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
125869851 12586985 1 I 201607 20160718 20160725 20160725 PER US-ELI_LILLY_AND_COMPANY-US201607006938 ELI LILLY AND CO 74.89 YR M Y 0.00000 20160725 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
125869851 12586985 1 PS CIALIS TADALAFIL 1 5 MG, QD U 21368 5 MG TABLET QD
125869851 12586985 2 SS CIALIS TADALAFIL 1 20 MG, PRN U C078087A 21368 20 MG TABLET
125869851 12586985 3 C SIMVASTATIN. SIMVASTATIN 1 Unknown UNK, UNKNOWN U U 0
125869851 12586985 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown UNK, UNKNOWN U U 0
125869851 12586985 5 C PRAVASTATIN. PRAVASTATIN 1 Unknown UNK, UNKNOWN U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125869851 12586985 1 Erectile dysfunction
125869851 12586985 2 Benign prostatic hyperplasia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125869851 12586985 Drug ineffective
125869851 12586985 Expired product administered

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
125869851 12586985 1 201407 0
125869851 12586985 2 201504 0