Ticagrelor side effects: what 31,704 FDA adverse event reports show
Drug class
P2Y12 Platelet Inhibitor
Who reports
31,704 reports · 76% serious · 3,436 with death outcome · 38% female
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.
What it is
Ticagrelor tablets contains ticagrelor, a cyclopentyltriazolopyrimidine, inhibitor of platelet activation and aggregation mediated by the P2Y 12 ADP-receptor.
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 ).
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). 1,128 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 |
|---|---|---|---|---|---|---|
| Diabetic macroangiopathy | 12 | 390.9 191.1–799.6ROR 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=12 | not reported in cached trials |
| Vascular stent occlusion | 151 | 390.4 319.2–477.5ROR 392.3 · calibrated p 1e-12 ✓ | 237.2 EB05 207.1 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious n=151 · 74% consumer | NCT01991795: 1/9,531 (0.0%) control (serious AE) |
| Vascular stent thrombosis | 723 | 366.9 335.2–401.6ROR 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=722 | not reported in cached trials |
| Vascular stent restenosis | 28 | 276.4 177.7–430.0ROR 276.7 · calibrated p 2e-10 ✓ | 171.8 EB05 124.7 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious n=25 | not reported in cached trials |
| Chronic coronary syndrome | 12 | 230.0 119.1–444.1ROR 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=12 | NCT01225562: 1/6,958 (0.0%) on Ticagrelor; 3/6,996 (0.0%) control (serious AE) |
| Vascular stent stenosis | 85 | 169.9 133.8–215.6ROR 170.3 · calibrated p 3e-9 ✓ | 131.0 EB05 109.3 · IC025 +5.9 3/3 methods agree | Not in label — unassessed | serious n=80 | NCT01991795: 6/9,562 (0.1%) on Ticagrelor; 4/9,531 (0.0%) control (serious AE) |
| Hypersensitivity myocarditis | 22 | 146.3 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% clinician | not reported in cached trials |
| Arterial restenosis | 19 | 123.8 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 — unassessed | serious n=18 | NCT01225562: 1/6,988 (0.0%) on Ticagrelor (serious AE) |
| Platelet aggregation inhibition | 13 | 108.6 60.4–195.3ROR 108.6 · calibrated p 5e-7 ✓ | 82.3 EB05 51.2 · IC025 +3.5 3/3 methods agree | Labeled (related wording) related wording | serious n=11 | not reported in cached trials |
| Ventricular asystole | 20 | 84.1 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 — unassessed | serious n=20 | NCT01991795: 1/9,562 (0.0%) on Ticagrelor (serious AE) |
| Stent malfunction | 20 | 74.5 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 — unassessed | serious n=19 | not reported in cached trials |
| Thrombosis in device | 335 | 74.4 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 — unassessed | serious n=335 · 94% clinician | not reported in cached trials |
| Ecg signs of myocardial ischaemia | 20 | 63.3 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=20 | not reported in cached trials |
| Coronary artery restenosis | 52 | 62.5 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=52 | NCT01991795: 1/9,531 (0.0%) control (serious AE) |
| Breath holding | 31 | 61.8 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 — unassessed | serious n=31 · 100% clinician | not reported in cached trials |
| Platelet function test abnormal | 19 | 60.1 37.6–96.1ROR 60.1 · calibrated p 1e-5 ✓ | 52.4 EB05 35.4 · IC025 +3.8 3/3 methods agree | Reporting / coding artifact | serious n=13 | not reported in cached trials |
| Sinus arrest | 112 | 51.6 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 — unassessed | serious n=107 · 100% clinician | NCT01225562: 1/6,988 (0.0%) on Ticagrelor (serious AE) |
| Myocardial rupture | 21 | 48.2 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=21 | NCT01225562: 1/6,996 (0.0%) control (serious AE) |
