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
125729862 12572986 2 F 20160713 20160720 20160720 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-059143 BRISTOL MYERS SQUIBB 76.00 YR M Y 0.00000 20160720 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
125729862 12572986 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown UNK MG, UNK U 21436
125729862 12572986 2 C PROZAC FLUOXETINE HYDROCHLORIDE 1 Unknown 20 MG, UNK U 0 20 MG
125729862 12572986 3 C PROZAC FLUOXETINE HYDROCHLORIDE 1 Unknown 80 MG, UNK U 0 80 MG
125729862 12572986 4 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 Unknown 350 MG, UNK U 0 350 MG
125729862 12572986 5 C CELEXA CITALOPRAM HYDROBROMIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125729862 12572986 1 Depression
125729862 12572986 2 Depression
125729862 12572986 4 Depression
125729862 12572986 5 Depression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125729862 12572986 Product use issue

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

no results found

Therapies reported

no results found