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
108929974 10892997 4 F 20160824 20150306 20160824 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-013990 BRISTOL MYERS SQUIBB 1.00 DY Y 0.00000 20160824 CN FR FR

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
108929974 10892997 1 PS ABILIFY ARIPIPRAZOLE 1 Transplacental U 21436
108929974 10892997 2 SS RISPERIDONE. RISPERIDONE 1 Transplacental U 0
108929974 10892997 3 SS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Transplacental U 0
108929974 10892997 4 SS SERTRALINE SERTRALINE HYDROCHLORIDE 1 Transplacental U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108929974 10892997 1 Product used for unknown indication
108929974 10892997 2 Product used for unknown indication
108929974 10892997 3 Product used for unknown indication
108929974 10892997 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
108929974 10892997 OT
108929974 10892997 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
108929974 10892997 Atrial septal defect
108929974 10892997 Foetal exposure during pregnancy

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

no results found

Therapies reported

no results found