| Cheyne-stokes respiration | 14 | 39.1 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=13 | not reported in cached trials |
| Acid base balance abnormal | 12 | 36.9 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 — unassessed | serious n=12 | not reported in cached trials |
| Coronary artery occlusion | 596 | 29.9 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% consumer | NCT01225562: 1/6,958 (0.0%) on Ticagrelor; 1/6,996 (0.0%) control (serious AE) |
| Cardiac ventricular thrombosis | 53 | 28.9 22.0–38.1ROR 29.0 · calibrated p 4e-4 ✓ | 27.5 EB05 21.8 · IC025 +4.0 3/3 methods agree | Labeled (related wording) related wording | serious n=53 · ♀ 15% (drug 38%) | NCT01225562: 1/6,988 (0.0%) on Ticagrelor; 3/6,996 (0.0%) control (serious AE) |
| Bleeding time prolonged | 50 | 28.4 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 marker | serious n=30 · 82% consumer | not reported in cached trials |
| Vascular occlusion | 86 | 28.0 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 — unassessed | serious n=80 · 85% consumer | NCT01225562: 1/6,996 (0.0%) control (serious AE) |
| Gastroduodenal ulcer | 17 | 27.9 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 — unassessed | serious n=17 | NCT01991795: 2/9,562 (0.0%) on Ticagrelor (serious AE) |
| Angina unstable | 258 | 27.0 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 — unassessed | serious n=258 | NCT01225562: 4/6,988 (0.1%) on Ticagrelor; 3/6,996 (0.0%) control (serious AE) |
| Coronary artery dissection | 33 | 26.8 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% clinician | not reported in cached trials |
| Coronary artery thrombosis | 79 | 26.8 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=79 | NCT01225562: 2/6,958 (0.0%) on Ticagrelor (serious AE) |
| Vascular graft occlusion | 14 | 25.6 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 — unassessed | serious n=14 | NCT01225562: 1/6,996 (0.0%) control (serious AE) |
| Coronary artery stenosis | 174 | 23.6 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=167 | NCT01225562: 6/6,988 (0.1%) on Ticagrelor; 3/6,996 (0.0%) control (serious AE) |
| Muscle necrosis | 31 | 23.4 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 — unassessed | serious n=31 · 100% clinician | not reported in cached trials |
| Sinoatrial block | 16 | 18.0 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 — unassessed | serious n=15 | NCT01225562: 1/6,988 (0.0%) on Ticagrelor (serious AE) |
| Arterial occlusive disease | 204 | 17.5 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 — unassessed | serious PRR 12.3 · 80% consumer | NCT01225562: 17/6,988 (0.2%) on Ticagrelor; 15/6,996 (0.2%) control (serious AE) |
| Venous occlusion | 45 | 16.6 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 — unassessed | serious n=45 · 100% consumer | not reported in cached trials |
| Acute coronary syndrome | 204 | 16.6 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 12.2 | NCT01225562: 1/6,958 (0.0%) on Ticagrelor; 3/6,996 (0.0%) control (serious AE) |
| Acute myocardial infarction | 720 | 16.5 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 12.1 | NCT01225562: 19/6,988 (0.3%) on Ticagrelor; 28/6,996 (0.4%) control (serious AE) |
| Suffocation feeling | 59 | 16.1 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 — unassessed | serious n=45 | not reported in cached trials |
| Asphyxia | 173 | 14.3 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 — unassessed | serious PRR 10.5 · 91% clinician | not reported in cached trials |
| Bradyarrhythmia | 34 | 14.0 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% clinician | NCT01225562: 2/6,988 (0.0%) on Ticagrelor (serious AE) |
| Retroperitoneal haematoma | 45 | 13.8 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 — unassessed | serious n=45 | 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 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).
