Product image of Methotrexate Accord Healthcare (Methotrexate) supplied by GNH India

Methotrexate Accord Healthcare

Active Ingredient:
Methotrexate
Origin:
EU

Methotrexate Accord Healthcare (Methotrexate)

Methotrexate, the active ingredient in Methotrexate Accord Healthcare, is an antimetabolite presented as an injectable solution for intra‑arterial, intramuscular, or intravenous use. It is employed to manage autoimmune disorders and certain cancers in adult and pediatric patients.
GNH India supplies Methotrexate Accord Healthcare as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Accord Healthcare Limited

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Indications & Clinical Uses

Methotrexate acts on rapidly dividing cells and immune pathways, making it useful across several disease families.

  • Rheumatoid arthritis: reduces joint inflammation and slows disease progression.
  • Psoriasis: limits skin cell proliferation, improving plaque severity.
  • Acute lymphoblastic leukemia: interferes with malignant lymphoblast replication.
  • Non‑Hodgkin lymphoma: hampers growth of lymphoma cells.
  • Gestational trophoblastic disease: induces remission by targeting trophoblastic tissue.

How It Works

  • Methotrexate inhibits dihydrofolate reductase, preventing conversion of dihydrofolate to tetrahydrofolate. This blockade reduces synthesis of purine nucleotides and thymidylate, leading to impaired DNA, RNA and protein production. The resulting inhibition of cell division affects rapidly proliferating immune cells and malignant cells, providing both immunosuppressive and antineoplastic effects.

Side Effects

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

Common Side Effects

  • Nausea and vomiting: gastrointestinal upset occurring shortly after administration.
  • Fatigue: persistent tiredness not relieved by rest.
  • Oral mucositis: painful mouth sores and ulceration.
  • Elevated liver enzymes: mild hepatic enzyme rise detectable on labs.
  • Cytopenias: reduced white blood cells or platelets.

Serious or Rare Side Effects

  • Severe hepatotoxicity: potential liver injury requiring monitoring.
  • Pulmonary fibrosis: interstitial lung disease with breathlessness.
  • Bone marrow aplasia: profound suppression of blood cell production.
  • Renal failure: impaired kidney function, especially with high doses.
  • Severe cutaneous reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Careful monitoring and patient education are essential when using Methotrexate.

  • Liver monitoring: perform baseline and periodic liver function tests.
  • Hematologic surveillance: check complete blood counts regularly.
  • Pregnancy avoidance: contraindicated in pregnancy; ensure effective contraception.
  • Renal function: assess creatinine clearance before dose adjustments.
  • Drug interactions: review concomitant medications for potential additive toxicity.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Methotrexate interacts with several medicines that can alter its safety or efficacy.

Major Interactions (Avoid)

  • NSAIDs (e.g., ibuprofen, naproxen): increase methotrexate toxicity by reducing renal clearance.
  • Trimethoprim‑sulfamethoxazole: heightens risk of bone‑marrow suppression.
  • Live vaccines: may cause uncontrolled infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • Penicillins (e.g., amoxicillin): may modestly raise methotrexate levels.
  • Azathioprine: additive immunosuppressive effect, requiring blood count monitoring.
  • Phenytoin: can reduce methotrexate efficacy, necessitating therapeutic assessment.

Frequently Asked Questions

Methotrexate Accord Healthcare is indicated for rheumatoid arthritis, psoriasis, acute lymphoblastic leukemia, non‑Hodgkin lymphoma, and gestational trophoblastic disease. In each case it works by inhibiting cell proliferation and modulating immune activity to control disease activity.

Methotrexate blocks the enzyme dihydrofolate reductase, which is essential for producing tetrahydrofolate. This disruption reduces the synthesis of nucleotides needed for DNA and RNA, thereby limiting the growth of rapidly dividing cells such as immune cells and cancer cells.

The specific dose and schedule are determined by the prescribing clinician based on the patient’s condition, weight, renal function and treatment goals. Healthcare providers tailor the regimen to achieve therapeutic benefit while minimizing toxicity.

Methotrexate is classified as pregnancy category X, meaning it is contraindicated in pregnancy due to a high risk of fetal malformations and miscarriage. It is also not recommended while breastfeeding because it can be excreted in milk and affect the infant.

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 (including cold‑chain if needed) and necessary import documentation.

Methotrexate shares a similar mechanism with drugs like pemetrexed and leflunomide, but differs in potency, dosing routes and specific approved indications. Compared with newer biologics for rheumatoid arthritis, methotrexate is less expensive and administered via injection or oral routes, though it may have a broader side‑effect profile.

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

The medication is supplied as an injectable solution and can be given intra‑arterially, intramuscularly, or intravenously by a qualified healthcare professional. The route and frequency are selected by the prescriber according to the therapeutic indication.

Serious risks include severe liver toxicity, pulmonary fibrosis, bone‑marrow suppression leading to pancytopenia, renal failure, and life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored regularly for early signs of these complications.

Methotrexate should not be used by individuals who are pregnant, planning pregnancy, or breastfeeding, as well as patients with severe hepatic or renal impairment, uncontrolled infections, or known hypersensitivity to methotrexate or its excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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