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
107710322 10771032 2 F 2000 20160623 20150206 20160711 PER US-JNJFOC-20150116361 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
107710322 10771032 1 SS RISPERDAL RISPERIDONE 1 Oral U U 0 UNSPECIFIED
107710322 10771032 2 SS RISPERDAL RISPERIDONE 1 Oral U U 0 UNSPECIFIED
107710322 10771032 3 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 UNSPECIFIED
107710322 10771032 4 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
107710322 10771032 1 Schizoaffective disorder
107710322 10771032 2 Psychotic disorder
107710322 10771032 3 Major depression
107710322 10771032 4 Schizoaffective disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
107710322 10771032 Abnormal weight gain
107710322 10771032 Galactorrhoea
107710322 10771032 Gynaecomastia
107710322 10771032 Hyperglycaemia
107710322 10771032 Hyperprolactinaemia

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
107710322 10771032 1 200005 0
107710322 10771032 2 200005 0
107710322 10771032 3 200005 0
107710322 10771032 4 200806 200808 0