Product image of Injexate (Methotrexate) supplied by GNH India

Injexate

Active Ingredient:
Methotrexate
Origin:
EU

Injexate (Methotrexate)

Methotrexate, the active ingredient in Injexate, is a folate antagonist antimetabolite presented as a subcutaneous injection for systemic use. It is employed as an immunosuppressant and disease‑modifying antirheumatic drug to treat autoimmune disorders and certain malignancies.

GNH India supplies Injexate as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. Our distribution network ensures consistent quality and regulatory compliance across EU and global markets, providing reliable access for healthcare providers. We partner with accredited logistics firms to maintain product integrity during transport.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Methotrexate is used in several autoimmune and oncologic disease pathways.

  • Rheumatoid arthritis: reduces joint inflammation and slows structural damage.
  • Psoriasis: improves skin lesions and decreases disease severity.
  • Acute lymphoblastic leukemia: contributes to remission by inhibiting malignant cell proliferation.
  • Non‑Hodgkin lymphoma: used as part of combination regimens to achieve tumor control.

How It Works

  • Methotrexate inhibits dihydrofolate reductase, blocking the conversion of dihydrofolate to tetrahydrofolate, a cofactor required for purine and pyrimidine synthesis. This disruption reduces DNA, RNA and protein production, limiting the proliferation of rapidly dividing cells such as activated lymphocytes and cancer cells. The drug also promotes the release of adenosine, which exerts anti‑inflammatory effects on immune pathways. Consequently, methotrexate modulates immune response and impairs tumor growth.

Side Effects

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

Common Side Effects

  • Nausea or vomiting: gastrointestinal upset occurring early in therapy.
  • Fatigue: general tiredness or reduced energy.
  • Mouth sores: ulceration of oral mucosa.
  • Elevated liver enzymes: mild hepatic irritation.
  • Low blood cell counts: mild leukopenia or anemia.

Serious or Rare Side Effects

  • Severe liver toxicity: potential for hepatitis or fibrosis.
  • Pulmonary fibrosis: interstitial lung disease with breathing difficulty.
  • Bone marrow suppression: profound pancytopenia.
  • Renal impairment: acute kidney injury from drug accumulation.

Precautions & Warnings

Before initiating methotrexate therapy, several safety considerations should be reviewed.

  • Pregnancy: contraindicated (Category X); avoid use in pregnant or planning patients.
  • Renal function: assess creatinine clearance and adjust if impaired.
  • Liver function: perform baseline transaminases and monitor regularly.
  • Hematologic status: obtain complete blood count prior to start and during treatment.
  • Concomitant vaccines: avoid live vaccines while on therapy.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

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

Major Interactions (Avoid)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may increase methotrexate serum levels and risk renal toxicity.
  • Proton pump inhibitors (e.g., omeprazole): can reduce renal clearance and raise drug exposure.
  • Trimethoprim‑sulfamethoxazole: potentiates bone marrow suppression.

Moderate Interactions (Monitor Closely)

  • Azathioprine or mycophenolate: additive immunosuppression may increase infection risk.
  • Live vaccines: may cause severe infection due to immunosuppression.
  • Alcohol: can exacerbate hepatic toxicity.

Frequently Asked Questions

Injexate contains methotrexate, which is prescribed for rheumatoid arthritis, moderate to severe plaque psoriasis, and as part of combination chemotherapy regimens for certain cancers such as acute lymphoblastic leukemia and non‑Hodgkin lymphoma.

Methotrexate blocks the enzyme dihydrofolate reductase, preventing the formation of tetrahydrofolate needed for DNA, RNA and protein synthesis. This limits the growth of rapidly dividing cells, including immune cells that drive inflammation and malignant cells in cancer.

The dose of methotrexate is individualized by the prescribing clinician based on the specific indication, patient weight, renal function and treatment response. No fixed regimen is provided here; the prescriber determines the appropriate amount and frequency.

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

To request Injexate, 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 any required import documentation.

Injexate (methotrexate) is a conventional synthetic DMARD that works by inhibiting cell proliferation, whereas biologic DMARDs such as etanercept or adalimumab target specific cytokines. Methotrexate is often used first‑line because of its broad efficacy, lower cost and extensive clinical experience, while biologics are reserved for patients who do not respond adequately.

Injexate should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability and potency.

Injexate is given by subcutaneous injection, typically into the abdomen or thigh. The injection site should be rotated, and the solution must be administered using aseptic technique as instructed by a healthcare professional.

The most critical adverse effects include severe liver toxicity (hepatitis or fibrosis), bone marrow suppression leading to pancytopenia, and pulmonary fibrosis or interstitial lung disease. Patients should be monitored regularly for liver enzymes, blood counts and respiratory symptoms.

Methotrexate is contraindicated in pregnant individuals, those planning pregnancy, patients with severe renal or hepatic impairment, and anyone with known hypersensitivity to methotrexate or its excipients. Caution is also advised for patients with active infections or uncontrolled immune disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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