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
125459361 12545936 1 I 2002 20151014 20160711 20160711 PER US-JNJFOC-20151018754 JANSSEN 0.00 C M Y 0.00000 20160711 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
125459361 12545936 1 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 UNSPECIFIED
125459361 12545936 2 SS INVEGA PALIPERIDONE 1 Oral U U 21999 OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125459361 12545936 1 Attention deficit/hyperactivity disorder
125459361 12545936 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125459361 12545936 Abnormal weight gain
125459361 12545936 Galactorrhoea
125459361 12545936 Gynaecomastia
125459361 12545936 Hyperprolactinaemia
125459361 12545936 Off label use
125459361 12545936 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
125459361 12545936 1 2002 2005 0