Selexipag side effects: what 25,665 FDA adverse event reports show
Drug class
Prostacyclin Receptor Agonist
Brand names
Uptravi, Uptravi Titration Pack
Who reports
25,665 reports · 75% serious · 4,847 with death outcome · 74% female
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.
What it is
UPTRAVI contains selexipag, a prostacyclin receptor agonist.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- Labeled adverse reaction The exact term appears in the label's warnings or adverse-reactions sections: a known, expected effect. The FAERS signal confirms the label rather than discovering anything.
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- Likely indication confounding The term appears in the label's indications: reports probably describe the disease being treated (or its progression), not a drug effect. Classic confounding by indication.
- Reporting / coding artifact An administrative, monitoring or exposure term (product issue, off-label use, 'test normal', overdose...). Not a biological reaction; a high PRR here reflects how reports are coded.
- Lab value / disease marker A laboratory result, investigation or disease-activity marker (antibody positive, CRP abnormal, swollen joint count) not described in the label. These usually mirror the monitored disease or testing protocol rather than a drug effect; not screened further.
- Not in label — unassessed Not found in the label text, not an artifact pattern. This is a genuine candidate for a formal causality assessment (Bradford Hill / WHO-UMC); it has NOT had one here.
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.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Right atrial pressure increased | 17 | 217.1 127.1–370.9ROR 217.3 · calibrated p 2e-9 ✓ | 143.9 EB05 95.1 · IC025 +4.1 3/3 methods agree | Lab value / disease marker | serious n=16 | not reported in cached trials |
| Cardiothoracic ratio increased | 11 | 170.2 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 marker | serious n=11 | not reported in cached trials |
| Intracardiac pressure increased | 13 | 143.3 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 marker | serious n=11 | not reported in cached trials |
| Atrial septal defect repair | 23 | 126.8 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% clinician | not reported in cached trials |
| Cardiac output increased | 23 | 126.8 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 marker | serious n=15 | NCT02558231: 1/119 (0.8%) on Selexipag (serious AE) |
| Pulmonary arterial wedge pressure increased | 22 | 120.4 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 marker | serious n=20 | NCT01106014: 1/577 (0.2%) control (serious AE) |
| Walking distance test abnormal | 49 | 118.8 88.0–160.3ROR 119.0 · calibrated p 6e-8 ✓ | 99.7 EB05 78.4 · IC025 +5.2 3/3 methods agree | Reporting / coding artifact | serious n=42 | NCT01106014: 1/577 (0.2%) control (serious AE) |
| Bendopnoea | 26 | 116.9 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 — unassessed | serious n=23 | not reported in cached trials |
| Pulmonary veno-occlusive disease | 84 | 112.1 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% clinician | NCT01106014: 2/575 (0.3%) on Selexipag; 1/577 (0.2%) control (serious AE) |
| Pulmonary arterial pressure increased | 194 | 109.9 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 marker | serious n=167 | NCT01106014: 1/577 (0.2%) control (serious AE) |
| Pulmonary arterial hypertension | 1,703 | 108.1 103.0–113.6ROR 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 74.2 | NCT01106014: 83/575 (14.4%) on Selexipag; 127/577 (22.0%) control (serious AE) |
| Ventilation perfusion mismatch | 31 | 103.1 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 — unassessed | serious n=29 | not reported in cached trials |
| Right-to-left cardiac shunt | 25 | 102.1 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 — unassessed | serious n=25 · 100% clinician | not reported in cached trials |
| Transplant evaluation | 56 | 100.6 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 — unassessed | serious n=56 | NCT01106014: 1/575 (0.2%) on Selexipag (serious AE) |
| Pulmonary hypertensive crisis | 26 | 88.3 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% clinician | not reported in cached trials |
| Oxygen consumption increased | 230 | 88.1 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 marker | serious n=192 | not reported in cached trials |
