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
123030924 12303092 4 F 200611 20160617 20160426 20160830 PER US-JNJFOC-20160322115 JANSSEN 4.85 YR 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
123030924 12303092 1 SS RISPERDAL RISPERIDONE 1 Oral U U UNKNOWN 0 UNSPECIFIED
123030924 12303092 2 PS RISPERDAL RISPERIDONE 1 Oral U U UNKNOWN 20272 UNSPECIFIED
123030924 12303092 3 SS RISPERDAL M-TAB RISPERIDONE 1 Oral U U 21444 TABLETS
123030924 12303092 4 SS DEPAKOTE DIVALPROEX SODIUM 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123030924 12303092 1 Attention deficit/hyperactivity disorder
123030924 12303092 2 Bipolar disorder
123030924 12303092 3 Product used for unknown indication
123030924 12303092 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123030924 12303092 Drug ineffective
123030924 12303092 Emotional disorder
123030924 12303092 Gynaecomastia
123030924 12303092 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
123030924 12303092 1 2006 2007 0
123030924 12303092 2 2006 2007 0