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
115895693 11589569 3 F 20080527 20160607 20151002 20160830 PER US-JNJFOC-20150911334 JANSSEN 15.88 YR T M Y 0.00000 20160830 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
115895693 11589569 1 SS RISPERDAL RISPERIDONE 1 Oral U U 0 1 MG UNSPECIFIED
115895693 11589569 2 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 2 MG UNSPECIFIED
115895693 11589569 3 SS RISPERIDONE. RISPERIDONE 1 Unknown U U 20272 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115895693 11589569 1 Autism
115895693 11589569 2 Autism
115895693 11589569 3 Autism

Outcome of event

Event ID CASEID OUTC COD
115895693 11589569 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115895693 11589569 Abnormal weight gain
115895693 11589569 Gynaecomastia
115895693 11589569 Hyperprolactinaemia
115895693 11589569 Off label use
115895693 11589569 Product use issue

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
115895693 11589569 1 20080527 20080626 0
115895693 11589569 2 20080527 20131212 0
115895693 11589569 3 20141105 20150423 0