Description

Tofacitinib is an oral Janus kinase (JAK) inhibitor for the treatment of rheumatoid
arthritis and psoriatic arthritis. Tofacitinib inhibits JAK dependent cytokine
signaling. JAKs are intracellular enzymes which transmit signals arising from
cytokine or growth factor-receptor interactions on the cellular membrane. JAKs
phosphorylate and activate Signal Transducers and Activators of Transcription
(STATs) which modulate intracellular activity including gene expression. Tofacitinib
prevents the phosphorylation and activation of STATs thus downregulates the
production of cytokines by inhibiting JAK.

Presentation

    Each extended release film coated tablet contains Tofacitinib Citrate INN 17.77 mg equivalent to Tofacitinib 11 mg.

Indications

    Rheumatoid Arthritis: Arthanib/Arthanib XR Tablet is indicated for the
    treatment of adult patients with moderate to severe rheumatoid arthritis. It may be
    used as monotherapy or in combination with methotrexate or other nonbiologic
    disease-modifying antirheumatic drugs (DMARDs).
    Psoriatic Arthritis: Arthanib/Arthanib XR Tablet is indicated for the treatment of
    adult patients with active psoriatic arthritis. It may be used in combination with
    methotrexate or other nonbiologic disease-modifying antirheumatic drugs
    (DMARDs).
    Ulcerative Colitis: Arthanib/Arthanib XR Tablet is indicated for the treatment of
    adult patients with moderately to severely active ulcerative colitis

Dosage & Administration

    Rheumatoid Arthritis & Psoriatic Arthritis patients: The recommended dose is
    Arthanib 5 mg twice daily or Arthanib XR 11 mg once daily with or without food.
    Ulcerative colitis patients: The recommended dose is Arthanib10 mg twice daily
    for at least 8 weeks; then Arthanib 5 or 10 mg twice daily

Contrainidications

    Contraindicated in patients with known hypersensitivity to Tofacitinib or any other
    component of this product. It is contraindicated in severe hepatic impaired patients.

Warning & Precautions

    Avoid use of Tofacitinib during an active serious infection, including localized
    infections. Use with caution in patients that may be at increased risk of astrointestinal Perforations. Avoid use of Tofacitinib concurrently with
    Immunizations - Live vaccines. Storage: Store below 300 C at dry place, protect from light and moisture. Keep out of the reach of children.

Side effects

    The most commonly reported adverse reactions are upper respiratory tract infections, headache, diarrhea and nasopharyngitis.

Drug interaction

    Tofacitinib exposure is increased when coadministered with potent inhibitors of
    cytochrome P450 (CYP) 3A4 (e.g., ketoconazole) & medications that result in
    both moderate inhibition of CYP3A4 and potent inhibition of CYP2C19 (e.g.,
    fluconazole). Tofacitinib exposure is decreased when coadministered with potent
    CYP3A4 inducers (e.g., rifampin). There is a risk of added immunosuppression
    when Tofacitinib is coadministered with potent immunosuppressive drugs (e.g.,
    azathioprine, tacrolimus, cyclosporine). Use of Tofacitinib in combination with
    biologic DMARDs or potent immunosuppressants such as azathioprine and
    cyclosporine is not recommended.

Use in special groups

    Use in pregnancy: Pregnancy Category C. There are no adequate and wellcontrolled studies in pregnant women. Tofacitinib should be used during
    pregnancy only if the potential benefit justifies the potential risk to the fetus.
    Use in lactation: It is not known whether Tofacitinib is excreted in human milk. A
    decision should be made whether to discontinue nursing or to discontinue the
    drug, taking into account the importance of the drug for the mother.
    Pediatric use: The safety and effectiveness of Tofacitinib in pediatric patients
    have not been established.
    Hepatic impairment: No dose adjustment is required in patients with mild hepatic
    impairment. For moderate hepatic impairment patients recommended dose is
    Tofacitinib 5 mg once daily. Use of Tofacitinib in patients with severe hepatic
    impairment is not recommended.
    Renal impairment: No dose adjustment is required in patients with mild renal
    impairment. For patients with moderate and severe renal impairment
    recommended dose is Tofacitinib 5 mg once daily

Packing

    Each box contains 10's tablets in alu-alu blister pack.