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
109448552 10944855 2 F 20160714 20150323 20160830 PER US-JNJFOC-20150305684 JANSSEN 0.00 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
109448552 10944855 1 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 UNSPECIFIED
109448552 10944855 2 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 TABLETS
109448552 10944855 3 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
109448552 10944855 1 Product used for unknown indication
109448552 10944855 2 Product used for unknown indication
109448552 10944855 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
109448552 10944855 Abnormal weight gain
109448552 10944855 Galactorrhoea
109448552 10944855 Gynaecomastia
109448552 10944855 Hyperprolactinaemia
109448552 10944855 Wrong technique in product usage process

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found