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
125225803 12522580 3 F 201606 20160822 20160701 20160901 EXP US-ACTELION-A-NJ2016-134552 ACTELION 69.00 YR E F Y 0.00000 20160901 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
125225803 12522580 1 PS TRACLEER BOSENTAN 1 Oral 125 MG, BID OP021P0101,OP023P0101,OP026P0101 21290 125 MG TABLET BID
125225803 12522580 2 C TYVASO TREPROSTINIL 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125225803 12522580 1 Pulmonary hypertension

Outcome of event

Event ID CASEID OUTC COD
125225803 12522580 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125225803 12522580 Arthritis
125225803 12522580 Infection
125225803 12522580 Joint swelling
125225803 12522580 Oedema peripheral
125225803 12522580 Pain in extremity
125225803 12522580 Pyrexia

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
125225803 12522580 1 20150911 0