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
125832791 12583279 1 I 20160715 20160722 20160722 EXP US-GLAXOSMITHKLINE-US2016GSK102538 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
125832791 12583279 1 PS WELLBUTRIN BUPROPION HYDROCHLORIDE 1 UNK Y 18644
125832791 12583279 2 C ABILIFY ARIPIPRAZOLE 1 2 MG, QD 0 2 MG QD
125832791 12583279 3 C ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125832791 12583279 1 Bipolar disorder
125832791 12583279 2 Bipolar disorder
125832791 12583279 3 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125832791 12583279 Abdominal discomfort
125832791 12583279 Depression
125832791 12583279 Drug ineffective
125832791 12583279 Off label use

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
125832791 12583279 1 2015 0
125832791 12583279 2 201411 0