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
125850481 12585048 1 I 20160710 20160716 20160723 20160723 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-059930 BRISTOL MYERS SQUIBB 45.85 YR M Y 0.00000 20160723 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
125850481 12585048 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown UNK 21436
125850481 12585048 2 SS ABILIFY ARIPIPRAZOLE 1 Unknown UNK 21436
125850481 12585048 3 SS ARIPIPRAZOLE. ARIPIPRAZOLE 1 Unknown UNK 0
125850481 12585048 4 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 Unknown U 0
125850481 12585048 5 C LAMOTRIGINE. LAMOTRIGINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125850481 12585048 1 Product used for unknown indication
125850481 12585048 3 Product used for unknown indication
125850481 12585048 4 Product used for unknown indication
125850481 12585048 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125850481 12585048 Abdominal discomfort
125850481 12585048 Anxiety
125850481 12585048 Drug withdrawal syndrome
125850481 12585048 Dyspnoea
125850481 12585048 Insomnia

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
125850481 12585048 1 201511 0
125850481 12585048 2 201512 20160708 0
125850481 12585048 3 20160708 0