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
100105432 10010543 2 F 20130923 20140324 20140314 20140331 EXP US-BRISTOL-MYERS SQUIBB COMPANY-20378584 BRISTOL MYERS SQUIBB 66.00 YR F Y 0.00000 20140331 N 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
100105432 10010543 1 PS ELIQUIS 1 ORAL D 2J69969A 202155 5 MG BID
100105432 10010543 2 C LIPITOR 1 D 0
100105432 10010543 3 C METOPROLOL 1 D 0
100105432 10010543 4 C MOBIC 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100105432 10010543 1 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
100105432 10010543 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100105432 10010543 Anosmia
100105432 10010543 Decreased appetite
100105432 10010543 Hypogeusia
100105432 10010543 Nausea
100105432 10010543 Rotator cuff syndrome
100105432 10010543 Weight decreased

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
100105432 10010543 1 20130312 0