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Treprostinil side effects: what 124,472 FDA adverse event reports show

Treprostinil · 1,239 reaction terms · 508,089 drug–reaction co-reports · data 2026-09-14
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Drug class

Prostacycline Vasodilator

FDA label (Established Pharmacologic Class)

Who reports

124,472 reports · 57% serious · 14,973 with death outcome · 74% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Treprostinil injection is a prostacyclin vasodilator indicated for: Treatment of pulmonary arterial hypertension (PAH; WHO Group 1) to diminish symptoms associated with exercise. Studies establishing effectiveness included patients with NYHA Functional.

FDA label, Indications and Usage

What it is

Treprostinil is a carboxylic acid and a carbotricyclic compound. It has a role as a cardiovascular drug, a vasodilator agent, an antihypertensive agent, a platelet aggregation inhibitor, a vitamin K antagonist and a human blood serum metabolite.

PubChem CID 6918140 (ChEBI)

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 2Labeled (related wording) 21Likely indication confounding 2Reporting / coding artifact 4Lab value / disease marker 3Not in label — unassessed 8
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). 1,199 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
Device wireless communication issue24413,408.8
4,294.7–41,864.6ROR 13,435.1 · calibrated p 5e-21 ✓
161.8 EB05 145.5 · IC025 +6.7
3/3 methods agree
Reporting / coding artifactserious n=72 · 100% consumernot reported in cached trials
Device maintenance issue453718.1
580.3–888.6ROR 720.7 · calibrated p 2e-15 ✓
134.1 EB05 124.1 · IC025 +6.7
3/3 methods agree
Reporting / coding artifactserious n=133 · 87% consumernot reported in cached trials
Unevaluable device issue56419.7
256.3–687.2ROR 419.8 · calibrated p 6e-12 ✓
114.5 EB05 91.5 · IC025 +5.4
3/3 methods agree
Not in label — unassessedserious n=32 · 100% consumernot reported in cached trials
Infusion site infection1,518348.1
318.6–380.3ROR 352.3 · calibrated p 2e-12 ✓
112.4 EB05 107.7 · IC025 +6.7
3/3 methods agree
Labeled adverse reaction
exact term
serious n=773NCT01027949: 11/894 (1.2%) on Treprostinil (serious AE)
Bendopnoea138339.6
253.6–454.6ROR 339.9 · calibrated p 8e-12 ✓
110.0 EB05 95.4 · IC025 +6.0
3/3 methods agree
Not in label — unassessedserious n=104 · 86% consumernot reported in cached trials
Administration site odour43221.5
140.2–350.1ROR 221.6 · calibrated p 1e-9 ✓
91.3 EB05 70.6 · IC025 +5.0
3/3 methods agree
Not in label — unassessed♀ 100% (drug 74%) · 100% consumernot reported in cached trials
Intracardiac pressure increased40143.4
93.8–219.0ROR 143.4 · calibrated p 3e-8 ✓
74.5 EB05 57.1 · IC025 +4.8
3/3 methods agree
Lab value / disease markerserious n=30 · 100% consumernot reported in cached trials
Infusion site pain5,691135.7
131.1–140.5ROR 142.2 · calibrated p 7e-9 ✓
74.9 EB05 73.3 · IC025 +6.2
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 116.5 · serious n=2,001 · 72% consumerNCT01027949: 28/894 (3.1%) on Treprostinil (serious AE)
Patient dissatisfaction with device102126.4
97.7–163.6ROR 126.5 · calibrated p 3e-8 ✓
71.1 EB05 60.2 · IC025 +5.4
3/3 methods agree
Not in label — unassessedserious n=32 · 100% consumernot reported in cached trials
Oxygen consumption increased967117.0
107.7–127.0ROR 117.9 · calibrated p 3e-8 ✓
68.7 EB05 65.2 · IC025 +5.9
3/3 methods agree
Lab value / disease markerserious n=551not reported in cached trials
Catheter site vesicles6892.7
68.8–124.7ROR 92.7 · calibrated p 4e-7 ✓
58.7 EB05 47.9 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=50 · ♀ 100% (drug 74%)not reported in cached trials
Walking distance test abnormal13691.5
74.2–112.8ROR 91.6 · calibrated p 3e-7 ✓
58.7 EB05 50.9 · IC025 +5.3
3/3 methods agree
Reporting / coding artifactserious n=67not reported in cached trials
Catheter site irritation10886.0
68.2–108.5ROR 86.1 · calibrated p 5e-7 ✓
56.3 EB05 48.0 · IC025 +5.2
3/3 methods agree
Not in label — unassessedserious n=79not reported in cached trials
Catheter site warmth4980.8
57.4–113.7ROR 80.8 · calibrated p 1e-6 ✓
53.5 EB05 42.0 · IC025 +4.7
3/3 methods agree
Not in label — unassessedserious n=34 · ♀ 100% (drug 74%)not reported in cached trials
Device infusion issue78178.7
72.2–85.6ROR 79.1 · calibrated p 6e-7 ✓
53.5 EB05 50.4 · IC025 +5.6
3/3 methods agree
Reporting / coding artifactserious n=286 · 75% consumernot reported in cached trials
Pulmonary hypertensive crisis8477.4
59.7–100.3ROR 77.4 · calibrated p 1e-6 ✓
52.4 EB05 43.6 · IC025 +5.0
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=84 · 100% cliniciannot reported in cached trials
Pulmonary arterial hypertension4,47574.5
72.0–77.2ROR 77.3 · calibrated p 7e-7 ✓
51.6 EB05 50.4 · IC025 +5.6
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
age-adj. PRR 66.9 · serious PRR 50.1NCT01027949: 3/894 (0.3%) on Treprostinil (serious AE)
Pulmonary arterial pressure abnormal8671.6
55.6–92.2ROR 71.7 · calibrated p 2e-6 ✓
49.7 EB05 41.5 · IC025 +4.9
3/3 methods agree
Lab value / disease markerserious n=55not reported in cached trials
Vascular device occlusion9768.0
53.7–86.2ROR 68.1 · calibrated p 2e-6 ✓
48.0 EB05 40.5 · IC025 +4.9
3/3 methods agree
Not in label — unassessedserious n=92not reported in cached trials

