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沙特阿拉伯王国政府所属的官方政府网站。
icon 周三 1 7月 2026
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沙特官方政府网站的域名以下列后缀结尾 gov.sa

沙特阿拉伯王国所有政府机构的官方网站均以 .gov.sa 结尾。

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政府网站使用以下协议。 HTTPS 用于加密和安全。

沙特阿拉伯王国所有政府机构的官方网站均以 .gov.sa 结尾。

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在数字政府管理局注册,编号:
20250831619
建议

Saudi Food and Drug Authority (SFDA) PRESS RELEASE – Safety of Pioglitazone - (Actos®)

Saudi Food and Drug Authority (SFDA) PRESS RELEASE – Safety of Pioglitazone - (Actos®)

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<p align="justify"><br />Recently, the French Medicine Agency has suspended marketing authorization of anti-diabetic drug Pioglitazone (Actos®). French agency action has been announced after the result of recent retrospective cohort study has become available. This study was carried out in France and suggested an excess increase in bladder cancer among pioglitazone and pioglitazone-containing product users, Adjusted Hazard Ration (HR) was (1.22 [95% CI: 1.05-1.43]).<br />The Study data were retrieved from French health insurance. All included patients were on anti-diabetic medicaments and were followed-up for four consecutive years (2006-2009).<br />On the other hand, The European Medicines Agency (EMA) has initiated a safety review of the pioglitazone and pioglitazone-containing product since March 2011. In addition, the Committee for Medicinal Products for Human Use (CHMP) is intended to enclose the recent French study recommendations with respect to pioglitazone safety within their next meeting agenda. Furthermore, the United States Food and Drug Administration (US-FDA) is currently reviewing a ten-year epidemiological study concerning the association between the increased risk of bladder cancer and use of pioglitazone.<br />At this time, SFDA is currently reviewing all data on this safety concern and will release the results of this review when it finished. SFDA advises all healthcare professionals to continue to follow the recommendations in the drug label. In addition, SFDA advises patients not to stop taking pioglitazone (Actos®) and to talk to their doctors and/or pharmacists if they have any concern or contact the SFDA National Drug and Poison Information Center on the internet at <br />Report Adverse Drug Reactions (ADRs) to the Saudi FDA <br />The SFDA urges both healthcare professionals and patients to report ADRs resulted from using such a medication and other medication to the SFDA either online, by regular mail or by fax, using the following contact information:<br />National Pharmacovigilance and Drug Safety Center (NPC)<br />Saudi Food and Drug Authority-Drug sector<br />3292 Northern Ring Road <br />Al Nafal District <br />Riyadh 13312 – 6288<br />Kingdom of Saudi Arabia <br />Tel: 012759222 ext. 2334, 2317, 2353, 2354, 2356<br />Fax: 012057662<br />Email: <br />Website: <br /></p>

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