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
75294304 7529430 4 F 20160823 20100805 20160829 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-15225881 BRISTOL MYERS SQUIBB 1.00 DY M Y 3.70000 KG 20160829 CN 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
75294304 7529430 1 PS ABILIFY ARIPIPRAZOLE 1 Transplacental 20MG U 21436 30 MG TABLET QD
75294304 7529430 2 SS LAROXYL AMITRIPTYLINE 1 Transplacental 50 MG, QD U 0 50 MG QD
75294304 7529430 3 SS LOXAPAC LOXAPINE SUCCINATE 1 Transplacental 20 MG, QD U 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
75294304 7529430 1 Product used for unknown indication
75294304 7529430 2 Product used for unknown indication
75294304 7529430 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
75294304 7529430 CA
75294304 7529430 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
75294304 7529430 Cryptorchism
75294304 7529430 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
75294304 7529430 1 2006 20091206 0
75294304 7529430 2 2006 20091206 0
75294304 7529430 3 20090304 20090611 0