Mygraf (500mg) 20 Tablets

Mygraf (500mg) 20 Tablets

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  • Manufacturer PLATINUM PHAMA
  • Generic Name Mycophenolate Mofetil

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Product Information

  • Description
  • Ingredients
  • Drug Class
  • Dosage Form
  • Uses
  • Dosage
  • In case of Overdose
  • Missed Dose
  • How To Use
  • When Not to Use
  • Side Effects
  • Precautions & Warnings
  • Drug Interactions
  • Food Interactions
  • Storage/Disposal
  • Quick Tips, if any
  • Laboratory Screening
  • Description

    Mycophenolate Mofetil, when administered, is rapidly metabolized in the liver and gut wall to mycophenolic acid (MPA), which is the active form of the drug. MPA acts as a non-competitive, selective, and reversible inhibitor of inosine-5'-monophosphate dehydrogenase (IMPDH). By blocking the activity of IMPDH, Mycophenolate Mofetil inhibits the de novo synthesis of guanosine nucleotides, which are essential for the proliferation of lymphocytes, especially T and B cells. This mechanism selectively suppresses the immune response by reducing the production of antibodies and inhibiting the activation and proliferation of T cells, thereby preventing the rejection of transplanted organs or tissues.

  • Ingredients

    Mycophenolate Mofetil
  • Drug Class

    Immunosuppressant

  • Dosage Form

    Tablet

  • Uses

    The following are the uses of Mycophenolate Mofetil 500mg Tablet:

    • Used for preventing organ rejection in transplant patients
    • Used for managing autoimmune conditions like lupus and psoriasis
    • Used to treat inflammatory bowel disease (IBD)
    • Used in rheumatoid arthritis to control inflammation
    • Used for suppressing overactive immune responses
    • Used in kidney, heart, and liver transplant recovery
    • Used to reduce the risk of graft rejection episodes
  • Dosage

    Tailoring Treatment for Optimal Health, Prescribed Medication Dosage is:

    • Renal Transplant- Starting dosage of 1000 mg twice daily, subject to change based on lab results and clinical response
    • Cardiac Transplant- Starting dosage ranges between 1,500 mg to 3,000 mg daily divided into three or four doses daily
    • Rheumatoid Arthritis- Starting dosage of 500 mg to 1000 mg daily, subject to increase based on severity of the disease and response to treatment
  • In case of Overdose

    In the case of an overdose of Mycophenolate Mofetil 500mg Tablets, individuals may experience severe gastrointestinal symptoms such as nausea, vomiting, and diarrhea. The severity of these symptoms can vary based on the amount ingested. Additionally, there is a risk of hematological complications, including leukopenia and thrombocytopenia. It is vital to seek medical assistance promptly, as doctors may employ specific treatments to manage the overdose, including gastric lavage and supportive care.

  • Missed Dose

    In the case of a missed dose of Mycophenolate Mofetil 500mg Tablet, it is generally recommended to take the missed dose as soon as you remember, provided it is not too close to the time of your next scheduled dose. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. However, do not double the dose to make up for a missed one, as this may increase the risk of side effects. It is important to maintain a consistent medication routine, and if you frequently miss doses, consult your healthcare provider for advice on how to improve adherence to your treatment plan.

  • How To Use

    To take Mycophenolate Mofetil 500mg Tablets, swallow the tablet whole with a full glass of water, usually twice a day or as directed by your doctor, and ensure you take it consistently at evenly spaced intervals for optimal effectiveness.

  • When Not to Use

    Here are the situations when Mycophenolate Mofetil 500mg Tablet should not be used:

    • Should not be used in individuals with a known allergy to Mycophenolate Mofetil or any of its components.
    • Contraindicated in patients with severe kidney disease or those undergoing dialysis.
    • Not recommended for individuals with severe liver impairment or liver disease.
    • Should not be used during pregnancy as it may cause harm to the fetus.
    • Contraindicated in breastfeeding mothers due to potential risks to the infant.
    • Avoid using if you have recently received a live vaccine, and inform your doctor about your vaccination history.
    • Not suitable for individuals with active infections or a history of severe or life-threatening infections.
    • Should not be used in patients with a known or suspected malignancy, as it can suppress the immune system.
    • Avoid using Mycophenolate Mofetil if you have gastrointestinal ulcers or gastrointestinal bleeding.
    • Not recommended for individuals with a history of severe or uncontrolled hypertension.
  • Side Effects

    The side effects of Mycophenolate Mofetil 500mg Tablet may include:

    • Nausea and vomiting
    • Diarrhea
    • Stomach pain or cramps
    • Headaches
    • Tremors or shaking
    • Increased risk of infections
    • Fatigue and weakness
    • Skin rashes or itching
  • Precautions & Warnings

    Following are the precautions and warnings for Mycophenolate Mofetil 500mg Tablet:

