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
126210291 12621029 1 I 20160420 20160727 20160804 20160804 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-063432 BRISTOL MYERS SQUIBB 24.21 YR F Y 0.00000 20160804 OT FR FR

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
126210291 12621029 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 10 MG, BID Y 21436 10 MG TABLET BID
126210291 12621029 2 SS RISPERIDONE. RISPERIDONE 1 Oral 3 MG, QD Y 0 3 MG TABLET QD
126210291 12621029 3 C RISPERDAL CONSTA RISPERIDONE 1 Unknown 75 MG, Q2WK U 0 75 MG INJECTION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126210291 12621029 1 Product used for unknown indication
126210291 12621029 2 Product used for unknown indication
126210291 12621029 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126210291 12621029 OT
126210291 12621029 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126210291 12621029 Delirium
126210291 12621029 Off label use
126210291 12621029 Paradoxical drug reaction
126210291 12621029 Psychotic disorder
126210291 12621029 Treatment failure

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
126210291 12621029 1 20160420 20160503 0
126210291 12621029 2 20160420 20160502 0
126210291 12621029 3 20160503 0