Product image of Mycophenolate Mofetil Teva (Mycophenolate Mofetil) supplied by GNH India

Mycophenolate Mofetil Teva

Active Ingredient:
Mycophenolate Mofetil
Origin:
EU

Mycophenolate Mofetil Teva (Mycophenolate Mofetil)

Mycophenolate Mofetil, the active ingredient in Mycophenolate Mofetil Teva, is an antimetabolite immunosuppressant presented as an oral dosage form for oral use. It is used to prevent organ transplant rejection and to treat lupus nephritis in appropriate patients.

GNH India supplies Mycophenolate Mofetil Teva as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Mycophenolate Mofetil is an antimetabolite immunosuppressant that acts on the adaptive immune response to reduce lymphocyte proliferation.

  • Organ transplant rejection: helps prevent acute and chronic rejection after solid‑organ transplantation.
  • Lupus nephritis: reduces renal inflammation and proteinuria in patients with systemic lupus erythematosus affecting the kidneys.
  • Maintenance therapy after transplantation: supports long‑term graft survival by sustaining immunosuppression.

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 suppressing the immune response required for graft rejection and autoimmune kidney injury.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: loose stools often occurring early in therapy.
  • Vomiting: occasional episodes, especially with rapid dose escalation.
  • Abdominal pain: cramping or discomfort in the stomach area.
  • Headache: transient mild to moderate pain.
  • Tremor: fine shaking of hands or limbs.

Serious or Rare Side Effects

  • Leukopenia or neutropenia: significant reduction in white blood cells.
  • Anemia: decreased red blood cell count leading to fatigue.
  • Severe infections: opportunistic bacterial, viral, or fungal infections.
  • Hepatotoxicity: elevated liver enzymes or liver injury.
  • Malignancies: increased risk of post‑transplant lymphoproliferative disorder.
  • Severe allergic reactions: rash, angioedema, or anaphylaxis.

Precautions & Warnings

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

  • Blood counts: monitor complete blood count regularly to detect leukopenia or anemia.
  • Renal function: assess serum creatinine and glomerular filtration rate periodically.
  • Liver enzymes: check hepatic function tests during treatment.
  • Live vaccines: avoid administration while on therapy due to infection risk.
  • Contraception: use effective birth control methods; drug may be teratogenic.
  • Store at below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Azathioprine: additive bone‑marrow suppression may lead to severe cytopenias.
  • Antacids containing magnesium or aluminum: reduce oral absorption of mycophenolic acid.
  • Cyclosporine: increases mycophenolate exposure, raising toxicity risk.
  • Rifampin or other strong inducers: markedly decrease mycophenolate plasma levels.
  • Live vaccines: heightened risk of disseminated infection.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: may exacerbate renal impairment when combined.
  • NSAIDs: increase risk of renal dysfunction and gastrointestinal irritation.
  • Vaccines (non‑live): monitor immune response effectiveness.
  • Cholesterol‑lowering agents (e.g., statins): watch for additive hepatic effects.
  • Hormonal contraceptives: possible reduced efficacy, advise backup method.

Frequently Asked Questions

Mycophenolate Mofetil Teva is prescribed to prevent rejection of transplanted organs and to treat lupus nephritis, a kidney manifestation of systemic lupus erythematosus. It helps maintain graft function and reduces renal inflammation by suppressing the immune system.

After oral administration, Mycophenolate Mofetil is converted to mycophenolic acid, which selectively inhibits the enzyme inosine monophosphate dehydrogenase (IMPDH). This inhibition blocks guanosine nucleotide synthesis, a pathway essential for the proliferation of T‑ and B‑lymphocytes, thereby dampening immune responses.

The dosage of Mycophenolate Mofetil Teva is individualized by the prescribing physician based on the specific indication, patient weight, renal function, and concomitant immunosuppressive regimen. Patients should follow the exact dosing instructions provided by their healthcare professional.

Mycophenolate Mofetil is generally contraindicated in pregnancy because it may cause fetal harm. Women of child‑bearing potential should use effective contraception. Limited data are available for breastfeeding, and the drug is usually avoided; consult a physician for personalized advice.

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 any cold‑chain requirements), 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 regimens to achieve synergistic immunosuppression while potentially reducing the dose‑related toxicities of each individual agent.

Store Mycophenolate Mofetil Teva at temperatures below 25 °C in its original packaging. Protect the product from moisture, excessive heat, and direct sunlight to maintain its stability and potency.

Mycophenolate Mofetil Teva is taken orally, usually with food or a glass of water to lessen gastrointestinal irritation. The exact dosing schedule—once or twice daily—depends on the prescribing clinician’s plan and the patient’s clinical situation.

Serious risks include bone‑marrow suppression leading to leukopenia or anemia, severe infections (including opportunistic pathogens), liver toxicity, and an increased risk of certain malignancies such as post‑transplant lymphoproliferative disorder. Patients should be monitored regularly for these complications.

Mycophenolate Mofetil is contraindicated in patients with known hypersensitivity to the drug or its components, in those receiving live vaccines, and in pregnant women unless the potential benefit justifies the risk. Caution is also advised for individuals with severe renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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