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
126246121 12624612 1 I 20160730 20160805 20160805 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-064176 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160805 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
126246121 12624612 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown 5 MG, QD N 21436 5 MG QD
126246121 12624612 2 SS ABILIFY ARIPIPRAZOLE 1 Unknown 2.5 MG, QD N 21436 2.5 MG QD
126246121 12624612 3 C LAMICTAL LAMOTRIGINE 1 Unknown U 0
126246121 12624612 4 C ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126246121 12624612 1 Major depression
126246121 12624612 2 Bipolar disorder
126246121 12624612 3 Product used for unknown indication
126246121 12624612 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126246121 12624612 Balance disorder
126246121 12624612 Dizziness
126246121 12624612 Dyskinesia
126246121 12624612 Fall
126246121 12624612 Memory impairment
126246121 12624612 Off label use
126246121 12624612 Vertigo

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
126246121 12624612 1 2005 0
126246121 12624612 2 2016 0