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
118183694 11818369 4 F 2007 20160701 20151210 20160830 PER US-JNJFOC-20151112189 JANSSEN 0.00 T 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
118183694 11818369 1 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 1 MG TABLETS
118183694 11818369 2 SS RISPERDAL M-TAB RISPERIDONE 1 Oral U U 21444 TABLETS
118183694 11818369 3 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20272 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118183694 11818369 1 Attention deficit/hyperactivity disorder
118183694 11818369 2 Product used for unknown indication
118183694 11818369 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118183694 11818369 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118183694 11818369 Gynaecomastia
118183694 11818369 Off label use
118183694 11818369 Product use issue
118183694 11818369 Weight increased

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
118183694 11818369 1 200706 200911 0