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
123166803 12316680 3 F 20160804 20160429 20160811 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-031863 BRISTOL MYERS SQUIBB 0.00 M Y 0.00000 20160811 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
123166803 12316680 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown 30 MG, UNK 21436 30 MG
123166803 12316680 2 SS ABILIFY ARIPIPRAZOLE 1 Unknown 20 MG, UNK 21436 20 MG
123166803 12316680 3 SS ABILIFY MAINTENA ARIPIPRAZOLE 1 Unknown 400 MG, UNK U 0 400 MG
123166803 12316680 4 SS ABILIFY MAINTENA ARIPIPRAZOLE 1 Unknown 400 MG, UNK U 0 400 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123166803 12316680 1 Product used for unknown indication
123166803 12316680 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123166803 12316680 HO
123166803 12316680 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123166803 12316680 Depressed mood
123166803 12316680 Flat affect
123166803 12316680 Hospitalisation
123166803 12316680 Off label use
123166803 12316680 Personality disorder

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
123166803 12316680 1 201603 0
123166803 12316680 3 20160404 0
123166803 12316680 4 20160713 0