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
118175073 11817507 3 F 1994 20160701 20151210 20160830 PER US-JNJFOC-20151107612 JANSSEN 0.00 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
118175073 11817507 1 PS RISPERDAL RISPERIDONE 1 Oral VARYING DOSES OF 1 MG TO 4 MG U U 20272 TABLETS
118175073 11817507 2 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20272 TABLETS
118175073 11817507 3 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118175073 11817507 1 Depression
118175073 11817507 2 Product used for unknown indication
118175073 11817507 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118175073 11817507 Gynaecomastia
118175073 11817507 Off label use
118175073 11817507 Product use issue
118175073 11817507 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
118175073 11817507 1 1994 2015 0