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
120664183 12066418 3 F 2009 20160907 20160210 20160929 PER US-JNJFOC-20150920116 JANSSEN 0.00 T M Y 0.00000 20160929 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
120664183 12066418 1 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 .5 MG UNSPECIFIED
120664183 12066418 2 SS INVEGA PALIPERIDONE 1 Oral U U 21999 5 MG OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET
120664183 12066418 3 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120664183 12066418 1 Autism
120664183 12066418 2 Autism
120664183 12066418 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
120664183 12066418 Abnormal weight gain
120664183 12066418 Gynaecomastia
120664183 12066418 Off label use
120664183 12066418 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
120664183 12066418 1 20090209 20140127 0
120664183 12066418 2 2009 2011 0