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
126052571 12605257 1 I 20160712 20160729 20160729 EXP DK-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-058922 BRISTOL MYERS SQUIBB 0.00 M Y 0.00000 20160729 CN DK DK

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
126052571 12605257 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown UNK U 21436
126052571 12605257 2 C ZYPREXA OLANZAPINE 1 Oral UNK 0
126052571 12605257 3 C CIPRAMIL /00582602/ CITALOPRAM HYDROBROMIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126052571 12605257 1 Psychotic disorder
126052571 12605257 2 Psychotic disorder
126052571 12605257 3 Psychotic disorder

Outcome of event

Event ID CASEID OUTC COD
126052571 12605257 HO
126052571 12605257 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126052571 12605257 Brain injury
126052571 12605257 Product use issue
126052571 12605257 Psychotic disorder

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
126052571 12605257 1 200906 0
126052571 12605257 2 20060808 200906 0
126052571 12605257 3 201105 2011 0