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
117408293 11740829 3 F 20110807 20160728 20151114 20160803 EXP AU-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-077513 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160803 CN AU AU

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
117408293 11740829 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown U 21436
117408293 11740829 2 SS RISPERDAL RISPERIDONE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117408293 11740829 1 Product used for unknown indication
117408293 11740829 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117408293 11740829 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117408293 11740829 Amnesia
117408293 11740829 Delusion
117408293 11740829 Infertility
117408293 11740829 Mental impairment
117408293 11740829 Weight abnormal

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found