Product image of Leflunomid Stada (Leflunomide) supplied by GNH India

Leflunomid Stada

Active Ingredient:
Leflunomide
Origin:
EU

Leflunomid Stada (Leflunomide)

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

Manufacturer / TM Owner

Stadapharm Gmbh

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Indications & Clinical Uses

Leflunomid Stada is a disease‑modifying antirheumatic drug that targets inflammatory pathways in autoimmune joint disorders.

  • Rheumatoid arthritis: reduces joint inflammation, pain and structural damage.
  • Psoriatic arthritis: improves skin lesions and joint symptoms, slowing disease progression.

How It Works

  • Leflunomide inhibits the mitochondrial enzyme dihydroorotate dehydrogenase, which blocks de novo pyrimidine synthesis. This limits the proliferation of activated lymphocytes and reduces the production of inflammatory cytokines, thereby modulating the immune response in autoimmune conditions.

Side Effects

Leflunomid Stada may cause a range of adverse reactions that vary in frequency and severity.

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 readings.

Serious or Rare Side Effects

  • Severe liver injury: potential hepatic failure requiring monitoring.
  • Bone marrow suppression: pancytopenia or anemia.
  • Pulmonary toxicity: interstitial lung disease or pneumonitis.
  • Severe infections: opportunistic bacterial or viral infections.
  • Stevens‑Johnson syndrome: severe skin and mucosal reactions.
  • Teratogenicity: fetal malformations if exposure occurs during pregnancy.

Precautions & Warnings

Before initiating therapy with Leflunomid Stada, several safety considerations should be observed.

  • Pregnancy contraindication: avoid use in women who are pregnant or may become pregnant.
  • Liver monitoring: perform baseline and periodic liver function tests.
  • Hematologic monitoring: check complete blood count regularly.
  • Live vaccines: avoid administration while on therapy due to immunosuppression.
  • Severe hepatic impairment: contraindicated in patients with existing liver disease.
  • Store at room temperature: keep in the original packaging, protect from moisture and heat.

Avoid Interactions

Leflunomid Stada can interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Statins: possible increase in muscle toxicity.
  • Antihypertensives: may enhance blood pressure lowering.
  • Oral contraceptives: reduced hormonal efficacy, consider alternative contraception.

Frequently Asked Questions

Leflunomid Stada contains leflunomide, which is prescribed for adults with rheumatoid arthritis and psoriatic arthritis to reduce joint inflammation, pain, and disease progression.

Leflunomide blocks dihydroorotate dehydrogenase, an enzyme needed for pyrimidine synthesis. This limits the proliferation of activated lymphocytes, thereby dampening the immune response that drives inflammation in autoimmune arthritis.

The dosing regimen for Leflunomid Stada is determined by the prescribing physician based on the patient’s clinical condition, laboratory results, and treatment guidelines. Patients should follow the prescriber’s instructions exactly.

Leflunomid Stada is classified as pregnancy category X, meaning it is contraindicated in pregnancy due to a high risk of fetal malformations. It is also not recommended while breastfeeding because it can be excreted in milk.

To request Leflunomid Stada, submit an enquiry on the product page at gnhindia.com with 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 necessary import documentation.

Leflunomide is an oral DMARD that offers a convenient dosing schedule compared with injectable biologics. It has a distinct mechanism—pyrimidine synthesis inhibition—while other conventional DMARDs like methotrexate target folate pathways. Efficacy and safety profiles differ, so choice depends on patient factors and physician judgment.

Leflunomid Stada tablets should be stored at room temperature, below 25 °C, in the original blister pack. Keep the container tightly closed, protect from moisture and direct sunlight to maintain product stability.

Leflunomid Stada is taken orally, usually with a full glass of water. The tablet should be swallowed whole and not crushed or chewed. Patients should follow the dosing schedule prescribed by their healthcare provider.

Serious risks include severe liver injury, bone marrow suppression leading to pancytopenia, pulmonary toxicity, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Regular laboratory monitoring is essential to detect these complications early.

Leflunomid Stada should not be used by pregnant women, individuals with severe hepatic impairment, patients with known hypersensitivity to leflunomide, or those taking contraindicated medications such as certain live vaccines.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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