The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5374942 6321316 I 5374942-7 20050701 20070515 20070629 EXP CA-SANOFI-SYNTHELABO-A01200705288 SANOFI-SYNTHELABO 47 YR M Y 20070629 OT CANADA

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5374942 1008647750 SS INTEGRILIN 1 INTRAVENOUS UNK
5374942 1008647751 SS HEPARIN 1 UNKNOWN UNK
5374942 1008647752 SS ASPIRIN 1 ORAL UNK
5374942 1008647753 PS PLAVIX 1 ORAL 020839

Indications of drugs used

Event ID DRUG SEQ INDI PT
5374942 1008647750 PERCUTANEOUS CORONARY INTERVENTION
5374942 1008647751 DRUG USE FOR UNKNOWN INDICATION
5374942 1008647752 DRUG USE FOR UNKNOWN INDICATION
5374942 1008647753 PERCUTANEOUS CORONARY INTERVENTION

Outcome of event

Event ID OUTC COD
5374942 DS
5374942 HO
5374942 LT

Reactions reported

Event ID PT
5374942 CEREBRAL ISCHAEMIA
5374942 CEREBROVASCULAR ACCIDENT
5374942 INJECTION SITE HAEMORRHAGE
5374942 MOUTH HAEMORRHAGE
5374942 MYOCARDIAL INFARCTION
5374942 THROMBOCYTOPENIA
5374942 THROMBOSIS

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5374942 1008647750 20050714 20050714 1 DAY