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
114419542 11441954 2 F 20160823 20150901 20160823 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2014-007937 BRISTOL MYERS SQUIBB 0.00 M Y 3.00000 KG 20160823 OT 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
114419542 11441954 1 PS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Transplacental UNK MG, UNK U 21436 TABLET
114419542 11441954 2 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Transplacental U 0 SUSPENSION FOR INJECTION
114419542 11441954 3 C COGENTIN BENZTROPINE MESYLATE 1 Transplacental UNK U 0
114419542 11441954 4 C VITAMIN VITAMINS 1 Transplacental U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114419542 11441954 1 Product used for unknown indication
114419542 11441954 2 Product used for unknown indication
114419542 11441954 3 Product used for unknown indication
114419542 11441954 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
114419542 11441954 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
114419542 11441954 Foetal exposure during pregnancy
114419542 11441954 Jaundice neonatal

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
114419542 11441954 1 20140410 20140602 0
114419542 11441954 3 20140424 20140512 0