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
85911894 8591189 4 F 20111212 20160824 20120601 20160825 EXP DE-BRISTOL-MYERS SQUIBB COMPANY-16612921 BRISTOL MYERS SQUIBB 0.00 N M Y 4.00000 KG 20160825 CN DE DE

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
85911894 8591189 1 PS ABILIFY ARIPIPRAZOLE 1 Transplacental 30 MG, QD U 21436 30 MG TABLET QD
85911894 8591189 2 SS AMISULPRIDE AMISULPRIDE 1 Transplacental 400 MG, BID U 0 400 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
85911894 8591189 1 Product used for unknown indication
85911894 8591189 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
85911894 8591189 OT
85911894 8591189 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
85911894 8591189 Cardiac hypertrophy
85911894 8591189 Cryptorchism
85911894 8591189 Cyanosis
85911894 8591189 Foetal exposure during pregnancy
85911894 8591189 Hypoglycaemia neonatal
85911894 8591189 Large for dates baby
85911894 8591189 Neonatal respiratory distress syndrome

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

no results found

Therapies reported

no results found