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
121913433 12191343 3 F 20160627 20160318 20160705 EXP US-ELI_LILLY_AND_COMPANY-US201603003642 ELI LILLY AND CO 0.00 M Y 60.32000 KG 20160704 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
121913433 12191343 1 PS ADCIRCA TADALAFIL 1 Unknown UNK, UNKNOWN U 21368 TABLET
121913433 12191343 2 SS ORENITRAM TREPROSTINIL 1 Oral 9 MG, TID U U 2100397 0 9 MG TID
121913433 12191343 3 SS ORENITRAM TREPROSTINIL 1 Oral 3 MG, TID U U 2100476 0 3 MG TID
121913433 12191343 4 SS ORENITRAM TREPROSTINIL 1 Oral 3 MG, TID U U 2100679 0 3 MG TID
121913433 12191343 5 C ADEMPAS RIOCIGUAT 1 Unknown UNK, UNKNOWN U 0
121913433 12191343 6 C NORVASC AMLODIPINE BESYLATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121913433 12191343 1 Product used for unknown indication
121913433 12191343 2 Pulmonary arterial hypertension
121913433 12191343 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121913433 12191343 OT
121913433 12191343 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121913433 12191343 Dyspnoea
121913433 12191343 Fluid retention
121913433 12191343 Renal failure
121913433 12191343 Systemic infection

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
121913433 12191343 2 20150901 0
121913433 12191343 3 20150901 0
121913433 12191343 4 20150901 0