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
70031595 7003159 5 F 20090111 20160907 20090527 20160908 EXP JP-BRISTOL-MYERS SQUIBB COMPANY-14636856 BRISTOL MYERS SQUIBB 0.00 DY M Y 3.35000 KG 20160908 MD JP JP

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
70031595 7003159 1 PS ABILIFY ARIPIPRAZOLE 1 Transplacental 6 MG, QD 21436 6 MG TABLET QD
70031595 7003159 2 SS ABILIFY ARIPIPRAZOLE 1 Transplacental 12 MG, QD 21436 12 MG TABLET QD
70031595 7003159 3 SS ABILIFY ARIPIPRAZOLE 1 Transmammary 12 MG, QD 21436 12 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
70031595 7003159 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
70031595 7003159 LT
70031595 7003159 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
70031595 7003159 Exposure during breast feeding
70031595 7003159 Foetal exposure during pregnancy
70031595 7003159 Neonatal asphyxia

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
70031595 7003159 1 20080315 0
70031595 7003159 2 20090110 0
70031595 7003159 3 20090111 0