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
119152253 11915225 3 F 20020204 20160823 20160114 20160829 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-10963080 BRISTOL MYERS SQUIBB 1.00 DY M Y 3.70000 KG 20160829 OT 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
119152253 11915225 1 PS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Transplacental 1 DF, QD 90 DF U 21436 1 DF TABLET QD
119152253 11915225 2 C LORAZEPAM. LORAZEPAM 1 Transplacental UNK U 0
119152253 11915225 3 C ADEPAL ETHINYL ESTRADIOLLEVONORGESTREL 1 Transplacental UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119152253 11915225 1 Product used for unknown indication
119152253 11915225 2 Product used for unknown indication
119152253 11915225 3 Contraception

Outcome of event

Event ID CASEID OUTC COD
119152253 11915225 CA
119152253 11915225 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119152253 11915225 Cytogenetic abnormality
119152253 11915225 Foetal exposure during pregnancy

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
119152253 11915225 1 20010411 20010709 0
119152253 11915225 2 20010403 20010605 0
119152253 11915225 3 199907 20010609 0