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
120008454 12000845 4 F 20160118 20160818 20160204 20160824 EXP US-UNITED THERAPEUTICS-UNT-2016-001166 UNITED THERAPEUTICS 54.84 YR F Y 61.68000 KG 20160824 PH 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
120008454 12000845 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.032 ?G/KG, CONTINUING U U 926118 21272 .032 UG/KG INJECTION
120008454 12000845 2 SS REMODULIN TREPROSTINIL 1 Subcutaneous 0.020 ?G/KG, CONTINUING U U 929006 21272 .02 UG/KG INJECTION
120008454 12000845 3 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120008454 12000845 1 Pulmonary arterial hypertension
120008454 12000845 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120008454 12000845 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
120008454 12000845 Infusion site pain
120008454 12000845 Liver transplant

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
120008454 12000845 1 20140709 0