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
125842161 12584216 1 I 20160722 20160722 20160722 EXP US-GLAXOSMITHKLINE-US2016GSK106600 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160722 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
125842161 12584216 1 PS WELLBUTRIN BUPROPION HYDROCHLORIDE 1 U 18644
125842161 12584216 2 SS ABILIFY ARIPIPRAZOLE 1 Oral 5 MG, QD Y 0 5 MG QD
125842161 12584216 3 SS ABILIFY ARIPIPRAZOLE 1 Oral 30 MG, QD Y 0 30 MG QD
125842161 12584216 4 SS ABILIFY ARIPIPRAZOLE 1 Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125842161 12584216 1 Product used for unknown indication
125842161 12584216 2 Major depression
125842161 12584216 3 Generalised anxiety disorder
125842161 12584216 4 Borderline personality disorder

Outcome of event

Event ID CASEID OUTC COD
125842161 12584216 HO
125842161 12584216 OT
125842161 12584216 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125842161 12584216 Condition aggravated
125842161 12584216 Disability
125842161 12584216 Hospitalisation
125842161 12584216 Insomnia
125842161 12584216 Mental disorder

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
125842161 12584216 2 1996 0
125842161 12584216 3 1998 0