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
125620601 12562060 1 I 20160624 20160715 20160715 PER US-ELI_LILLY_AND_COMPANY-US201606009142 ELI LILLY AND CO 78.00 YR M Y 0.00000 20160715 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
125620601 12562060 1 PS CIALIS TADALAFIL 1 Oral 20 MG, PRN U U C497101A 21368 20 MG TABLET
125620601 12562060 2 C DOXAZOSIN DOXAZOSINDOXAZOSIN MESYLATE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125620601 12562060 1 Erectile dysfunction
125620601 12562060 2 Benign prostatic hyperplasia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125620601 12562060 Drug ineffective
125620601 12562060 Headache
125620601 12562060 Nasal congestion
125620601 12562060 Rhinorrhoea

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found