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
125913152 12591315 2 F 20160402 20160503 20160726 20160727 PER US-UNITED THERAPEUTICS-UNT-2016-005537 UNITED THERAPEUTICS 55.18 YR M Y 94.33000 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
125913152 12591315 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.007 ?G/KG, CONTINUING U U 926618 21272 .007 UG/KG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125913152 12591315 1 Pulmonary hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125913152 12591315 Device dislocation
125913152 12591315 Drug dose omission
125913152 12591315 Flushing
125913152 12591315 Injection site discomfort
125913152 12591315 Injection site erythema
125913152 12591315 Injection site pruritus
125913152 12591315 Sluggishness

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
125913152 12591315 1 20160209 0