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
122416802 12241680 2 F 20160715 20160406 20160715 PER US-BRISTOL-MYERS SQUIBB COMPANY-21396676 BRISTOL MYERS SQUIBB 0.00 F Y 72.56000 KG 20160715 CN JP 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
122416802 12241680 1 PS ABILIFY ARIPIPRAZOLE 1 Oral UNK U 21436 TABLET
122416802 12241680 2 SS ABILIFY MAINTENA ARIPIPRAZOLE 1 Intramuscular 300MG U 0 400 MG QD
122416802 12241680 3 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122416802 12241680 1 Product used for unknown indication
122416802 12241680 2 Bipolar disorder
122416802 12241680 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122416802 12241680 Drooling
122416802 12241680 Dysphagia
122416802 12241680 Fatigue
122416802 12241680 Hypopnoea
122416802 12241680 Narcolepsy
122416802 12241680 Sedation
122416802 12241680 Somnolence
122416802 12241680 Weight increased

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
122416802 12241680 2 20140723 0