BOXED WARNING Hepatotoxicity — measure aminotransferases before and monthly during treatment; embryo-fetal toxicity — contraindicated in pregnancy, exclude pregnancy before start; available only through a restricted REMS program.
FDA dosing
Population
Start
Target
Max
Pulmonary arterial hypertension (WHO Group 1)
>12 yr and >40 kg
62.5 mg BID
125 mg BID (after 4 wk)
125 mg BID
Pulmonary arterial hypertension
≤12 yr (weight-based per Table 1)
weight-based (Table 1)
weight-based (Table 1)
weight-based (Table 1)
Titration Increase to maintenance dose after 4 weeks
Renal No adjustment needed
Hepatic Not studied in severe impairment (Child-Pugh C); exposure increased in moderate (Child-Pugh B) — avoid in moderate-to-severe impairment; reduce dose or discontinue if aminotransferases >3× ULN
Instructions
Enroll in Bosentan REMS; monthly liver aminotransferase monitoring; exclude pregnancy before initiation
May be taken with or without food
Reduce dose and closely monitor if aminotransferases >3× ULN
Pulmonary veno-occlusive disease — consider if pulmonary edema occurs
Decreased sperm counts
Decreased hemoglobin/hematocrit — monitor at 1 and 3 months, then every 3 months
Adverse reactions
Respiratory tract infection
Anemia
Pregnancy Contraindicated — may cause fetal harm/birth defects (boxed); exclude pregnancy before start and use reliable contraception
Lactation Discontinue either breastfeeding or bosentan
Cost
Bosentan (TRACLEER)
Strength
#/mo
generic $/mo
CostPlus
32 mg
tab
60 BID
not offered
62.5 mg
tab
60 BID
not offered
125 mg
tab
60 BID
not offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Bosentan is dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.
Defining liabilityGenerally tolerated at therapeutic doses; clinically important risks are agent-specific and increase with interactions or organ impairment.