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
118190703 11819070 3 F 2002 20160622 20151210 20160707 EXP US-JNJFOC-20151107846 JANSSEN 54.00 YR A M Y 0.00000 20160707 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
118190703 11819070 1 SS RISPERDAL RISPERIDONE 1 Oral U U 0 UNSPECIFIED
118190703 11819070 2 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 2 MG UNSPECIFIED
118190703 11819070 3 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20272 2 MG UNSPECIFIED
118190703 11819070 4 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 2 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118190703 11819070 1 Depression
118190703 11819070 2 Depression
118190703 11819070 3 Schizophrenia
118190703 11819070 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118190703 11819070 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118190703 11819070 Gynaecomastia
118190703 11819070 Off label use
118190703 11819070 Product use issue
118190703 11819070 Weight increased

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
118190703 11819070 2 2002 2015 0