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

Micofenolato De Mofetilo Tillomed

Active Ingredient:
Mycophenolate Mofetil
Origin:
EU

Micofenolato De Mofetilo Tillomed (Mycophenolate Mofetil)

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

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

Manufacturer / TM Owner

Laboratorios Tillomed Spain, S.L.U

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Indications & Clinical Uses

Mycophenolate Mofetil acts on the immune system to inhibit lymphocyte proliferation, making it useful in several immunologically mediated conditions.

  • Prevention of organ transplant rejection: lowers the risk of acute and chronic graft rejection after kidney, heart or liver transplantation.
  • Treatment of lupus nephritis: reduces renal inflammation and helps preserve kidney function in systemic lupus erythematosus.
  • Management of certain autoimmune diseases: suppresses immune activity in disorders such as vasculitis or dermatomyositis.

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 pathway essential for the proliferation of T and B lymphocytes, thereby dampening the adaptive immune response while sparing other cell types.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Diarrhea: increased bowel movements, sometimes watery.
  • Headache: transient cranial discomfort.
  • Abdominal pain: cramping or discomfort in the stomach area.
  • Infections: higher susceptibility to common viral or bacterial infections.

Serious or Rare Side Effects

  • Leukopenia: significant reduction in white blood cells.
  • Severe infections: opportunistic infections such as Pneumocystis jirovecii pneumonia.
  • Hepatotoxicity: elevated liver enzymes or liver injury.
  • Malignancy risk: increased incidence of certain cancers with long‑term use.
  • Progressive multifocal leukoencephalopathy (PML): rare demyelinating disease of the brain.

Precautions & Warnings

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

  • Monitor blood counts: regular CBC to detect leukopenia or anemia.
  • Monitor liver function: periodic LFTs to identify hepatotoxicity.
  • Avoid in pregnancy: drug is contraindicated; effective contraception required.
  • Use caution in renal impairment: dose adjustment may be needed.
  • Counsel on infection risk: advise prompt reporting of fever or signs of infection.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Other immunosuppressants (e.g., azathioprine, tacrolimus): increase risk of bone marrow suppression.
  • ACE inhibitors or ARBs: may worsen renal function when combined.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): elevate risk of kidney injury.
  • Vaccines (non‑live): monitor immune response effectiveness.

Frequently Asked Questions

Micofenolato De Mofetilo Tillomed contains mycophenolate mofetil, which is prescribed to prevent rejection after organ transplantation, to treat lupus nephritis, and to manage certain autoimmune diseases where suppression of the immune system is required.

Mycophenolate mofetil is converted to mycophenolic acid, which selectively blocks the enzyme inosine monophosphate dehydrogenase. This inhibition reduces the synthesis of guanosine nucleotines, a critical step for the proliferation of T and B lymphocytes, thereby dampening the immune response.

The specific dose and dosing schedule are determined by the prescribing physician based on the patient’s condition, weight, renal function and other clinical factors. Patients should follow the exact regimen provided by their healthcare professional.

Mycophenolate mofetil is contraindicated in pregnancy because it can cause fetal malformations and miscarriage. Women of child‑bearing potential must use effective contraception. It is also not recommended while breastfeeding, as it may be excreted in breast 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 necessary import documentation.

Compared with calcineurin inhibitors such as cyclosporine or tacrolimus, mycophenolate mofetil offers a different mechanism—targeting nucleotide synthesis rather than calcineurin signaling. It is often used in combination regimens to provide synergistic immunosuppression while potentially reducing nephrotoxicity associated with calcineurin inhibitors.

The product should be stored at room temperature, below 25 °C, in its original packaging. Keep it away from moisture, direct sunlight and sources of heat to maintain stability and potency.

Micofenolato De Mofetilo Tillomed is taken orally, usually with food or a glass of water to improve tolerability. The exact administration instructions, including timing relative to other medications, are provided by the prescribing clinician.

Serious risks include severe infections, leukopenia or other blood dyscrasias, liver injury, and an increased long‑term risk of certain malignancies. Patients should be monitored regularly for signs of infection, abnormal blood counts and liver function abnormalities.

The drug is contraindicated in pregnant women, individuals with known hypersensitivity to mycophenolate mofetil or its excipients, and patients with severe, uncontrolled infections. Caution is also advised for those with significant renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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