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
118169602 11816960 2 F 2011 20160706 20151210 20160830 PER US-JNJFOC-20151115377 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
118169602 11816960 1 SS RISPERDAL RISPERIDONE 1 Oral IN VARYING DOSES OF 0.5 MG TO 1.0 MG U 0 SOLUTION
118169602 11816960 2 PS RISPERDAL RISPERIDONE 1 Oral IN VARYING DOSES OF 0.5 MG TO 1.0 MG U 20588 SOLUTION
118169602 11816960 3 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20272 TABLETS
118169602 11816960 4 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20588 SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118169602 11816960 1 Abnormal behaviour
118169602 11816960 2 Autism
118169602 11816960 3 Product used for unknown indication
118169602 11816960 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118169602 11816960 Abnormal weight gain
118169602 11816960 Gynaecomastia

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
118169602 11816960 1 2008 2011 0
118169602 11816960 2 2008 2011 0