The Safety Rates Drug Report

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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
124199762 12419976 2 F 201603 20160726 20160531 20160803 PER US-ELI_LILLY_AND_COMPANY-US201605008914 ELI LILLY AND CO 64.11 YR M Y 104.00000 KG 20160803 MD 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
124199762 12419976 1 PS AXIRON TESTOSTERONE 1 Topical 4 PUMPS, QD 1682610 22504 120 MG ORAL LIQUID QD
124199762 12419976 2 SS AXIRON TESTOSTERONE 1 22504 ORAL LIQUID
124199762 12419976 3 SS CIALIS TADALAFIL 1 Oral 5 MG, QD 0 5 MG TABLET QD
124199762 12419976 4 SS CIALIS TADALAFIL 1 0 TABLET
124199762 12419976 5 SS CIALIS TADALAFIL 1 0 TABLET
124199762 12419976 6 SS CIALIS TADALAFIL 1 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124199762 12419976 1 Blood testosterone decreased
124199762 12419976 2 Testicular failure
124199762 12419976 3 Benign prostatic hyperplasia
124199762 12419976 4 Testicular failure
124199762 12419976 5 Psychosexual disorder
124199762 12419976 6 Erectile dysfunction

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124199762 12419976 Prostatic specific antigen increased

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
124199762 12419976 1 20120905 0
124199762 12419976 3 20110721 0