← All drugs
Drug · FAERS side-effect profile with label screen

Ticagrelor side effects: what 31,704 FDA adverse event reports show

Ticagrelor · 1,168 reaction terms · 94,044 drug–reaction co-reports · data 2026-09-14
Share: X Facebook Reddit Email

Drug class

P2Y12 Platelet Inhibitor

FDA label (Established Pharmacologic Class)

Who reports

31,704 reports · 76% serious · 3,436 with death outcome · 38% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Ticagrelor tablets are a P2Y 12 platelet inhibitor indicated to reduce the risk of cardiovascular (CV) death, myocardial infarction (MI), and stroke in patients with acute coronary syndrome (ACS) or a history of MI. For at least the first 12 months following ACS, it is superior to clopidogrel. Ticagrelor tablets also reduces the risk of stent thrombosis in patients who have been stented for treatment of ACS.

FDA label, Indications and Usage

What it is

Ticagrelor tablets contains ticagrelor, a cyclopentyltriazolopyrimidine, inhibitor of platelet activation and aggregation mediated by the P2Y 12 ADP-receptor.

FDA label, Description section

Boxed warning

BLEEDING RISK Ticagrelor tablets, like other antiplatelet agents, can cause significant, sometimes fatal bleeding ( 5.1 , 6.1 ). Do not use ticagrelor tablets in patients with active pathological bleeding or a history of intracranial hemorrhage ( 4.1 , 4.2 ).

