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
81810506 8181050 6 F 20110929 20160823 20111014 20160825 EXP JP-BRISTOL-MYERS SQUIBB COMPANY-16155558 BRISTOL MYERS SQUIBB 0.00 DY M Y 1.00000 KG 20160825 CN 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
81810506 8181050 1 PS ABILIFY ARIPIPRAZOLE 1 Transplacental 12 MG, QD U 21436 12 MG TABLET QD
81810506 8181050 2 C BIPERIDEN HCL BIPERIDEN HYDROCHLORIDE 1 Transplacental TABS U 0 1 MG
81810506 8181050 3 C LENDORMIN BROTIZOLAM 1 Transplacental TABS U 0 .25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
81810506 8181050 1 Product used for unknown indication
81810506 8181050 2 Product used for unknown indication
81810506 8181050 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
81810506 8181050 CA
81810506 8181050 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
81810506 8181050 Cardiac arrest
81810506 8181050 Congenital aortic valve stenosis
81810506 8181050 Congenital hand malformation
81810506 8181050 Congenital hydrocephalus
81810506 8181050 Foetal exposure during pregnancy
81810506 8181050 Premature baby
81810506 8181050 Pulmonary function test decreased
81810506 8181050 Pulmonary valve stenosis congenital
81810506 8181050 Trisomy 18
81810506 8181050 Ventricular septal defect

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
81810506 8181050 1 20110929 0
81810506 8181050 2 20110414 0
81810506 8181050 3 20110331 0