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How does patient response impact cosentyx adjustment?



Cosentyx is a biologic medication used to treat several autoimmune diseases, including psoriasis, psoriatic arthritis, and ankylosing spondylitis. The active ingredient in Cosentyx is secukinumab, which targets and blocks a specific protein that causes inflammation [1]. The medication is administered via injection, either subcutaneously or intravenously, depending on the condition being treated [3].

The response of patients to Cosentyx can impact the adjustment of the medication. According to a study published in the Journal of Clinical and Aesthetic Dermatology, patients with psoriasis who responded well to Cosentyx showed significant improvement in their symptoms, including skin clearance and quality of life. These patients typically received the recommended dosage of 300mg subcutaneously once a week for the first five weeks, followed by 300mg every four weeks [2].

However, some patients may not respond as well to Cosentyx or may experience side effects. In these cases, the dosage or frequency of administration may need to be adjusted. The European Medicines Agency (EMA) recommends that patients who do not respond to Cosentyx after 16 weeks of treatment should be re-evaluated, and the treatment plan should be adjusted accordingly. The EMA also advises that patients who experience severe side effects should discontinue treatment with Cosentyx [3].

In summary, patient response to Cosentyx can impact the adjustment of the medication. Patients who respond well to the medication typically receive the recommended dosage and frequency of administration. However, patients who do not respond or experience side effects may require adjustments to their treatment plan, including changes to dosage or frequency of administration. It is important for patients to communicate any concerns or issues with their healthcare provider to ensure that they receive the most effective treatment for their condition.

Sources:
[1] https://www.drugpatentwatch.com/p/biologics/tradename/COSENTYX
[2] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935619/
[3] https://www.ema.europa.eu/en/documents/product-information/cosentyx-epar-product-information_en.pdf



Follow-up:   Increase or decrease cosentyx dosage? Any side effects with cosentyx adjustment? How long until cosentyx adjustment takes effect?





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