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
125579543 12557954 3 F 20160706 20160810 20160714 20160818 EXP US-UNITED THERAPEUTICS-UNT-2016-011131 UNITED THERAPEUTICS 68.01 YR F Y 68.93000 KG 20160818 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
125579543 12557954 1 PS TYVASO TREPROSTINIL 1 54 -126 ?G, QID U U 2100810 22387 INHALATION GAS QID
125579543 12557954 2 SS TYVASO TREPROSTINIL 1 UNK U U 2100817 22387 INHALATION GAS
125579543 12557954 3 C ADCIRCA TADALAFIL 1 UNK 0
125579543 12557954 4 C OPSUMIT MACITENTAN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125579543 12557954 1 Pulmonary arterial hypertension
125579543 12557954 3 Product used for unknown indication
125579543 12557954 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125579543 12557954 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125579543 12557954 Fluid overload
125579543 12557954 Fluid retention
125579543 12557954 Product use issue
125579543 12557954 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
125579543 12557954 1 20130712 0