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
126793601 12679360 1 I 20160526 0 20160823 20160823 DIR 91.00 YR M N 61.20000 KG 20160721 N OT 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
126793601 12679360 1 PS ASPIRIN. ASPIRIN 1 Oral Y D 0 81 MG QD
126793601 12679360 2 SS CLOPIDOGREL CLOPIDOGREL BISULFATE 1 Oral Y D 0 75 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126793601 12679360 1 Cerebrovascular accident prophylaxis
126793601 12679360 2 Cerebrovascular accident prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126793601 12679360 RI
126793601 12679360 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126793601 12679360 Atrioventricular block
126793601 12679360 Blood urea increased
126793601 12679360 Faeces discoloured
126793601 12679360 Gastric haemorrhage
126793601 12679360 Gastrointestinal haemorrhage
126793601 12679360 Haemoglobin decreased
126793601 12679360 Orthostatic hypotension
126793601 12679360 Sinus arrest

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

Event ID CASEID RPSR COD
126793601 12679360 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126793601 12679360 1 20101215 20160526 0
126793601 12679360 2 20101215 20160526 0