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
124561223 12456122 3 F 20160409 20160629 20160610 20160706 EXP RU-SA-2016SA093788 AVENTIS 63.00 YR A M Y 90.00000 KG 20160706 CN RU RU

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
124561223 12456122 1 PS PLAVIX CLOPIDOGREL BISULFATE 1 Oral DOSE AND FREQUENCY :: 300 MG -SINGLE DOSE Y 5A463 20839 FILM-COATED TABLET
124561223 12456122 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral DOSE AND FREQUENCY :: 300 MG -SINGLE DOSE Y 5A463 20839 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124561223 12456122 1 Acute coronary syndrome
124561223 12456122 2 Acute myocardial infarction

Outcome of event

Event ID CASEID OUTC COD
124561223 12456122 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124561223 12456122 Chest pain
124561223 12456122 Coronary artery thrombosis
124561223 12456122 Off label use
124561223 12456122 Vascular stent thrombosis

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
124561223 12456122 1 20160409 20160409 0
124561223 12456122 2 20160409 20160409 0