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
124132876 12413287 6 F 201605 20160725 20160527 20160803 EXP JP-UNITED THERAPEUTICS-UNT-2016-008492 UNITED THERAPEUTICS 47.09 YR F Y 35.00000 KG 20160803 PH JP JP

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
124132876 12413287 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous UNK Y 21272 INJECTION
124132876 12413287 2 C TRACLEER BOSENTAN 1 Oral 250 MG DAILY DOSE 0
124132876 12413287 3 C FLOLAN EPOPROSTENOL SODIUM 1 Intravenous drip UNK 0
124132876 12413287 4 C REVATIO SILDENAFIL CITRATE 1 Oral 60 MG DAILY DOSE 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124132876 12413287 1 Pulmonary arterial hypertension
124132876 12413287 2 Pulmonary arterial hypertension
124132876 12413287 3 Pulmonary arterial hypertension
124132876 12413287 4 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
124132876 12413287 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124132876 12413287 Hyperthyroidism
124132876 12413287 Infusion site pain
124132876 12413287 Pain in extremity

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
124132876 12413287 1 20160430 20160608 0
124132876 12413287 2 20060609 0
124132876 12413287 3 20050927 20120506 0
124132876 12413287 4 20080507 0