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
125912472 12591247 2 F 201603 20160713 20160726 20160727 PER US-UNITED THERAPEUTICS-UNT-2016-005454 UNITED THERAPEUTICS 34.41 YR F Y 73.16000 KG 20160727 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
125912472 12591247 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.002 ?G/KG, CONTINUING U U 926618 21272 .002 UG/KG INJECTION
125912472 12591247 2 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.01 ?G/KG,CONTINUING U U 926618 21272 .01 UG/KG INJECTION
125912472 12591247 3 SS LETAIRIS AMBRISENTAN 1 Unknown 5 MG, QD SBFS 0 5 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125912472 12591247 1 Pulmonary arterial hypertension
125912472 12591247 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125912472 12591247 Dermatitis contact
125912472 12591247 Infusion site erythema
125912472 12591247 Infusion site haemorrhage
125912472 12591247 Infusion site pain
125912472 12591247 Infusion site pruritus
125912472 12591247 Infusion site rash

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
125912472 12591247 1 20160302 0
125912472 12591247 2 20160302 0
125912472 12591247 3 20150501 0