| Right ventricular enlargement | 30 | 85.6 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 — unassessed | serious n=30 | not reported in cached trials |
| Pulmonary arterial pressure abnormal | 27 | 84.5 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 marker | serious n=23 · 100% clinician | NCT01106014: 1/577 (0.2%) control (serious AE) |
| Cardiac failure high output | 21 | 79.0 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 — unassessed | serious n=21 | NCT02558231: 1/119 (0.8%) on Selexipag (serious AE) |
| Pain in jaw | 2,434 | 76.7 73.7–79.8ROR 84.6 · calibrated p 4e-7 ✓ | 70.0 EB05 67.7 · IC025 +6.0 3/3 methods agree | Labeled (related wording) related wording | serious PRR 59.8 | NCT01106014: 5/575 (0.9%) on Selexipag; 4/577 (0.7%) control (serious AE) |
| Right ventricular failure | 601 | 75.9 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 — unassessed | serious PRR 53.3 | NCT01106014: 2/575 (0.3%) on Selexipag; 5/577 (0.9%) control (serious AE) |
| Catheterisation cardiac abnormal | 22 | 72.5 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 — unassessed | serious n=16 | NCT01106014: 3/575 (0.5%) on Selexipag; 1/577 (0.2%) control (serious AE) |
| Pulmonary endarterectomy | 12 | 72.1 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 — unassessed | serious n=12 | not reported in cached trials |
| Endarterectomy | 17 | 66.4 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 — unassessed | serious n=17 | not reported in cached trials |
| Paracentesis | 42 | 59.5 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 — unassessed | serious n=42 · 100% clinician | not reported in cached trials |
| Mineral supplementation | 29 | 56.9 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 — unassessed | serious n=27 | not reported in cached trials |
| Brain natriuretic peptide abnormal | 14 | 56.6 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 marker | serious n=14 | NCT01106014: 1/577 (0.2%) control (serious AE) |
| Crest syndrome | 15 | 54.9 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 — unassessed | serious n=15 | NCT01106014: 1/577 (0.2%) control (serious AE) |
| Right ventricular dilatation | 36 | 54.8 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 — unassessed | serious n=36 | not reported in cached trials |
| Catheter management | 55 | 52.9 40.3–69.5ROR 53.0 · calibrated p 1e-5 ✓ | 48.9 EB05 39.0 · IC025 +4.7 3/3 methods agree | Reporting / coding artifact | serious n=53 · 100% clinician | not reported in cached trials |
| Pulmonary artery dilatation | 21 | 52.6 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 — unassessed | serious n=21 | NCT01106014: 1/577 (0.2%) control (serious AE) |
| Brain natriuretic peptide increased | 181 | 50.9 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 marker | serious n=177 | NCT01106014: 1/577 (0.2%) control (serious AE) |
| Right ventricular systolic pressure increased | 18 | 49.6 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 marker | serious n=17 | not reported in cached trials |
| Oxygen therapy | 93 | 49.4 40.1–60.9ROR 49.6 · calibrated p 2e-5 ✓ | 46.2 EB05 38.8 · IC025 +4.9 3/3 methods agree | Reporting / coding artifact | serious n=83 | NCT01106014: 1/575 (0.2%) on Selexipag (serious AE) |
| Systemic scleroderma | 41 | 49.3 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 — unassessed | serious n=40 | NCT02558231: 1/119 (0.8%) on Selexipag (serious AE) |
| Abdominal cavity drainage | 24 | 49.0 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 — unassessed | serious n=24 | not reported in cached trials |
| Pericardial drainage | 13 | 46.7 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 — unassessed | serious n=13 | NCT02558231: 1/127 (0.8%) control (serious AE) |
| N-terminal prohormone brain natriuretic peptide increased | 73 | 44.8 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 marker | serious n=72 · 90% clinician | not reported in cached trials |
| Catheterisation cardiac | 231 | 44.8 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 — unassessed | serious n=222 | NCT01106014: 3/575 (0.5%) on Selexipag; 1/577 (0.2%) control (serious AE) |
| Catheter site irritation | 16 | 43.1 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 — unassessed | serious n=16 | not 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).
