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
118077362 11807736 2 F 20160720 20151207 20160722 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-082215 BRISTOL MYERS SQUIBB 44.00 YR 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
118077362 11807736 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown 5 MG, QD N 21436 5 MG QD
118077362 11807736 2 SS ABILIFY ARIPIPRAZOLE 1 N 21436
118077362 11807736 3 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118077362 11807736 1 Bipolar disorder
118077362 11807736 2 Depression
118077362 11807736 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118077362 11807736 Hypocalcaemia
118077362 11807736 Presyncope
118077362 11807736 Weight decreased
118077362 11807736 Weight increased

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
118077362 11807736 1 2010 201502 0