سلامة دواء أداليموماب: تحليل قاعدة بيانات نظام الإبلاغ عن الآثار الجانبية

المؤلفون

  • Buthainah Ghanem Department of Pharmaceutical Economics and Policy, School of Pharmacy, Chapman University, Irvine, CA, USA.

DOI:

https://doi.org/10.35516/jjps.v16i3.629

الكلمات المفتاحية:

أداليموماب، الآثار الجانبية شديدة الخطورة، قاعدة ببانات، أمراض الروماتيزم، هوميرا

الملخص

Not Applicable

الهدف: تحديد مدى سلامة دواء أداليموماب و بدائله الحيوية لكل إستخدام معتمد من خلال تحليل الأثار الجانبية التي تم الإبلاغ عنها إلى قاعدة بيانات نظام الإبلاغ عن الآثار الجانبية التابعة لإدارة الغذاء و الدواء الأمريكية

الطريقة: قمنا بإجراء تحليل إحصائي رجعي لتقارير الآثار الجانبية الموثقة من عام 2002 الى عام 2022. كما قمنا بمقارنة تقارير الآثار الجانبية لدواء الأدابيموماب و بدائله الحيوية مع البدائل الأخرى المتاحة حاليا لكل إستخدام.

النتائج: بالمجمل، تم الإبلاغ عن 543.873 تقرير لدواء الأداليموماب. من بين هؤلاء كان هناك 49.8٪؜ من الحالات شديدة الخطورة. الحاجة للذهاب إلى المستشفى كان أكثر الأثار الجانبية شيوعا. الذكور، وكبار السن (<60)، وإستخدام أكثر من دواء في نفس الوقت كانوا أكثر العوامل إرتباطا بالآثار الجانبية شديدة الخطورة.

الخلاصة: تشير نتائج هذه الدراسة إلى أن دواء أداليموماب يعتبر أكثر أمانا مقارنة بالبدائل البيولوجية المتاحة حاليا.

السيرة الشخصية للمؤلف

Buthainah Ghanem، Department of Pharmaceutical Economics and Policy, School of Pharmacy, Chapman University, Irvine, CA, USA.

كلية الصيدلة، جامعة تشابمان، كاليفورنيا، الولايات المتحدة الامريكية.

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التنزيلات

منشور

2023-09-23

كيفية الاقتباس

Ghanem, B. (2023). سلامة دواء أداليموماب: تحليل قاعدة بيانات نظام الإبلاغ عن الآثار الجانبية. Jordan Journal of Pharmaceutical Sciences, 16(3), 517–528. https://doi.org/10.35516/jjps.v16i3.629

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