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 tablet for oral use. It helps prevent organ transplant rejection and treats certain autoimmune diseases such as lupus nephritis.

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 used in conditions that involve immune‑mediated tissue injury or autoimmunity.

  • Organ transplant rejection: reduces the risk of acute and chronic graft rejection by inhibiting lymphocyte proliferation.
  • Lupus nephritis: controls renal inflammation and helps preserve kidney function in systemic lupus erythematosus.
  • Other autoimmune disorders: provides immunosuppression for diseases where T‑ and B‑cell activity drives pathology.

How It Works

  • Mycophenolate Mofetil is converted intracellularly to mycophenolic acid, which selectively inhibits inosine monophosphate dehydrogenase (IMPDH). This blocks de novo guanosine nucleotide synthesis, a pathway essential for proliferation of activated T and B lymphocytes, thereby dampening the adaptive immune response.

Side Effects

Adverse reactions may range from mild to severe and should be monitored during therapy.

Common Side Effects

  • Nausea and vomiting: gastrointestinal discomfort that may improve with food.
  • Diarrhea: frequent loose stools, sometimes requiring fluid replacement.
  • Headache: mild to moderate intensity.
  • Tremor: fine shaking of the hands or limbs.
  • Hypertension: elevated blood pressure readings.

Serious or Rare Side Effects

  • Infections: increased susceptibility to bacterial, viral or fungal infections.
  • Bone marrow suppression: leukopenia, anemia or thrombocytopenia.
  • Malignancy: heightened risk of lymphoproliferative disorders.
  • Severe liver injury: elevated transaminases or hepatitis.
  • Progressive multifocal leukoencephalopathy (PML): rare demyelinating disease.

Precautions & Warnings

Before initiating therapy, clinicians should assess baseline health status and monitor patients regularly.

  • Monitor blood counts: perform complete blood count to detect leukopenia or anemia.
  • Assess renal function: check serum creatinine and eGFR, especially in transplant recipients.
  • Avoid use in pregnancy: potential teratogenic effects require contraception for women of child‑bearing potential.
  • Evaluate infection risk: screen for latent infections and vaccinate before treatment when possible.
  • Adjust dose in hepatic impairment: consider reduced exposure in patients with liver dysfunction.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Mycophenolate Mofetil can interact with several drug classes, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Live vaccines: may cause uncontrolled infection due to immunosuppression.
  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): markedly reduce mycophenolate exposure.
  • Antacids containing aluminum or magnesium: decrease absorption when taken simultaneously.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: combined use may increase risk of hyperkalemia and renal dysfunction.
  • Warfarin: may alter INR, requiring more frequent coagulation monitoring.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): can exacerbate nephrotoxicity, especially in patients with compromised kidney function.

Frequently Asked Questions

Mycophenolate Mofetil Teva is prescribed to prevent rejection of transplanted organs and to treat autoimmune kidney disease such as lupus nephritis. It works by suppressing the activity of T and B lymphocytes, which are key drivers of immune‑mediated tissue damage.

After oral administration, Mycophenolate Mofetil is converted to mycophenolic acid, which blocks the enzyme inosine monophosphate dehydrogenase. This inhibition stops the synthesis of guanosine nucleotides needed for the proliferation of activated T and B cells, thereby reducing the immune response.

The specific dose of Mycophenolate Mofetil Teva is determined by the prescribing physician based on the patient’s condition, weight, renal function and other clinical factors. Patients should follow the dosage instructions provided by their healthcare professional.

The safety of Mycophenolate Mofetil in pregnancy is not established and the drug may cause fetal harm. Women of child‑bearing potential should use effective contraception. Limited data are available for breastfeeding, so a risk‑benefit assessment with a clinician is essential.

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, Mycophenolate Mofetil offers a different mechanism by targeting nucleotide synthesis rather than calcineurin signaling. It is often used in combination regimens to provide synergistic immunosuppression while potentially reducing the dose‑related toxicities of other agents.

Mycophenolate Mofetil Teva tablets should be stored at room temperature, below 25 °C, in the original blister pack or bottle. Protect the product from moisture, excessive heat and direct sunlight to maintain potency.

The medication 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 assessment of the patient’s therapeutic needs.

Serious risks include severe infections due to immunosuppression, bone‑marrow suppression leading to low blood counts, and an increased long‑term risk of certain malignancies. Patients should be monitored regularly for signs of infection, anemia, leukopenia and liver dysfunction.

Mycophenolate Mofetil is contraindicated in patients with known hypersensitivity to the drug, in pregnant women, and in individuals with uncontrolled infections. Caution is also advised for patients with severe hepatic impairment or those receiving live vaccines.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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