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
125459321 12545932 1 I 201003 20150811 20160711 20160711 PER US-JNJFOC-20150810728 JANSSEN 18.24 YR T M Y 0.00000 20160711 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
125459321 12545932 1 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 1 MG UNSPECIFIED
125459321 12545932 2 SS INVEGA PALIPERIDONE 1 Oral U U 21999 3 MG OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125459321 12545932 1 Attention deficit/hyperactivity disorder
125459321 12545932 2 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125459321 12545932 Abnormal weight gain
125459321 12545932 Galactorrhoea
125459321 12545932 Gynaecomastia
125459321 12545932 Hyperprolactinaemia
125459321 12545932 Off label use
125459321 12545932 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
125459321 12545932 1 201105 201410 0
125459321 12545932 2 201003 201007 0