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
125419822 12541982 2 F 20160713 20160708 20160725 EXP US-ACTELION-A-US2015-114320 ACTELION 55.00 YR A F Y 0.00000 20160726 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
125419822 12541982 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID IP053P0101,IP060P0101, OP023P0101 21290 125 MG TABLET BID
125419822 12541982 2 C SILDENAFIL. SILDENAFIL 1 U 0
125419822 12541982 3 C COUMADIN WARFARIN SODIUM 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125419822 12541982 1 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
125419822 12541982 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125419822 12541982 Anaemia
125419822 12541982 Blood iron
125419822 12541982 Cardiac failure congestive
125419822 12541982 Chest pain
125419822 12541982 Diverticulitis intestinal haemorrhagic
125419822 12541982 Dyspnoea
125419822 12541982 Fatigue
125419822 12541982 Oxygen saturation decreased
125419822 12541982 Ulcer haemorrhage

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
125419822 12541982 1 20060531 0