Product image of Mycophenolat Mofetil Tillomed (Mycophenolate Mofetil) supplied by GNH India

Mycophenolat Mofetil Tillomed

Active Ingredient:
Mycophenolate Mofetil
Origin:
EU

Mycophenolat Mofetil Tillomed (Mycophenolate Mofetil)

Mycophenolate Mofetil, the active ingredient in Mycophenolat Mofetil Tillomed, is an immunosuppressant presented as an oral formulation for oral use. It is employed to prevent rejection of transplanted organs and to treat lupus nephritis in adult patients.
GNH India supplies Mycophenolat Mofetil Tillomed as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide.

Manufacturer / TM Owner

Tillomed Pharma Gmbh

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Indications & Clinical Uses

  • Mycophenolate Mofetil is used in conditions where immune suppression is required to protect transplanted tissue or control autoimmune kidney disease.
  • Kidney transplant: helps prevent acute and chronic graft rejection.
  • Heart transplant: reduces the risk of organ rejection after surgery.
  • Lupus nephritis: improves renal function and reduces proteinuria in patients with systemic lupus erythematosus.

How It Works

  • Mycophenolate Mofetil is a pro‑drug that is converted to mycophenolic acid, which selectively inhibits inosine monophosphate dehydrogenase (IMPDH). This enzyme is essential for de novo guanosine nucleotide synthesis in lymphocytes, leading to reduced proliferation of T and B cells and thereby dampening the immune response.

Side Effects

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

Common Side Effects

  • Gastrointestinal upset (nausea, diarrhea, abdominal pain).
  • Hematologic changes (leukopenia, anemia, thrombocytopenia).
  • Headache or dizziness.
  • Elevated liver enzymes.

Serious or Rare Side Effects

  • Opportunistic infections (e.g., cytomegalovirus, fungal infections).
  • Progressive multifocal leukoencephalopathy (PML).
  • Severe hypersensitivity reactions (rash, Stevens‑Johnson syndrome).
  • Pregnancy‑related teratogenicity and fetal loss.

Precautions & Warnings

  • Before initiating therapy, clinicians should assess baseline laboratory values and consider patient‑specific risk factors.
  • Monitor blood counts: perform regular CBC to detect leukopenia or anemia.
  • Assess renal function: adjust therapy if creatinine clearance declines.
  • Avoid use in pregnancy: drug is contraindicated (Category X).
  • Screen for infections: treat active infections before starting.
  • Consider hepatic impairment: dose may need adjustment.
  • Store at ambient temperature: keep below 25 °C, in original packaging, protected from moisture.

Avoid Interactions

Mycophenolate Mofetil interacts with several agents that can alter its exposure or increase infection risk.

Major Interactions (Avoid)

  • Antacids containing magnesium or aluminum: reduce absorption of mycophenolic acid.
  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): markedly lower drug levels.

Moderate Interactions (Monitor Closely)

  • Azathioprine or other myelosuppressants: increase risk of bone‑marrow suppression.
  • Live vaccines: may cause uncontrolled infection.
  • Concomitant nephrotoxic agents (e.g., calcineurin inhibitors): require renal function monitoring.

Frequently Asked Questions

Mycophenolat Mofetil Tillomed contains mycophenolate mofetil, an immunosuppressant indicated for preventing rejection after kidney, heart or liver transplantation and for treating lupus nephritis, a kidney manifestation of systemic lupus erythematosus.

The drug is converted to mycophenolic acid, which blocks inosine monophosphate dehydrogenase (IMPDH). This enzyme is crucial for making guanosine nucleotides in lymphocytes, so its inhibition reduces T‑ and B‑cell proliferation and dampens the immune response.

Dosing is individualized by the prescribing clinician based on the specific indication, patient weight, renal function and concomitant immunosuppressants. The prescriber determines the appropriate dose and schedule.

Mycophenolate mofetil is classified as Pregnancy Category X because it can cause fetal malformations and loss. It is contraindicated in pregnancy, and breastfeeding is not recommended due to potential drug exposure to the infant.

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 required import documentation.

Compared with calcineurin inhibitors such as cyclosporine, mycophenolate mofetil offers a different mechanism—IMPDH inhibition—resulting in less nephrotoxicity but a higher risk of gastrointestinal and hematologic side effects. It is often used in combination regimens to balance efficacy and safety.

Store the product at ambient temperature, below 25 °C, in its original packaging. Protect it from moisture and direct sunlight to maintain stability.

The medication is taken orally, usually as whole tablets or capsules, with or without food as directed by the prescriber. Swallow the dose whole; do not crush or split unless instructed.

Serious risks include severe infections (including opportunistic pathogens), progressive multifocal leukoencephalopathy, life‑threatening bone‑marrow suppression, and teratogenic effects if exposure occurs during pregnancy.

Patients who are pregnant, planning pregnancy, or breastfeeding should avoid the drug. It is also contraindicated in individuals with known hypersensitivity to mycophenolate mofetil or its excipients, and in those with uncontrolled infections.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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