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Drugs or medicines may be withdrawn from c … Drugs or medicines may be withdrawn from commercial markets because of risks to patients, but also because of commercial reasons (e.g. lack of demand and relatively high production costs). Where risks or harms is the reason for withdrawal, this will usually have been prompted by unexpected adverse effects that were not detected during Phase III clinical trials, i.e. they were only made apparent from postmarketing surveillance data collected from the wider community over longer periods of time. This list is not limited to drugs that were ever approved by the FDA. Some of them (lumiracoxib, rimonabant, tolrestat, ximelagatran and ximelidine, for example) were approved to be marketed in Europe but had not yet been approved for marketing in the US, when side effects became clear and their developers pulled them from the market. Some drugs in this list (e.g. LSD) were never approved for marketing in the US or Europe.pproved for marketing in the US or Europe.
, بعض الأدوية يصادق على استخدامها وتسوق في ب … بعض الأدوية يصادق على استخدامها وتسوق في بعض البلدان أو في بلدان العالم كافة، ثم تظهر عليها أعراض جانبية ومخاطر في الاستخدام لم تظهر في التجارب السريرية لذلك تقوم المؤسسات الحكومية المختصة بسحبها من الأسواق. وكالة الأدوية الأوروبية هي المسؤولة عن إجراءات المصادقة أو عدمها وحتى سحب الدواء من الأسواق في الإتحاد الأوروبي، بينما في الولايات المتحدة فإدارة الغذاء والدواء هي المسؤولة عن ذلك. في بعض الأحيان تسوق بعض الأدوية في الاتحاد الأوروبي ثم تسحب وهي لم تصل مرحلة المصادقة عليها في الولايات المتحدة، والعكس صحيح أيضاً.ها في الولايات المتحدة، والعكس صحيح أيضاً.
, 因为对患者有一定风险，有些药品已经退出市场。通常这些副作用在第三期临床试验中并未发现，在市场销售后的临床监视期发现。 本列表不止包含美国食品药品监督管理局(FDA)没有批准的药物。其中一些被批准在欧洲市场销售，但尚未在美国批准上市，随着副作用的发现撤出市场的药品（例如：、）。同样LSD从未在美国批准上市。
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因为对患者有一定风险，有些药品已经退出市场。通常这些副作用在第三期临床试验中并未发现，在市场销售后的临床监视期发现。 本列表不止包含美国食品药品监督管理局(FDA)没有批准的药物。其中一些被批准在欧洲市场销售，但尚未在美国批准上市，随着副作用的发现撤出市场的药品（例如：、）。同样LSD从未在美国批准上市。
, بعض الأدوية يصادق على استخدامها وتسوق في ب … بعض الأدوية يصادق على استخدامها وتسوق في بعض البلدان أو في بلدان العالم كافة، ثم تظهر عليها أعراض جانبية ومخاطر في الاستخدام لم تظهر في التجارب السريرية لذلك تقوم المؤسسات الحكومية المختصة بسحبها من الأسواق. وكالة الأدوية الأوروبية هي المسؤولة عن إجراءات المصادقة أو عدمها وحتى سحب الدواء من الأسواق في الإتحاد الأوروبي، بينما في الولايات المتحدة فإدارة الغذاء والدواء هي المسؤولة عن ذلك. في بعض الأحيان تسوق بعض الأدوية في الاتحاد الأوروبي ثم تسحب وهي لم تصل مرحلة المصادقة عليها في الولايات المتحدة، والعكس صحيح أيضاً.ها في الولايات المتحدة، والعكس صحيح أيضاً.
, Drugs or medicines may be withdrawn from c … Drugs or medicines may be withdrawn from commercial markets because of risks to patients, but also because of commercial reasons (e.g. lack of demand and relatively high production costs). Where risks or harms is the reason for withdrawal, this will usually have been prompted by unexpected adverse effects that were not detected during Phase III clinical trials, i.e. they were only made apparent from postmarketing surveillance data collected from the wider community over longer periods of time.der community over longer periods of time.
|
| rdfs:label |
قائمة الأدوية المسحوبة
, List of withdrawn drugs
, 撤回药品列表
|
