Anti Cancer Medicine

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• Accurate composition
• Quick results
• Safe to use

• It is very important that your doctor check your progress at regular visits to make sure that this medicine is working properly. Blood and urine tests may be needed to check for unwanted effects
• Using this medicine while you are pregnant can harm your unborn baby. Use an effective form of birth control while you are using this medicine and for at least 8 weeks after stopping treatment. If you think you have become pregnant while using the medicine, tell your doctor right away
• If you are a plan to have children, talk with your doctor before using this medicine. This medicine may decrease fertility in men and women
• This medicine may cause a serious lung problem called noninfectious pneumonitis. Check with your doctor right away if you have chest pain, chills, a cough, a fever, shortness of breath, or trouble breathing

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We are counted among the leading suppliers, importers and exporters of a wide array of Aprepitant capsules. Superior grade ingredients are used to process the offered range. In addition to this, we pack these products using the premium quality material to retain the effectiveness.

Uses:
Aprepitant is used with other medications to help prevent nausea and vomiting caused by cancer drug treatment (chemotherapy). This medication is also used to prevent nausea and vomiting after surgery. Aprepitant works by blocking one of the body's natural substances that cause vomiting.

Overdose:
Overdose symptoms may include drowsiness and headache.

Precautions and Warning:
Before using aprepitant, tell your doctor or pharmacist if you are allergic to it; or to fosaprepitant or if you have any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.
Before using this medication, tell your doctor or pharmacist your medical history, especially of: liver problems.
During pregnancy, this medication should be used only when clearly needed. Discuss the risks and benefits with your doctor.
It is not known if this drug passes into breast milk. Consult your doctor before breast-feeding.
 

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• Breast cancer
• Stomach cancer Canmab Injection Uses and Benefits

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• Longer shelf life
• Free from impurities
• Fewer side effects

• Agitation
• Loss of balance
• Seizure
• Loss of coordination

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• Long shelf life
• Pure

The highest dose of afatinib studied in a limited number of patients in Phase I clinical trials was 160 mg once daily for 3 days and 100 mg once daily for 2 weeks. The adverse reactions observed at these doses were primarily dermatological (rash/acne) and gastrointestinal events (especially diarrhoea). Overdose in 2 healthy adolescents involving the ingestion of 360 mg each of afatinib (as part of a mixed drug ingestion) was associated with adverse events of nausea, vomiting, asthenia, dizziness, headache, abdominal pain and elevated amylase (< 1.5 times ULN). Both individuals recovered from these adverse events.

Treatment:

There is no specific antidote for overdose with this medicinal product. In cases of suspected overdose, GIOTRIF should be withheld and supportive care initiated.

When assessing the EGFR mutation status of a patient, it is important that a well-validated and robust methodology is chosen to avoid false negative or false positive determinations.

Diarrhoea

Diarrhoea, including severe diarrhoea, has been reported during treatment with GIOTRIF (see section 4.8). Diarrhoea may result in dehydration with or without renal impairment, which in rare cases has resulted in fatal outcomes. Diarrhoea usually occurred within the first 2 weeks of treatment. Grade 3 diarrhoea most frequently occurred within the first 6 weeks of treatment.

Proactive management of diarrhoea including adequate hydration combined with anti-diarrhoeal medicinal products especially within the first 6 weeks of the treatment is important and should start at first signs of diarrhoea. Antidiarrhoeal medicinal products (e.g. ) should be used and if necessary their dose should be escalated to the highest recommended approved dose. Anti-diarrhoeal medicinal products should be readily available to the patients so that treatment can be initiated at first signs of diarrhoea and continued until loose bowel movements cease for 12 hours. Patients with severe diarrhoea may require interruption and dose reduction or discontinuation of therapy with GIOTRIF (see section 4.2). Patients who become dehydrated may require administration of intravenous electrolytes and fluids.

Skin related adverse events:

Rash/acne has been reported in patients treated with this medicinal product (see section 4.8). In general, rash manifests as a mild or moderate erythematous and acneiform rash, which may occur or worsen in areas exposed to the sun. For patients who are exposed to the sun, protective clothing, and use of sun screen are advisable. Early intervention (such as emollients, ) of dermatologic reactions can facilitate continuous GIOTRIF treatment. Patients with severe skin reactions may also require temporary interruption of therapy, dose reduction (see section 4.2), additional therapeutic intervention, and referral to a specialist with expertise in managing these dermatologic effects.

Additional Information:

• Item Code: GIOTRIF

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• Accurate composition
• Precise pH value
• Longer shelf life

• Symptoms of overdose associated with temonat may include chills, persistent sore throat or persistent fever; or severe bleeding or bruising.

