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
103920503 10392050 3 F 20140805 20140901 20140819 20160907 EXP AT-UNITED THERAPEUTICS-UNT-2014-005552 UNITED THERAPEUTICS 27.29 YR F Y 48.00000 KG 20160907 CN AT OM

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
103920503 10392050 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.012 ?G/KG, UNK 21272 .012 UG/KG INJECTION
103920503 10392050 2 C TRACLEER BOSENTAN 1 Oral 125 MG, BID U 0 125 MG BID
103920503 10392050 3 C SILDENAFIL. SILDENAFIL 1 Oral UNK U 0 TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103920503 10392050 1 Pulmonary arterial hypertension
103920503 10392050 2 Pulmonary arterial hypertension
103920503 10392050 3 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
103920503 10392050 DE
103920503 10392050 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
103920503 10392050 Cardiac failure
103920503 10392050 Cardiac failure acute
103920503 10392050 Drug ineffective
103920503 10392050 Oedema peripheral

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
103920503 10392050 1 20140802 20140807 0
103920503 10392050 2 20140807 0
103920503 10392050 3 20140807 0