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
127650881 12765088 1 I 20160914 20160921 20160921 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-076553 BRISTOL MYERS SQUIBB 0.00 Y 0.00000 20160921 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
127650881 12765088 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown 2 MG, UNK U 21436 2 MG TABLET
127650881 12765088 2 SS ABILIFY ARIPIPRAZOLE 1 U 21436 TABLET
127650881 12765088 3 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Unknown 2 MG, UNK U 0 2 MG
127650881 12765088 4 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127650881 12765088 1 Mania
127650881 12765088 2 Bipolar I disorder
127650881 12765088 3 Mania
127650881 12765088 4 Bipolar I disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127650881 12765088 Insomnia
127650881 12765088 Off label use
127650881 12765088 Restlessness
127650881 12765088 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

no results found