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

Micofenolato De Mofetilo Cinfa

Active Ingredient:
Mycophenolate Mofetil
Origin:
EU

Micofenolato De Mofetilo Cinfa (Mycophenolate Mofetil)

Mycophenolate Mofetil, the active ingredient in Micofenolato De Mofetilo Cinfa, is an antimetabolite immunosuppressant presented as an oral formulation for oral use. It is employed to prevent acute organ transplant rejection and to treat lupus nephritis in appropriate patients.

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

Manufacturer / TM Owner

Laboratorios Cinfa S.A.

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Indications & Clinical Uses

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

  • Kidney transplant: helps prevent acute rejection of the transplanted organ.
  • Heart transplant: reduces the risk of early graft rejection.
  • Lupus nephritis: decreases renal inflammation and preserves kidney function.

How It Works

  • Mycophenolate Mofetil is a selective inhibitor of inosine monophosphate dehydrogenase (IMPDH). By blocking IMPDH, it limits guanosine nucleotide synthesis, which is essential for the proliferation of T‑ and B‑lymphocytes. The resulting reduction in lymphocyte replication dampens the immune response, providing immunosuppression in transplant and autoimmune settings.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: loose stools that may affect hydration.
  • Abdominal pain: cramping or discomfort in the stomach area.
  • Headache: transient pain in the head region.
  • Vomiting: occasional expulsion of stomach contents.
  • Tremor: mild shaking of the hands or limbs.

Serious or Rare Side Effects

  • Opportunistic infections: increased susceptibility to fungal, viral, or bacterial pathogens.
  • Bone marrow suppression: leukopenia, anemia, or thrombocytopenia.
  • Malignancy: heightened risk of certain cancers with long‑term use.
  • Severe liver injury: elevated transaminases or hepatitis.
  • Progressive multifocal leukoencephalopathy (PML): rare demyelinating brain disease.
  • Pregnancy complications: fetal toxicity and loss.

Precautions & Warnings

Patients should be monitored closely for safety concerns before and during therapy.

  • Blood count monitoring: perform regular CBC to detect leukopenia or anemia.
  • Renal function assessment: evaluate serum creatinine and eGFR periodically.
  • Liver enzyme testing: check ALT/AST levels for hepatic toxicity.
  • Pregnancy avoidance: drug is category D; use effective contraception.
  • Dose adjustment in renal impairment: consider reduced dosing when clearance is decreased.
  • Store at below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Azathioprine: additive bone‑marrow suppression increases risk of cytopenias.
  • Cyclosporine: raises mycophenolate exposure, potentially intensifying toxicity.
  • Tacrolimus: similar increase in systemic levels, requiring dose review.
  • Live vaccines: heightened risk of infection due to immunosuppression.
  • Cholesterol‑binding resins (e.g., cholestyramine): reduce mycophenolate absorption.

Moderate Interactions (Monitor Closely)

  • Antacids (aluminum or magnesium): may lower oral bioavailability; separate dosing by at least 2 hours.
  • Rifampin: induces metabolism, decreasing mycophenolate concentrations.
  • Warfarin: possible increase in INR; monitor coagulation parameters.
  • ACE inhibitors: combined renal effects may require closer kidney function monitoring.

Frequently Asked Questions

Micofenolato De Mofetilo Cinfa contains mycophenolate mofetil, which is prescribed to prevent acute rejection after solid‑organ transplants such as kidney or heart transplants, and to treat lupus nephritis by reducing kidney inflammation.

Mycophenolate mofetil selectively inhibits the enzyme inosine monophosphate dehydrogenase (IMPDH). This blocks the synthesis of guanosine nucleotides, a critical building block for T‑ and B‑lymphocyte proliferation, thereby dampening the immune response.

The exact dose and dosing schedule are determined by the prescribing clinician based on the patient’s transplant type, renal function, and overall clinical condition. Dosage should never be altered without medical guidance.

Mycophenolate mofetil is classified as pregnancy category D, indicating evidence of fetal risk. It should be avoided in pregnant women and those planning pregnancy. Breastfeeding is not recommended because the drug is excreted in milk.

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 required import documentation.

Compared with calcineurin inhibitors such as cyclosporine or tacrolimus, mycophenolate mofetil offers a different mechanism—targeting lymphocyte proliferation rather than calcineurin signaling. It is often used in combination regimens to achieve synergistic immunosuppression while allowing lower doses of each agent.

Store the product at temperatures below 25 °C, in its original packaging, and protect it from moisture and direct sunlight. Do not refrigerate or freeze unless the label specifically indicates otherwise.

The medication is taken orally, usually as whole tablets or capsules, with or without food as directed by the prescriber. Swallow the dose whole; do not crush or split unless instructed.

Serious risks include opportunistic infections, bone‑marrow suppression leading to low blood counts, potential development of malignancies, severe liver injury, and rare neurological complications such as progressive multifocal leukoencephalopathy.

Patients with known hypersensitivity to mycophenolate mofetil or any component of the formulation, those who are pregnant, and individuals with severe uncontrolled infections should avoid this medication. Clinicians should also assess renal and hepatic function before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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