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 delayed‑release tablet for oral use. It is employed to prevent acute organ rejection in renal, cardiac and hepatic transplantation and as adjunct therapy for certain autoimmune disorders such as lupus nephritis and vasculitis.

GNH India supplies Myfortic as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide.

Manufacturer / TM Owner

Novartis Hungária Kft.

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Indications & Clinical Uses

Myfortic is an antimetabolite immunosuppressant used in several transplant and autoimmune pathways.

  • Renal transplantation: helps prevent acute graft rejection after kidney transplant.
  • Cardiac transplantation: reduces the risk of early heart‑transplant rejection.
  • Hepatic transplantation: supports maintenance of liver graft function by limiting immune attack.
  • Lupus nephritis: used as adjunct therapy to control renal inflammation in systemic lupus.
  • Vasculitis: added to standard regimens to suppress immune‑mediated vessel inflammation.

How It Works

  • Mycophenolic acid selectively and reversibly inhibits inosine monophosphate dehydrogenase (IMPDH), a key enzyme in the de novo synthesis of guanosine nucleotides. This inhibition depletes guanosine pools, impairing proliferation of T‑ and B‑lymphocytes while sparing most other cell types, thereby dampening the adaptive immune response essential for graft rejection and autoimmune activity.

Side Effects

Adverse reactions may range from mild to severe and should be monitored during therapy.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: frequent loose stools.
  • Vomiting: occasional emesis.
  • Abdominal pain: cramping or discomfort.
  • Headache: transient head pain.
  • Tremor: fine shaking of hands.

Serious or Rare Side Effects

  • Infections: increased susceptibility to bacterial, viral or fungal infections.
  • Leukopenia: marked reduction in white blood cells.
  • Anemia: decreased red blood cell count.
  • Lymphopenia: low lymphocyte levels.
  • Malignancy: rare reports of post‑transplant lymphoproliferative disorders.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.

Precautions & Warnings

Careful monitoring and patient education are essential when using Myfortic.

  • Monitor blood counts: regular CBC to detect leukopenia or anemia.
  • Assess renal function: check serum creatinine and eGFR periodically.
  • Avoid in pregnancy: teratogenic risk; contraindicated for women who are pregnant or may become pregnant.
  • Counsel on infection risk: advise patients to report fever, cough or unusual infections promptly.
  • Dose adjustment in hepatic impairment: consider reduced dosing in patients with significant liver disease.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Myfortic may interact with several medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Cyclosporine: increases mycophenolic acid exposure, raising toxicity risk.
  • Tacrolimus: synergistic immunosuppression may lead to excessive immune suppression.
  • Rifampin: induces metabolism and reduces mycophenolic acid levels, compromising effectiveness.

Moderate Interactions (Monitor Closely)

  • Azathioprine: combined bone‑marrow suppression can exacerbate cytopenias.
  • NSAIDs: concurrent use may increase risk of nephrotoxicity, especially in transplant recipients.

Frequently Asked Questions

Myfortic is prescribed to prevent acute rejection after kidney, heart and liver transplantation and as an adjunct therapy for autoimmune disorders such as lupus nephritis and certain types of vasculitis. It works by suppressing the immune response that can damage the transplanted organ or inflamed tissues.

Mycophenolic Acid inhibits the enzyme inosine monophosphate dehydrogenase (IMPDH), which is essential for the synthesis of guanosine nucleotides. This blocks the proliferation of T‑ and B‑lymphocytes, the immune cells responsible for graft rejection and autoimmune inflammation, thereby reducing immune activity.

The dose of Myfortic is individualized by the prescribing clinician based on the type of transplant, patient weight, renal function and concomitant immunosuppressants. The prescriber determines the appropriate strength and dosing schedule for each patient.

Myfortic is classified as Pregnancy Category X, indicating it is contraindicated in pregnancy because it can cause fetal harm. It is also not recommended during breastfeeding, as the drug may be excreted in milk and affect the infant.

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 (mycophenolic acid) selectively inhibits lymphocyte proliferation via IMPDH blockade, offering a more targeted mechanism than azathioprine, which interferes with DNA synthesis broadly. Myfortic often provides better control of acute rejection with a different side‑effect profile, though both require careful monitoring of blood counts.

Myfortic tablets should be stored at temperatures below 25 °C in their original container, protected from moisture and direct sunlight. Keeping the packaging sealed helps maintain tablet integrity and potency throughout its shelf life.

Myfortic is taken orally as a delayed‑release tablet, usually once or twice daily as directed by the prescriber. The tablet should be swallowed whole with water and not crushed, chewed, or split, to preserve its delayed‑release properties.

The most serious risks include severe infections due to immune suppression, hematologic abnormalities such as leukopenia or anemia, and rare cases of malignancy. Patients should be monitored regularly for signs of infection, blood‑cell changes and any unusual symptoms.

Myfortic is contraindicated in pregnant women, individuals with known hypersensitivity to mycophenolic acid or any tablet components, and patients with severe hepatic impairment unless dose adjustments are made. It should also be avoided in patients with active, uncontrolled infections.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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