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

Micofenolato De Mofetilo Stada

Active Ingredient:
Mycophenolate Mofetil
Origin:
EU

Micofenolato De Mofetilo Stada (Mycophenolate Mofetil)

Mycophenolate Mofetil, the active ingredient in Micofenolato De Mofetilo Stada, 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 patient populations.

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

Manufacturer / TM Owner

Laboratorio Stada, S.L.

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Indications & Clinical Uses

Mycophenolate Mofetil is used in immunosuppressive regimens targeting organ transplantation and autoimmune kidney disease.

  • Acute organ transplant rejection: helps prevent rejection episodes after solid‑organ transplantation.
  • Kidney transplant: reduces the risk of graft loss and improves long‑term graft survival.
  • Lupus nephritis: diminishes renal inflammation and slows disease progression in systemic lupus erythematosus patients.

How It Works

  • Mycophenolate Mofetil is converted intracellularly to mycophenolic acid, which selectively inhibits inosine monophosphate dehydrogenase (IMPDH). This blockade curtails guanosine nucleotide synthesis, a pathway essential for lymphocyte proliferation, thereby suppressing the immune response without markedly affecting other cell types.

Side Effects

Mycophenolate Mofetil may cause a range of adverse reactions, from mild to severe.

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.
  • Vomiting: occasional emesis, especially after dose initiation.
  • Infections: increased susceptibility to bacterial, viral, or fungal infections.

Serious or Rare Side Effects

  • Leukopenia: significant reduction in white blood cell count.
  • Anemia: decreased red blood cell levels causing fatigue.
  • Severe infections: opportunistic infections such as Pneumocystis jirovecii pneumonia.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Malignancy risk: potential increased risk of lymphoproliferative disorders.
  • Progressive multifocal leukoencephalopathy (PML): rare but life‑threatening brain infection.

Precautions & Warnings

Patients receiving Mycophenolate Mofetil should be monitored closely for safety and efficacy.

  • Blood counts: monitor complete blood count regularly to detect leukopenia or anemia.
  • Renal function: assess serum creatinine and glomerular filtration rate, especially in transplant recipients.
  • Pregnancy: avoid use during pregnancy; drug is classified as Category D.
  • Contraception: ensure effective contraception for both male and female patients of reproductive potential.
  • Drug interactions: review concomitant medications that may affect mycophenolate exposure.
  • Storage: Store at below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Mycophenolate Mofetil interacts with several agents that may alter its efficacy or safety.

Major Interactions (Avoid)

  • Azathioprine: additive bone‑marrow suppression.
  • Cyclosporine or tacrolimus: increased risk of nephrotoxicity and infections.
  • Cholestyramine or colestipol: reduces oral absorption of mycophenolic acid.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may potentiate renal impairment.
  • Warfarin: possible alteration of anticoagulant effect.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): increased risk of gastrointestinal irritation.
  • Live vaccines: heightened risk of vaccine‑derived infection.

Frequently Asked Questions

Micofenolato De Mofetilo Stada contains Mycophenolate Mofetil and is indicated for the prevention of acute organ transplant rejection and for the treatment of lupus nephritis, an autoimmune kidney disease.

Mycophenolate Mofetil is converted to mycophenolic acid, which selectively inhibits the enzyme inosine monophosphate dehydrogenase (IMPDH). This blocks guanosine nucleotide synthesis, a critical pathway for lymphocyte proliferation, thereby suppressing the immune response.

The specific dose of Micofenolato De Mofetilo Stada is determined by the prescribing clinician based on the patient’s condition, weight, renal function, and other individual factors. Patients should follow the dose prescribed by their healthcare provider.

Mycophenolate Mofetil is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should not be used during pregnancy, and effective contraception is required. Breastfeeding is also 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.

Mycophenolate Mofetil offers a selective mechanism targeting lymphocyte proliferation, which can result in a different side‑effect profile compared with calcineurin inhibitors such as cyclosporine or tacrolimus. Choice of therapy depends on the transplant protocol, patient tolerance, and physician preference.

Store the product at below 25 °C in its original packaging, protecting it from moisture and direct sunlight. Do not expose the tablets or capsules to excessive heat or humidity to maintain potency.

The medication is taken orally, usually with food or a glass of water to reduce gastrointestinal irritation. The exact dosing schedule and whether it is taken once or twice daily are determined by the prescribing clinician.

Serious risks include severe infections, leukopenia, anemia, hepatic dysfunction, and rare but life‑threatening conditions such as progressive multifocal leukoencephalopathy (PML). Patients should be monitored regularly for these adverse events.

Patients with known hypersensitivity to Mycophenolate Mofetil or any component of the formulation, those who are pregnant, or individuals with uncontrolled infections should avoid this medication. Clinicians must assess each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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