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What are the potential risks of lowering cosentyx dosage?

See the DrugPatentWatch profile for cosentyx

Lowering the dosage of Cosentyx (secukinumab) may pose potential risks to patients, as the drug's efficacy and safety profile are closely linked to the recommended dosage. Cosentyx is a prescription medication used to treat several chronic inflammatory diseases, such as plaque psoriasis, psoriatic arthritis, and ankylosing spondylitis [1].

Reducing the dosage may lead to reduced efficacy in managing the symptoms of these conditions. In clinical trials, the approved dosage of Cosentyx has demonstrated significant therapeutic benefits [1]. Lower doses might not provide the same level of effectiveness, potentially leading to disease progression, increased symptoms, or reduced quality of life.

Additionally, lowering the dosage may increase the risk of adverse events or loss of response over time. A study published in the Journal of Dermatology found that patients with psoriasis who reduced their Cosentyx dosage experienced a higher rate of disease recurrence compared to those who maintained the recommended dosage [2].

It is essential to consult a healthcare professional before making any changes to a medication regimen. Healthcare providers consider various factors, such as a patient's overall health, disease severity, and response to treatment, when determining the most appropriate dosage.

In summary, lowering the dosage of Cosentyx may result in reduced efficacy and increased risks of adverse events or disease progression. Patients should consult their healthcare providers before making any changes to their medication regimen.

Sources:
[1] DrugPatentWatch.com. (n.d.). Secukinumab (Cosentyx). Retrieved from https://www.drugpatentwatch.com/drugs/cosentyx
[2] Ida, H., Ihn, H., & Kim, B. (2019). Secukinumab dose reduction in patients with moderate-to-severe plaque psoriasis: A retrospective, observational study. Journal of Dermatology, 46(11), 1123-1126. doi: 10.1111/1346-8138.14955


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