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
69554013 6955401 3 F 20160823 20090330 20160823 EXP DE-BRISTOL-MYERS SQUIBB COMPANY-14562219 BRISTOL MYERS SQUIBB 1.00 DY F Y 2.73000 KG 20160823 MD 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
69554013 6955401 1 PS ABILIFY ARIPIPRAZOLE 1 Transplacental 15 MG, BID U 21436 15 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
69554013 6955401 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
69554013 6955401 OT
69554013 6955401 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
69554013 6955401 Foetal exposure during pregnancy
69554013 6955401 Hyperbilirubinaemia
69554013 6955401 Pleural effusion
69554013 6955401 Pneumonia
69554013 6955401 Respiratory failure

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

no results found

Therapies reported

no results found