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
125264631 12526463 1 I 201603 20160627 20160705 20160705 PER US-ELI_LILLY_AND_COMPANY-US201606009934 ELI LILLY AND CO 0.00 M Y 0.00000 20160705 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
125264631 12526463 1 PS CIALIS TADALAFIL 1 Unknown 5 MG, UNKNOWN (6 DAYS IN MARCH) Y Y 21368 5 MG TABLET
125264631 12526463 2 SS CIALIS TADALAFIL 1 Unknown 5 MG, UNKNOWN (6 DAYS IN APRIL) Y Y 21368 5 MG TABLET
125264631 12526463 3 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown 1 DF, UNKNOWN U 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125264631 12526463 1 Erectile dysfunction
125264631 12526463 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125264631 12526463 Back pain
125264631 12526463 Blood testosterone decreased
125264631 12526463 Drug ineffective Drug ineffective
125264631 12526463 Headache

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
125264631 12526463 1 201603 201603 0
125264631 12526463 2 201604 201604 0