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
118181192 11818119 2 F 2001 20160913 20151210 20160929 PER US-JNJFOC-20151014065 JANSSEN 0.00 C M Y 0.00000 20160929 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
118181192 11818119 1 PS RISPERDAL RISPERIDONE 1 Oral RISPERDAL WAS GIVEN AT A UNKNOWN DOSE. U U 20272 UNSPECIFIED
118181192 11818119 2 SS INVEGA PALIPERIDONE 1 Oral U U 21999 3 MG OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118181192 11818119 1 Attention deficit/hyperactivity disorder
118181192 11818119 2 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118181192 11818119 Gynaecomastia
118181192 11818119 Off label use
118181192 11818119 Product use issue
118181192 11818119 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
118181192 11818119 1 2001 2008 0
118181192 11818119 2 2007 0