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

Micofenolato De Mofetil Aristo

Active Ingredient:
Mycophenolate Mofetil
Origin:
EU

Micofenolato De Mofetil Aristo (Mycophenolate Mofetil)

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

GNH India supplies Micofenolato De Mofetil Aristo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide. The company adheres to stringent quality standards and provides regulatory documentation for global distribution, including batch release certificates and stability data, to ensure compliance.

Manufacturer / TM Owner

Aristo Pharma Iberia, S.L.

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Indications & Clinical Uses

Mycophenolate Mofetil is an antimetabolite immunosuppressant used in specific transplant and autoimmune conditions.

  • Organ transplant rejection: helps prevent acute graft rejection and maintain graft survival.
  • Lupus nephritis: reduces proteinuria and preserves kidney function in patients with systemic lupus erythematosus.
  • Kidney transplant: supports long‑term graft acceptance and decreases incidence of chronic rejection.

How It Works

  • Mycophenolate Mofetil selectively and reversibly inhibits inosine monophosphate dehydrogenase (IMPDH), the key enzyme for de novo guanosine nucleotide synthesis. This inhibition lowers intracellular guanosine pools, suppressing proliferation of T‑ and B‑lymphocytes that rely on this pathway, thereby reducing immune responses.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhea: loose stools, sometimes watery.
  • Vomiting: occasional emesis.
  • Abdominal pain: cramping or discomfort.
  • Headache: mild to moderate.
  • Infections: increased susceptibility to viral or bacterial infections.

Serious or Rare Side Effects

  • Leukopenia: significant drop in white blood cells.
  • Anemia: reduced red blood cell count.
  • Severe infections: opportunistic or systemic infections.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Malignancy risk: potential increased risk of certain cancers.
  • Teratogenicity: fetal harm if exposure occurs during pregnancy.

Precautions & Warnings

Patients should be monitored closely for safety and efficacy.

  • Monitor blood counts: regular CBC to detect leukopenia or anemia.
  • Monitor liver function: periodic LFTs for hepatic safety.
  • Avoid in pregnancy: contraindicated due to teratogenic risk; ensure effective contraception.
  • Use caution in renal impairment: dose adjustment may be required.
  • Counsel on infection risk: advise prompt reporting of fever or signs of infection.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Mycophenolate Mofetil may interact with several medicines.

Major Interactions (Avoid)

  • Azathioprine: additive bone‑marrow suppression.
  • Cyclosporine: increased mycophenolate exposure, risk of toxicity.
  • Tacrolimus: similar risk of heightened exposure.
  • Ribavirin: enhanced hematologic toxicity.
  • Live vaccines: risk of uncontrolled infection.

Moderate Interactions (Monitor Closely)

  • Antacids: may reduce absorption; separate dosing.
  • Cholestyramine: can bind drug, lowering efficacy.
  • Warfarin: potential alteration of INR; monitor coagulation.
  • Phenytoin: may affect drug metabolism.
  • Fluconazole: possible increase in mycophenolate levels.

Frequently Asked Questions

Micofenolato De Mofetil Aristo contains mycophenolate mofetil, an immunosuppressant indicated to prevent organ transplant rejection and to treat lupus nephritis, a kidney complication of systemic lupus erythematosus.

Mycophenolate mofetil inhibits the enzyme inosine monophosphate dehydrogenase, blocking de novo guanosine synthesis. This limits the proliferation of T‑ and B‑lymphocytes, which depend on this pathway, thereby suppressing the immune response.

The prescribed dose is determined by the treating physician based on the specific indication, patient weight, renal function, and other clinical factors. Patients should follow the exact dosing instructions provided by their healthcare professional.

Mycophenolate mofetil is classified as pregnancy category X because it can cause fetal harm. It is contraindicated in pregnancy, and effective contraception is required. Breastfeeding is not recommended while using this medication.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Mycophenolate mofetil offers a distinct mechanism—IMP dehydrogenase inhibition—different from calcineurin inhibitors like cyclosporine or tacrolimus. It is often used in combination regimens and may have a more favorable side‑effect profile for certain patients, but choice depends on individual clinical circumstances.

Store the product below 25 °C in its original packaging, protecting it from moisture and direct sunlight. Do not freeze. Follow any additional handling instructions provided on the label.

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

Serious risks include severe infections, leukopenia, anemia, hepatic dysfunction, potential malignancy, and teratogenic effects. Patients should be monitored regularly for blood counts, liver enzymes, and signs of infection, and must avoid pregnancy.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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