Treprostinil side effects: what 124,472 FDA adverse event reports show
Drug class
Prostacycline Vasodilator
Who reports
124,472 reports · 57% serious · 14,973 with death outcome · 74% female
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.
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.
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). 1,199 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 |
|---|---|---|---|---|---|---|
| Device wireless communication issue | 244 | 13,408.8 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 artifact | serious n=72 · 100% consumer | not reported in cached trials |
| Infusion site pustule | 108 | 1,047.4 628.1–1,746.6ROR 1,048.3 · calibrated p 9e-16 ✓ | 139.8 EB05 119.0 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=26 · 76% consumer | not reported in cached trials |
| Device maintenance issue | 453 | 718.1 580.3–888.6ROR 720.7 · calibrated p 2e-15 ✓ | 134.1 EB05 124.1 · IC025 +6.7 3/3 methods agree | Reporting / coding artifact | serious n=133 · 87% consumer | not reported in cached trials |
| Unevaluable device issue | 56 | 419.7 256.3–687.2ROR 419.8 · calibrated p 6e-12 ✓ | 114.5 EB05 91.5 · IC025 +5.4 3/3 methods agree | Not in label — unassessed | serious n=32 · 100% consumer | not reported in cached trials |
| Infusion site infection | 1,518 | 348.1 318.6–380.3ROR 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=773 | NCT01027949: 11/894 (1.2%) on Treprostinil (serious AE) |
| Bendopnoea | 138 | 339.6 253.6–454.6ROR 339.9 · calibrated p 8e-12 ✓ | 110.0 EB05 95.4 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=104 · 86% consumer | not reported in cached trials |
| Administration site odour | 43 | 221.5 140.2–350.1ROR 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% consumer | not reported in cached trials |
| Infusion site discharge | 915 | 195.1 177.4–214.7ROR 196.6 · calibrated p 5e-10 ✓ | 89.7 EB05 85.0 · IC025 +6.3 3/3 methods agree | Labeled (related wording) related wording | serious n=256 · 76% consumer | not reported in cached trials |
| Infusion site scab | 64 | 185.1 129.5–264.5ROR 185.2 · calibrated p 2e-9 ✓ | 85.6 EB05 69.4 · IC025 +5.3 3/3 methods agree | Labeled (related wording) related wording | 100% consumer | not reported in cached trials |
| Infusion site warmth | 584 | 159.7 142.5–178.9ROR 160.4 · calibrated p 3e-9 ✓ | 81.4 EB05 76.0 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=182 · 73% consumer | not reported in cached trials |
| Infusion site irritation | 585 | 150.2 134.3–168.0ROR 150.9 · calibrated p 5e-9 ✓ | 78.9 EB05 73.7 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=200 · 77% consumer | not reported in cached trials |
| Infusion site cellulitis | 236 | 147.9 124.1–176.3ROR 148.2 · calibrated p 6e-9 ✓ | 78.0 EB05 70.0 · IC025 +5.9 3/3 methods agree | Labeled (related wording) related wording | serious n=188 | NCT01027949: 8/894 (0.9%) on Treprostinil (serious AE) |
| Intracardiac pressure increased | 40 | 143.4 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 marker | serious n=30 · 100% consumer | not reported in cached trials |
| Infusion site induration | 651 | 142.7 128.5–158.5ROR 143.5 · calibrated p 7e-9 ✓ | 76.8 EB05 72.0 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=203 · 75% consumer | not reported in cached trials |
| Infusion site injury | 77 | 142.6 105.1–193.5ROR 142.7 · calibrated p 1e-8 ✓ | 75.5 EB05 62.4 · IC025 +5.3 3/3 methods agree | Labeled (related wording) related wording | 100% consumer | NCT01027949: 37/894 (4.1%) on Treprostinil (serious AE) |
| Infusion site pain | 5,691 | 135.7 131.1–140.5ROR 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% consumer | NCT01027949: 28/894 (3.1%) on Treprostinil (serious AE) |
| Infusion site haemorrhage | 1,402 | 128.6 120.0–137.9ROR 130.1 · calibrated p 1e-8 ✓ | 72.6 EB05 69.5 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=420 · 78% consumer | NCT01027949: 12/894 (1.3%) on Treprostinil (serious AE) |
| Infusion site oedema | 356 | 127.0 110.6–145.9ROR 127.4 · calibrated p 2e-8 ✓ | 71.9 EB05 65.9 · IC025 +5.9 3/3 methods agree | Labeled (related wording) related wording | serious n=105 · 76% consumer | NCT01027949: 5/894 (0.6%) on Treprostinil (serious AE) |
| Patient dissatisfaction with device | 102 | 126.4 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 — unassessed | serious n=32 · 100% consumer | not reported in cached trials |
| Infusion site abscess | 200 | 119.5 99.6–143.3ROR 119.7 · calibrated p 4e-8 ✓ | 69.2 EB05 61.6 · IC025 +5.7 3/3 methods agree | Labeled (related wording) related wording | serious n=142 | not reported in cached trials |
| Infusion site inflammation | 277 | 117.4 100.6–136.9ROR 117.7 · calibrated p 4e-8 ✓ | 68.7 EB05 62.1 · IC025 +5.7 3/3 methods agree | Labeled (related wording) related wording | serious n=104 · 77% consumer | NCT01027949: 1/894 (0.1%) on Treprostinil (serious AE) |
