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Selexipag side effects: what 25,665 FDA adverse event reports show

Selexipag · Uptravi, Uptravi Titration Pack · 1,128 reaction terms · 145,959 drug–reaction co-reports · data 2026-09-14
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Drug class

Prostacyclin Receptor Agonist

FDA label (Established Pharmacologic Class)

Brand names

Uptravi, Uptravi Titration Pack

openFDA label

Who reports

25,665 reports · 75% serious · 4,847 with death outcome · 74% female

openFDA FAERS counts, all years, deduplication not applied

Used for

UPTRAVI is a prostacyclin receptor agonist indicated for the treatment of pulmonary arterial hypertension (PAH, WHO Group I): In adults to delay disease progression and reduce the risk of hospitalization for PAH. ( 1.1 ) In pediatric patients aged 2 years and older. UPTRAVI reduces NT-proBNP and is expected to delay disease progression and reduce the risk of hospitalization for PAH.

FDA label, Indications and Usage

What it is

UPTRAVI contains selexipag, a prostacyclin receptor agonist.

FDA label, Description section

Boxed warning

None in the current label

How to read this page. FAERS is a spontaneous-reporting system: counts are not incidence rates and a signal is not proof of causation. Each reaction below is run through an automated screen — is the term in the FDA label (known), in the indications (the disease being treated), an administrative/coding term, or none of these (unlabeled)? That screen is mechanical text matching, not a causality assessment. The 30 hand-written Bradford Hill assessments are on the causality assessment page. Not medical advice.

Causality screen of the 40 strongest signals

Labeled adverse reaction 1Labeled (related wording) 1Likely indication confounding 3Reporting / coding artifact 3Lab value / disease marker 12Not in label — unassessed 20
What the badges mean

Strongest disproportionality signals

Flagged terms (PRR ≥ 2, χ² ≥ 4, n ≥ 10), ranked by PRR; infinite PRRs (no comparator reports) excluded. The EBGM column is a second, shrinkage-based estimate (MGPS) with its 5th percentile EB05 and the BCPNN IC025; a pair flagged by PRR alone is marked PRR-only and should be read as fragile. The strata column recomputes the PRR on serious reports only (and, for the 300 most-reported drugs, adjusted for age band), and flags pairs whose reports are unusually skewed by sex or come mostly from consumers. Each row also shows the PRR against the other drugs of the same FDA class, which removes most confounding by the condition being treated, and a calibrated p-value: on validation, known non-causes average an ROR of about 2, so significance is judged against that empirical null (✓ = p < 0.05 after calibration). 1,088 further terms are in the interactive explorer. Reaction links open the term's cross-drug page.

