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
112909602 11290960 2 F 201501 20150717 20150722 20160928 EXP US-UNITED THERAPEUTICS-UNT-2015-000163 UNITED THERAPEUTICS 44.01 YR M Y 77.98000 KG 20160928 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
112909602 11290960 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.0515 ?G/KG, CONTINUING U U 924065 21272 .051 UG/KG INJECTION
112909602 11290960 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip 0.060 ?G/KG, CONTINUING U U 2100499 21272 .06 UG/KG INJECTION
112909602 11290960 3 SS LETAIRIS AMBRISENTAN 1 10 MG, QD 1309762A 0 10 MG QD
112909602 11290960 4 SS LETAIRIS AMBRISENTAN 1 0
112909602 11290960 5 C ADCIRCA TADALAFIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112909602 11290960 1 Pulmonary arterial hypertension
112909602 11290960 3 Pulmonary hypertension
112909602 11290960 4 Drug abuse
112909602 11290960 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
112909602 11290960 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
112909602 11290960 Dermatitis contact
112909602 11290960 Device related infection
112909602 11290960 Dyspnoea
112909602 11290960 Infection
112909602 11290960 Injection site infection

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
112909602 11290960 1 20140516 0
112909602 11290960 2 20140516 0
112909602 11290960 3 20111130 0