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
117421893 11742189 3 F 20160707 20151116 20160713 PER US-ACTELION PHARMACEUTICALS US, INC.-A-NJ2014-97265 ACTELION 56.00 YR A F Y 0.00000 20160713 OT 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
117421893 11742189 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID IP045P0101/EP099P0101/IP032P0101 21290 125 MG TABLET BID
117421893 11742189 2 SS TRACLEER BOSENTAN 1 Oral 125 MG, BID OP023P0101 21290 125 MG TABLET BID
117421893 11742189 3 C RIOCIGUAT RIOCIGUAT 1 U 0
117421893 11742189 4 C SILDENAFIL. SILDENAFIL 1 U 0
117421893 11742189 5 C COUMADIN WARFARIN SODIUM 1 U 0
117421893 11742189 6 C DIGOXIN. DIGOXIN 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117421893 11742189 1 Pulmonary arterial hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
117421893 11742189 Cough
117421893 11742189 Dizziness
117421893 11742189 Dyspnoea
117421893 11742189 Fatigue
117421893 11742189 Headache
117421893 11742189 Hernia
117421893 11742189 Hypotension
117421893 11742189 Nausea
117421893 11742189 Oedema
117421893 11742189 Palpitations
117421893 11742189 Vomiting

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
117421893 11742189 1 20101115 0