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
125249971 12524997 1 I 20160628 20160704 20160704 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-054398 BRISTOL MYERS SQUIBB 10.00 YR F Y 0.00000 20160704 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
125249971 12524997 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown 21436
125249971 12524997 2 SS ABILIFY ARIPIPRAZOLE 1 21436
125249971 12524997 3 SS ABILIFY ARIPIPRAZOLE 1 21436
125249971 12524997 4 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125249971 12524997 1 Autism
125249971 12524997 2 Abnormal behaviour
125249971 12524997 3 Anger
125249971 12524997 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125249971 12524997 Abdominal discomfort
125249971 12524997 Nausea
125249971 12524997 Product use issue
125249971 12524997 Vomiting
125249971 12524997 Withdrawal syndrome

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found