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
125910792 12591079 2 F 201512 20151214 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015853 UNITED THERAPEUTICS 49.24 YR F Y 93.65000 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
125910792 12591079 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.002 ?G/KG/MIN, CONTINUING U U 926118 21272 .002 UG/KG INJECTION
125910792 12591079 2 SS REMODULIN TREPROSTINIL 1 0.022 ?G/KG/MIN, CONTINUING U U 21272 .022 UG/KG INJECTION
125910792 12591079 3 C OPSUMIT MACITENTAN 1 0
125910792 12591079 4 C DILTIAZEM. DILTIAZEM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125910792 12591079 1 Pulmonary arterial hypertension
125910792 12591079 3 Product used for unknown indication
125910792 12591079 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125910792 12591079 Asthenia
125910792 12591079 Chills
125910792 12591079 Constipation
125910792 12591079 Cough
125910792 12591079 Dizziness
125910792 12591079 Infusion site erythema
125910792 12591079 Infusion site pain
125910792 12591079 Infusion site pruritus
125910792 12591079 Malaise
125910792 12591079 Nausea
125910792 12591079 Oral pain
125910792 12591079 Oropharyngeal pain
125910792 12591079 Pain
125910792 12591079 Tachycardia
125910792 12591079 Wheezing

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
125910792 12591079 1 20151203 0