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
126735871 12673587 1 I 2008 20151027 20160822 20160822 EXP US-JNJFOC-20151103357 JANSSEN 0.00 A M Y 0.00000 20160822 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
126735871 12673587 1 PS RISPERDAL RISPERIDONE 1 Oral VARIED DOSES OF 1 MG AND 2 MG U 20272 TABLETS
126735871 12673587 2 SS RISPERIDONE. RISPERIDONE 1 Unknown U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126735871 12673587 1 Drug therapy
126735871 12673587 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126735871 12673587 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126735871 12673587 Galactorrhoea
126735871 12673587 Gynaecomastia
126735871 12673587 Hyperprolactinaemia
126735871 12673587 Obesity
126735871 12673587 Off label use
126735871 12673587 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
126735871 12673587 1 2008 2010 0