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
125974621 12597462 1 I 201601 20160106 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-000238 UNITED THERAPEUTICS 50.35 YR F Y 97.52000 KG 20160726 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
125974621 12597462 1 PS TYVASO TREPROSTINIL 1 18-54 MICROGRAMS, QID U U 2100695 22387 INHALATION GAS QID
125974621 12597462 2 SS ADCIRCA TADALAFIL 1 U U 0
125974621 12597462 3 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD 1500226A 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125974621 12597462 1 Pulmonary hypertension
125974621 12597462 2 Product used for unknown indication
125974621 12597462 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125974621 12597462 Cough
125974621 12597462 Skin induration
125974621 12597462 Weight 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
125974621 12597462 1 20160105 0
125974621 12597462 3 20151231 0