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
126925281 12692528 1 I 20160818 20160829 20160829 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-069473 BRISTOL MYERS SQUIBB 0.00 M Y 0.00000 20160829 CN US US

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
126925281 12692528 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown UNK Y 21436 TABLET
126925281 12692528 2 SS LUNESTA ESZOPICLONE 1 Unknown UNK Y 0
126925281 12692528 3 SS HALDOL HALOPERIDOL 1 Unknown UNK Y 0
126925281 12692528 4 SS REXULTI BREXPIPRAZOLE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126925281 12692528 1 Delusion
126925281 12692528 2 Product used for unknown indication
126925281 12692528 3 Product used for unknown indication
126925281 12692528 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126925281 12692528 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126925281 12692528 Electrocardiogram QT prolonged
126925281 12692528 Off label use

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
126925281 12692528 1 2014 0
126925281 12692528 4 201608 0