Uploaded on Dec 29, 2021
Apremilast specifically is an orally-active small molecule which blocks phosphodiesterase-4 (PDE4). On behalf of carried out clinical trials, apremilast in psoriatic arthritis (PsA) and psoriasis have demonstrated its efficacy and safety. Apremilast comes in the form of tablets, which should be swallowed whole; do not split/chew/crush them. A health specialist will probably start you on a low apremilast dose and gradually increase the dose once a day for the initial 5 days of treatment. The established therapeutic options have variable effectiveness across the different domains of psoriatic disease.
Apremilast: An Orally-Active Small Molecule
HOW APREMILAST TABLETS IS USEFUL IN PSORIATIC ARTHRITIS Otezla 30 mg (apremilast tablet) is used to treat patients with psoriatic arthritis and moderate to severe plaque psoriasis who are candidates for the treatment of the skin with an ultraviolet light source. Apremilast 30 mg blocks the production of an enzyme called phosphodiesterase 4 (PDE4) and leads to a reduction in inflammation. Apremilast is typically prescribed to patients with failure of one or more disease-modifying drugs (DMARDs) but are not suitable for biologic therapies. Apremilast is an oral first-in-class phosphodiesterase 4 inhibitor that was approved by the FDA for the treatment of adults with active psoriatic arthritis and adults with moderate to severe plaque psoriasis. The recommended daily dose is 30 mg twice daily and initial doses should be titrated over the course of about a week to reduce gastrointestinal adverse reactions. Apremilast was shown to be moderately effective in clinical trials at reducing symptoms of psoriatic arthritis including tender and swollen joints and physical functioning (ACR20) in patients who have failed previous treatments. Concomitant treatment with methotrexate or other conventional systemic disease-modifying antirheumatic drugs (DMARDs) was allowed. Results from 4 clinical trials showed NNTs ranging from 4-10 with 30 mg twice daily dosing. Apremilast tablet was shown to be moderately effective in clinical trials at improving symptoms and quality of life for patients with plaque psoriasis. Results from two clinical trials showed statistically significant improvements in 75% improvement in Psoriasis Area and Severity Index (PASI-75) with 20 mg twice daily and 30 mg twice daily dosing. Depression may develop or worsen during therapy; educate patients and use caution in patients with a history of depression or suicidality. The most common adverse reactions reported were diarrhea, headache, nausea, and upper respiratory tract infection. There is moderate quality evidence consistently showing apremilast to be a safe and effective medication in the treatment of adults with moderate to severe psoriatic arthritis or plaque psoriasis. For psoriatic arthritis, the clinical trials showed improvement in clinical symptoms such as tender or swollen joints, however, they did not evaluate improvements in or slowed progression of radiographic damage to affected joints. The major benefit of otezla 30 mg are convenient administration and lack of monitoring. Apremilast appears to be safe in short-term studies. These advantages need to be weighed against cost, lack of long-term safety data, and lack of radiographic evaluation. Direct comparisons with active therapies, long-term studies beyond 1 year and radiographic outcome measures are needed to determine its role in therapy. Cost of Apremilast: Availability of low-cost apremilast tablet or otezla 30mg sounds good. A respective patient can purchase this medication from only a registered and certified pharmaceutical company. Source: http://the-indian-pharma.over-blog.com/how-apremilast-tablets-is-useful-in- psoriatic-arthritis.html
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