Asa Safety Questions, Asa Answers
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Asa Safety Reports
Total Asa reports: 3.Asa FDA safety alerts: 2001 2003 2004 2005 2006 2007 .
Reported deaths: 2 Reported hospitalizations: 46.
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Reported Asa Side Effects: respiratory distress, vessel puncture site haematoma, hypoventilation, platelet function test abnormal, gingival bleeding.
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Pharmacist from UNITED STATES reported ASA problem on Oct 02, 2006. Male patient, 61 years of age, was diagnosed with cerebrovascular disorder and was treated with ASA. After drug was administered, patient experienced the following problems/side effects: gingival bleeding, platelet function test abnormal. ASA dosage: 25/200 MG BID PO. During the same period patient was treated with DIPYRIDAMOLE. Patient was hospitalized. Patient recovered.
ASA problem was reported by a Health Professional from UNITED STATES on July 03, 2007. Male patient, weighting 381.0 lb, was diagnosed with acute coronary syndrome and was treated with ASA. After drug was administered, patient experienced the following problems/side effects: respiratory distress. ASA dosage: AT LEAST 300 MG D1; 300-325 MG FROM D2 TO D30. During the same period patient was treated with CLOPIDOGREL, CITALOPRAM HYDROBROMIDE, DEMADEX, NITROGLYCERIN, ALLOPURINOL, TOPROL, ALDACTONE. Patient was hospitalized. Patient recovered.
Health Professional from UNITED STATES reported ASA problem on July 11, 2007. Male patient, weighting 381.0 lb, was diagnosed with acute coronary syndrome and was treated with ASA. After drug was administered, patient experienced the following problems/side effects: hypoventilation, respiratory distress, vessel puncture site haematoma. ASA dosage: AT LEAST 300 MG D1; 300-325 MG FROM D2 TO D30. During the same period patient was treated with CLOPIDOGREL, CITALOPRAM HYDROBROMIDE, DEMADEX, NITROGLYCERIN, ALLOPURINOL, TOPROL, ALDACTONE. Patient was hospitalized. Patient recovered.