Show:
ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Right atrial pressure increased17217.1
127.1–370.9ROR 217.3 · calibrated p 2e-9 ✓
143.9 EB05 95.1 · IC025 +4.1
3/3 methods agree
Lab value / disease markerserious n=16not reported in cached trials
Cardiothoracic ratio increased11170.2
88.8–326.2ROR 170.3 · calibrated p 4e-8 ✓
113.5 EB05 67.6 · IC025 +3.3
3/3 methods agree
Lab value / disease markerserious n=11not reported in cached trials
Intracardiac pressure increased13143.3
79.4–258.5ROR 143.4 · calibrated p 8e-8 ✓
103.7 EB05 64.5 · IC025 +3.5
3/3 methods agree
Lab value / disease markerserious n=11not reported in cached trials
Atrial septal defect repair23126.8
81.7–196.7ROR 126.9 · calibrated p 7e-8 ✓
100.7 EB05 70.7 · IC025 +4.4
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=23 · 100% cliniciannot reported in cached trials
Cardiac output increased23126.8
81.7–196.7ROR 126.9 · calibrated p 7e-8 ✓
100.7 EB05 70.7 · IC025 +4.4
3/3 methods agree
Lab value / disease markerserious n=15NCT02558231: 1/119 (0.8%) on Selexipag (serious AE)
Pulmonary arterial wedge pressure increased22120.4
76.9–188.5ROR 120.5 · calibrated p 1e-7 ✓
96.3 EB05 67.1 · IC025 +4.3
3/3 methods agree
Lab value / disease markerserious n=20NCT01106014: 1/577 (0.2%) control (serious AE)
Walking distance test abnormal49118.8
88.0–160.3ROR 119.0 · calibrated p 6e-8 ✓
99.7 EB05 78.4 · IC025 +5.2
3/3 methods agree
Reporting / coding artifactserious n=42NCT01106014: 1/577 (0.2%) control (serious AE)
Bendopnoea26116.9
77.5–176.3ROR 117.0 · calibrated p 1e-7 ✓
95.2 EB05 68.3 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=23not reported in cached trials
Pulmonary veno-occlusive disease84112.1
89.2–140.8ROR 112.5 · calibrated p 7e-8 ✓
96.4 EB05 80.3 · IC025 +5.6
3/3 methods agree
Labeled adverse reaction
exact term
serious n=82 · 90% clinicianNCT01106014: 2/575 (0.3%) on Selexipag; 1/577 (0.2%) control (serious AE)
Pulmonary arterial pressure increased194109.9
94.7–127.7ROR 110.8 · calibrated p 6e-8 ✓
95.9 EB05 85.1 · IC025 +6.0
3/3 methods agree
Lab value / disease markerserious n=167NCT01106014: 1/577 (0.2%) control (serious AE)
Pulmonary arterial hypertension1,703108.1
103.0–113.6ROR 115.7 · calibrated p 4e-8 ✓
95.3 EB05 91.6 · IC025 +6.5
3/3 methods agree
Likely indication confounding
term in indications
serious PRR 74.2NCT01106014: 83/575 (14.4%) on Selexipag; 127/577 (22.0%) control (serious AE)
Ventilation perfusion mismatch31103.1
70.9–149.8ROR 103.2 · calibrated p 2e-7 ✓
86.7 EB05 64.0 · IC025 +4.6
3/3 methods agree
Not in label — unassessedserious n=29not reported in cached trials
Right-to-left cardiac shunt25102.1
67.4–154.8ROR 102.2 · calibrated p 3e-7 ✓
85.0 EB05 60.6 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=25 · 100% cliniciannot reported in cached trials
Transplant evaluation56100.6
76.2–132.8ROR 100.8 · calibrated p 2e-7 ✓
86.9 EB05 69.5 · IC025 +5.2
3/3 methods agree
Not in label — unassessedserious n=56NCT01106014: 1/575 (0.2%) on Selexipag (serious AE)
Pulmonary hypertensive crisis2688.3
58.9–132.3ROR 88.4 · calibrated p 8e-7 ✓
75.4 EB05 54.1 · IC025 +4.3
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=26 · 100% cliniciannot reported in cached trials
Oxygen consumption increased23088.1
77.0–100.9ROR 88.9 · calibrated p 3e-7 ✓
79.0 EB05 70.8 · IC025 +5.9
3/3 methods agree
Lab value / disease markerserious n=192not reported in cached trials
Right ventricular enlargement3085.6
58.8–124.7ROR 85.7 · calibrated p 8e-7 ✓
74.0 EB05 54.3 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=30not reported in cached trials
Pulmonary arterial pressure abnormal2784.5
56.9–125.6ROR 84.6 · calibrated p 1e-6 ✓
72.8 EB05 52.5 · IC025 +4.4
3/3 methods agree
Lab value / disease markerserious n=23 · 100% clinicianNCT01106014: 1/577 (0.2%) control (serious AE)
Cardiac failure high output2179.0
50.4–123.6ROR 79.0 · calibrated p 2e-6 ✓
67.7 EB05 46.7 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=21NCT02558231: 1/119 (0.8%) on Selexipag (serious AE)
