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
120946933 12094693 3 F 20160209 20160622 20160219 20160701 EXP US-ELI_LILLY_AND_COMPANY-US201602003967 ELI LILLY AND CO 27.92 YR M Y 0.00000 20160630 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
120946933 12094693 1 PS ADCIRCA TADALAFIL 1 Unknown 2 DF, QD C459623A 21368 2 DF TABLET QD
120946933 12094693 2 SS ADCIRCA TADALAFIL 1 Unknown 20 MG, BID C464095A 21368 20 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120946933 12094693 1 Cor pulmonale chronic

Outcome of event

Event ID CASEID OUTC COD
120946933 12094693 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
120946933 12094693 Ascites
120946933 12094693 Asthenia
120946933 12094693 Chills
120946933 12094693 Oedema peripheral
120946933 12094693 Pyrexia

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
120946933 12094693 1 201503 0