Ruxolitinib, a Janus kinase (JAK) inhibitor, inhibits JAK1 and JAK2, which mediate the signaling of a number of cytokines and growth factors that are important for hematopoiesis and immune function. JAK signaling involves recruitment of STATs (signal transducers and activators of transcription) to cytokine receptors, activation and subsequent localization of STATs to the nucleus, leading to modulation of gene expression. The relevance of inhibition of specific JAK enzymes to therapeutic effectiveness is not currently known.
100% Genuine Products, Guaranteed
Safe & Secure Payments, Always
Fast, Secure & Efficient Delivery
Proper Packaging
Ruxonib is a Janus kinase (JAK) inhibitor, which is indicated for atopic dermatitis and vitiligo.
- Absorption: Plasma concentrations of Ruxolitinib were quantifiable in all subjects. There is no evidence of Ruxolitinib accumulation after daily application of Ruxolitinib for 28 days in subjects with atopic dermatitis.
- Distribution: Plasma protein binding is approximately 97%.
- Elimination: The mean terminal half-life of Ruxolitinib following topical application of Ruxolitinib is approximately 116 hours.
- Metabolism: Ruxolitinib is primarily metabolized by CYP3A4 and to a lesser extent by CYP2C9 in vitro.
- Excretion: Ruxolitinib and its metabolites are primarily excreted by urine (74%) and feces (22%). Less than 1% is excreted as unchanged drug.
ওয়েবসাইট থেকে অর্ডার করার সহজ ভিডিও গাইড।
অ্যাপ থেকে অর্ডারের সহজ ভিডিও গাইড
অ্যাপ ডাউনলোডDownload ePharma App বিস্তারিত গাইড ›Detailed App Ordering GuideRuxonib is known to be a substrate for cytochrome P450 3A4 (CYP3A4). Inhibitors of CYP3A4 may increase Ruxonib systemic concentrations, whereas inducers of CYP3A4 may decrease Ruxonib systemic concentrations.
Strong Inhibitors of CYP3A4: Co-administration of Ruxonib should be avoided with strong inhibitors of CYP3A4, as there is a potential to increase the systemic exposure of Ruxonib and could increase the risk of Ruxonib adverse reactions.
Because of the serious adverse findings in adults, including risks of serious infections, thrombocytopenia, anemia, and neutropenia, women should not breastfeed during treatment with Ruxolitinib and for approximately four weeks after the last dose.
In atopic dermatitis, the most common side effects are nasopharyngitis, diarrhea, bronchitis, ear infection, increased eosinophil count, urticaria, folliculitis, tonsillitis, and rhinorrhea.
In nonsegmental vitiligo, the most common side effects are application site acne, application site pruritus, nasopharyngitis, headache, urinary tract infection, application site erythema, and pyrexia.
It is contraindicated in patients with known hypersensitivity to the drug or any of its components.
Store below 30°C in a dry place, away from sunlight & keep out of reach of children.
⚠️Disclaimer:
At ePharma, we’re committed to providing accurate and accessible health information. However, all content is intended for informational purposes only and should not replace medical advice from a qualified physician. Please consult your healthcare provider for personalized guidance. We aim to support, not substitute, the doctor-patient relationship.