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
119438872 11943887 2 F 201510 20160126 20160125 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-013927 UNITED THERAPEUTICS 6.93 YR F Y 16.78000 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
119438872 11943887 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.011 ?G/KG, CONTINUING U U 926115 21272 .011 UG/KG INJECTION
119438872 11943887 2 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.012 ?G/KG, CONTINUING U U 924061 21272 .012 UG/KG INJECTION
119438872 11943887 3 C TRACLEER BOSENTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119438872 11943887 1 Pulmonary arterial hypertension
119438872 11943887 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119438872 11943887 Infusion site erythema
119438872 11943887 Infusion site oedema
119438872 11943887 Infusion site pain
119438872 11943887 Infusion site warmth
119438872 11943887 Syncope

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
119438872 11943887 1 20151028 0