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
119483743 11948374 3 F 20150923 20160718 20160125 20160718 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-004178 BRISTOL MYERS SQUIBB 7.80 YR M Y 0.00000 20160718 OT 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
119483743 11948374 1 PS ABILIFY ARIPIPRAZOLE 1 Oral 2.5 MG, QD 21436 2.5 MG TABLET QD
119483743 11948374 2 SS RISPERIDONE. RISPERIDONE 1 Unknown 0.5 MG, UNK 0 .5 MG
119483743 11948374 3 SS RITALIN METHYLPHENIDATE HYDROCHLORIDE 1 Unknown 0
119483743 11948374 4 C GUANFACINE. GUANFACINE 1 Unknown U 0
119483743 11948374 5 C VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119483743 11948374 1 Oppositional defiant disorder
119483743 11948374 2 Product used for unknown indication
119483743 11948374 3 Product used for unknown indication
119483743 11948374 4 Product used for unknown indication
119483743 11948374 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119483743 11948374 Off label use
119483743 11948374 Wrong technique in product usage process

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
119483743 11948374 1 20150923 0