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
126981691 12698169 1 I 2008 20160613 20160830 20160830 PER US-JNJFOC-20160619773 JANSSEN 0.00 C 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
126981691 12698169 1 SS RISPERDAL RISPERIDONE 1 Oral U 0 UNSPECIFIED
126981691 12698169 2 PS RISPERDAL RISPERIDONE 1 Oral U 20272 UNSPECIFIED
126981691 12698169 3 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20272 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126981691 12698169 1 Abnormal behaviour
126981691 12698169 2 Abnormal behaviour
126981691 12698169 3 Abnormal behaviour

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126981691 12698169 Emotional disorder
126981691 12698169 Gynaecomastia
126981691 12698169 Obesity

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
126981691 12698169 1 200809 200902 0
126981691 12698169 2 200809 201003 0
126981691 12698169 3 200809 200901 0