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
125748401 12574840 1 I 20150811 20160720 20160720 PER US-ASTELLAS-2015US029647 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
125748401 12574840 1 PS VESICARE SOLIFENACIN SUCCINATE 1 Unknown HALF OF THE TABLET, EVERY OTHER NIGHT 21518 TABLET
125748401 12574840 2 SS VESICARE SOLIFENACIN SUCCINATE 1 Unknown 1/3 OF THE TABLET, ONCE DAILY U 21518 TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125748401 12574840 1 Urinary incontinence

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125748401 12574840 Constipation
125748401 12574840 Inappropriate schedule of drug administration
125748401 12574840 Wrong technique in product usage process

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
125748401 12574840 2 201508 0