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
6698195 7367250 F 6698195-2 20100306 20100419 20100427 EXP US-SANOFI-AVENTIS-2010SA020799 SANOFI-AVENTIS 70 YR F Y 86 KG 20100427 MD 20100407 UNITED STATES

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
6698195 1013574963 PS CLOPIDOGREL BISULFATE 1 ORAL 020839
6698195 1013574964 SS CLOPIDOGREL BISULFATE 1 ORAL 020839
6698195 1013574965 C ASPIRIN 1
6698195 1013574966 C PERINDOPRIL 2
6698195 1013574967 C AMLODIPINE 1
6698195 1013574968 C TRIMETAZIDINE 2
6698195 1013574969 C CANDESARTAN 2
6698195 1013574970 C CARVEDILOL 1
6698195 1013574971 C PANTOPRAZOLE 1
6698195 1013574972 C GLYCERYL TRINITRATE 2
6698195 1013574973 C INSULIN 2
6698195 1013574974 C ALDACTONE 1
6698195 1013574975 C ATORVASTATIN 2
6698195 1013574976 C RAMIPRIL 1
6698195 1013574977 C TRAZODONE HCL 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6698195 1013574963 ACUTE CORONARY SYNDROME

Outcome of event

Event ID OUTC COD
6698195 DE
6698195 HO

Reactions reported

Event ID PT
6698195 ANGINA UNSTABLE
6698195 MYOCARDIAL INFARCTION

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
6698195 1013574963 20090623 20100307
6698195 1013574964 20100319 20100324
6698195 1013574965 20070212
6698195 1013574966 20090622
6698195 1013574967 20090225
6698195 1013574968 20090623
6698195 1013574969 20090623
6698195 1013574970 20090623
6698195 1013574971 20090623
6698195 1013574972 20090623
6698195 1013574973 19890101
6698195 1013574974 20090630
6698195 1013574975 20090920
6698195 1013574976 20090920
6698195 1013574977 20091129