The Safety Rates Drug Report

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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
125453561 12545356 1 I 20160630 20160711 20160711 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-055060 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160711 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
125453561 12545356 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown 5 MG, UNK Y 21436 5 MG TABLET
125453561 12545356 2 SS ABILIFY ARIPIPRAZOLE 1 Unknown 30 MG, UNK Y 21436 30 MG TABLET
125453561 12545356 3 SS ABILIFY ARIPIPRAZOLE 1 Y 21436 TABLET
125453561 12545356 4 SS WELLBUTRIN BUPROPION HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125453561 12545356 1 Major depression
125453561 12545356 2 Generalised anxiety disorder
125453561 12545356 3 Borderline personality disorder
125453561 12545356 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125453561 12545356 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125453561 12545356 Insomnia
125453561 12545356 Mental 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
125453561 12545356 1 1996 0
125453561 12545356 2 1998 0