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
63664922 6366492 2 F 20070620 20160901 20070725 20160906 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-13853429 BRISTOL MYERS SQUIBB 0.00 DY F Y 2.10000 KG 20160906 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
63664922 6366492 1 PS ABILIFY ARIPIPRAZOLE 1 Transplacental 15 MG, QD U 21436 15 MG QD
63664922 6366492 2 SS SEROPLEX ESCITALOPRAM OXALATE 1 Transplacental 10 MG, QD U 0 10 MG QD
63664922 6366492 3 SS DEPAMIDE VALPROMIDE 1 Transplacental 1200 MG, QD U 0 1200 MG QD
63664922 6366492 4 SS SERESTA OXAZEPAM 1 Transplacental UNK U 0
63664922 6366492 5 SS LARGACTIL CHLORPROMAZINE 1 Transplacental 50 MG, QD U 0 50 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
63664922 6366492 1 Product used for unknown indication
63664922 6366492 2 Product used for unknown indication
63664922 6366492 3 Product used for unknown indication
63664922 6366492 4 Product used for unknown indication
63664922 6366492 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
63664922 6366492 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
63664922 6366492 Foetal exposure during pregnancy
63664922 6366492 Premature baby

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
63664922 6366492 1 20050624 200612 0
63664922 6366492 2 20051017 200612 0
63664922 6366492 3 2001 200612 0
63664922 6366492 4 20061221 20070620 0
63664922 6366492 5 20061221 20070620 0