Nebenwirkungen · Clopidogrel Taw Pharma (previously Clopidogrel Mylan)
Clopidogrel Taw Pharma 75 mg film-coated tablets · Abschnitt 4.8 · PDF-Seite 10
HOS-212103 · Präparat HOS-154824
In ACTIVE A, the rate of major bleeding was greater in the clopidogrel + ASA group than in the placebo + ASA group (6.7% versus 4.3%). Major bleeding was mostly of extracranial origin in both groups (5.3% in the clopidogrel + ASA group; 3.5% in the placebo +ASA group), mainly from the gastrointestinal tract (3.5% vs. 1.8%). There was an excess of intracranial bleeding in the clopidogrel + ASA treatment group compared to the placebo + ASA group (1.4% versus 0.8%, respectively). There was no statistically significant difference in the rates of fatal bleeding (1.1% in the clopidogrel + ASA group and 0.7% in the placebo +ASA group) and haemorrhagic stroke (0.8% and 0.6%, respectively) between groups.
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Version 2023-12-19T13:48:00Z · SHA-256 b3992d2973f4ae730e07521176d9e9c00fa2564f1a5afd425a7a1ce9b1db9a91 · Passage 6012dd48a7389e0316d3721ef96192e0b1bff7014667c7d35a7ec568d2728abf · Zeichen 1679–2384 im Abschnitt