Product image of Methotrexate Medac (Methotrexate) supplied by GNH India

Methotrexate Medac

Active Ingredient:
Methotrexate
Origin:
EU

Methotrexate Medac (Methotrexate)

Methotrexate, the active ingredient in Methotrexate Medac, is an antimetabolite (folate antagonist) presented as a sterile injectable for intraarterial, intramuscular and intravenous use. It is employed to treat various malignant and autoimmune conditions in adult and pediatric patients.

GNH India supplies Methotrexate Medac as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Medac Gesellschaft Für Klinische Spezialpräparate Mbh (Wedel)

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Indications & Clinical Uses

Methotrexate Medac acts as a folate antagonist and is indicated for several oncologic and autoimmune disease pathways.

  • Rheumatoid arthritis: reduces joint inflammation and slows disease progression.
  • Psoriasis: improves skin lesions and decreases scaling.
  • Acute lymphoblastic leukemia: induces remission by inhibiting malignant cell proliferation.
  • Non‑Hodgkin lymphoma: contributes to tumor control as part of combination therapy.
  • Breast cancer: used in multi‑drug regimens to limit tumor growth.

How It Works

  • Methotrexate inhibits dihydrofolate reductase, preventing the regeneration of tetrahydrofolate. This blocks the synthesis of purine nucleotides and thymidylate, impairing DNA, RNA and protein production. The resulting cytotoxic effect preferentially targets rapidly dividing cells and also suppresses immune cell proliferation, providing both antineoplastic and immunosuppressive actions.

Side Effects

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

Common Side Effects

  • Nausea and vomiting.
  • Fatigue and malaise.
  • Mucositis (mouth sores).
  • Alopecia (hair loss).
  • Elevated liver enzymes.
  • Mild skin rash.

Serious or Rare Side Effects

  • Bone marrow suppression leading to pancytopenia.
  • Severe infections due to immunosuppression.
  • Pulmonary toxicity (interstitial pneumonitis).
  • Hepatotoxicity with fibrosis or cirrhosis.
  • Renal toxicity, especially with high doses.
  • Life‑threatening cutaneous reactions such as Stevens‑Johnson syndrome.

Precautions & Warnings

Before initiating therapy, clinicians should assess baseline status and monitor patients regularly.

  • Monitor blood counts: perform complete blood count before each dose.
  • Assess liver function: check transaminases and bilirubin regularly.
  • Evaluate renal function: monitor serum creatinine and adjust dose if needed.
  • Avoid use in active infections: treat infections prior to dosing.
  • Use effective contraception: methotrexate is teratogenic.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Methotrexate interacts with several medicines that may increase toxicity or reduce efficacy.

Major Interactions (Avoid)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): increase methotrexate serum levels.
  • Penicillins (e.g., ampicillin): may reduce renal clearance.
  • Sulfonamide antibiotics: additive bone‑marrow suppression.
  • Live vaccines: risk of severe infection.

Moderate Interactions (Monitor Closely)

  • Azathioprine: enhanced immunosuppression.
  • Cyclosporine: increased risk of nephrotoxicity.
  • Proton‑pump inhibitors: may affect renal elimination.
  • Warfarin: potential for altered anticoagulant effect.

Frequently Asked Questions

Methotrexate Medac is indicated for rheumatoid arthritis, psoriasis, acute lymphoblastic leukemia, non‑Hodgkin lymphoma and breast cancer. It is used to control autoimmune inflammation and as part of chemotherapy regimens for certain malignancies.

Methotrexate blocks the enzyme dihydrofolate reductase, stopping the formation of tetrahydrofolate needed for DNA, RNA and protein synthesis. This interferes with the growth of rapidly dividing cells and suppresses immune cell activity.

The dose is individualized by the prescribing clinician based on the specific indication, patient weight, renal and hepatic function, and treatment protocol. No standard dose can be provided without a medical prescription.

Methotrexate is classified as teratogenic and is contraindicated in pregnancy. Women of child‑bearing potential must use effective contraception. It is also not recommended while breastfeeding because it can be excreted in milk.

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 import documentation.

Methotrexate is a folate antagonist, whereas many other chemotherapeutics target microtubules, DNA cross‑linking or kinase pathways. Its oral and injectable forms allow flexible dosing, but it requires careful monitoring for bone‑marrow and organ toxicity, unlike some agents with different safety profiles.

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

Methotrexate Medac is supplied as a sterile injectable solution and may be given intra‑arterially, intramuscularly or intravenously by a qualified healthcare professional according to the prescribed regimen.

Serious risks include bone‑marrow suppression leading to pancytopenia, severe infections, pulmonary toxicity, hepatotoxicity with possible fibrosis, renal impairment and life‑threatening skin reactions such as Stevens‑Johnson syndrome.

Patients with active infections, severe liver or kidney disease, known hypersensitivity to methotrexate, pregnant or breastfeeding women, and those taking contraindicated medications (e.g., certain NSAIDs or live vaccines) should not receive Methotrexate Medac.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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