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

Mofetilmikofenolat Tillomed

Active Ingredient:
Mycophenolate Mofetil
Origin:
EU

Mofetilmikofenolat Tillomed (Mycophenolate Mofetil)

Mycophenolate Mofetil, the active ingredient in Mofetilmikofenolat Tillomed, is an antimetabolite presented as an oral formulation for oral use. It is employed to prevent organ transplant rejection and to treat certain autoimmune kidney disorders in adult patients.

GNH India supplies Mofetilmikofenolat 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 the management of immune‑mediated conditions where suppression of lymphocyte activity is required.

  • Organ transplant rejection (kidney, heart, liver): helps prevent acute and chronic graft rejection.
  • Lupus nephritis: reduces renal inflammation and proteinuria in systemic lupus erythematosus.
  • Certain autoimmune diseases (e.g., vasculitis, dermatomyositis): controls disease activity by limiting immune cell proliferation.

How It Works

  • Mycophenolate Mofetil is a selective inhibitor of inosine monophosphate dehydrogenase (IMPDH). By blocking IMPDH, it reduces de novo synthesis of guanosine nucleotides, which are essential for DNA replication in activated T‑ and B‑lymphocytes, thereby suppressing their proliferation and dampening the immune response.

Side Effects

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

Common Side Effects

  • Nausea or vomiting
  • Diarrhea or abdominal pain
  • Headache
  • Tremor or dizziness
  • Hypertension
  • Upper respiratory tract infection

Serious or Rare Side Effects

  • Bone marrow suppression (leukopenia, anemia, thrombocytopenia)
  • Opportunistic infections (e.g., CMV, PCP)
  • Increased risk of malignancy (skin cancers, lymphomas)
  • Hepatic toxicity (elevated transaminases, hepatitis)
  • Severe allergic reactions (rash, Stevens‑Johnson syndrome)
  • Pregnancy‑related teratogenicity (category X).

Precautions & Warnings

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

  • Blood counts: monitor complete blood count regularly to detect marrow suppression.
  • Renal function: assess serum creatinine and glomerular filtration rate before and during therapy.
  • Pregnancy: contraindicated; ensure effective contraception for women of child‑bearing potential.
  • Drug interactions: avoid concomitant use with live vaccines and other potent immunosuppressants.
  • Dose adjustments: consider renal impairment when determining the prescribed dose.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Live attenuated vaccines: may cause severe infection.
  • Azathioprine or cyclophosphamide: additive bone‑marrow toxicity.
  • Cholestyramine or colestipol: reduces drug absorption.

Moderate Interactions (Monitor Closely)

  • Antacids containing aluminum or magnesium: may decrease bioavailability.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): increase plasma levels.
  • NSAIDs: may exacerbate renal impairment.
  • ACE inhibitors or ARBs: heightened risk of hyperkalemia when combined with renal dysfunction.

Frequently Asked Questions

Mofetilmikofenolat Tillomed contains Mycophenolate Mofetil, an immunosuppressant used to prevent rejection after kidney, heart or liver transplantation and to treat lupus nephritis and selected autoimmune disorders by limiting lymphocyte proliferation.

Mycophenolate Mofetil selectively inhibits the enzyme inosine monophosphate dehydrogenase, which is essential for the synthesis of guanosine nucleotides. This blocks DNA synthesis in activated T‑ and B‑cells, reducing their proliferation and dampening the immune response.

The prescribed dose of Mycophenolate Mofetil is individualized by the treating physician based on the specific indication, patient weight, renal function and concomitant therapies. Patients should follow the dosing instructions provided by their healthcare professional.

Mycophenolate Mofetil is classified as pregnancy category X because it can cause fetal malformations and embryonic loss. It is contraindicated in pregnancy, and women of child‑bearing potential must use effective contraception. Breastfeeding is 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.

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 agents.

Store the product at ambient temperature, preferably below 25 °C, in the original packaging. Protect it from moisture, excessive heat and direct sunlight to maintain stability and potency throughout its shelf life.

The medication is taken orally, usually as tablets or capsules, with or without food as directed by the prescriber. Swallow the dose whole with a glass of water and do not crush or chew unless specifically instructed.

Serious risks include bone‑marrow suppression leading to severe infections, opportunistic infections such as cytomegalovirus or Pneumocystis pneumonia, increased risk of certain cancers, and teratogenic effects if exposure occurs during pregnancy.

Patients with known hypersensitivity to Mycophenolate Mofetil or any component of the formulation, pregnant women, and individuals with severe renal impairment without dose adjustment should avoid this medication. Contraindications are also present for those receiving live vaccines.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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