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
118198263 11819826 3 F 200507 20160622 20151210 20160711 PER US-JNJFOC-20151107845 JANSSEN 18.45 YR T 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
118198263 11819826 1 PS RISPERDAL RISPERIDONE 1 Oral IN VARYING DOSE OG 1 MG TO 3 MG U 20272 TABLETS
118198263 11819826 2 SS INVEGA PALIPERIDONE 1 Oral IN VARYING DOSE OF 6 TO 9 MG U U 21999 OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET
118198263 11819826 3 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20272 TABLETS
118198263 11819826 4 SS RISPERDAL M-TAB RISPERIDONE 1 Oral U U 21444 TABLETS
118198263 11819826 5 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118198263 11819826 1 Schizophrenia
118198263 11819826 2 Schizophrenia
118198263 11819826 3 Product used for unknown indication
118198263 11819826 4 Product used for unknown indication
118198263 11819826 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118198263 11819826 Blood prolactin increased
118198263 11819826 Dry mouth
118198263 11819826 Gynaecomastia
118198263 11819826 Obesity
118198263 11819826 Sensory disturbance

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
118198263 11819826 1 2003 2011 0
118198263 11819826 2 2009 2012 0