Rutinib Cream contains Ruxolitinib, a Janus kinase (JAK) inhibitor that selectively blocks JAK1 and JAK2 enzymes, which are critical in the signaling of cytokines and growth factors involved in hematopoiesis and immune responses. By inhibiting JAK-STAT signaling, Ruxolitinib reduces inflammation, abnormal immune activity, and the progression of inflammatory skin conditions.
Rutinib is a topical formulation intended for the treatment of atopic dermatitis and nonsegmental vitiligo, providing targeted local effects while minimizing systemic exposure. The cream has been shown to improve skin lesions, reduce itching, and support repigmentation in affected areas.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Rutinib Cream is indicated for:
Atopic Dermatitis:
Reduction of inflammation, redness, and itching associated with mild to moderate disease
Management of affected skin areas up to 20% of body surface area
Nonsegmental Vitiligo:
Supports repigmentation of depigmented areas
Treatment of affected areas up to 10% of body surface area
Note: Safety and efficacy in pediatric patients under 12 years have not been established.
Pyrrolopyrimidines (JAK inhibitor)
Ruxolitinib inhibits JAK1 and JAK2, preventing activation of STAT transcription factors and modulating gene expression.
Plasma protein binding: ~97%
Terminal half-life: ~116 hours after topical application
Metabolized primarily via CYP3A4 and to a lesser extent CYP2C9
Excretion: ~74% urine, 22% feces; <1% unchanged drug
Atopic Dermatitis: Apply a thin layer twice daily to affected areas, up to 20% body surface area. Maximum: 60 g/week or 100 g/2 weeks. Discontinue when symptoms resolve; reassess if no improvement in 8 weeks.
Nonsegmental Vitiligo: Apply a thin layer twice daily to affected areas, up to 10% body surface area. Treatment may continue for over 24 weeks if clinically meaningful repigmentation occurs; reassess if ineffective by 24 weeks.
Topical use only – do not apply intraocularly, orally, or intravaginally.
Substrate of CYP3A4: Strong inhibitors (e.g., ketoconazole, clarithromycin) may increase systemic exposure and risk of adverse reactions
Strong inducers (e.g., rifampicin, carbamazepine) may decrease effectiveness
Known hypersensitivity to Ruxolitinib or any excipients in the cream
Atopic Dermatitis:
Nasopharyngitis, diarrhea, bronchitis, ear infection, increased eosinophils, urticaria, folliculitis, tonsillitis, rhinorrhea
Nonsegmental Vitiligo:
Application site acne or pruritus, nasopharyngitis, headache, urinary tract infection, application site erythema, pyrexia
Serious infections: Avoid use in active infections; interrupt therapy if infection occurs
Cardiovascular risk: Monitor in patients with risk factors; avoid in patients with history of myocardial infarction or stroke
Skin cancer: Periodic examination recommended; limit UV exposure
Hematologic effects: Thrombocytopenia, anemia, neutropenia; monitor CBC as clinically indicated
Thromboembolism: Discontinue if thrombosis occurs
Breastfeeding should be avoided during treatment and for ~4 weeks after last dose due to risk of serious adverse effects
Store below 30°C in a dry place, protected from sunlight
Keep out of reach of children.
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