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
119911603 11991160 3 F 1999 20160630 20160203 20160714 EXP US-JNJFOC-20160104938 JANSSEN 18.80 YR C M Y 0.00000 20160714 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
119911603 11991160 1 PS RISPERDAL RISPERIDONE 1 Oral N 20272 2 MG TABLETS BID
119911603 11991160 2 SS RISPERIDONE. RISPERIDONE 1 Oral N 20272 2 MG TABLETS QD
119911603 11991160 3 SS RISPERIDONE. RISPERIDONE 1 Oral 0 2 MG TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119911603 11991160 1 Attention deficit/hyperactivity disorder
119911603 11991160 2 Product used for unknown indication
119911603 11991160 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119911603 11991160 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119911603 11991160 Gynaecomastia
119911603 11991160 Obesity
119911603 11991160 Off label use
119911603 11991160 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
119911603 11991160 1 1999 2011 0