FDA 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) 2Likely indication confounding 13Reporting / coding artifact 1Lab value / disease marker 1Not in label — unassessed 21
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). 1,128 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
Diabetic macroangiopathy12390.9
191.1–799.6ROR 391.1 · calibrated p 1e-10 ✓
176.5 EB05 107.6 · IC025 +3.5
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=12not reported in cached trials
Vascular stent occlusion151390.4
319.2–477.5ROR 392.3 · calibrated p 1e-12 ✓
237.2 EB05 207.1 · IC025 +6.8
3/3 methods agree
Not in label — unassessedserious n=151 · 74% consumerNCT01991795: 1/9,531 (0.0%) control (serious AE)
Vascular stent thrombosis723366.9
335.2–401.6ROR 375.4 · calibrated p 1e-12 ✓
233.6 EB05 219.7 · IC025 +7.5
3/3 methods agree
Likely indication confounding
term in indications
serious n=722not reported in cached trials
Vascular stent restenosis28276.4
177.7–430.0ROR 276.7 · calibrated p 2e-10 ✓
171.8 EB05 124.7 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=25not reported in cached trials
Chronic coronary syndrome12230.0
119.1–444.1ROR 230.0 · calibrated p 5e-9 ✓
134.4 EB05 81.9 · IC025 +3.5
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=12NCT01225562: 1/6,958 (0.0%) on Ticagrelor; 3/6,996 (0.0%) control (serious AE)
Vascular stent stenosis85169.9
133.8–215.6ROR 170.3 · calibrated p 3e-9 ✓
131.0 EB05 109.3 · IC025 +5.9
3/3 methods agree
Not in label — unassessedserious n=80NCT01991795: 6/9,562 (0.1%) on Ticagrelor; 4/9,531 (0.0%) control (serious AE)
Hypersensitivity myocarditis22146.3
92.1–232.2ROR 146.4 · calibrated p 3e-8 ✓
108.6 EB05 75.6 · IC025 +4.3
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=22 · ♀ 100% (drug 38%) · 100% cliniciannot reported in cached trials
Arterial restenosis19123.8
75.8–202.2ROR 123.9 · calibrated p 1e-7 ✓
94.6 EB05 64.0 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=18NCT01225562: 1/6,988 (0.0%) on Ticagrelor (serious AE)
Ventricular asystole2084.1
52.8–133.9ROR 84.1 · calibrated p 1e-6 ✓
69.8 EB05 47.7 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=20NCT01991795: 1/9,562 (0.0%) on Ticagrelor (serious AE)
Stent malfunction2074.5
46.9–118.3ROR 74.5 · calibrated p 3e-6 ✓
63.1 EB05 43.1 · IC025 +3.9
3/3 methods agree
Not in label — unassessedserious n=19not reported in cached trials
Thrombosis in device33574.4
66.5–83.3ROR 75.2 · calibrated p 1e-6 ✓
66.7 EB05 60.9 · IC025 +5.7
3/3 methods agree
Not in label — unassessedserious n=335 · 94% cliniciannot reported in cached trials
Ecg signs of myocardial ischaemia2063.3
40.0–100.1ROR 63.3 · calibrated p 8e-6 ✓
54.9 EB05 37.5 · IC025 +3.8
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=20not reported in cached trials
Coronary artery restenosis5262.5
47.0–83.1ROR 62.6 · calibrated p 5e-6 ✓
56.0 EB05 44.4 · IC025 +4.8
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=52NCT01991795: 1/9,531 (0.0%) control (serious AE)
Breath holding3161.8
42.7–89.3ROR 61.8 · calibrated p 7e-6 ✓
54.7 EB05 40.4 · IC025 +4.3
3/3 methods agree
Not in label — unassessedserious n=31 · 100% cliniciannot reported in cached trials
Platelet function test abnormal1960.1
37.6–96.1ROR 60.1 · calibrated p 1e-5 ✓
52.4 EB05 35.4 · IC025 +3.8
3/3 methods agree
Reporting / coding artifactserious n=13not reported in cached trials
Sinus arrest11251.6
42.6–62.5ROR 51.8 · calibrated p 1e-5 ✓
47.5 EB05 40.6 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=107 · 100% clinicianNCT01225562: 1/6,988 (0.0%) on Ticagrelor (serious AE)
Myocardial rupture2148.2
30.9–75.0ROR 48.2 · calibrated p 4e-5 ✓
43.3 EB05 29.9 · IC025 +3.7
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=21NCT01225562: 1/6,996 (0.0%) control (serious AE)
Cheyne-stokes respiration1439.1
22.8–67.1ROR 39.2 · calibrated p 2e-4 ✓
35.4 EB05 22.4 · IC025 +3.1
3/3 methods agree
Labeled adverse reaction
exact term
serious n=13not reported in cached trials
Acid base balance abnormal1236.9
20.6–66.0ROR 36.9 · calibrated p 3e-4 ✓
