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
106954068 10695406 8 F 200609 20160620 20150107 20160704 EXP US-JNJFOC-20150101722 JANSSEN 9.87 YR C M Y 0.00000 20160704 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
106954068 10695406 1 PS RISPERDAL RISPERIDONE 1 Oral IN VARYING DOSES OF 0.5 MG AND 1.5 MG N N 20272 UNSPECIFIED
106954068 10695406 2 SS INVEGA PALIPERIDONE 1 Oral U U 21999 1.5 MG OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET
106954068 10695406 3 SS ABILIFY ARIPIPRAZOLE 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106954068 10695406 1 Autism
106954068 10695406 2 Autism
106954068 10695406 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
106954068 10695406 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106954068 10695406 Galactorrhoea
106954068 10695406 Gynaecomastia
106954068 10695406 Hyperprolactinaemia
106954068 10695406 Obesity

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
106954068 10695406 1 2003 0
106954068 10695406 2 20140226 20140723 0
106954068 10695406 3 2006 0