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
125909933 12590993 3 F 2015 20151212 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-015413 UNITED THERAPEUTICS 0.00 A M Y 0.00000 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
125909933 12590993 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.060 ?G/KG, CONTINUING 21272 .06 UG/KG INJECTION
125909933 12590993 2 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.060 ?G/KG, Q72H 21272 .06 UG/KG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125909933 12590993 1 Pulmonary arterial hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125909933 12590993 Activities of daily living impaired
125909933 12590993 Decreased appetite
125909933 12590993 Feeling of despair
125909933 12590993 Lethargy
125909933 12590993 Muscle atrophy
125909933 12590993 Musculoskeletal pain
125909933 12590993 Nausea
125909933 12590993 Pain in extremity
125909933 12590993 Weight decreased

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
125909933 12590993 1 20150908 0