The Safety Rates Drug Report

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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
119651782 11965178 2 F 201412 20160808 20160127 20160811 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-004894 BRISTOL MYERS SQUIBB 58.06 YR F Y 0.00000 20160811 MD 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
119651782 11965178 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 15 MG, QD N 21436 15 MG QD
119651782 11965178 2 SS ABILIFY ARIPIPRAZOLE 1 N 21436
119651782 11965178 3 C LEXAPRO ESCITALOPRAM OXALATE 1 Unknown 20 MG, UNK U 0 20 MG
119651782 11965178 4 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 Unknown 300 OTHER, BID U 0 300 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119651782 11965178 1 Depression
119651782 11965178 2 Bipolar disorder
119651782 11965178 3 Product used for unknown indication
119651782 11965178 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119651782 11965178 Off label use
119651782 11965178 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
119651782 11965178 1 20140303 20151015 0
119651782 11965178 3 20140423 20151015 0
119651782 11965178 4 20140423 0