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Treprostinil vs Selexipag: side effects in FDA adverse event reports

How to read this page. FAERS report counts have no denominator; the comparison is of reporting patterns, not of risk. Signals are screened against each FDA label (badges) but not causally assessed. Not medical advice.

At a glance

TreprostinilSelexipag
Drug classProstacycline VasodilatorProstacyclin Receptor Agonist
Brand names–Uptravi, Uptravi Titration Pack
FAERS reports124,47225,665
Serious57%75%
Death outcome14,9734,847
Boxed warningNoNo

Signals both drugs share

ReactionTreprostinilSelexipagLabel screen (A / B)
Pulmonary arterial hypertension4,475 · PRR 74.51,703 · PRR 108.1Likely indication confounding / Likely indication confounding
Bendopnoea138 · PRR 339.626 · PRR 116.9Not in label — unassessed / Not in label — unassessed
Catheter site irritation108 · PRR 86.016 · PRR 43.1Not in label — unassessed / Not in label — unassessed
Pulmonary hypertensive crisis84 · PRR 77.426 · PRR 88.3Likely indication confounding / Likely indication confounding

Labeled signals distinctive to Treprostinil

Labeled signals distinctive to Selexipag

Common questions

Which has more reported side effects, Treprostinil or Selexipag?

Treprostinil has 124,472 FAERS reports and Selexipag 25,665. More reports does not mean more dangerous: volume follows how widely and how long a drug has been used, prescription vs over-the-counter status, and publicity. The seriousness share (57% vs 75%) is a better like-for-like signal of the kind of problems reported.

Which side effects do Treprostinil and Selexipag share?

Both drugs carry disproportionality signals for pulmonary arterial hypertension, bendopnoea, catheter site irritation, pulmonary hypertensive crisis. Shared signals often reflect a shared drug class or the condition both are used for.

Is Treprostinil or Selexipag safer?

FAERS cannot answer that: it has no denominator and no comparator. Use this page to see which risks are already on each label and which signals are unlabeled, then check the prescribing information and your clinician for your situation.

Sources: openFDA FAERS pair statistics (OpenPV build 2026-09-14), FDA labels via openFDA, openFDA count queries for seriousness and deaths. Pair chosen because it is a commonly searched comparison. Generated 2026-10-08.