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
112827844 11282784 4 F 20160825 20150720 20160905 EXP US-JNJFOC-20150713510 JANSSEN 0.00 M Y 0.00000 20160905 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
112827844 11282784 1 SS RISPERDAL RISPERIDONE 1 Oral U U 0 UNSPECIFIED
112827844 11282784 2 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 UNSPECIFIED
112827844 11282784 3 SS INVEGA PALIPERIDONE 1 Oral U U 21999 OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET
112827844 11282784 4 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 2 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112827844 11282784 1 Psychomotor hyperactivity
112827844 11282784 2 Attention deficit/hyperactivity disorder
112827844 11282784 3 Product used for unknown indication
112827844 11282784 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
112827844 11282784 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112827844 11282784 Abnormal weight gain
112827844 11282784 Diabetes mellitus
112827844 11282784 Gynaecomastia
112827844 11282784 Hyperprolactinaemia
112827844 11282784 Off label use
112827844 11282784 Product use issue

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

no results found

Therapies reported

no results found