    • Do not take this medication if you are allergic to mycophenolate mofetil or any of its ingredients.
    • Regular blood tests are required to monitor kidney function and blood cell counts while on this medication.
    • Patients with a history of kidney problems should be closely monitored, as dosage adjustments may be necessary.
    • Avoid live vaccines during treatment and consult your doctor before any vaccination.
    • Women of childbearing age should use effective contraception while taking this medication and for 6 weeks after stopping treatment.
    • This medication can cause birth defects, so it should not be used during pregnancy unless the potential benefits outweigh the risks.
    • Breastfeeding is not recommended while taking Mycophenolate Mofetil due to potential risks to the infant.
    • Patients should report any signs of infection, unusual bleeding, or any other new symptoms to their healthcare provider immediately.
  • Drug Interactions

    Following are the drug interactions for Mycophenolate Mofetil 500mg Tablet:

    • Live vaccines should be avoided due to potential risk of infection or decreased vaccine efficacy.
    • Co-administration with azathioprine may increase risk of myelosuppression and infections.
    • Drug interaction with acyclovir can increase mycophenolic acid levels, potentially leading to myelotoxicity.
    • Use with antacids containing magnesium or aluminum can reduce absorption of mycophenolate mofetil.
    • When taken with cyclosporine, increased risk of infection and lymphoproliferative disorders may occur.
    • Mycophenolate mofetil may increase the levels of sirolimus, potentially causing toxicity.
    • Concomitant use with trimethoprim/sulfamethoxazole can increase mycophenolic acid concentrations, requiring dosage adjustments.
  • Food Interactions

    Following are the food interactions for Mycophenolate Mofetil 500mg Tablet:

    • Avoid grapefruit and grapefruit juice as they can increase drug levels in the blood, potentially leading to increased side effects.
    • Alcohol consumption should be limited or avoided as it may increase the risk of gastrointestinal side effects.
    • Live vaccines, found in some dairy products, should be avoided due to potential immune system interactions.
    • High-fat meals can increase the absorption of Mycophenolate Mofetil, potentially requiring dosage adjustments.
    • Ensure adequate fluid intake to reduce the risk of gastrointestinal side effects.
    • Avoid black cohosh supplements as they may interact with the medication's metabolism.
    • Herbal teas containing St. John's Wort should be avoided as it can affect the medication's effectiveness.
    • Consult your doctor before taking any vitamins or supplements to ensure they won't interfere with the medication's function.
  • Storage/Disposal

    Mycophenolate Mofetil 500mg Tablets should be stored in a secure and dry location, away from direct sunlight and moisture. It is crucial to keep the medication in its original container, tightly sealed, to maintain its integrity and prevent contamination. Avoid storing the tablets in the bathroom or near heat-emitting appliances, as temperature fluctuations can impact their effectiveness. Pay attention to the expiration date on the packaging, and discard any unused or expired tablets appropriately. Do not dispose of them in sinks or toilets; instead, consult your pharmacist or healthcare professional for guidance on safe disposal practices. Always keep medications out of children's reach to prevent accidental consumption.

  • Quick Tips, if any

    Following are the quick tips for Mycophenolate Mofetil 500mg Tablet:

    • Ensure you take the tablet as directed by your doctor for the best results.
    • Take the tablet with a full glass of water to aid in swallowing.
    • Maintain a consistent daily routine for taking the medication.
    • Consider taking the tablet with food to minimize stomach-related side effects.
    • Avoid crushing or chewing the tablet; swallow it whole.
    • Store the medication in a cool, dry place, away from direct sunlight.
    • Regularly monitor your blood cell counts and kidney function while on this medication.
    • Inform your doctor about all medications you are taking to avoid potential drug interactions.
  • Laboratory Screening

    Mycophenolate Mofetil is an immunosuppressant drug that is commonly used to prevent organ rejection in transplants. To ensure the safety and effectiveness of the drug, several essential laboratory tests are required. First, regular complete blood count (CBC) monitoring detects abnormalities in blood components, such as white blood cells, red blood cells, and platelets. Low white blood cell counts indicate immunosuppression, while low red blood cell counts may indicate anemia. Second, since Mycophenolate Mofetil can cause kidney damage, regular tests assess kidney function, including blood levels of creatinine and blood urea nitrogen (BUN) to determine creatinine clearance or estimated glomerular filtration rate (eGFR). Third, to ensure the drug does not cause undue stress to the liver, tests such as alanine aminotransferase (ALT), aspartate aminotransferase (AST), and bilirubin may be monitored. Additionally, specific levels of Mycophenolate Mofetil in the blood may be measured to ensure therapeutic concentration, particularly in the early stages of therapy or if there is a reason to suspect a compliance issue. Given the drug's potential to cause elevated potassium levels in the blood, periodic monitoring of potassium levels is recommended, especially in those with risk factors for hyperkalemia. Moreover, since concurrent use with certain immunosuppressants can lead to elevated calcium levels, occasional monitoring of calcium levels in the blood is recommended to rule out the risk of adverse events. Overall, these comprehensive tests help ensure the safe and effective use of Mycophenolate Mofetil in transplant patients.

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