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
103647575 10364757 5 F 2004 20160624 20140806 20160711 PER US-JNJFOC-20140800547 JANSSEN 0.00 A 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
103647575 10364757 1 PS RISPERDAL RISPERIDONE 1 Oral VARIED DOSES OF 2 MG AND 4 MG Y U 20272 TABLETS
103647575 10364757 2 SS INVEGA SUSTENNA PALIPERIDONE PALMITATE 1 Intramuscular VARIED DOSES OF 117 MG TO 234 MG U U 22264 INJECTION
103647575 10364757 3 SS RISPERDAL CONSTA RISPERIDONE 1 Intramuscular N 21346 MICROSPHERES
103647575 10364757 4 SS INVEGA PALIPERIDONE 1 Oral VARIED DOSES OF 117 MG TO 234 MG U U 21999 OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103647575 10364757 1 Psychotic disorder
103647575 10364757 2 Product used for unknown indication
103647575 10364757 3 Psychotic disorder
103647575 10364757 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
103647575 10364757 OT
103647575 10364757 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
103647575 10364757 Blood testosterone decreased
103647575 10364757 Dystonia
103647575 10364757 Fatigue
103647575 10364757 Gynaecomastia
103647575 10364757 Hyperprolactinaemia
103647575 10364757 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
103647575 10364757 1 2004 0