develop high blood pressure or your high blood pressure gets worse, your healthcare provider may lower your dose of Caprelsa or tell you to stop taking Caprelsa until your blood pressure is under control. Your healthcare provider may prescribe another medicine to control your high blood pressure. Reversible Posterior Leukoencephalopathy Syndrome (RPLS). A condition called reversible posterior leukoencephalopathy syndrome can happen while taking Caprelsa. Call your healthcare provider right away if you have: headaches seizures confusion changes in vision problems thinking The most common side effects of Caprelsa include: diarrhea rash acne nausea high blood pressure headache feeling tired loss of appetite upper respiratory tract infections stomach (abdominal) pain 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 Caprelsa. For more information, ask your healthcare provider or pharmacist.

Approx. Rs 1,000 / BoxGet Latest Price

Product BrochureProduct Details:

Eudemine (Diazoxide 50 Mg) Tablets are used orally in the treatment of intractable hypoglycaemia.

Diazoxide also causes salt and water retention.

Hypoglycaemia: Eudemine administered orally is indicated for the treatment of intractable hypoglycaemia with severe symptoms from a variety of causes including: idiopathic hypoglycaemia in infancy, leucine-sensitive or unclassified; functional islet cell tumours both malignant and benign if inoperable, extra-pancreatic neoplasms producing hypoglycaemia; glycogen storage disease; hypoglycaemia of unknown origin.

Posology and method of administration
Hypoglycaemia: In hypoglycaemia, the dosage schedule of Eudemine tablets is determined according to the clinical needs and the response of the individual patient. For both adults and children a starting oral dose of 5mg/kg body weight divided into 2 or 3 equal doses per 24 hours will establish the patient's response and thereafter the dose can be increased until the symptoms and blood glucose level respond satisfactorily. Regular determinations of the blood glucose in the initial days of treatment are essential. The usual maintenance dose is 3 - 8mg/kg/day given in two or three divided doses.

Reduced doses may be required in patients with impaired renal function.

In children with leucine-sensitive hypoglycaemia, a dosage range of 15- 20mg/kg/day is suggested.

In adults with benign or malignant islet-cell tumours producing large quantities of insulin, high dosages of up to 1,000mg per day have been used.

Contraindications
In the treatment of hypoglycaemia, Eudemine is contraindicated in all cases which are amenable to surgery or other specific therapy.

Hypersensitivity to any component of the preparation or other thiazides.

Special warnings and precautions for use
In the treatment of hypoglycaemia it is necessary that the blood pressure be monitored regularly.

Retention of sodium and water is likely to necessitate therapy with an oral diuretic such as frusemide or ethacrynic acid. The dosage of either of the diuretics mentioned may be up to 1g daily. It must be appreciated that if diuretics are employed then both the hypotensive and hyperglycaemic activities of diazoxide will be potentiated and it is likely that the dosage of diazoxide will require adjustment downwards. In patients with severe renal failure it is desirable to maintain, with diuretic therapy, urinary volumes in excess of 1 litre daily. Hypokalaemia should be avoided by adequate potassium replacement.

Diazoxide should be used with caution in patients with cardiac failure or impaired cardiac reserve in whom sodium and water retention may worsen or precipitate congestive heart failure. A direct effect on myocardium and cardiac function cannot be excluded.

Diazoxide should be used with care in patients with impaired cardiac or cerebral circulation and in patients with aortic coarctation, aortic stenosis, arteriovenous shunt, heart failure or other cardiovascular disorders in which an increase in cardiac output could be detrimental.

Diazoxide should be administered with caution to patients with hyperuricaemia or a history of gout, and it is advisable to monitor serum uric acid concentration.

Whenever Eudemine is given over a prolonged period regular haematological examinations are indicated to exclude changes in white blood cell and platelet counts.

Also in children there should be regular assessment of growth, bone and psychological maturation.

The very rapid, almost complete protein binding of diazoxide requires cautious dosage to be used in patients whose plasma proteins may be lower than normal.

Approx. Rs 2,000 / StripeGet Latest Price

Product BrochureProduct Details:

PIRFENEX (Pirfenidone 200 Mg) Tablet is a prescription medicine used in the treatment of idiopathic pulmonary fibrosis. It reduces scarring and swelling in the lungs and helps to breathe better. Pirfenex Tablet is best taken with food. Take it at the same time every day to get the most benefits. The dose and how often you take it depends on what you are taking it for. Your doctor will decide how much you need to improve your symptoms. You should take this medicine for as long as it is prescribed for you. The most common side effects of this medicine include insomnia, headache, and dizziness. To overcome dizziness, avoid driving or attention-seeking activity. Some people may experience weight loss and other side effects. Monitor your weight regularly or ask for the doctor's advice in such cases. Your doctor also may perform a liver function test while on treatment with this medicine. Before taking this medicine, let your doctor know if you have liver or kidney disease. Your doctor should also know about all other medicines you are taking as many of these may make this medicine less effective or change the way it works. It makes your skin sun-sensitive, wear protective clothing or apply sunscreen while in direct contact with the sun. Inform your doctor if you are pregnant or breastfeeding.