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
125452574 12545257 4 F 201606 20160824 20160711 20160830 EXP US-UNITED THERAPEUTICS-UNT-2016-009656 UNITED THERAPEUTICS 37.49 YR F Y 80.00000 KG 20160830 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
125452574 12545257 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.009 ?G/KG, CONTINUING U U 2100954 21272 .009 UG/KG INJECTION
125452574 12545257 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip 0.017 ?G/KG, CONTINUING U U 21272 .017 UG/KG INJECTION
125452574 12545257 3 C ADCIRCA TADALAFIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125452574 12545257 1 Pulmonary hypertension
125452574 12545257 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125452574 12545257 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125452574 12545257 Diarrhoea
125452574 12545257 Headache
125452574 12545257 Hypotension
125452574 12545257 Lethargy
125452574 12545257 Pneumonia
125452574 12545257 Pulmonary arterial hypertension
125452574 12545257 Renal disorder

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
125452574 12545257 1 20160609 0