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
124614512 12461451 2 F 20160816 20160613 20160824 EXP KR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-046004 BRISTOL MYERS SQUIBB 62.00 YR Y 0.00000 20160824 CN KR KR

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
124614512 12461451 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown 5 MG, UNK U 21436 5 MG
124614512 12461451 2 SS ABILIFY ARIPIPRAZOLE 1 Unknown 5 MG U 21436 5 MG
124614512 12461451 3 SS ABILIFY ARIPIPRAZOLE 1 Unknown 5 MG, UNK U 21436 5 MG
124614512 12461451 4 C PROPRANOLOL PROPRANOLOLPROPRANOLOL HYDROCHLORIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124614512 12461451 1 Depression
124614512 12461451 2 Insomnia
124614512 12461451 4 Depression

Outcome of event

Event ID CASEID OUTC COD
124614512 12461451 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124614512 12461451 Abulia
124614512 12461451 Asthenia
124614512 12461451 Dizziness
124614512 12461451 Feeling abnormal
124614512 12461451 Insomnia
124614512 12461451 Palpitations
124614512 12461451 Stupor

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
124614512 12461451 1 20110526 20110601 0
124614512 12461451 2 20110602 20110622 0
124614512 12461451 3 20110623 20110713 0