Product image of Myfortic (Mycophenolic Acid) supplied by GNH India

Myfortic

Active Ingredient:
Mycophenolic Acid
Origin:
EU

Myfortic (Mycophenolic Acid)

Mycophenolic Acid, the active ingredient in Myfortic, is an immunosuppressant presented as an oral tablet for oral use. It is used to prevent organ rejection in patients who have undergone kidney, heart, or liver transplantation.
GNH India supplies Myfortic as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide.

Manufacturer / TM Owner

Novartis Europharm Limited

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Indications & Clinical Uses

  • Myfortic is an immunosuppressant that works by inhibiting lymphocyte proliferation, making it essential in transplant medicine.
  • Kidney transplantation: helps prevent acute and chronic rejection of the transplanted kidney.
  • Heart transplantation: reduces the risk of graft rejection and improves long‑term graft survival.
  • Liver transplantation: supports maintenance of graft function by suppressing immune‑mediated damage.

How It Works

  • Myfortic (mycophenolate sodium) is converted to mycophenolic acid, which selectively inhibits inosine monophosphate dehydrogenase (IMPDH). This blocks de novo synthesis of guanosine nucleotides, a pathway critical for proliferation of T and B lymphocytes, thereby dampening the adaptive immune response that leads to organ rejection.

Side Effects

Myfortic may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: frequent loose stools, often self‑limiting.
  • Vomiting: occasional episodes, especially early in therapy.
  • Abdominal pain: crampy discomfort in the stomach area.
  • Headache: transient, usually resolves without intervention.
  • Infections: increased susceptibility to bacterial, viral, or fungal infections.

Serious or Rare Side Effects

  • Leukopenia: significant reduction in white blood cells, raising infection risk.
  • Anemia: decreased red blood cell count leading to fatigue.
  • Severe infection: opportunistic infections such as Pneumocystis jirovecii pneumonia.
  • Malignancy: heightened risk of lymphoproliferative disorders.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Progressive multifocal leukoencephalopathy (PML): rare but potentially fatal brain infection.

Precautions & Warnings

Before initiating Myfortic, clinicians should assess patient-specific risk factors and monitor for adverse events.

  • Monitor blood counts: perform regular complete blood counts to detect leukopenia or anemia.
  • Assess renal function: adjust therapy if creatinine clearance is reduced.
  • Screen for infections: evaluate for active infections and vaccinate appropriately before treatment.
  • Avoid in pregnancy: potential teratogenic effects; use effective contraception.
  • Store at room temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

Myfortic interacts with several medicines that can alter its efficacy or safety.

Major Interactions (Avoid)

  • Azathioprine: additive bone‑marrow suppression.
  • Live vaccines: increased risk of vaccine‑derived infection.
  • Cholestyramine: binds drug and reduces absorption.
  • Rifampin: strong CYP3A4 inducer that lowers mycophenolic acid levels.
  • Antacids containing aluminum or magnesium: may decrease bioavailability.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: may enhance nephrotoxic potential.
  • NSAIDs: increase risk of renal impairment.
  • Warfarin: may affect INR and bleeding risk.
  • Ganciclovir: potential additive myelosuppression.
  • Diuretics: monitor electrolytes and renal function.

Frequently Asked Questions

Myfortic (mycophenolate sodium) is prescribed to prevent rejection of transplanted organs such as kidneys, hearts, and livers. By suppressing the immune response, it helps maintain graft function and improves long‑term transplant outcomes.

Mycophenolic Acid, the active moiety of Myfortic, inhibits the enzyme inosine monophosphate dehydrogenase (IMPDH). This blocks the synthesis of guanosine nucleotides needed for T‑ and B‑lymphocyte proliferation, thereby reducing the immune response that can attack a transplanted organ.

The specific dose of Myfortic is determined by the prescribing physician based on the patient’s transplant type, renal function, and other clinical factors. Dosage adjustments are individualized and should follow the prescriber’s instructions.

The safety of Myfortic in pregnancy and lactation has not been definitively established. It is generally advised to avoid use during pregnancy unless the potential benefit justifies the risk, and breastfeeding decisions should be made in consultation with a healthcare professional.

To place an order, submit an enquiry on the Myfortic product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Myfortic belongs to the antimetabolite class and offers a different mechanism than calcineurin inhibitors like tacrolimus. It is often used in combination regimens to provide synergistic immunosuppression while potentially reducing the dose‑related toxicity of other agents.

Myfortic should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

Myfortic is taken orally, usually as tablets, with or without food as directed by the prescriber. The exact timing and frequency depend on the individualized dosing schedule established by the treating physician.

Serious risks include severe infections, leukopenia, anemia, hepatic dysfunction, and rare occurrences of progressive multifocal leukoencephalopathy (PML). Patients should be monitored regularly for blood count changes and signs of infection.

Myfortic is contraindicated in patients with known hypersensitivity to mycophenolate or any component of the formulation, and it should be avoided in individuals with active, uncontrolled infections or severe hepatic impairment. Pregnant women should only use it if clearly needed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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