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
111665264 11166526 4 F 20160829 20150605 20160912 EXP US-JNJFOC-20150504643 JANSSEN 0.00 C M Y 0.00000 20160912 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
111665264 11166526 1 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 SOLUTION
111665264 11166526 2 PS RISPERIDONE. RISPERIDONE 1 Oral U 20588 SOLUTION
111665264 11166526 3 SS RISPERDAL RISPERIDONE 1 Oral U U 20272 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111665264 11166526 1 Psychomotor hyperactivity
111665264 11166526 2 Psychomotor hyperactivity
111665264 11166526 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
111665264 11166526 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111665264 11166526 Emotional distress
111665264 11166526 Gynaecomastia
111665264 11166526 Obesity
111665264 11166526 Psychotic behaviour

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
111665264 11166526 2 2009 2010 0