- NCT01106014 — Selexipag (ACT-293987) in Pulmonary Arterial Hypertension (N=1156, PHASE3; 379 AE terms posted; arms: Selexipag; Placebo)
- NCT02558231 — The Efficacy and Safety of Initial Triple Versus Initial Dual Oral Combination Therapy in Patients With Newly (N=247, PHASE3; 244 AE terms posted; arms: Triple Oral Therapy (Macitentan, Tadalaf; Double Oral Therapy (Macitentan, Tadalaf)
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.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Headache | 6,740 | 8.9 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 9.4 | NCT01106014: 2/575 (0.3%) on Selexipag (serious AE) |
| Diarrhoea (diarrhea) | 5,173 | 6.6 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 6.4 | NCT01106014: 3/575 (0.5%) on Selexipag; 3/577 (0.5%) control (serious AE) |
| Dyspnoea (shortness of breath) | 4,774 | 6.9 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 — unassessed | serious PRR 6.2 | NCT01106014: 17/575 (3.0%) on Selexipag; 13/577 (2.3%) control (serious AE) |
| Nausea | 4,103 | 4.3 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 4.5 | NCT01106014: 1/575 (0.2%) on Selexipag (serious AE) |
| Fatigue (tiredness) | 2,601 | 2.7 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 — unassessed | serious PRR 3.0 | NCT01106014: 1/577 (0.2%) control (serious AE) |
| Death | 2,528 | 2.4 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 reaction | serious PRR 1.8 | NCT01106014: 1/575 (0.2%) on Selexipag; 2/577 (0.3%) control (serious AE) |
| Pain in jaw | 2,434 | 76.7 73.7–79.8ROR 84.6 · calibrated p 4e-7 ✓ | 70.0 EB05 67.7 · IC025 +6.0 3/3 methods agree | Labeled (related wording) related wording | serious PRR 59.8 | NCT01106014: 5/575 (0.9%) on Selexipag; 4/577 (0.7%) control (serious AE) |
| Dizziness | 2,304 | 3.8 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 — unassessed | serious PRR 4.0 | NCT01106014: 1/575 (0.2%) on Selexipag (serious AE) |
| Pain | 2,218 | 3.0 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 2.5 | NCT01106014: 5/575 (0.9%) on Selexipag; 4/577 (0.7%) control (serious AE) |
| Pain in extremity | 2,129 | 5.9 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 5.5 | NCT01106014: 2/575 (0.3%) on Selexipag (serious AE) |
| Myalgia (muscle pain) | 1,981 | 9.6 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 8.9 | NCT01106014: 2/575 (0.3%) on Selexipag (serious AE) |
| Vomiting | 1,953 | 3.4 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 3.0 | NCT01106014: 2/575 (0.3%) on Selexipag; 2/577 (0.3%) control (serious AE) |
| Pneumonia (lung infection) | 1,813 | 4.6 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 — unassessed | serious PRR 3.6 | NCT01106014: 1/577 (0.2%) control (serious AE) |
| Malaise (feeling unwell) | 1,802 | 3.4 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 — unassessed | serious PRR 3.4 | not reported in cached trials |
| Hypotension (low blood pressure) | 1,726 | 7.1 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 5.5 | NCT01106014: 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.
- Bendopnoea — n=26, PRR 116.9
- Ventilation perfusion mismatch — n=31, PRR 103.1
- Right-to-left cardiac shunt — n=25, PRR 102.1
- Transplant evaluation — n=56, PRR 100.6 (also seen in trial arm)
- Right ventricular enlargement — n=30, PRR 85.6
- Cardiac failure high output — n=21, PRR 79.0 (also seen in trial arm)
- Right ventricular failure — n=601, PRR 75.9 (also seen in trial arm)
- Catheterisation cardiac abnormal — n=22, PRR 72.5 (also seen in trial arm)
- Paracentesis — n=42, PRR 59.5
- Mineral supplementation — n=29, PRR 56.9
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
- FDA label via openFDA (set ID a7a23b87-f892-4e2c-8e2e-ebf841220f90, effective 20260528; matched on
openfda.generic_name.exact:"SELEXIPAG") - Bayesian shrinkage measures computed offline over all 1,317,300 cached pairs: BCPNN information component (IC, with Norén closed-form IC025) and MGPS empirical-Bayes geometric mean (EBGM, EB05) with a two-component gamma prior fitted by maximum marginal likelihood (α₁=0.57, β₁=0.02, α₂=1.42, β₂=0.70, w=0.17); unstratified
- FAERS pair statistics from the OpenPV build of 2026-09-14 (openFDA
count=aggregation, fieldpatient.drug.openfda.generic_name.exact, 1,128 reaction terms, min 3 co-reports); PRR/ROR with 95% CI, chi-square with Yates correction - Serious-only and stratified counts (serious:1, patient.patientsex, primarysource.qualification) from openFDA count queries; serious-only PRR uses the drug serious report total and the term global serious total (N_serious=11,882,979); strata shown only when n ≥ 20
- Seriousness and sex counts from openFDA
count=serious,patient.patientsex,seriousnessdeath - ClinicalTrials.gov API v2 (query
SELEXIPAG, results-bearing studies sorted by enrollment)
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.