Clinical concept groups

MedDRA splits one clinical problem across several terms (e.g. "neutropenia", "neutrophil count decreased", "agranulocytosis"), which dilutes term-level signals. These rows count reports with any term in a concept group (an exact union, not a sum), compared with all other drugs. Groups are hand-built and listed in the methods.

ConceptReportsPRR 95% CIReading
Heart failure3,1413.02.9–3.1signal
Serious infection9,7082.12.1–2.2signal
Gi bleeding1,6401.51.4–1.6raised
Interstitial lung disease8511.51.4–1.6raised
Fall / fracture3,2531.41.4–1.5raised
Arrhythmia / qt1,5511.31.3–1.4raised
Anaemia2,2111.21.2–1.3raised
Venous thromboembolism1,0120.80.7–0.8lower than other drugs
Kidney injury1,9420.70.7–0.7lower than other drugs
Hyponatraemia3380.70.6–0.8lower than other drugs
Opportunistic infection5400.70.6–0.7lower than other drugs
Thrombocytopenia7830.60.6–0.6lower than other drugs
Depression8850.50.5–0.6lower than other drugs
Hypoglycaemia3010.50.5–0.6lower than other drugs
Myocardial infarction5960.50.5–0.5lower than other drugs
Stroke6710.50.4–0.5lower than other drugs

