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
125909492 12590949 2 F 20151201 20151201 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015274 UNITED THERAPEUTICS 33.06 YR M Y 67.57000 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
125909492 12590949 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.080 ?G/KG/MIN, CONTINUING U U 2100582 21272 .08 UG/KG INJECTION
125909492 12590949 2 C LETAIRIS AMBRISENTAN 1 0
125909492 12590949 3 C SILDENAFIL. SILDENAFIL 1 0
125909492 12590949 4 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125909492 12590949 1 Pulmonary arterial hypertension
125909492 12590949 2 Product used for unknown indication
125909492 12590949 3 Product used for unknown indication
125909492 12590949 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125909492 12590949 Device dislocation
125909492 12590949 Drug dose omission
125909492 12590949 Infusion site erythema
125909492 12590949 Infusion site pustule

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
125909492 12590949 1 20130515 0