| Oxygen consumption increased | 967 | 117.0 107.7–127.0ROR 117.9 · calibrated p 3e-8 ✓ | 68.7 EB05 65.2 · IC025 +5.9 3/3 methods agree | Lab value / disease marker | serious n=551 | not reported in cached trials |
| Infusion site erythema | 3,287 | 110.7 106.0–115.7ROR 113.7 · calibrated p 4e-8 ✓ | 66.6 EB05 64.7 · IC025 +6.0 3/3 methods agree | Labeled (related wording) related wording | serious n=1,097 · 74% consumer | not reported in cached trials |
| Infusion site vesicles | 198 | 102.7 86.0–122.6ROR 102.8 · calibrated p 1e-7 ✓ | 63.3 EB05 56.2 · IC025 +5.5 3/3 methods agree | Labeled (related wording) related wording | serious n=54 · 74% consumer | not reported in cached trials |
| Catheter site vesicles | 68 | 92.7 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 — unassessed | serious n=50 · ♀ 100% (drug 74%) | not reported in cached trials |
| Walking distance test abnormal | 136 | 91.5 74.2–112.8ROR 91.6 · calibrated p 3e-7 ✓ | 58.7 EB05 50.9 · IC025 +5.3 3/3 methods agree | Reporting / coding artifact | serious n=67 | not reported in cached trials |
| Catheter site pruritus | 298 | 86.8 75.4–99.9ROR 87.0 · calibrated p 4e-7 ✓ | 57.0 EB05 51.8 · IC025 +5.5 3/3 methods agree | Labeled (related wording) related wording | serious n=224 | not reported in cached trials |
| Infusion site discolouration | 293 | 86.7 75.3–99.9ROR 86.9 · calibrated p 4e-7 ✓ | 57.0 EB05 51.7 · IC025 +5.5 3/3 methods agree | Labeled (related wording) related wording | serious n=77 · 73% consumer | not reported in cached trials |
| Catheter site irritation | 108 | 86.0 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 — unassessed | serious n=79 | not reported in cached trials |
| Infusion site hypersensitivity | 39 | 82.4 56.1–121.1ROR 82.5 · calibrated p 1e-6 ✓ | 53.9 EB05 41.1 · IC025 +4.5 3/3 methods agree | Labeled (related wording) related wording | 100% consumer | NCT01027949: 2/894 (0.2%) on Treprostinil (serious AE) |
| Catheter site warmth | 49 | 80.8 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 — unassessed | serious n=34 · ♀ 100% (drug 74%) | not reported in cached trials |
| Device infusion issue | 781 | 78.7 72.2–85.6ROR 79.1 · calibrated p 6e-7 ✓ | 53.5 EB05 50.4 · IC025 +5.6 3/3 methods agree | Reporting / coding artifact | serious n=286 · 75% consumer | not reported in cached trials |
| Pulmonary hypertensive crisis | 84 | 77.4 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% clinician | not reported in cached trials |
| Pulmonary arterial hypertension | 4,475 | 74.5 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 50.1 | NCT01027949: 3/894 (0.3%) on Treprostinil (serious AE) |
| Infusion site swelling | 1,871 | 73.3 69.5–77.4ROR 74.4 · calibrated p 1e-6 ✓ | 51.0 EB05 49.1 · IC025 +5.6 3/3 methods agree | Labeled (related wording) related wording | serious n=627 · 72% consumer | not reported in cached trials |
| Infusion site nodule | 270 | 71.9 62.3–83.0ROR 72.1 · calibrated p 1e-6 ✓ | 50.2 EB05 45.4 · IC025 +5.3 3/3 methods agree | Labeled (related wording) related wording | serious n=67 · 78% consumer | not reported in cached trials |
| Pulmonary arterial pressure abnormal | 86 | 71.6 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 marker | serious n=55 | not reported in cached trials |
| Acute right ventricular failure | 49 | 69.6 49.9–97.2ROR 69.7 · calibrated p 3e-6 ✓ | 48.4 EB05 38.0 · IC025 +4.6 3/3 methods agree | Labeled (related wording) related wording | serious n=49 · ♀ 100% (drug 74%) · 100% clinician | NCT01027949: 129/894 (14.4%) on Treprostinil (serious AE) |
| Infusion site discomfort | 295 | 68.1 59.5–78.0ROR 68.3 · calibrated p 2e-6 ✓ | 48.4 EB05 43.9 · IC025 +5.3 3/3 methods agree | Labeled (related wording) related wording | serious n=105 · 74% consumer | NCT01027949: 2/894 (0.2%) on Treprostinil (serious AE) |
| Vascular device occlusion | 97 | 68.0 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 — unassessed | serious n=92 | not 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.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Heart failure | 3,141 | 3.02.9–3.1 | signal |
| Serious infection | 9,708 | 2.12.1–2.2 | signal |
| Gi bleeding | 1,640 | 1.51.4–1.6 | raised |
| Interstitial lung disease | 851 | 1.51.4–1.6 | raised |
| Fall / fracture | 3,253 | 1.41.4–1.5 | raised |
| Arrhythmia / qt | 1,551 | 1.31.3–1.4 | raised |
| Anaemia | 2,211 | 1.21.2–1.3 | raised |
| Venous thromboembolism | 1,012 | 0.80.7–0.8 | lower than other drugs |
| Kidney injury | 1,942 | 0.70.7–0.7 | lower than other drugs |
| Hyponatraemia | 338 | 0.70.6–0.8 | lower than other drugs |
| Opportunistic infection | 540 | 0.70.6–0.7 | lower than other drugs |
| Thrombocytopenia | 783 | 0.60.6–0.6 | lower than other drugs |
| Depression | 885 | 0.50.5–0.6 | lower than other drugs |
| Hypoglycaemia | 301 | 0.50.5–0.6 | lower than other drugs |
| Myocardial infarction | 596 | 0.50.5–0.5 | lower than other drugs |
| Stroke | 671 | 0.50.4–0.5 | lower 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).