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Treprostinil 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 (11 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
Dyspnoea (shortness of breath)21,3626.6
6.5–6.6ROR 7.7 · calibrated p 0.074
6.3 EB05 6.3 · IC025 +2.6
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 5.9 · serious PRR 5.9NCT01027949: 41/894 (4.6%) on Treprostinil (serious AE)
Headache17,2834.7
4.7–4.8ROR 5.3 · calibrated p 0.200
4.6 EB05 4.6 · IC025 +2.2
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 4.2 · serious PRR 4.1NCT01027949: 7/894 (0.8%) on Treprostinil (serious AE)
Diarrhoea (diarrhea)13,8223.7
3.6–3.7ROR 4.0 · calibrated p 0.377
3.6 EB05 3.6 · IC025 +1.8
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 3.1 · serious PRR 3.1NCT01027949: 13/894 (1.5%) on Treprostinil (serious AE)
Nausea12,4132.7
2.6–2.7ROR 2.9 · calibrated p 0.675
2.6 EB05 2.6 · IC025 +1.4
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 2.4 · serious PRR 2.5NCT01027949: 11/894 (1.2%) on Treprostinil (serious AE)
Cough11,6597.3
7.1–7.4ROR 7.9 · calibrated p 0.069
7.0 EB05 6.9 · IC025 +2.8
3/3 methods agree
Not in label — unassessedage-adj. PRR 5.5 · serious PRR 5.2 · 74% consumerNCT01027949: 1/894 (0.1%) on Treprostinil (serious AE)
Dizziness9,5203.3
3.2–3.3ROR 3.4 · calibrated p 0.498
3.2 EB05 3.2 · IC025 +1.7
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 2.9 · serious PRR 2.9NCT01027949: 5/894 (0.6%) on Treprostinil (serious AE)
Fatigue (tiredness)9,4282.1
2.0–2.1ROR 2.1 · calibrated p 0.982
2.0 EB05 2.0 · IC025 +1.0
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 1.8 · serious PRR 1.9NCT01027949: 3/894 (0.3%) on Treprostinil (serious AE)
Death8,9891.8
1.7–1.8ROR 1.8 · calibrated p 0.843
1.8 EB05 1.7 · IC025 +0.8Outcome field, not a reactionage-adj. PRR 2.4 · serious PRR 1.8NCT01027949: 15/894 (1.7%) on Treprostinil (serious AE)
Vomiting6,3242.3
2.2–2.3ROR 2.4 · calibrated p 0.878
2.3 EB05 2.2 · IC025 +1.1
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 2.1 · serious PRR 2.0NCT01027949: 10/894 (1.1%) on Treprostinil (serious AE)
Hypotension (low blood pressure)5,7274.9
4.8–5.0ROR 5.1 · calibrated p 0.223
4.8 EB05 4.7 · IC025 +2.2
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 4.2 · serious PRR 4.0NCT01027949: 23/894 (2.6%) on Treprostinil (serious AE)
Infusion site pain5,691135.7
131.1–140.5ROR 142.2 · calibrated p 7e-9 ✓
74.9 EB05 73.3 · IC025 +6.2
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 116.5 · serious n=2,001 · 72% consumerNCT01027949: 28/894 (3.1%) on Treprostinil (serious AE)
Malaise (feeling unwell)5,5892.2
2.1–2.2ROR 2.2 · calibrated p 0.949
2.1 EB05 2.1 · IC025 +1.1
3/3 methods agree
Not in label — unassessedage-adj. PRR 2.2 · serious PRR 1.9not reported in cached trials
Fluid retention5,07218.5
18.0–19.1ROR 19.3 · calibrated p 0.002 ✓
16.8 EB05 16.4 · IC025 +4.0
3/3 methods agree
Not in label — unassessedage-adj. PRR 19.4 · serious PRR 19.0NCT01027949: 4/894 (0.4%) on Treprostinil (serious AE)
Oxygen saturation decreased4,95716.3
15.8–16.8ROR 16.9 · calibrated p 0.004 ✓
14.9 EB05 14.6 · IC025 +3.9
3/3 methods agree
Lab value / disease markerage-adj. PRR 13.1 · serious PRR 12.3not reported in cached trials

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.

✓ A hand-written Bradford Hill causality assessment exists for this drug: Treprostinil ↔ Headache.

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 Treprostinil?

In FDA FAERS, the most frequently co-reported reaction terms for Treprostinil are dyspnoea, headache, diarrhoea, nausea, cough, dizziness. 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 Treprostinil have an FDA boxed warning?

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

Do FAERS signals prove that Treprostinil 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.