33.3 EB05 20.3 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=12not reported in cached trials
Coronary artery occlusion59629.9
27.5–32.4ROR 30.4 · calibrated p 2e-4 ✓
28.6 EB05 26.7 · IC025 +4.7
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious PRR 21.6 · 73% consumerNCT01225562: 1/6,958 (0.0%) on Ticagrelor; 1/6,996 (0.0%) control (serious AE)
Bleeding time prolonged5028.4
21.4–37.7ROR 28.5 · calibrated p 4e-4 ✓
27.0 EB05 21.3 · IC025 +4.0
3/3 methods agree
Lab value / disease markerserious n=30 · 82% consumernot reported in cached trials
Vascular occlusion8628.0
22.6–34.8ROR 28.1 · calibrated p 4e-4 ✓
26.8 EB05 22.4 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=80 · 85% consumerNCT01225562: 1/6,996 (0.0%) control (serious AE)
Gastroduodenal ulcer1727.9
17.2–45.3ROR 27.9 · calibrated p 8e-4 ✓
26.1 EB05 17.2 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=17NCT01991795: 2/9,562 (0.0%) on Ticagrelor (serious AE)
Angina unstable25827.0
23.9–30.6ROR 27.3 · calibrated p 5e-4 ✓
26.0 EB05 23.4 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=258NCT01225562: 4/6,988 (0.1%) on Ticagrelor; 3/6,996 (0.0%) control (serious AE)
Coronary artery dissection3326.8
19.0–38.0ROR 26.9 · calibrated p 7e-4 ✓
25.5 EB05 19.0 · IC025 +3.7
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=33 · 100% cliniciannot reported in cached trials
Coronary artery thrombosis7926.8
21.4–33.6ROR 26.9 · calibrated p 5e-4 ✓
25.7 EB05 21.2 · IC025 +4.1
3/3 methods agree
Likely indication confounding
term in indications
serious n=79NCT01225562: 2/6,958 (0.0%) on Ticagrelor (serious AE)
Vascular graft occlusion1425.6
15.0–43.7ROR 25.6 · calibrated p 0.001 ✓
23.9 EB05 15.0 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=14NCT01225562: 1/6,996 (0.0%) control (serious AE)
Coronary artery stenosis17423.6
20.3–27.4ROR 23.7 · calibrated p 9e-4 ✓
22.8 EB05 20.1 · IC025 +4.2
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=167NCT01225562: 6/6,988 (0.1%) on Ticagrelor; 3/6,996 (0.0%) control (serious AE)
Muscle necrosis3123.4
16.3–33.4ROR 23.4 · calibrated p 0.001 ✓
22.3 EB05 16.4 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=31 · 100% cliniciannot reported in cached trials
Sinoatrial block1618.0
10.9–29.5ROR 18.0 · calibrated p 0.005 ✓
16.9 EB05 10.6 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious n=15NCT01225562: 1/6,988 (0.0%) on Ticagrelor (serious AE)
Arterial occlusive disease20417.5
15.2–20.1ROR 17.6 · calibrated p 0.004 ✓
17.0 EB05 15.2 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious PRR 12.3 · 80% consumerNCT01225562: 17/6,988 (0.2%) on Ticagrelor; 15/6,996 (0.2%) control (serious AE)
Venous occlusion4516.6
12.4–22.4ROR 16.7 · calibrated p 0.005 ✓
16.1 EB05 12.5 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=45 · 100% consumernot reported in cached trials
Acute coronary syndrome20416.6
14.4–19.0ROR 16.7 · calibrated p 0.005 ✓
16.1 EB05 14.4 · IC025 +3.7
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious PRR 12.2NCT01225562: 1/6,958 (0.0%) on Ticagrelor; 3/6,996 (0.0%) control (serious AE)
Acute myocardial infarction72016.5
15.3–17.7ROR 16.8 · calibrated p 0.004 ✓
16.1 EB05 15.1 · IC025 +3.9
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious PRR 12.1NCT01225562: 19/6,988 (0.3%) on Ticagrelor; 28/6,996 (0.4%) control (serious AE)
Suffocation feeling5916.1
12.4–20.8ROR 16.1 · calibrated p 0.006 ✓
15.6 EB05 12.5 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=45not reported in cached trials
Asphyxia17314.3
12.3–16.6ROR 14.4 · calibrated p 0.009 ✓
13.9 EB05 12.3 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious PRR 10.5 · 91% cliniciannot reported in cached trials
Bradyarrhythmia3414.0
9.9–19.6ROR 14.0 · calibrated p 0.011 ✓
13.4 EB05 9.8 · IC025 +3.0
3/3 methods agree
Labeled adverse reaction
exact term
serious n=32 · 100% clinicianNCT01225562: 2/6,988 (0.0%) on Ticagrelor (serious AE)
Retroperitoneal haematoma4513.8
10.3–18.6ROR 13.8 · calibrated p 0.011 ✓
13.3 EB05 10.2 · IC025 +3.1
3/3 methods agree
Not in label — unassessedserious n=45not reported in cached trials

