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
125751971 12575197 1 I 20160119 20160720 20160720 PER US-ASTELLAS-2016US002280 ASTELLAS 0.00 F Y 0.00000 20160720 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
125751971 12575197 1 PS VESICARE SOLIFENACIN SUCCINATE 1 Oral U 21518 5 MG TABLET QD
125751971 12575197 2 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 Oral U 0 30 MG TABLET QD
125751971 12575197 3 C CRESTOR ROSUVASTATIN CALCIUM 1 Oral U 0 5 MG FORMULATION UNKNOWN QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125751971 12575197 1 Product used for unknown indication
125751971 12575197 2 Product used for unknown indication
125751971 12575197 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125751971 12575197 Constipation
125751971 12575197 Drug effect incomplete
125751971 12575197 Dry eye

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
125751971 12575197 1 201512 0