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
118169022 11816902 2 F 20081125 20160613 20151210 20160830 PER US-JNJFOC-20151107665 JANSSEN 9.77 YR 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
118169022 11816902 1 PS RISPERDAL RISPERIDONE 1 Oral 0.25 MG, 1 MG N 20272 TABLETS
118169022 11816902 2 SS RISPERIDONE. RISPERIDONE 1 Oral U U 20272 TABLETS
118169022 11816902 3 SS RISPERIDONE. RISPERIDONE 1 Unknown U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118169022 11816902 1 Attention deficit/hyperactivity disorder
118169022 11816902 2 Product used for unknown indication
118169022 11816902 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118169022 11816902 Abnormal weight gain
118169022 11816902 Gynaecomastia
118169022 11816902 Off label use
118169022 11816902 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
118169022 11816902 1 20081125 20110819 0