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
123674932 12367493 2 F 2016 20160706 20160513 20160712 EXP US-UNITED THERAPEUTICS-UNT-2016-006657 UNITED THERAPEUTICS 41.81 YR F Y 53.97000 KG 20160712 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
123674932 12367493 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.049 ?G/KG, CONTINUING U U 926116 21272 .049 UG/KG INJECTION
123674932 12367493 2 C LETAIRIS AMBRISENTAN 1 0
123674932 12367493 3 C REVATIO SILDENAFIL CITRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123674932 12367493 1 Pulmonary arterial hypertension
123674932 12367493 2 Product used for unknown indication
123674932 12367493 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123674932 12367493 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123674932 12367493 Fluid retention
123674932 12367493 Haemoptysis
123674932 12367493 Pulmonary arterial hypertension

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
123674932 12367493 1 20140107 0