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
126823901 12682390 1 I 20160812 20160825 20160825 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-069951 BRISTOL MYERS SQUIBB 49.00 YR M Y 0.00000 20160825 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
126823901 12682390 1 PS ABILIFY ARIPIPRAZOLE 1 Oral UNK, QD N 21436 TABLET QD
126823901 12682390 2 C LAMICTAL LAMOTRIGINE 1 Unknown U 0
126823901 12682390 3 C INSULIN INSULIN NOS 1 Unknown U 0
126823901 12682390 4 C GLYBURIDE. GLYBURIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126823901 12682390 1 Bipolar II disorder
126823901 12682390 2 Product used for unknown indication
126823901 12682390 3 Product used for unknown indication
126823901 12682390 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126823901 12682390 Decreased appetite
126823901 12682390 Depressed mood
126823901 12682390 Erythema
126823901 12682390 Head discomfort
126823901 12682390 Product use issue

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
126823901 12682390 1 2016 0