Product image of Micofenolato De Mofetil Accord (Mycophenolate Mofetil) supplied by GNH India

Micofenolato De Mofetil Accord

Active Ingredient:
Mycophenolate Mofetil
Origin:
EU

Micofenolato De Mofetil Accord (Mycophenolate Mofetil)

Mycophenolate Mofetil, the active ingredient in Micofenolato De Mofetil Accord, is an antimetabolite immunosuppressant presented as an oral formulation for systemic use. It is employed to prevent organ transplant rejection and to treat lupus nephritis by suppressing lymphocyte proliferation.

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

Manufacturer / TM Owner

Accord Healthcare S.L.U.

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Indications & Clinical Uses

Mycophenolate Mofetil is used in the management of immune‑mediated conditions where inhibition of lymphocyte proliferation is required.

  • Kidney transplant: helps prevent acute and chronic graft rejection.
  • Heart transplant: reduces the risk of organ rejection post‑surgery.
  • Liver transplant: supports long‑term graft survival by suppressing immune response.
  • Lupus nephritis: diminishes renal inflammation and preserves kidney function.

How It Works

  • Mycophenolate Mofetil is converted intracellularly to mycophenolic acid, which selectively inhibits inosine monophosphate dehydrogenase (IMPDH). This blockade reduces guanosine nucleotide synthesis, a critical pathway for the proliferation of T and B lymphocytes, thereby attenuating the immune response that leads to graft rejection or autoimmune kidney damage.

Side Effects

Adverse reactions may occur with Mycophenolate Mofetil therapy.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: frequent loose stools, sometimes leading to dehydration.
  • Headache: transient cranial discomfort.
  • Abdominal pain: cramping or discomfort in the stomach area.
  • Tremor: fine shaking of the hands or limbs.

Serious or Rare Side Effects

  • Leukopenia: significant reduction in white blood cells, increasing infection risk.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Opportunistic infections: severe infections such as cytomegalovirus or fungal disease.
  • Malignancy: increased risk of certain cancers with long‑term use.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.

Precautions & Warnings

Patients receiving Mycophenolate Mofetil should be monitored closely for safety concerns.

  • Monitor blood counts: regular CBC to detect leukopenia or anemia.
  • Assess liver function: periodic liver enzyme tests for hepatotoxicity.
  • Avoid in pregnancy: drug is Category D; use effective contraception.
  • Use caution in renal impairment: dose adjustment may be required.
  • Counsel on infection risk: advise prompt reporting of fever or signs of infection.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Mycophenolate Mofetil can interact with several medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Azathioprine: additive bone‑marrow suppression.
  • Cyclosporine: increased mycophenolate exposure, raising toxicity risk.
  • Tacrolimus: synergistic immunosuppression, heightening infection risk.
  • Live vaccines: may cause severe infection; avoid administration.

Moderate Interactions (Monitor Closely)

  • Antacids (aluminum or magnesium): may reduce absorption of mycophenolic acid.
  • Rifampin: induces metabolism, decreasing drug levels.
  • Cholestyramine: binds drug in gut, lowering systemic exposure.
  • NSAIDs: can exacerbate renal toxicity when combined.

Frequently Asked Questions

Micofenolato De Mofetil Accord contains Mycophenolate Mofetil, an immunosuppressant prescribed to prevent rejection after kidney, heart or liver transplantation and to treat lupus nephritis by reducing abnormal immune activity.

Mycophenolate Mofetil is converted to mycophenolic acid, which selectively blocks the enzyme inosine monophosphate dehydrogenase (IMPDH). This inhibition limits guanosine nucleotide synthesis, a key step for T‑ and B‑cell proliferation, thereby dampening the immune response.

The exact dose and dosing schedule are determined by the prescribing clinician based on the patient’s condition, transplant type, renal function and other individual factors. Patients should follow the prescriber’s instructions precisely.

Mycophenolate Mofetil is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should be avoided in pregnancy unless no safer alternative exists, and effective contraception is required. Breastfeeding is not recommended while taking this medication.

To place an order, 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.

Compared with calcineurin inhibitors such as cyclosporine or tacrolimus, Mycophenolate Mofetil offers a different mechanism—IMPDH inhibition—resulting in a distinct side‑effect profile. It is often used in combination regimens to achieve synergistic immunosuppression while allowing lower doses of each agent.

Store the product at below 25 °C in its original container, protecting it from moisture and direct sunlight. Do not expose the tablets or capsules to excessive heat or humidity, and keep them out of reach of children.

The medication is taken orally, usually with food or a glass of water to reduce gastrointestinal irritation. The exact frequency (once or twice daily) and dose are set by the prescriber based on the therapeutic indication and patient factors.

Serious risks include severe infections due to immune suppression, leukopenia or anemia, liver toxicity, and an increased long‑term risk of certain malignancies. Patients should be monitored regularly for blood count changes, liver function abnormalities and signs of infection.

Patients with known hypersensitivity to Mycophenolate Mofetil or any component of the formulation should avoid it. It is contraindicated in pregnant women unless absolutely necessary, and caution is advised in individuals with severe renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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