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 a sterile intravenous solution for Intravenous use. It is employed to prevent acute rejection in organ transplantation and to treat selected autoimmune disorders such as lupus nephritis.

GNH India supplies Micofenolato De Mofetil Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution, including temperature‑controlled shipping where required.

Manufacturer / TM Owner

Accord Healthcare S.L.U.

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Indications & Clinical Uses

  • Mycophenolate Mofetil is used in transplant medicine and certain autoimmune diseases to suppress immune‑mediated damage.
  • Kidney transplantation: prevents acute graft rejection and supports graft survival.
  • Heart transplantation: reduces risk of early rejection episodes.
  • Liver transplantation: helps maintain long‑term graft function.
  • Lupus nephritis: diminishes renal inflammation and proteinuria.
  • ANCA‑associated vasculitis: controls systemic vasculitic activity.

How It Works

  • Mycophenolate Mofetil selectively inhibits inosine monophosphate dehydrogenase (IMPDH), the key enzyme for de novo synthesis of guanosine nucleotides. By depleting guanosine pools, it blocks proliferation of T‑ and B‑lymphocytes, which rely on this pathway for clonal expansion, while sparing most other cell types. The effect is reversible upon drug discontinuation, allowing restoration of normal lymphocyte function.

Side Effects

Mycophenolate Mofetil may cause a range of adverse reactions, classified as common or serious.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Diarrhea: loose stools that may affect hydration.
  • Vomiting: occasional episodes of emesis.
  • Headache: transient cranial discomfort.

Serious or Rare Side Effects

  • Severe infection: opportunistic bacterial, viral or fungal infections.
  • Leukopenia: significant reduction in white blood cells.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Monitor blood counts: perform regular complete blood count to detect leukopenia or anemia.
  • Assess liver function: check hepatic enzymes periodically for signs of dysfunction.
  • Adjust dose in renal impairment: reduce dosage in patients with reduced kidney function.
  • Contraindicated in pregnancy: avoid use in pregnant women; use effective contraception.
  • Avoid live vaccines: do not administer live attenuated vaccines while on therapy.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Mycophenolate Mofetil can interact with several medicines, requiring caution.

Major Interactions (Avoid)

  • Azathioprine: additive bone‑marrow suppression.
  • Cyclosporine: increased mycophenolate exposure, risk of toxicity.
  • Tacrolimus: increased exposure, may require dose adjustment.
  • Live vaccines: risk of severe infection.

Moderate Interactions (Monitor Closely)

  • Antacids (e.g., aluminum‑magnesium): may reduce absorption.
  • Cholestyramine: can bind drug and lower plasma levels.
  • Valganciclovir: additive myelosuppression risk.

Frequently Asked Questions

Micofenolato De Mofetil Accord contains mycophenolate mofetil, an immunosuppressive agent used to prevent acute rejection after organ transplantation (kidney, heart, liver) and to treat certain autoimmune conditions such as lupus nephritis and ANCA‑associated vasculitis.

Mycophenolate mofetil inhibits the enzyme inosine monophosphate dehydrogenase (IMPDH), which is essential for de novo guanosine nucleotide synthesis. This blocks the proliferation of T‑ and B‑lymphocytes, reducing the immune response that leads to graft rejection and autoimmune inflammation.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s condition, weight, renal function and other factors. Dosage instructions are provided on the prescription label and should be followed exactly as directed.

Mycophenolate mofetil is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should be avoided in pregnant women and those planning pregnancy. Breastfeeding is not recommended because the drug is excreted in milk and may affect the infant.

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 (including cold‑chain if needed) and necessary import documentation.

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

The product should be stored at ambient temperature, below 25 °C, in its original packaging. Protect it from moisture, direct sunlight and extreme temperatures. Do not freeze the solution. Follow any additional handling instructions provided on the label.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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