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
125910562 12591056 2 F 201512 20160217 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015705 UNITED THERAPEUTICS 62.77 YR M Y 89.80000 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
125910562 12591056 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.070 ?G/KG/MIN, CONTINUING U U 2100665 21272 .07 UG/KG INJECTION
125910562 12591056 2 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.067 ?G/KG/MIN, UNK U U 2100666 21272 .067 UG/KG INJECTION
125910562 12591056 3 SS LETAIRIS AMBRISENTAN 1 Unknown 5 MG, QD SBFP 0 5 MG TABLET QD
125910562 12591056 4 SS ADCIRCA TADALAFIL 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125910562 12591056 1 Pulmonary arterial hypertension
125910562 12591056 3 Product used for unknown indication
125910562 12591056 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125910562 12591056 Chest pain
125910562 12591056 Device occlusion
125910562 12591056 Drug dose omission
125910562 12591056 Infusion site erythema
125910562 12591056 Infusion site pain
125910562 12591056 Pain in extremity

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
125910562 12591056 1 20150529 0
125910562 12591056 3 20130624 0