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• Longer shelf life
• Effective
• Instant relief

• The recommended dose of Temonat is usually once daily for 5 days. The treatment may be repeated every 28 days.

• Symptoms of overdose associated with temonat may include chills, persistent sore throat or persistent fever; or severe bleeding or bruising.

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• Longer shelf life
• Purity
• Effective

• Muscle aches
• Low blood potassium levels*
• Less common
• Hot flashes
• Diarrhea
• Cough
• High blood pressure*
• Abnormal heart rhythm
• Upset stomach
• Chest pain
• Heart failure*
• Adrenal gland problems

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Additional Information:

• Item Code: CAPNAT-500

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• Longer shelf life
• Pure

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Advice women of child bearing potential to use an effective method of
contraception while using everolimus for upto 8 weeks after ending treatment

Lactation:
Whether to discontinue breast feeding or the drug taking into consideration the importance of the drug to the mother.

Children:
Safety and efficacy in children have not been established

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• Longer shelf life
• Accurate composition

• Gleevac is often associated with oedema (swelling) and serious fluid retention (holding water). It is important that patients be weighed and monitored regularly for signs and symptoms of serious fluid retention or unexpected weight gain. Patients experiencing unexpected, rapid weight gain should speak to their doctor about appropriate supportive care treatment. Studies have shown that oedema tended to occur more often among patients who are 65 and older or those taking higher doses of GLEEVEC. If you experience severe fluid retention, your doctor may treat you with diuretics and may stop your GLEEVEC treatment until the fluid retention has been managed. Treatment can be resumed as appropriate depending on the initial severity of the event
• Cytopenias (reduction or lack of certain cell elements in blood circulation) have occurred. Your doctor will test your blood weekly for the first month, biweekly for the second month, and periodically thereafter. In most cases, your doctor will reduce or interrupt your GLEEVEC therapy; in rare cases, if the cytopenia is severe, your doctor may discontinue treatment
• Congestive heart failure (impaired ability of the heart to pump blood) and left ventricular dysfunction (impaired functioning of the left side of the heart) have been reported, particularly in patients with other health issues and risk factors. Patients with heart disease or risk factors for heart disease or history of renal failure will be monitored and treated for the condition
• Severe liver problems (hepatotoxicity) may occur. Cases of fatal liver failure and severe liver injury requiring liver transplants have been reported with both short-term and long-term use of GLEEVEC. Your doctor will check your liver function before beginning treatment and continue to monitor liver function as needed. If you experience severe liver problems, your doctor may stop your treatment with GLEEVEC until the liver problem has been managed
• Bleeding may occur. Severe gastrointestinal (GI) bleeding has been reported in patients with Ph+ CML and KIT+ GIST. GI tumor sites may be the cause of this bleeding

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• Leukopenia
• anaemia
• thrombocytopenia
• nausea and vomiting
• Diarrhea

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Our company specializes in importing and exporting excellent quality Pemetrexed Injection 100mg. The offered range of injection is formulated under the strict supervision of diligent and dexterous professionals to meet the medical industry standards. 
Features:

• Effective
  
• Accurate composition
  
• Instant relief
  

Indication:
Pemnat may also be used for the treatment of non-small cell lung cancer (NSLC).
Pemnat is used with for the treatment of malignant pleural mesothelioma (a type of cancer that affects the inside lining of the chest cavity) who cannot be treated with surgery.

Mechanism of action:
Pemnat interferes with the growth of cancer cells and slows their growth and spread in the body

Overdose:
Symptoms of overdose associated with pemnat may include rash, flu symptoms, sores and/or redness in the mouth or throat or on the lips, unusual bleeding or bruising, sore throat, fever, chills, cough or other signs of infection, extreme tiredness, weakness, pale skin, body ache, dizziness, confusion, fast heartbeat, difficulty falling asleep or staying asleep, severe diarrhea.

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With firm commitment to the quality, we are importing and exporting a wide range of supreme quality Regorafenib 40mg Tablet. Processed using high-quality ingredients, these tablets are used for the treatment of symptoms of cancer.

Features:

• Long shelf Life
• Purity
  
• Effective
  

Overdose:
The highest dose of Regorafenib studied clinically was 220 mg per day. The most frequently observed adverse drug reactions at this dose were dermatological events, dysphonia, diarrhoea, mucosal inflammation, dry mouth, decreased appetite, hypertension, and fatigue.
There is no specific antidote for Regorafenib overdose. In the event of suspected overdose, Regorafenib should be discontinued immediately, with best supportive care initiated by a medical professional, and the patient should be observed until clinical stabilisation.
 