Right ventricular failure60175.9
69.9–82.5ROR 77.7 · calibrated p 7e-7 ✓
69.3 EB05 64.8 · IC025 +5.9
3/3 methods agree
Not in label — unassessedserious PRR 53.3NCT01106014: 2/575 (0.3%) on Selexipag; 5/577 (0.9%) control (serious AE)
Catheterisation cardiac abnormal2272.5
46.9–112.2ROR 72.6 · calibrated p 3e-6 ✓
63.2 EB05 44.0 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=16NCT01106014: 3/575 (0.5%) on Selexipag; 1/577 (0.2%) control (serious AE)
Pulmonary endarterectomy1272.1
39.9–130.1ROR 72.1 · calibrated p 7e-6 ✓
60.2 EB05 36.7 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious n=12not reported in cached trials
Endarterectomy1766.4
40.5–108.9ROR 66.4 · calibrated p 7e-6 ✓
57.7 EB05 38.1 · IC025 +3.7
3/3 methods agree
Not in label — unassessedserious n=17not reported in cached trials
Paracentesis4259.5
43.5–81.4ROR 59.6 · calibrated p 7e-6 ✓
54.2 EB05 41.8 · IC025 +4.6
3/3 methods agree
Not in label — unassessedserious n=42 · 100% cliniciannot reported in cached trials
Mineral supplementation2956.9
39.1–82.9ROR 57.0 · calibrated p 1e-5 ✓
51.5 EB05 37.6 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=27not reported in cached trials
Brain natriuretic peptide abnormal1456.6
32.9–97.3ROR 56.6 · calibrated p 2e-5 ✓
49.6 EB05 31.4 · IC025 +3.3
3/3 methods agree
Lab value / disease markerserious n=14NCT01106014: 1/577 (0.2%) control (serious AE)
Crest syndrome1554.9
32.5–92.5ROR 54.9 · calibrated p 3e-5 ✓
48.5 EB05 31.2 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=15NCT01106014: 1/577 (0.2%) control (serious AE)
Right ventricular dilatation3654.8
39.1–76.7ROR 54.8 · calibrated p 1e-5 ✓
50.1 EB05 37.8 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=36not reported in cached trials
Catheter management5552.9
40.3–69.5ROR 53.0 · calibrated p 1e-5 ✓
48.9 EB05 39.0 · IC025 +4.7
3/3 methods agree
Reporting / coding artifactserious n=53 · 100% cliniciannot reported in cached trials
Pulmonary artery dilatation2152.6
33.9–81.8ROR 52.7 · calibrated p 2e-5 ✓
47.5 EB05 32.8 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=21NCT01106014: 1/577 (0.2%) control (serious AE)
Brain natriuretic peptide increased18150.9
43.8–59.1ROR 51.3 · calibrated p 1e-5 ✓
47.7 EB05 42.2 · IC025 +5.2
3/3 methods agree
Lab value / disease markerserious n=177NCT01106014: 1/577 (0.2%) control (serious AE)
Right ventricular systolic pressure increased1849.6
30.8–79.8ROR 49.6 · calibrated p 4e-5 ✓
44.7 EB05 29.9 · IC025 +3.6
3/3 methods agree
Lab value / disease markerserious n=17not reported in cached trials
Oxygen therapy9349.4
40.1–60.9ROR 49.6 · calibrated p 2e-5 ✓
46.2 EB05 38.8 · IC025 +4.9
3/3 methods agree
Reporting / coding artifactserious n=83NCT01106014: 1/575 (0.2%) on Selexipag (serious AE)
Systemic scleroderma4149.3
36.0–67.6ROR 49.4 · calibrated p 2e-5 ✓
45.6 EB05 35.0 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=40NCT02558231: 1/119 (0.8%) on Selexipag (serious AE)
Abdominal cavity drainage2449.0
32.5–74.0ROR 49.1 · calibrated p 3e-5 ✓
44.7 EB05 31.6 · IC025 +3.9
3/3 methods agree
Not in label — unassessedserious n=24not reported in cached trials
Pericardial drainage1346.7
26.7–81.7ROR 46.7 · calibrated p 7e-5 ✓
41.7 EB05 25.9 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=13NCT02558231: 1/127 (0.8%) control (serious AE)
N-terminal prohormone brain natriuretic peptide increased7344.8
35.4–56.7ROR 44.9 · calibrated p 3e-5 ✓
42.1 EB05 34.6 · IC025 +4.7
3/3 methods agree
Lab value / disease markerserious n=72 · 90% cliniciannot reported in cached trials
Catheterisation cardiac23144.8
39.2–51.1ROR 45.2 · calibrated p 3e-5 ✓
42.3 EB05 37.9 · IC025 +5.1
3/3 methods agree
Not in label — unassessedserious n=222NCT01106014: 3/575 (0.5%) on Selexipag; 1/577 (0.2%) control (serious AE)
Catheter site irritation1643.1
26.0–71.2ROR 43.1 · calibrated p 9e-5 ✓
39.2 EB05 25.6 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=16not reported in cached trials

