The Safety Rates Drug Report

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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
125940061 12594006 1 I 201509 20150924 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-012088 UNITED THERAPEUTICS 38.50 YR F Y 73.47000 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
125940061 12594006 1 PS TYVASO TREPROSTINIL 1 18-54 MICROGRAMS, QID N 2100672 22387 INHALATION GAS QID
125940061 12594006 2 SS TYVASO TREPROSTINIL 1 UNK N 2100697 22387 INHALATION GAS
125940061 12594006 3 C SILDENAFIL. SILDENAFIL 1 0
125940061 12594006 4 C WARFARIN WARFARIN 1 0
125940061 12594006 5 C ADEMPAS RIOCIGUAT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125940061 12594006 1 Pulmonary hypertension
125940061 12594006 3 Product used for unknown indication
125940061 12594006 4 Product used for unknown indication
125940061 12594006 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125940061 12594006 Adverse event
125940061 12594006 Rash
125940061 12594006 Throat irritation

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
125940061 12594006 1 20150902 0