Precaution and Warning:
Abnormalities of liver function tests (alanine aminotransferase [ALT], aspartate aminotransferase [AST] and bilirubin) have been frequently observed in patients treated with Stivarga. Severe liver function test abnormalities (Grade 3 to 4) and hepatic dysfunction with clinical manifestations (including fatal outcomes) have been reported in a small proportion of patients (see section 4.8). In clinical trials, a higher incidence of severe liver function test abnormalities and hepatic dysfunction was observed in Asian (in particular Japanese) patients treated with Stivarga as compared with Caucasians (see section 4.2).
It is recommended to perform liver function tests (ALT, AST and bilirubin) before initiation of treatment with Stivarga and monitor closely (at least every two weeks) during the first 2 months of treatment. Thereafter, periodic monitoring should be continued at least monthly and as clinically indicated.

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Additional Information:

• Item Code: Temoside-100

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We are glad to know you that we have export and import the medicine for our client Votrient 400mg. Optimum-grade ingredients are used to process these tablets following standards and norms of the pharmaceutical industry.

Features:

Renal cell cancer and soft tissue sarcoma

Side Effects:

 Excessive fatigue, High blood pressure

Precaution and Warning:
This medicine can cause potentially life-threatening liver problems. Your healthcare provider will monitor your liver function with blood tests before you start Votrient, every month for the first four months, and then periodically throughout the remainder of treatment.

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• There have been no reports of overdose of Xbira acetate during clinical studies
• There is no specific antidote. In the event of an overdose, stop abiraterone acetate, undertake general supportive measures, including monitoring for arrhythmias and cardiac failure, and assess liver function 

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• Fever or chills
• Tiredness
• Redness, tenderness, swelling or warmth of area of skin
• Ear drainage or severe pain
• Frequent or urgent need to urinate
• burning feeling when you urinate
• Pain, numbness, swelling, or drainage from mouth, teeth, or jaw
• Slow healing of the mouth or jaw
• Severe abdominal pain
• Ongoing pain that begins in the stomach area, but may spread to the back
• Fast heart rate

Additional Information:

• Item Code: XGEVA-120

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• Low level of potassium in blood
• Fluid retention in the body
• High blood pressure
• Urinary Tract Infection
• Diarrhea
• Erratic heart beat
• Signs of urinary incontinence
• Abnormal swelling in joints accompanied by muscle ache
• Flatulence
• Brittle bones, resulting in frequent fractures
• A cough and cold

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• Longer shelf life
• Effective
• Purity

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• Long shelf life
• Purity
• Effective

• Joint swelling or pain
• Muscle aches
• Hot flushes
• Diarrhea
• Urinary tract infection
• Cough
• Irregular heartbeats
• Urinate more often than normal
• Need to get up at night to urinate
• Heartburn

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• Accurate composition
• Precise pH value
• Longer shelf life

• Weakness, unusual bruising or bleeding, blurred vision, pinpoint red spots on your skin, and fainting

• Patients are advised not to take any immunization during this period, without doctor’s consent
• Drug Interactions
• Carbamazepine
• Dexamethasone
• Phenytoin
• St. John's wort
• erythromycin or telithromycin)

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Sofosbuvir is a prescription medication used with other antiviral medicines to treat chronic hepatitis C viral infection in adults.

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• Long shelf life
• Effective
• Purity

The only time's medicines should be injected are:

WHAT TO DO WHEN THE DOCTOR PRESCRIBES INJECTIONS:

Doctors and other health workers sometimes prescribe injections when they are not needed. After all, they can charge more money for injections. They forget the problems and dangers of giving injections in rural areas.

1. If a health worker or healer wants to give you an injection, be sure the medicine is appropriate and that she takes all the necessary precautions.

2. If a doctor prescribes injections, explain that you live where no one is well trained to give injections and ask if it would be possible to prescribe a medicine to take by mouth.

3. If a doctor wants to prescribe injections of vitamins, liver extract, or vitamin B₁₂ but has not had your blood tested, tell him you would prefer to see another doctor.

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• Unusual bleeding or bruising
• Sore throat, fever, chills, cough, or other signs of infection

• Tell your doctor and pharmacist if you are allergic to decitabine or any other medications.
• Tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Your doctor may need to change the doses of your medications or monitor you carefully for side effects.
• Tell your doctor if you have kidney or liver disease.
• Tell your doctor if you are pregnant or plan to become pregnant, or if you plan to father a child. You or your partner should not become pregnant while you are using decitabine. You should use birth control to prevent pregnancy in yourself or your partner during your treatment with decitabine and for 2 months afterwards. Talk to your doctor about birth control methods that will work for you. If you or your partner becomes pregnant while using decitabine, call your doctor. Decitabine may harm the fetus.
• Tell your doctor if you are breast-feeding.

