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
124357662 12435766 2 F 20160728 20160603 20160810 EXP US-ACTELION-A-NJ2016-137136 ACTELION 77.00 YR E F Y 0.00000 20160810 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
124357662 12435766 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID OP023P0101 21290 125 MG TABLET BID
124357662 12435766 2 SS ADCIRCA TADALAFIL 1 Unknown 20 MG, QD 0 20 MG QD
124357662 12435766 3 SS COUMADIN WARFARIN SODIUM 1 Unknown 3-6 MG, QD U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124357662 12435766 1 Pulmonary arterial hypertension
124357662 12435766 2 Product used for unknown indication
124357662 12435766 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124357662 12435766 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124357662 12435766 Diverticulum
124357662 12435766 Gastrointestinal haemorrhage
124357662 12435766 Headache

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
124357662 12435766 1 20060505 0