- NCT01027949 — An Open-Label Extension Trial of UT-15C Sustained-release (SR) in Subjects With Pulmonary Arterial Hypertensio (N=894, PHASE3; 460 AE terms posted; arms: Oral Treprostinil)
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 |
|---|---|---|---|---|---|---|
| Dyspnoea (shortness of breath) | 21,362 | 6.6 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 5.9 | NCT01027949: 41/894 (4.6%) on Treprostinil (serious AE) |
| Headache | 17,283 | 4.7 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 4.1 | NCT01027949: 7/894 (0.8%) on Treprostinil (serious AE) |
| Diarrhoea (diarrhea) | 13,822 | 3.7 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 3.1 | NCT01027949: 13/894 (1.5%) on Treprostinil (serious AE) |
| Nausea | 12,413 | 2.7 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 2.5 | NCT01027949: 11/894 (1.2%) on Treprostinil (serious AE) |
| Cough | 11,659 | 7.3 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 — unassessed | age-adj. PRR 5.5 · serious PRR 5.2 · 74% consumer | NCT01027949: 1/894 (0.1%) on Treprostinil (serious AE) |
| Dizziness | 9,520 | 3.3 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 2.9 | NCT01027949: 5/894 (0.6%) on Treprostinil (serious AE) |
| Fatigue (tiredness) | 9,428 | 2.1 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 1.9 | NCT01027949: 3/894 (0.3%) on Treprostinil (serious AE) |
| Death | 8,989 | 1.8 1.7–1.8ROR 1.8 · calibrated p 0.843 | 1.8 EB05 1.7 · IC025 +0.8 | Outcome field, not a reaction | age-adj. PRR 2.4 · serious PRR 1.8 | NCT01027949: 15/894 (1.7%) on Treprostinil (serious AE) |
| Vomiting | 6,324 | 2.3 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 2.0 | NCT01027949: 10/894 (1.1%) on Treprostinil (serious AE) |
| Hypotension (low blood pressure) | 5,727 | 4.9 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 4.0 | NCT01027949: 23/894 (2.6%) on Treprostinil (serious AE) |
| Infusion site pain | 5,691 | 135.7 131.1–140.5ROR 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% consumer | NCT01027949: 28/894 (3.1%) on Treprostinil (serious AE) |
| Pneumonia (lung infection) | 5,644 | 3.0 2.9–3.0ROR 3.1 · calibrated p 0.606 | 2.9 EB05 2.9 · IC025 +1.5 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 3.0 · serious PRR 3.0 | NCT01027949: 63/894 (7.0%) on Treprostinil (serious AE) |
| Malaise (feeling unwell) | 5,589 | 2.2 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 — unassessed | age-adj. PRR 2.2 · serious PRR 1.9 | not reported in cached trials |
| Fluid retention | 5,072 | 18.5 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 — unassessed | age-adj. PRR 19.4 · serious PRR 19.0 | NCT01027949: 4/894 (0.4%) on Treprostinil (serious AE) |
| Oxygen saturation decreased | 4,957 | 16.3 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 marker | age-adj. PRR 13.1 · serious PRR 12.3 | not 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.
- Unevaluable device issue — n=56, PRR 419.7
- Bendopnoea — n=138, PRR 339.6
- Administration site odour — n=43, PRR 221.5
- Patient dissatisfaction with device — n=102, PRR 126.4
- Catheter site vesicles — n=68, PRR 92.7
- Catheter site irritation — n=108, PRR 86.0
- Catheter site warmth — n=49, PRR 80.8
- Vascular device occlusion — n=97, PRR 68.0
✓ 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
- FDA label via openFDA (set ID 33050ee2-519b-1f0b-d4df-9e14dd329c57, effective 20211223; matched on
openfda.generic_name.exact:"TREPROSTINIL" AND openfda.product_type:"HUMAN PRESCRIPTION DRUG") - PubChem CID 6918140 description (ChEBI)
- 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, 1,239 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
TREPROSTINIL, 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.