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
123037373 12303737 3 F 20160912 20160426 20160929 PER US-JNJFOC-20160412887 JANSSEN 0.00 M Y 0.00000 20160929 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
123037373 12303737 1 PS RISPERDAL RISPERIDONE 1 Oral U U 20272 TABLETS
123037373 12303737 2 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 TABLETS
123037373 12303737 3 SS RISPERIDONE. RISPERIDONE 1 Oral U 0 TABLETS
123037373 12303737 4 SS INVEGA PALIPERIDONE 1 Oral U U 21999 OROS (ORAL OSMOTIC) THERAPEUTIC SYSTEM TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123037373 12303737 1 Product used for unknown indication
123037373 12303737 2 Product used for unknown indication
123037373 12303737 3 Product used for unknown indication
123037373 12303737 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123037373 12303737 Adverse event

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
123037373 12303737 1 20080709 20080809 0
123037373 12303737 2 20080804 20090601 0
123037373 12303737 3 20110706 20140911 0