Product image of Leflunomida Tillomed (Leflunomide) supplied by GNH India

Leflunomida Tillomed

Active Ingredient:
Leflunomide
Origin:
EU

Leflunomida Tillomed (Leflunomide)

Leflunomide, the active ingredient in Leflunomida Tillomed, 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, helping to reduce inflammation and slow disease progression.

GNH India supplies Leflunomida Tillomed as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution. Customers benefit from consistent product availability and regulatory compliance across multiple markets.

Manufacturer / TM Owner

Laboratorios Tillomed Spain, S.L.U

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Indications & Clinical Uses

Leflunomide, a disease‑modifying antirheumatic drug (DMARD), acts on inflammatory pathways in autoimmune joint diseases.

  • Rheumatoid arthritis: reduces joint inflammation, pain, and swelling while slowing radiographic progression and improving physical function.
  • Psoriatic arthritis: improves both skin lesions and joint symptoms, helping to control disease activity and prevent joint damage.
  • Active adult disease: assists patients with moderate to severe disease in achieving clinical remission and maintaining functional ability.
  • Inadequate response to methotrexate: provides an alternative therapeutic option for adults whose disease remains active despite standard therapy.

How It Works

  • Leflunomide is converted in vivo to its active metabolite teriflunomide, which selectively inhibits the mitochondrial enzyme dihydroorotate dehydrogenase. This blockade reduces de novo pyrimidine synthesis, limiting the proliferation of activated lymphocytes. By decreasing the pool of nucleotides required for DNA replication, the drug dampens the immune response that drives joint inflammation in rheumatoid and psoriatic arthritis.

Side Effects

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

Common Side Effects

  • Diarrhea: loose stools or increased frequency.
  • Nausea: feeling of sickness or upset stomach.
  • Alopecia: thinning or loss of hair.
  • Elevated liver enzymes: mild increase in hepatic transaminases.

Serious or Rare Side Effects

  • Severe liver injury: hepatitis or hepatic failure requiring monitoring.
  • Bone marrow suppression: anemia, leukopenia, or thrombocytopenia.
  • Pulmonary toxicity: interstitial lung disease or pneumonitis.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

When prescribing Leflunomida Tillomed, clinicians should observe several safety precautions to minimize risk.

  • Liver function monitoring: assess transaminases before treatment and periodically during therapy.
  • Blood pressure assessment: monitor for hypertension, especially in patients with cardiovascular risk.
  • Pregnancy avoidance: drug is contraindicated in pregnancy; ensure effective contraception for women of childbearing potential.
  • Breastfeeding restriction: not recommended for nursing mothers due to potential infant exposure.
  • Infection vigilance: screen for active infections and avoid live vaccines during treatment.
  • Store at below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Warfarin: may increase INR and bleeding risk.
  • Methotrexate: combined use can heighten hepatic toxicity.
  • Live vaccines: immunosuppression raises risk of severe infection.

Moderate Interactions (Monitor Closely)

  • Statins: increased risk of myopathy and elevated creatine kinase.
  • Azathioprine: additive bone marrow suppression potential.
  • Sulfasalazine: may further elevate liver enzymes.

Frequently Asked Questions

Leflunomida Tillomed contains leflunomide, which is approved for the treatment of rheumatoid arthritis and psoriatic arthritis in adult patients. It helps to reduce joint inflammation, pain, and structural damage, and can also be used when disease activity remains high despite other conventional therapies.

Leflunomide is metabolised to teriflunomide, an inhibitor of dihydroorotate dehydrogenase. By blocking this enzyme, the drug suppresses de novo pyrimidine synthesis, limiting the proliferation of activated T‑lymphocytes. The resulting reduction in immune cell activity dampens the inflammatory processes that drive joint damage in arthritis.

The dosage of Leflunomida Tillomed is individualized by the prescribing clinician based on the patient’s disease severity, response to therapy, and laboratory monitoring. The prescriber decides the appropriate starting dose, any titration steps, and the maintenance dose, following local prescribing guidelines.

Leflunomida Tillomed is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy because of a high risk of fetal malformations and embryotoxicity. It is also not recommended for breastfeeding mothers, as the drug can be excreted in breast milk and may harm the infant.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity of Leflunomida Tillomed. 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.

Compared with methotrexate, another first‑line DMARD, leflunomide offers a once‑daily oral regimen and may be preferred when patients cannot tolerate methotrexate’s hepatic or gastrointestinal side effects. Both drugs suppress immune activity, but leflunomide’s mechanism targets pyrimidine synthesis, whereas methotrexate inhibits folate pathways.

Leflunomida Tillomed should be stored at temperatures below 25 °C. Keep the tablets in the original container, protect them from moisture and direct light, and ensure the packaging remains sealed until use to maintain product stability.

The medication is taken orally, usually with a full glass of water. It can be taken with or without food, but patients should follow the prescribing clinician’s instructions regarding timing and any required loading doses or titration schedules.

The most serious adverse events include severe liver injury, bone‑marrow suppression leading to anemia or low white‑blood‑cell counts, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should report signs of jaundice, unexplained bruising, persistent fever, or severe rash immediately to their healthcare provider.

Leflunomida Tillomed is contraindicated in pregnant women, individuals with severe liver disease, active infections, or known hypersensitivity to leflunomide or its metabolites. Caution is also advised for patients with pre‑existing immunodeficiency, uncontrolled hypertension, or those receiving live vaccines.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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