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
126339991 12633999 1 I 20160803 20160809 20160809 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-065048 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160809 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
126339991 12633999 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 5 MG, QD 21436 5 MG TABLET QD
126339991 12633999 2 SS ABILIFY ARIPIPRAZOLE 1 21436 TABLET
126339991 12633999 3 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Unknown 5 MG, UNK 0 5 MG
126339991 12633999 4 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Unknown 10 UNK, UNK 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126339991 12633999 1 Bipolar disorder
126339991 12633999 2 Mania
126339991 12633999 3 Bipolar disorder
126339991 12633999 4 Mania

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126339991 12633999 Drug ineffective
126339991 12633999 Off label use
126339991 12633999 Wrong technique in product usage process

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
126339991 12633999 1 2014 201601 0
126339991 12633999 3 201601 0
126339991 12633999 4 201603 0