- NCT01225562 — Prevention of Cardiovascular Events (eg, Death From Heart or Vascular Disease, Heart Attack, or Stroke) in Pat (N=21379, PHASE3; 1433 AE terms posted; arms: Placebo; Ticagrelor 60mg bd; Ticagrelor 90mg bd)
- NCT01991795 — A Study Comparing Cardiovascular Effects of Ticagrelor Versus Placebo in Patients With Type 2 Diabetes Mellitu (N=19271, PHASE3; 1344 AE terms posted; arms: Ticagrelor 60 mg; Ticagrelor Placebo)
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) | 4,009 | 4.7 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 3.2 | NCT01225562: 29/6,988 (0.4%) on Ticagrelor; 12/6,996 (0.2%) control (serious AE) |
| Myocardial infarction (heart attack) | 2,777 | 10.6 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 7.9 | NCT01225562: 19/6,988 (0.3%) on Ticagrelor; 28/6,996 (0.4%) control (serious AE) |
| Death | 1,725 | 1.3 1.3–1.4ROR 1.3 · calibrated p 0.538 | 1.3 EB05 1.3 · IC025 +0.3 | Outcome field, not a reaction boxed warning mentions mortality | serious PRR 1.0 | NCT01225562: 1/6,988 (0.0%) on Ticagrelor; 1/6,996 (0.0%) control (serious AE) |
| Fatigue (tiredness) | 1,549 | 1.3 1.3–1.4ROR 1.3 · calibrated p 0.532 | 1.3 EB05 1.3 · IC025 +0.3 | Not in label — unassessed | serious PRR 1.0 · 72% consumer | NCT01225562: 1/6,996 (0.0%) control (serious AE) |
| Off label use (used outside approved label) | 1,525 | 1.2 1.1–1.2ROR 1.2 · calibrated p 0.420 | 1.2 EB05 1.1 · IC025 +0.1 | Reporting / coding artifact | serious PRR 1.2 | not reported in cached trials |
| Chest pain | 1,469 | 5.3 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 — unassessed | serious PRR 4.3 | NCT01225562: 6/6,988 (0.1%) on Ticagrelor; 4/6,996 (0.1%) control (serious AE) |
| Dizziness | 1,250 | 1.7 1.6–1.8ROR 1.7 · calibrated p 0.763 | 1.7 EB05 1.6 · IC025 +0.6 | Labeled adverse reaction exact term | serious PRR 1.5 | NCT01225562: 9/6,988 (0.1%) on Ticagrelor; 2/6,996 (0.0%) control (serious AE) |
| Contusion | 1,088 | 7.6 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 — unassessed | serious PRR 5.5 · ♀ 59% (drug 38%) · 87% consumer | NCT01225562: 1/6,988 (0.0%) on Ticagrelor (serious AE) |
| Drug interaction | 960 | 4.0 3.8–4.3ROR 4.1 · calibrated p 0.357 | 4.0 EB05 3.8 · IC025 +1.9 3/3 methods agree | Reporting / coding artifact | serious PRR 3.2 · 92% clinician | not reported in cached trials |
| Asthenia (weakness) | 918 | 1.6 1.5–1.7ROR 1.6 · calibrated p 0.728 | 1.6 EB05 1.5 · IC025 +0.6 | Not in label — unassessed | serious PRR 1.2 | NCT01225562: 2/6,988 (0.0%) on Ticagrelor; 1/6,996 (0.0%) control (serious AE) |
| Malaise (feeling unwell) | 894 | 1.3 1.3–1.4ROR 1.4 · calibrated p 0.546 | 1.3 EB05 1.3 · IC025 +0.3 | Not in label — unassessed | serious PRR 0.9 · 74% consumer | NCT01225562: 1/6,988 (0.0%) on Ticagrelor; 1/6,996 (0.0%) control (serious AE) |
| Haemorrhage | 879 | 5.6 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 4.0 | NCT01225562: 1/6,958 (0.0%) on Ticagrelor (serious AE) |
| Drug ineffective (drug did not work) | 859 | 0.4 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 artifact | serious PRR 0.8 | not reported in cached trials |
| Nausea | 857 | 0.7 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 0.7 | NCT01225562: 2/6,988 (0.0%) on Ticagrelor (serious AE) |
| Chest discomfort | 773 | 5.0 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 — unassessed | serious PRR 4.8 | NCT01225562: 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.
- Vascular stent occlusion — n=151, PRR 390.4 (also seen in trial arm)
- Vascular stent restenosis — n=28, PRR 276.4
- Vascular stent stenosis — n=85, PRR 169.9 (also seen in trial arm)
- Ventricular asystole — n=20, PRR 84.1 (also seen in trial arm)
- Stent malfunction — n=20, PRR 74.5
- Thrombosis in device — n=335, PRR 74.4
- Breath holding — n=31, PRR 61.8
- Sinus arrest — n=112, PRR 51.6 (also seen in trial arm)
- Vascular occlusion — n=86, PRR 28.0 (also seen in trial arm)
- Angina unstable — n=258, PRR 27.0 (also seen in trial arm)
✓ 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
- FDA label via openFDA (set ID 3225098b-3138-4aec-a866-de94c3006e8e, effective 20251029; matched on
openfda.generic_name.exact:"TICAGRELOR") - 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, 1,168 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
TICAGRELOR, 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.