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
124865092 12486509 2 F 201603 20160623 20160621 20160701 EXP ZA-ELI_LILLY_AND_COMPANY-ZA201606005308 ELI LILLY AND CO 64.00 YR M Y 0.00000 20160630 CN ZA ZA

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
124865092 12486509 1 PS CIALIS TADALAFIL 1 Unknown 20 MG, UNKNOWN N U 21368 20 MG TABLET
124865092 12486509 2 SS CIALIS TADALAFIL 1 Unknown 5 MG, QD N U 21368 5 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124865092 12486509 1 Erectile dysfunction

Outcome of event

Event ID CASEID OUTC COD
124865092 12486509 OT
124865092 12486509 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124865092 12486509 Cerebral malaria
124865092 12486509 Coma
124865092 12486509 Erectile dysfunction
124865092 12486509 Fall
124865092 12486509 Penis disorder
124865092 12486509 Urethral injury
124865092 12486509 Urethral stenosis

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

no results found

Therapies reported

no results found