Product image of Leflunomide Aurobindo (Leflunomide) supplied by GNH India

Leflunomide Aurobindo

Active Ingredient:
Leflunomide
Origin:
EU

Leflunomide Aurobindo (Leflunomide)

Leflunomide, the active ingredient in Leflunomide Aurobindo, is an immunomodulatory agent presented as a tablet for oral use. It is used to treat rheumatoid arthritis and psoriatic arthritis in adult patients.
GNH India supplies Leflunomide Aurobindo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Aurobindo Pharma B.V.

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Indications & Clinical Uses

  • Leflunomide is a disease‑modifying antirheumatic drug that acts on autoimmune joint disorders.
  • Rheumatoid arthritis: reduces joint inflammation, pain and slows structural damage.
  • Psoriatic arthritis: improves skin lesions and joint symptoms, helping maintain function.

How It Works

  • Leflunomide inhibits the mitochondrial enzyme dihydroorotate dehydrogenase, which blocks de novo pyrimidine synthesis. This limits the proliferation of activated T‑lymphocytes and other immune cells, thereby reducing the autoimmune response that drives joint inflammation and damage.

Side Effects

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

Common Side Effects

  • Diarrhoea: loose stools occurring during early therapy.
  • Nausea: feeling of sickness or upset stomach.
  • Alopecia: thinning or loss of hair.
  • Rash: skin redness or itching.
  • Elevated liver enzymes: mild increase in ALT/AST.
  • Hypertension: rise in blood pressure.

Serious or Rare Side Effects

  • Severe liver injury: jaundice, hepatic failure.
  • Stevens‑Johnson syndrome: severe skin blistering.
  • Bone marrow suppression: low blood cell counts.
  • Interstitial lung disease: breathing difficulty, cough.
  • Severe infections: opportunistic bacterial or viral infections.
  • Teratogenicity: birth defects if exposure occurs during pregnancy.

Precautions & Warnings

  • Before initiating Leflunomide, clinicians should evaluate several safety parameters.
  • Pregnancy contraindication: avoid use in women who are pregnant or may become pregnant.
  • Liver function monitoring: check ALT/AST before start and periodically thereafter.
  • Blood count monitoring: assess complete blood count regularly.
  • Hypertension surveillance: monitor blood pressure throughout treatment.
  • Infection risk: screen for active infections and avoid live vaccines.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Leflunomide can alter the activity of several co‑administered medicines.

Major Interactions (Avoid)

  • Warfarin: increased anticoagulant effect, risk of bleeding.
  • Teriflunomide: additive toxicity, especially hepatic.
  • Live vaccines: risk of uncontrolled infection.
  • Immunosuppressants (e.g., cyclosporine): heightened immunosuppression.
  • Cholesterol‑binding resins (e.g., cholestyramine): reduced Leflunomide absorption.

Moderate Interactions (Monitor Closely)

  • Statins: possible increase in muscle toxicity.
  • Antihypertensives: additive blood‑pressure lowering.
  • Oral contraceptives: reduced efficacy, consider alternative methods.
  • NSAIDs: may increase liver enzyme elevations.
  • Methotrexate: combined bone‑marrow suppression risk.

Frequently Asked Questions

Leflunomide Aurobindo is prescribed for adult patients with rheumatoid arthritis and psoriatic arthritis. In both conditions it helps reduce joint inflammation, pain, and slows the progression of structural damage, improving overall functional ability.

Leflunomide blocks the enzyme dihydroorotate dehydrogenase, which is essential for making new pyrimidine nucleotides. By limiting pyrimidine synthesis, the drug reduces the proliferation of activated lymphocytes, thereby dampening the immune response that drives joint inflammation.

The specific dose of Leflunomide Aurobindo is determined by the prescribing clinician based on the patient’s condition, disease severity, and individual health factors. Only a qualified healthcare professional should set the dosage regimen.

Leflunomide is classified as pregnancy category X, meaning it is contraindicated in pregnancy because of a high risk of fetal malformations. Women of child‑bearing potential must use effective contraception, and the drug should not be used while breastfeeding.

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 and any necessary import documentation.

Leflunomide differs from conventional synthetic DMARDs such as methotrexate by targeting pyrimidine synthesis rather than folate pathways. It offers an oral alternative with a distinct safety profile, but clinicians often consider patient‑specific factors, comorbidities and potential drug interactions when choosing between agents.

Leflunomide Aurobindo tablets should be stored below 25 °C in their original packaging, protected from moisture and direct sunlight. Maintaining a stable, room‑temperature environment helps preserve product potency throughout its shelf life.

Leflunomide Aurobindo is taken orally, usually as a tablet swallowed whole with water. The exact timing and whether it should be taken with food are determined by the prescribing physician based on individual tolerability and therapeutic goals.

The most serious risks include severe liver injury, life‑threatening skin reactions such as Stevens‑Johnson syndrome, bone‑marrow suppression leading to low blood counts, interstitial lung disease, and teratogenic effects if exposure occurs during pregnancy.

Leflunomide Aurobindo should be avoided in pregnant women, women planning pregnancy, patients with severe liver disease, uncontrolled hypertension, active infections, or those who have had hypersensitivity reactions to Leflunomide or related compounds.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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