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• Act upon non-small lung cancer

• Severe lung disease. Rarely, some patients have developed interstitial lung disease (ILD), or scarring of lung tissue. Some cases have been fatal. Tell your doctor if you develop symptoms such as cough, difficulty breathing, and fever.
• Increased liver enzymes or liver damage. Your doctor may periodically monitor your liver function with simple blood tests. Liver disease may cause gefitinib blood levels to increase as gefitinib is cleared from the body by the liver.

Do not take gefitinib if you are allergic to any of its ingredients.

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Safety and efficacy have not been established in combination with direct acting antiviral agents approved for treatment of chronic hepatitis C infection.

Risk of hepatotoxicity:

Revolade administration can cause abnormal liver function. In the controlled clinical studies in chronic ITP with eltrombopag, increases in serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) and bilirubin were observed.

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• Purity
• Effectiveness
• Compositional accuracy

• Low white blood cell count with increased risk of infection*
• Cough
• Rash, itching
• Nausea
• Vomiting
• Diarrhea
• Muscle aches
• Runny nose
• Sinus infection

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• Accurate composition
• Effective
• Longer shelf life

• if you are pregnant, planning to become pregnant, or are breast-feeding
• if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement
• if you have allergies to medicines, foods, or other substances
• if you have a history of skin cancer or uncontrolled muscle movements (eg, twitching of the face and tongue and involuntary movements of the arms and legs)
• if you have a history of liver problems, kidney problems, sleep problems, or high or low blood pressure
• if you have certain adrenal gland problems (pheochromocytoma) or a history of mental or mood problems

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• long shelf life
• purity
• effective

• Joint swelling or pain
• Muscle aches
• Hot flushes
• Diarrhea
• Urinary tract infection
• Cough
• Irregular heartbeats
• Urinate more often than normal
• Need to get up at night to urinate

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MyHep LVIR Medicines Ledipasvir & Sofosbuvir is a prescription medicine used with other antiviral medicines to treat chronic (lasting a long time) Hepatitis C (Hep C) infection in adults.

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Overdose:
In animal studies, Afinitor showed a low acute toxic potential. No lethality or severe toxicity was observed in either mice or rats given single oral doses of 2000 mg/kg (limit test).
Reported experience with overdose in humans is very limited. Single doses of up to 70 mg have been administered. The acute toxicity profile observed with the 70 mg dose was consistent with that for the 10 mg dose.

Precaution and Warning:
Non-infectious pneumonitis is a class effect of rapamycin derivatives, including AFINITOR. Non-infectious pneumonitis was reported in up to 19% of patients treated with AFINITOR in clinical trials. The incidence of Common Terminology Criteria (CTC) Grade 3 and 4 non-infectious pneumonitis was up to 4.0% and up to 0.2%, respectively [see ADVERSE REACTIONS]. Fatal outcomes have been observed.

Consider a diagnosis of non-infectious pneumonitis in patients presenting with non-specific respiratory signs and symptoms such as hypoxia, pleural effusion, cough, or dyspnea, and in whom infectious, neoplastic, and other causes have been excluded by means of appropriate investigations. Opportunistic infections such as pneumocystis jiroveci pneumonia (PJP) should be considered in the differential diagnosis. Advise patients to report promptly any new or worsening respiratory symptoms. 

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We have put forth for our esteemed customers an effective range of Tykerb Tablets. The range we offer to customers is processed under the strict surveillance of medical experts. To cater to the variegated requirements of customers, we offer these tablets in a spectrum of specifications at market leading prices.

Features:

• Longer shelf life
• Pure
• Safe to consume

• Red, Painful Hands And Feet
• Nausea
• Rash
• Vomiting
• Tiredness Or Weakness
• Mouth Sores
• Loss Of Appetite
• Indigestion
• Unusual Hair Loss Or Thinning

• Heart problems including, decreased pumping of blood from the heart and an abnormal heartbeat. Signs and symptoms of an abnormal heartbeat include:
  • feeling like your heart is pounding or racing
  • dizziness
  • tiredness
  • feeling lightheaded
  • shortness of breath
    • Your doctor should check your heart function before you start taking lapatinib and during treatment.
• Liver problems. Signs and symptoms of liver problems include:
  • itching
  • yellow eyes or skin
  • dark urine
  • pain or discomfort in the right upper stomach area
  • death
    • Your doctor should do blood tests to check your liver before you start taking lapatinib and during treatment.
• Diarrhea, which may cause you to become dehydrated. Follow your doctors instructions for what to do to help prevent diarrhea. Call your doctor immediately at the first sign of diarrhea, as it is important that this is treated right away.
• Lung problems. Symptoms of a lung problem with lapatinib include a cough that will not go away or shortness of breath.

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• Nausea
• Vomiting
• Weakness
• Dizziness
• Headache
• Stomach Pain

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