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 antimetabolite presented as an oral tablet for oral use. It is employed to reduce the risk of organ rejection in transplant recipients, particularly those receiving a kidney graft.
GNH India supplies Myfortic as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide.

Manufacturer / TM Owner

Novartis S.R.O.,

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Indications & Clinical Uses

Myfortic is an antimetabolite immunosuppressant used in solid‑organ transplantation to inhibit lymphocyte proliferation.

  • Renal transplant: helps prevent graft rejection in kidney recipients.
  • Cardiac transplant: reduces the incidence of heart‑graft rejection.
  • Liver transplant: supports long‑term graft survival by suppressing immune response.

How It Works

  • Mycophenolic acid selectively inhibits inosine monophosphate dehydrogenase (IMPDH), a key enzyme in the de novo synthesis of guanosine nucleotides. By limiting guanosine availability, the drug suppresses proliferation of activated T and B lymphocytes, which rely heavily on this pathway, thereby dampening the 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 upset stomach.
  • Diarrhea: frequent loose stools.
  • Vomiting: occasional emesis.
  • Abdominal pain: cramping or discomfort.
  • Headache: transient mild headache.
  • Increased infection risk: higher susceptibility to common infections.

Serious or Rare Side Effects

  • Leukopenia: significant reduction in white blood cells.
  • Anemia: decreased red blood cell count.
  • Severe infections: opportunistic or life‑threatening infections.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Malignancy: increased risk of certain cancers with long‑term use.
  • Gastrointestinal perforation: rare but serious bowel injury.

Precautions & Warnings

Patients receiving Myfortic should be monitored closely for safety and efficacy.

  • Blood counts: monitor complete blood count regularly to detect leukopenia or anemia.
  • Liver function: assess hepatic enzymes periodically.
  • Live vaccines: avoid administration while on therapy due to immunosuppression.
  • Renal function: adjust dosing in patients with impaired kidney function.
  • Infection signs: report fever, cough, or unusual symptoms promptly.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Myfortic can interact with several medicines, altering its effectiveness or safety profile.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: may reduce absorption of mycophenolic acid.
  • Cholestyramine or colestipol: can bind the drug and lower systemic exposure.
  • Cyclosporine or tacrolimus: may increase mycophenolic acid levels, raising toxicity risk.

Moderate Interactions (Monitor Closely)

  • Azathioprine: additive bone‑marrow suppression; monitor blood counts closely.
  • Live attenuated vaccines: heightened infection risk; consider alternative immunizations.

Frequently Asked Questions

Myfortic contains mycophenolic acid and is prescribed to prevent rejection of transplanted organs, especially kidneys. It works by suppressing the immune system’s response to the foreign graft, helping maintain graft function and prolong patient survival.

Mycophenolic acid blocks the enzyme inosine monophosphate dehydrogenase, which is essential for making guanosine nucleotides. Lymphocytes rely on this pathway for proliferation, so the drug limits T‑ and B‑cell growth, reducing the immune attack on a transplanted organ.

The exact dose of Myfortic is individualized by the prescribing clinician based on the patient’s transplant type, kidney function, and other medications. Dosage decisions are made by the treating physician and should follow the approved prescribing information.

The safety of Myfortic in pregnancy and lactation has not been definitively established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the healthcare provider.

To request Myfortic, submit an enquiry on the 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 required import documentation.

Myfortic (mycophenolic acid) is an antimetabolite, differing from calcineurin inhibitors such as cyclosporine or tacrolimus, which act on T‑cell activation pathways. Myfortic offers a distinct mechanism that can be combined with other agents for synergistic immunosuppression, often providing a favorable side‑effect profile for certain patients.

Myfortic tablets should be stored at room temperature, below 25 °C, in the original packaging. Keep them away from moisture, heat and direct sunlight to maintain product stability throughout its shelf life.

Myfortic is taken orally, usually with food to improve tolerability. The tablets are swallowed whole with a glass of water and should be taken exactly as prescribed by the healthcare professional.

Serious risks include severe infections, leukopenia (low white‑blood‑cell count), anemia, liver dysfunction, and a potential increased risk of certain malignancies with long‑term use. Patients should be monitored regularly for these complications.

Myfortic is contraindicated in individuals with known hypersensitivity to mycophenolic acid or any component of the formulation. It should also be avoided in patients with uncontrolled severe infections or active, untreated malignancies unless specifically directed by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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