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
125325002 12532500 2 F 20160810 20160706 20160822 EXP US-ACTELION-A-US2016-138653 ACTELION 54.00 YR A F Y 0.00000 20160822 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
125325002 12532500 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID OP023P0101, OP026P0101 21290 125 MG TABLET BID
125325002 12532500 2 C RIOCIGUAT RIOCIGUAT 1 U 0
125325002 12532500 3 C REMODULIN TREPROSTINIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125325002 12532500 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
125325002 12532500 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125325002 12532500 Dizziness
125325002 12532500 Dyspnoea exertional
125325002 12532500 Hypotension
125325002 12532500 Localised infection
125325002 12532500 Oedema peripheral
125325002 12532500 Osteomyelitis
125325002 12532500 Wound

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
125325002 12532500 1 20081107 0