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
127268781 12726878 1 I 20160831 20160908 20160908 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-073236 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160908 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
127268781 12726878 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 5 MG, QD 21436 5 MG QD
127268781 12726878 2 SS ABILIFY ARIPIPRAZOLE 1 21436
127268781 12726878 3 C CELEXA CITALOPRAM HYDROBROMIDE 1 Unknown U 0
127268781 12726878 4 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127268781 12726878 1 Bipolar disorder
127268781 12726878 2 Depression
127268781 12726878 3 Product used for unknown indication
127268781 12726878 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127268781 12726878 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127268781 12726878 Depression
127268781 12726878 Epilepsy
127268781 12726878 Head injury
127268781 12726878 Memory impairment

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found