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
108795732 10879573 2 F 201107 20160726 20150302 20160815 PER US-ELI_LILLY_AND_COMPANY-US201109004910 ELI LILLY AND CO 78.00 YR M Y 0.00000 20160815 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
108795732 10879573 1 PS CIALIS TADALAFIL 1 Unknown 20 MG, UNKNOWN U U 21368 20 MG TABLET
108795732 10879573 2 SS CIALIS TADALAFIL 1 Unknown 5 MG, UNKNOWN U U 21368 5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108795732 10879573 1 Erectile dysfunction

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
108795732 10879573 Abdominal discomfort
108795732 10879573 Drug ineffective
108795732 10879573 Dyspepsia
108795732 10879573 Spontaneous penile erection
108795732 10879573 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

no results found