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Baricitinib is a prescription JAK inhibitor used to treat rheumatoid arthritis, atopic dermatitis, COVID-19, and alopecia areata in adults and certain pediatric patients.
Baricitinib is a prescription JAK inhibitor used to treat rheumatoid arthritis, atopic dermatitis, COVID-19, and alopecia areata in adults and certain pediatric patients.
Baricitinib is an orally administered medication belonging to the class of Janus kinase (JAK) inhibitors. It selectively blocks specific enzymes involved in inflammatory signaling pathways in the body. Marketed under the brand name Olumiant® by Eli Lilly and Company, it is available as film-coated tablets and is typically taken once daily.
Baricitinib is approved for several immune-mediated conditions:
Baricitinib acts as a selective inhibitor of JAK1 and JAK2 enzymes. These enzymes are key components of the JAK-STAT signaling pathway, which mediates the effects of many cytokines (immune system messenger molecules). By blocking this pathway, baricitinib reduces excessive inflammatory responses without completely suppressing the immune system.
Compared to other JAK inhibitors, baricitinib demonstrates particularly high selectivity for JAK1 and JAK2, which underpins its effectiveness across the approved indications.
The recommended dose depends on the condition being treated and individual patient factors:
Dose adjustments may be necessary in patients with renal impairment or other comorbidities. The treating physician will determine the appropriate dose for each patient.
Like all medications, baricitinib can cause side effects. Common side effects include:
Less common but serious side effects may include:
Patients should undergo regular medical monitoring during treatment.
Baricitinib must not be used in the following situations:
Prior to initiating therapy, infectious diseases (in particular tuberculosis and hepatitis) should be excluded. Concomitant use of other immunosuppressive agents requires special caution.
Baricitinib is a prescription-only medication and must only be taken under medical supervision. Patients should not alter or discontinue the dose on their own. If symptoms such as fever, signs of infection, or unusual complaints arise, medical advice should be sought promptly.
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