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
123669153 12366915 3 F 201605 20160718 20160513 20160722 EXP US-UNITED THERAPEUTICS-UNT-2016-007483 UNITED THERAPEUTICS 0.00 A F Y 0.00000 20160722 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
123669153 12366915 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.056 ?G/KG, Q72H 21272 .056 UG/KG INJECTION
123669153 12366915 2 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.049 ?G/KG, CONTINUING 21272 .049 UG/KG INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123669153 12366915 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
123669153 12366915 DE
123669153 12366915 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123669153 12366915 Dyspnoea
123669153 12366915 Pulmonary arterial hypertension
123669153 12366915 Right ventricular failure
123669153 12366915 Urine output 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
123669153 12366915 1 201602 0
123669153 12366915 2 20160522 0