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 a delayed‑release tablet for oral use. It is employed to prevent acute rejection of transplanted organs in patients who have received kidney, heart or liver transplants.

GNH India supplies Myfortic as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and transplant centres worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches to meet global demand. Customers benefit from reliable logistics, comprehensive documentation, and responsive technical support.

Manufacturer / TM Owner

Novartis (Hellas) S.A.C.I.

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Indications & Clinical Uses

Myfortic, an antimetabolite immunosuppressant, is indicated to reduce immune‑mediated rejection in solid‑organ transplantation.

  • Renal transplantation: helps prevent acute graft rejection, improves graft survival, and facilitates stable kidney function post‑surgery.
  • Heart transplantation: reduces the incidence of early rejection episodes, supporting cardiac graft performance and patient recovery.
  • Liver transplantation: maintains graft viability by suppressing immune activation, thereby decreasing the risk of acute hepatic rejection.

How It Works

  • Myfortic delivers mycophenolic acid, which selectively inhibits inosine monophosphate dehydrogenase (IMPDH), a key enzyme in the de novo synthesis of guanosine nucleotides. By limiting guanosine availability, the drug impairs proliferation of T‑ and B‑lymphocytes, which rely on this pathway for clonal expansion, thereby attenuating the immune response that leads to organ rejection. The inhibition is reversible and preferentially affects activated lymphocytes while sparing resting cells, contributing to its targeted immunosuppressive profile.

Side Effects

Myfortic may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea
  • Diarrhea
  • Vomiting
  • Abdominal pain
  • Headache
  • Upper respiratory tract infection

Serious or Rare Side Effects

  • Leukopenia or neutropenia
  • Anemia or pancytopenia
  • Severe or opportunistic infections
  • Hepatic dysfunction
  • Malignancies such as lymphomas
  • Progressive multifocal leukoencephalopathy (rare)

Precautions & Warnings

When prescribing Myfortic, clinicians should observe several safety precautions to minimize risks.

  • Monitor blood counts: perform regular complete blood count tests to detect leukopenia or anemia early.
  • Assess renal function: adjust dosing in patients with impaired kidney function and monitor creatinine levels.
  • Avoid use in pregnancy: the drug is category D and may cause fetal harm; contraception is recommended.
  • Counsel on infection risk: advise patients to report fevers or signs of infection promptly.
  • Review vaccinations: live vaccines should be avoided during therapy.
  • Store at room temperature: keep below 25 °C in the original packaging, protected from moisture.

Avoid Interactions

Myfortic can interact with several medicines, altering its exposure or increasing toxicity.

Major Interactions (Avoid)

  • Cyclosporine: co‑administration markedly increases mycophenolic acid plasma concentrations.
  • Tacrolimus: similar effect, leading to higher exposure and potential toxicity.
  • Antacids or cholestyramine: reduce absorption of mycophenolic acid, decreasing efficacy.
  • Live vaccines: heightened risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • Azathioprine: additive bone‑marrow suppression may require dose adjustments.
  • Ribavirin: combined use can increase risk of anemia.
  • NSAIDs: may exacerbate renal impairment when used with Myfortic.

Frequently Asked Questions

Myfortic is prescribed to prevent acute rejection of transplanted organs. It is used in patients who have undergone kidney, heart, or liver transplantation to suppress the immune response that can damage the new graft.

Mycophenolic Acid selectively blocks the enzyme inosine monophosphate dehydrogenase, which is essential for making guanosine nucleotides. This limits the proliferation of T‑ and B‑lymphocytes, reducing the immune activity that leads to organ rejection.

The dose of Myfortic is individualized by the prescribing physician based on factors such as the type of transplant, patient weight, kidney function, and concurrent immunosuppressive therapy. No standard dose is provided here.

Myfortic is classified as pregnancy category D, indicating evidence of fetal risk. It should be avoided in pregnancy, and effective contraception is recommended. Limited data are available for breastfeeding, so use is generally not advised.

To order 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 necessary import documentation.

The primary alternative is mycophenolate mofetil (CellCept), which delivers the same active moiety but in a different salt form. Both provide comparable immunosuppressive efficacy; Myfortic’s delayed‑release formulation may improve gastrointestinal tolerability for some patients.

Myfortic tablets should be stored at room temperature, below 25 °C, in the original blister pack to protect them 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 as a delayed‑release tablet. It is usually swallowed whole with a glass of water, with or without food, as directed by the healthcare provider. Do not crush, chew, or split the tablet.

Serious risks include severe infections, bone‑marrow suppression leading to leukopenia or anemia, liver toxicity, and an increased long‑term risk of certain malignancies such as lymphomas. Patients should be monitored regularly for these complications.

Myfortic should not be used by individuals with known hypersensitivity to mycophenolic acid or any tablet components, pregnant women, patients with active severe infections, or those with uncontrolled severe liver disease without careful medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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