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
73734484 7373448 4 F 20160823 20100503 20160823 EXP AT-BRISTOL-MYERS SQUIBB COMPANY-14955686 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160823 CN AT AT

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
73734484 7373448 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 15 MG, QD 21436 15 MG TABLET QD
73734484 7373448 2 SS LITHIUM. LITHIUM 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
73734484 7373448 1 Schizoaffective disorder
73734484 7373448 2 Schizoaffective disorder

Outcome of event

Event ID CASEID OUTC COD
73734484 7373448 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
73734484 7373448 Caesarean section
73734484 7373448 Gestational diabetes
73734484 7373448 Live birth
73734484 7373448 Maternal exposure during pregnancy
73734484 7373448 Premature separation of placenta

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
73734484 7373448 1 200707 0
73734484 7373448 2 2007 0