Product image of Leflunomide Aspire Pharma (Malta) (Leflunomide) supplied by GNH India

Leflunomide Aspire Pharma (Malta)

Active Ingredient:
Leflunomide
Origin:
EU

Leflunomide Aspire Pharma (Malta) (Leflunomide)

Leflunomide, the active ingredient in Leflunomide Aspire Pharma, is a dihydroorotate dehydrogenase inhibitor presented as a strength/form for oral use. It treats rheumatoid arthritis and psoriatic arthritis in adult patients.

GNH India supplies Leflunomide Aspire Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Aspire Pharma (Malta) Limited

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Indications & Clinical Uses

  • Leflunomide is a disease‑modifying antirheumatic drug that acts on immune‑mediated joint diseases.
  • Rheumatoid arthritis: reduces disease activity, slows joint damage and improves functional capacity.
  • Psoriatic arthritis: alleviates joint inflammation and may improve associated skin lesions.

How It Works

  • Leflunomide inhibits the mitochondrial enzyme dihydroorotate dehydrogenase, which blocks de novo pyrimidine synthesis. This limits the proliferation of activated lymphocytes, thereby reducing the autoimmune response that drives inflammation in rheumatoid and psoriatic arthritis.

Side Effects

Leflunomide may cause a range of adverse reactions.

Common Side Effects

  • Diarrhea: mild to moderate gastrointestinal upset.
  • Nausea: occasional feeling of queasiness.
  • Alopecia: reversible hair thinning.
  • Rash: skin irritation or erythema.
  • Elevated liver enzymes: mild transaminase rise.
  • Hypertension: increase in blood pressure.

Serious or Rare Side Effects

  • Severe liver injury: hepatitis or hepatic failure.
  • Stevens‑Johnson syndrome/toxic epidermal necrolysis: severe skin reactions.
  • Bone marrow suppression: anemia, leukopenia, or thrombocytopenia.
  • Interstitial lung disease: pulmonary inflammation and fibrosis.

Precautions & Warnings

  • Before initiating therapy, clinicians should assess baseline health and monitor regularly.
  • Monitor liver function: obtain baseline and periodic ALT/AST tests.
  • Assess blood pressure: check regularly during treatment.
  • Screen for infections: evaluate for active infections before starting.
  • Avoid in pregnancy: contraindicated due to teratogenic risk.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture.

Avoid Interactions

Leflunomide can interact with several medicines; careful review is required.

Major Interactions (Avoid)

  • Warfarin: increased anticoagulant effect, risk of bleeding.
  • Teriflunomide: additive toxicity, especially hepatic.
  • Live vaccines: heightened risk of infection.
  • Methotrexate: enhanced hepatotoxicity.

Moderate Interactions (Monitor Closely)

  • Statins: increased risk of myopathy.
  • Carbamazepine: reduces leflunomide plasma levels.
  • Oral contraceptives: may diminish contraceptive efficacy.

Frequently Asked Questions

Leflunomide Aspire Pharma is prescribed for adult patients with rheumatoid arthritis and psoriatic arthritis. In both conditions it helps reduce inflammation, slow joint damage, and improve functional ability by modulating the immune response.

Leflunomide blocks the enzyme dihydroorotate dehydrogenase, which is essential for making pyrimidine nucleotides. This limits the replication of activated lymphocytes, decreasing the autoimmune activity that drives joint inflammation in rheumatoid and psoriatic arthritis.

The exact dose of leflunomide is determined by the prescribing physician based on the patient’s clinical condition, renal and hepatic function, and other individual factors. Dosage adjustments are made according to therapeutic response and safety monitoring.

Leflunomide is classified as pregnancy category X because it can cause fetal malformations and embryotoxicity. It is contraindicated in pregnancy and women of child‑bearing potential must use effective contraception. Breastfeeding is not recommended while on therapy.

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 is an oral synthetic DMARD that differs from biologic agents such as TNF‑α inhibitors. It offers the convenience of once‑daily dosing and does not require injection, but it carries a distinct safety profile, especially regarding liver toxicity and teratogenicity, which must be weighed against efficacy.

Leflunomide tablets should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original container, protect it from moisture and direct sunlight, and ensure the packaging remains tightly closed until use.

Leflunomide is taken orally, usually as a tablet swallowed whole with water. The medication may be taken with or without food, but patients should follow the specific instructions provided by their healthcare professional.

The most serious risks include severe liver injury, life‑threatening skin reactions such as Stevens‑Johnson syndrome, bone‑marrow suppression leading to anemia or neutropenia, and pulmonary toxicity. Prompt medical attention is required if any of these symptoms arise.

Leflunomide should not be used by pregnant women, women planning pregnancy, or those who are not using reliable contraception. It is also contraindicated in patients with severe liver disease, uncontrolled hypertension, or known hypersensitivity to the drug.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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