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
119332184 11933218 4 F 2014 20160628 20160121 20160712 EXP FR-ACTELION-A-CH2016-130139 ACTELION 86.00 YR E F Y 0.00000 20160712 MD FR FR

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
119332184 11933218 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID 21290 125 MG TABLET BID
119332184 11933218 2 SS TRACLEER BOSENTAN 1 Oral 62.5 MG, BID 21290 62.5 MG TABLET BID
119332184 11933218 3 C LASILIX FUROSEMIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119332184 11933218 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
119332184 11933218 DE
119332184 11933218 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119332184 11933218 Cardiac failure
119332184 11933218 Dyspnoea exertional
119332184 11933218 General physical health deterioration
119332184 11933218 Haematemesis
119332184 11933218 Hypertension
119332184 11933218 Pulmonary arterial hypertension
119332184 11933218 Transfusion

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
119332184 11933218 1 20140415 20141217 0
119332184 11933218 2 20140114 20140414 0