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
126235653 12623565 3 F 20160724 20160824 20160804 20160906 PER US-ACTELION-A-US2016-140281 ACTELION 43.00 YR A F Y 0.00000 20160907 MD 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
126235653 12623565 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID 21290 125 MG TABLET BID
126235653 12623565 2 SS UPTRAVI SELEXIPAG 1 Oral 600 MCG, BID U U 207947 600 UG TABLET BID
126235653 12623565 3 SS UPTRAVI SELEXIPAG 1 Oral 800 MCG, BID U U 207947 800 UG TABLET BID
126235653 12623565 4 C ADCIRCA TADALAFIL 1 U 0
126235653 12623565 5 C METOLAZONE. METOLAZONE 1 U 0
126235653 12623565 6 C POTASSIUM POTASSIUM 1 U 0
126235653 12623565 7 C DIGOXIN. DIGOXIN 1 U 0
126235653 12623565 8 C LASIX FUROSEMIDE 1 U 0
126235653 12623565 9 C SPIRONOLACTONE. SPIRONOLACTONE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126235653 12623565 1 Pulmonary arterial hypertension
126235653 12623565 2 Pulmonary arterial hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126235653 12623565 Fluid retention
126235653 12623565 Flushing
126235653 12623565 Headache
126235653 12623565 Myalgia
126235653 12623565 Nausea
126235653 12623565 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
126235653 12623565 1 20160116 0
126235653 12623565 2 20160706 0