Product image of Metoject Pen (Methotrexate) supplied by GNH India

Metoject Pen

Active Ingredient:
Methotrexate
Origin:
EU

Metoject Pen (Methotrexate)

Methotrexate, the active ingredient in Metoject Pen, is an antimetabolite presented as a pre‑filled pen injector for subcutaneous use. It is employed to manage autoimmune conditions such as rheumatoid arthritis, psoriatic arthritis and severe psoriasis by modulating immune activity. It is approved in the European Union and is available only by prescription.

GNH India supplies Metoject Pen as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to Good Distribution Practice and provides regulatory support for cross‑border shipments. Clients receive dedicated technical assistance and product documentation to ensure safe handling. All shipments are tracked with temperature monitoring where required.

Manufacturer / TM Owner

Medac Gesellschaft Für Klinische Spezialpräparate Mbh (Wedel)

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Indications & Clinical Uses

Methotrexate, an antimetabolite immunosuppressant, is indicated for several chronic inflammatory and autoimmune conditions.

  • Rheumatoid arthritis: decreases joint inflammation, alleviates pain, and helps prevent joint damage.
  • Psoriatic arthritis: controls joint swelling and skin lesions, improving functional ability.
  • Severe psoriasis: suppresses rapid skin cell growth, leading to reduction of plaques and scaling.
  • Juvenile idiopathic arthritis: used in pediatric patients to control joint inflammation when other therapies are insufficient.

How It Works

  • Methotrexate inhibits the enzyme dihydrofolate reductase, preventing conversion of dihydrofolate to tetrahydrofolate, a cofactor required for synthesis of purine nucleotides and thymidylate. This blockade reduces DNA synthesis and cell proliferation, particularly affecting rapidly dividing immune cells. The resulting immunosuppression diminishes cytokine production and inflammatory responses in target tissues. Additionally, methotrexate interferes with the adhesion of leukocytes to endothelium and modulates adenosine release, further contributing to its anti‑inflammatory effect.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Fatigue: feeling of tiredness or low energy.
  • Mouth ulcers: painful sores in the oral cavity.
  • Elevated liver enzymes: mild, reversible increase in hepatic enzymes.

Serious or Rare Side Effects

  • Bone marrow suppression: decreased blood cell production leading to anemia, infection risk.
  • Severe liver toxicity: hepatitis or fibrosis with prolonged use.
  • Pulmonary toxicity: interstitial pneumonitis presenting with cough and shortness of breath.

Precautions & Warnings

When using Methotrexate, several precautions should be observed to minimize risks and ensure safe therapy.

  • Baseline testing: obtain complete blood count, liver and renal function before starting.
  • Monitoring: repeat laboratory tests regularly to detect toxicity early.
  • Pregnancy: avoid use in pregnancy; effective contraception required for women of childbearing potential.
  • Drug interactions: review concomitant medications for potential additive toxicity.
  • Infection risk: monitor for signs of infection and postpone dosing if active infection present.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Methotrexate can interact with several medicines, altering its efficacy or increasing toxicity.

Major Interactions (Avoid)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may increase risk of gastrointestinal ulceration and renal toxicity.
  • Proton pump inhibitors: can raise methotrexate plasma levels, especially at high doses.
  • Trimethoprim‑sulfamethoxazole: may potentiate bone marrow suppression.

Moderate Interactions (Monitor Closely)

  • Azathioprine or mycophenolate: combined immunosuppression may heighten infection risk.
  • Live vaccines: reduced efficacy and potential for infection; avoid during therapy.
  • Vitamin supplements containing folic acid: may diminish therapeutic effect; adjust under physician guidance.

Frequently Asked Questions

Metoject Pen contains methotrexate and is prescribed for chronic autoimmune disorders such as rheumatoid arthritis, psoriatic arthritis and severe psoriasis. By suppressing abnormal immune activity, it helps reduce joint inflammation, skin plaque formation and disease progression in these conditions.

Methotrexate blocks the enzyme dihydrofolate reductase, which is essential for folate metabolism and DNA synthesis. This inhibition limits the proliferation of rapidly dividing immune cells and reduces inflammatory cytokine production, providing an overall immunosuppressive and anti‑inflammatory effect.

The dose of Metoject Pen is individualized by the prescribing physician based on the patient’s disease severity, weight, renal function and response to therapy. Only a qualified health professional should determine the appropriate dosing schedule.

Methotrexate is generally contraindicated in pregnancy because it can cause fetal harm. Women of childbearing potential should use effective contraception. Breastfeeding is also discouraged unless the prescriber determines that the benefits outweigh potential risks to the infant.

To request Metoject Pen, 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 where required) and necessary import documentation.

Metoject Pen (methotrexate) is a conventional disease‑modifying antirheumatic drug (DMARD) that is less expensive than many biologic agents. While biologics target specific cytokines, methotrexate provides broad immunosuppression and is often used as first‑line therapy or in combination with biologics for enhanced efficacy.

Metoject Pen must be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. If a pen is inadvertently exposed to temperatures outside this range, it should be discarded and a new unit used.

Metoject Pen is a pre‑filled, single‑use pen designed for subcutaneous injection. The patient or caregiver removes the protective cap, selects the prescribed dose by pressing the dose selector, and injects the medication into the thigh, abdomen or upper arm following aseptic technique.

The most serious adverse effects include bone marrow suppression leading to anemia or infection, severe liver toxicity such as hepatitis or fibrosis, and pulmonary toxicity manifesting as interstitial pneumonitis. Prompt medical evaluation is required if symptoms such as unexplained bruising, jaundice or persistent cough develop.

Metoject Pen should be avoided in patients with known hypersensitivity to methotrexate, severe hepatic impairment, significant renal dysfunction, active infections, or in women who are pregnant or planning pregnancy without reliable contraception. A thorough medical assessment is essential before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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