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Selexipag as a study intervention. The right-hand column of the signal table shows whether each FAERS term was also recorded in these trials, with a real denominator (20 of 40 signal terms matched).

Caveats: trial populations, doses and follow-up differ from the reporting population; AE terms are sponsor-coded and matched here by wording; absence from a trial list means the term was not reported above the sponsor's frequency threshold, not that it cannot occur.

Most frequently reported reactions

By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Headache6,7408.9
8.7–9.1ROR 11.7 · calibrated p 0.019 ✓
8.8 EB05 8.6 · IC025 +3.1
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 9.4NCT01106014: 2/575 (0.3%) on Selexipag (serious AE)
Diarrhoea (diarrhea)5,1736.6
6.5–6.8ROR 8.0 · calibrated p 0.066
6.6 EB05 6.4 · IC025 +2.7
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 6.4NCT01106014: 3/575 (0.5%) on Selexipag; 3/577 (0.5%) control (serious AE)
Dyspnoea (shortness of breath)4,7746.9
6.8–7.1ROR 8.3 · calibrated p 0.059
6.9 EB05 6.7 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious PRR 6.2NCT01106014: 17/575 (3.0%) on Selexipag; 13/577 (2.3%) control (serious AE)
Nausea4,1034.3
4.1–4.4ROR 4.9 · calibrated p 0.247
4.2 EB05 4.1 · IC025 +2.0
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 4.5NCT01106014: 1/575 (0.2%) on Selexipag (serious AE)
Fatigue (tiredness)2,6012.7
2.6–2.8ROR 2.9 · calibrated p 0.648
2.7 EB05 2.6 · IC025 +1.4
3/3 methods agree
Not in label — unassessedserious PRR 3.0NCT01106014: 1/577 (0.2%) control (serious AE)
Death2,5282.4
2.3–2.5ROR 2.6 · calibrated p 0.791
2.4 EB05 2.3 · IC025 +1.2
3/3 methods agree
Outcome field, not a reactionserious PRR 1.8NCT01106014: 1/575 (0.2%) on Selexipag; 2/577 (0.3%) control (serious AE)
Dizziness2,3043.8
3.6–3.9ROR 4.1 · calibrated p 0.366
3.8 EB05 3.6 · IC025 +1.8
3/3 methods agree
Not in label — unassessedserious PRR 4.0NCT01106014: 1/575 (0.2%) on Selexipag (serious AE)
Pain2,2183.0
2.8–3.1ROR 3.1 · calibrated p 0.584
2.9 EB05 2.8 · IC025 +1.5
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 2.5NCT01106014: 5/575 (0.9%) on Selexipag; 4/577 (0.7%) control (serious AE)
Pain in extremity2,1295.9
5.7–6.2ROR 6.4 · calibrated p 0.128
5.9 EB05 5.7 · IC025 +2.5
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 5.5NCT01106014: 2/575 (0.3%) on Selexipag (serious AE)
Myalgia (muscle pain)1,9819.6
9.2–10.0ROR 10.3 · calibrated p 0.029 ✓
9.5 EB05 9.2 · IC025 +3.2
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 8.9NCT01106014: 2/575 (0.3%) on Selexipag (serious AE)
Vomiting1,9533.4
3.3–3.6ROR 3.6 · calibrated p 0.459
3.4 EB05 3.3 · IC025 +1.7
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.0NCT01106014: 2/575 (0.3%) on Selexipag; 2/577 (0.3%) control (serious AE)
Pneumonia (lung infection)1,8134.6
4.4–4.8ROR 4.9 · calibrated p 0.249
4.6 EB05 4.4 · IC025 +2.1
3/3 methods agree
Not in label — unassessedserious PRR 3.6NCT01106014: 1/577 (0.2%) control (serious AE)
Malaise (feeling unwell)1,8023.4
3.2–3.5ROR 3.5 · calibrated p 0.476
3.3 EB05 3.2 · IC025 +1.7
3/3 methods agree
Not in label — unassessedserious PRR 3.4not reported in cached trials
Hypotension (low blood pressure)1,7267.1
6.8–7.4ROR 7.5 · calibrated p 0.080
7.0 EB05 6.8 · IC025 +2.7
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 5.5NCT01106014: 3/575 (0.5%) on Selexipag; 3/577 (0.5%) control (serious AE)

Unlabeled candidate signals

These flagged terms were not found in the FDA label text and do not match an artifact pattern. They are the pairs that would merit a structured assessment (temporality, dose-response, biological plausibility, consistency across databases, trial or cohort evidence). The screen has not done that; string-matching misses label wording, and a strong PRR can still be stimulated reporting, co-medication, or the disease itself.

Want to assess one of these properly? The runbook describes the Bradford Hill / trial-evidence workflow used on the assessment page, and handoff_top1000_signals.csv lists the strongest unassessed pairs across all drugs.

Common questions

What are the most reported side effects of Selexipag?

In FDA FAERS, the most frequently co-reported reaction terms for Selexipag are headache, diarrhoea, dyspnoea, nausea, fatigue, pain in jaw. These are report counts, not rates: FAERS has no denominator, reporting is voluntary and uneven, and a term can be reported because of the illness being treated rather than the drug.

Does Selexipag have an FDA boxed warning?

No. The FDA label retrieved for Selexipag has no boxed warning; see the label's Warnings and Precautions for the recognised risks.

Do FAERS signals prove that Selexipag causes these side effects?

No. A disproportionality signal (PRR, ROR) means a reaction is reported more often with this drug than with others in the database. That can reflect a real effect, but also the disease being treated, stimulated reporting after news or litigation, co-medications, or how reports are coded. Causality needs temporality, dose-response, biological plausibility, consistency across data sources and, ideally, trial or cohort evidence. This page screens each term against the FDA label and ClinicalTrials.gov results; it does not establish causation.

Sources & methods

Page generated 2026-10-14. Label and PubChem text are retrieved automatically and may lag the current label; always check the current prescribing information. OpenPV is a beta research tool of the Open Source Medicine Foundation.