GNH USA

Europe — EMA

Micofenolato De Mofetil Accord

GNH USA supplies Micofenolato De Mofetil Accord (Mycophenolate Mofetil), a antimetabolite immunosuppressant for organ transplant rejection prevention

Mycophenolate Mofetil

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What is Mycophenolate Mofetil?

Mycophenolate Mofetil, the active ingredient in Micofenolato De Mofetil Accord, is an antimetabolite immunosuppressant presented as an oral formulation for systemic use. It is employed to prevent organ transplant rejection and to treat lupus nephritis by suppressing lymphocyte proliferation.

GNH USA supplies Micofenolato De Mofetil Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide.

What is Mycophenolate Mofetil used for?

Mycophenolate Mofetil is used in the management of immune‑mediated conditions where inhibition of lymphocyte proliferation is required.

- Kidney transplant: helps prevent acute and chronic graft rejection. - Heart transplant: reduces the risk of organ rejection post‑surgery. - Liver transplant: supports long‑term graft survival by suppressing immune response. - Lupus nephritis: diminishes renal inflammation and preserves kidney function.

What are the side effects of Mycophenolate Mofetil?

Adverse reactions may occur with Mycophenolate Mofetil therapy.

Common Side Effects: - Nausea: mild to moderate gastrointestinal upset. - Diarrhea: frequent loose stools, sometimes leading to dehydration. - Headache: transient cranial discomfort. - Abdominal pain: cramping or discomfort in the stomach area. - Tremor: fine shaking of the hands or limbs.

Serious or Rare Side Effects: - Leukopenia: significant reduction in white blood cells, increasing infection risk. - Hepatic dysfunction: elevated liver enzymes or hepatitis. - Opportunistic infections: severe infections such as cytomegalovirus or fungal disease. - Malignancy: increased risk of certain cancers with long‑term use. - Severe allergic reaction: rash, swelling, or anaphylaxis.

What precautions apply to Mycophenolate Mofetil?

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

- Monitor blood counts: regular CBC to detect leukopenia or anemia. - Assess liver function: periodic liver enzyme tests for hepatotoxicity. - Avoid in pregnancy: drug is Category D; use 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 at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

What does Mycophenolate Mofetil interact with?

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

Major Interactions (Avoid): - Azathioprine: additive bone‑marrow suppression. - Cyclosporine: increased mycophenolate exposure, raising toxicity risk. - Tacrolimus: synergistic immunosuppression, heightening infection risk. - Live vaccines: may cause severe infection; avoid administration.

Moderate Interactions (Monitor Closely): - Antacids (aluminum or magnesium): may reduce absorption of mycophenolic acid. - Rifampin: induces metabolism, decreasing drug levels. - Cholestyramine: binds drug in gut, lowering systemic exposure. - NSAIDs: can exacerbate renal toxicity when combined.

Frequently asked questions

What is Micofenolato De Mofetil Accord used for?+
Micofenolato De Mofetil Accord contains Mycophenolate Mofetil, an immunosuppressant prescribed to prevent rejection after kidney, heart or liver transplantation and to treat lupus nephritis by reducing abnormal immune activity.
How does Mycophenolate Mofetil work?+
Mycophenolate Mofetil is converted to mycophenolic acid, which selectively blocks the enzyme inosine monophosphate dehydrogenase (IMPDH). This inhibition limits guanosine nucleotide synthesis, a key step for T‑ and B‑cell proliferation, thereby dampening the immune response.
What is the usual dose of Micofenolato De Mofetil Accord?+
The exact dose and dosing schedule are determined by the prescribing clinician based on the patient’s condition, transplant type, renal function and other individual factors. Patients should follow the prescriber’s instructions precisely.
Is Micofenolato De Mofetil safe during pregnancy or breastfeeding?+
Mycophenolate Mofetil is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should be avoided in pregnancy unless no safer alternative exists, and effective contraception is required. Breastfeeding is not recommended while taking this medication.
How do I order Micofenolato De Mofetil from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA 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.
How does Micofenolato De Mofetil compare with other immunosuppressants?+
Compared with calcineurin inhibitors such as cyclosporine or tacrolimus, Mycophenolate Mofetil offers a different mechanism—IMPDH inhibition—resulting in a distinct side‑effect profile. It is often used in combination regimens to achieve synergistic immunosuppression while allowing lower doses of each agent.
What are the storage and handling requirements for Micofenolato De Mofetil?+
Store the product at below 25 °C in its original container, protecting it from moisture and direct sunlight. Do not expose the tablets or capsules to excessive heat or humidity, and keep them out of reach of children.
How is Micofenolato De Mofetil administered?+
The medication is taken orally, usually with food or a glass of water to reduce gastrointestinal irritation. The exact frequency (once or twice daily) and dose are set by the prescriber based on the therapeutic indication and patient factors.
What are the most serious risks associated with Micofenolato De Mofetil?+
Serious risks include severe infections due to immune suppression, leukopenia or anemia, liver toxicity, and an increased long‑term risk of certain malignancies. Patients should be monitored regularly for blood count changes, liver function abnormalities and signs of infection.
Who should not use Micofenolato De Mofetil?+
Patients with known hypersensitivity to Mycophenolate Mofetil or any component of the formulation should avoid it. It is contraindicated in pregnant women unless absolutely necessary, and caution is advised in individuals with severe renal or hepatic impairment.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Mycophenolate Mofetil
Route
Oral Use
Manufacturer
Accord Healthcare S.L.U.
Origin
EU

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