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Ticagrelor 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 (21 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)4,0094.7
4.6–4.9ROR 5.3 · calibrated p 0.209
4.7 EB05 4.6 · IC025 +2.2
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 3.2NCT01225562: 29/6,988 (0.4%) on Ticagrelor; 12/6,996 (0.2%) control (serious AE)
Myocardial infarction (heart attack)2,77710.6
10.2–11.0ROR 11.5 · calibrated p 0.020 ✓
10.4 EB05 10.1 · IC025 +3.3
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 7.9NCT01225562: 19/6,988 (0.3%) on Ticagrelor; 28/6,996 (0.4%) control (serious AE)
Death1,7251.3
1.3–1.4ROR 1.3 · calibrated p 0.538
1.3 EB05 1.3 · IC025 +0.3Outcome field, not a reaction
boxed warning mentions mortality
serious PRR 1.0NCT01225562: 1/6,988 (0.0%) on Ticagrelor; 1/6,996 (0.0%) control (serious AE)
Fatigue (tiredness)1,5491.3
1.3–1.4ROR 1.3 · calibrated p 0.532
1.3 EB05 1.3 · IC025 +0.3Not in label — unassessedserious PRR 1.0 · 72% consumerNCT01225562: 1/6,996 (0.0%) control (serious AE)
Off label use (used outside approved label)1,5251.2
1.1–1.2ROR 1.2 · calibrated p 0.420
1.2 EB05 1.1 · IC025 +0.1Reporting / coding artifactserious PRR 1.2not reported in cached trials
Chest pain1,4695.3
5.0–5.5ROR 5.5 · calibrated p 0.189
5.2 EB05 5.0 · IC025 +2.3
3/3 methods agree
Not in label — unassessedserious PRR 4.3NCT01225562: 6/6,988 (0.1%) on Ticagrelor; 4/6,996 (0.1%) control (serious AE)
Dizziness1,2501.7
1.6–1.8ROR 1.7 · calibrated p 0.763
1.7 EB05 1.6 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 1.5NCT01225562: 9/6,988 (0.1%) on Ticagrelor; 2/6,996 (0.0%) control (serious AE)
Contusion1,0887.6
7.1–8.0ROR 7.8 · calibrated p 0.072
7.5 EB05 7.1 · IC025 +2.8
3/3 methods agree
Not in label — unassessedserious PRR 5.5 · ♀ 59% (drug 38%) · 87% consumerNCT01225562: 1/6,988 (0.0%) on Ticagrelor (serious AE)
Drug interaction9604.0
3.8–4.3ROR 4.1 · calibrated p 0.357
4.0 EB05 3.8 · IC025 +1.9
3/3 methods agree
Reporting / coding artifactserious PRR 3.2 · 92% cliniciannot reported in cached trials
Asthenia (weakness)9181.6
1.5–1.7ROR 1.6 · calibrated p 0.728
1.6 EB05 1.5 · IC025 +0.6Not in label — unassessedserious PRR 1.2NCT01225562: 2/6,988 (0.0%) on Ticagrelor; 1/6,996 (0.0%) control (serious AE)
Malaise (feeling unwell)8941.3
1.3–1.4ROR 1.4 · calibrated p 0.546
1.3 EB05 1.3 · IC025 +0.3Not in label — unassessedserious PRR 0.9 · 74% consumerNCT01225562: 1/6,988 (0.0%) on Ticagrelor; 1/6,996 (0.0%) control (serious AE)
Haemorrhage8795.6
5.2–6.0ROR 5.7 · calibrated p 0.169
5.5 EB05 5.2 · IC025 +2.4
3/3 methods agree
Labeled — boxed warning
exact term
serious PRR 4.0NCT01225562: 1/6,958 (0.0%) on Ticagrelor (serious AE)
Drug ineffective (drug did not work)8590.4
0.4–0.5ROR 0.4 · calibrated p 0.026 ✓
0.4 EB05 0.4 · IC025 -1.3
PRR-only: not supported by EBGM or IC
Reporting / coding artifactserious PRR 0.8not reported in cached trials
Nausea8570.7
0.7–0.8ROR 0.7 · calibrated p 0.136
0.7 EB05 0.7 · IC025 -0.6
PRR-only: not supported by EBGM or IC
Labeled adverse reaction
exact term
serious PRR 0.7NCT01225562: 2/6,988 (0.0%) on Ticagrelor (serious AE)
Chest discomfort7735.0
4.7–5.4ROR 5.1 · calibrated p 0.220
5.0 EB05 4.7 · IC025 +2.2
3/3 methods agree
Not in label — unassessedserious PRR 4.8NCT01225562: 2/6,988 (0.0%) on Ticagrelor; 2/6,996 (0.0%) 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.

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

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 Ticagrelor?

In FDA FAERS, the most frequently co-reported reaction terms for Ticagrelor are dyspnoea, myocardial infarction, fatigue, chest pain, dizziness, contusion. 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 Ticagrelor have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: BLEEDING RISK Ticagrelor tablets, like other antiplatelet agents, can cause significant, sometimes fatal bleeding ( 5.1 , 6.1 ). Do not use ticagrelor tablets in patients with active pathological bleeding or a history of intracranial hemorrhage ( 4.1 , 4.2 ).

Do FAERS signals prove that Ticagrelor 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.