The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
98099423 9809942 3 F 201111 20160810 20140110 20160819 EXP US-SANOFI-AVENTIS-2013SA068250 AVENTIS 61.39 YR A M Y 0.00000 20160819 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
98099423 9809942 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown U UNKNOWN 20839 75 MG TABLET QD
98099423 9809942 2 C ASPIRIN. ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98099423 9809942 1 Stent placement

Outcome of event

Event ID CASEID OUTC COD
98099423 9809942 OT
98099423 9809942 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
98099423 9809942 Gastric disorder
98099423 9809942 Gastrointestinal haemorrhage
98099423 9809942 Lung neoplasm malignant
98099423 9809942 Ulcer haemorrhage

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
98099423 9809942 1 2006 20111121 0