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
105304833 10530483 3 F 20111106 20160803 20141021 20160812 EXP US-SA-2014SA142399 AVENTIS 75.00 YR E F Y 0.00000 20160812 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
105304833 10530483 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Oral U UNK 20839 75 MG TABLET QD
105304833 10530483 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral U UNK 20839 75 MG TABLET QD
105304833 10530483 3 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral U UNK 20839 75 MG TABLET QD
105304833 10530483 4 C ASPIRIN. ASPIRIN 1 0 81 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105304833 10530483 1 Prophylaxis
105304833 10530483 2 Acute coronary syndrome
105304833 10530483 3 Myocardial infarction

Outcome of event

Event ID CASEID OUTC COD
105304833 10530483 HO
105304833 10530483 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105304833 10530483 Gastrointestinal haemorrhage
105304833 10530483 Multiple injuries

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
105304833 10530483 1 2005 201201 0
105304833 10530483 2 2005 201201 0
105304833 10530483 3 2005 201201 0