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
109737802 10973780 2 F 2006 20160615 20150401 20160830 PER US-JNJFOC-20150311629 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
109737802 10973780 1 PS RISPERDAL RISPERIDONE 1 Oral 0.25-0.50 MG U 20272 TABLETS
109737802 10973780 2 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109737802 10973780 1 Attention deficit/hyperactivity disorder
109737802 10973780 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
109737802 10973780 Abnormal weight gain
109737802 10973780 Aggression
109737802 10973780 Galactorrhoea
109737802 10973780 Gynaecomastia
109737802 10973780 Hyperprolactinaemia
109737802 10973780 Off label use
109737802 10973780 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
109737802 10973780 1 2006 2011 0