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
109448812 10944881 2 F 2009 20160620 20150323 20160830 PER US-JNJFOC-20150305692 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
109448812 10944881 1 PS RISPERDAL RISPERIDONE 1 Oral 0.25 MG TO 0.5 MG U U 20272 UNSPECIFIED
109448812 10944881 2 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20272 TABLETS
109448812 10944881 3 SS RISPERIDONE. RISPERIDONE 1 U 0 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109448812 10944881 1 Attention deficit/hyperactivity disorder
109448812 10944881 2 Product used for unknown indication
109448812 10944881 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
109448812 10944881 Abnormal weight gain
109448812 10944881 Galactorrhoea
109448812 10944881 Gynaecomastia
109448812 10944881 Hyperprolactinaemia
109448812 10944881 Off label use
109448812 10944881 Product use issue

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
109448812 10944881 1 2009 2015 0