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
124456002 12445600 2 F 2010 20160621 20160608 20160830 PER US-JNJFOC-20151101641 JANSSEN 0.00 C 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
124456002 12445600 1 SS RISPERDAL RISPERIDONE 1 Oral U U 0 .25 MG TABLETS
124456002 12445600 2 SS RISPERDAL RISPERIDONE 1 Oral U U 0 .25 MG TABLETS
124456002 12445600 3 SS RISPERDAL RISPERIDONE 1 Oral U U 0 .25 MG TABLETS
124456002 12445600 4 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 .25 MG TABLETS
124456002 12445600 5 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124456002 12445600 1 Aggression
124456002 12445600 2 Anger
124456002 12445600 3 Attention deficit/hyperactivity disorder
124456002 12445600 4 Depression
124456002 12445600 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124456002 12445600 Abnormal weight gain
124456002 12445600 Galactorrhoea
124456002 12445600 Gynaecomastia
124456002 12445600 Hyperprolactinaemia
124456002 12445600 Off label use
124456002 12445600 Product use issue
124456002 12445600 Treatment noncompliance

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
124456002 12445600 1 2010 2016 0
124456002 12445600 2 2010 2016 0
124456002 12445600 3 2010 2016 0
124456002 12445600 4 2010 2016 0