Epinephrine side effects: what 65,037 FDA adverse event reports show
Drug class
alpha-Adrenergic Agonist, beta-Adrenergic Agonist, Catecholamine
Who reports
65,037 reports · 57% serious · 4,076 with death outcome · 67% female
Used for
Epinephrine is a non-selective alpha and beta adrenergic agonist indicated: • To increase mean arterial blood pressure in adult patients with hypotension associated with septic shock. ( 1.1 ) • For emergency treatment of allergic reactions (Type 1), including anaphylaxis. ( 1.2 ) • For induction and maintenance of mydriasis during intraocular surgery.
What it is
Epinephrine Injection USP, 1 mg/mL is supplied as a sterile aqueous solution with a pH range of 2.2 to 5.0, that is colorless and nonpyrogenic. Each milliliter contains 1 mg epinephrine, sodiu.
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.
- 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). 1,190 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 |
|---|---|---|---|---|---|---|
| No device malfunction | 60 | 19,013.4 2,635.0–137,193.6ROR 19,030.9 · calibrated p 2e-13 ✓ | 284.3 EB05 228.9 · IC025 +6.0 3/3 methods agree vs other alpha-Adrenergic Agonists: only this drug | Not in label — unassessed | ♀ 0% (drug 67%) · 100% consumer | no trial arm names this drug |
| Injection site pallor | 127 | 212.9 170.1–266.6ROR 213.4 · calibrated p 4e-10 ✓ | 125.4 EB05 108.1 · IC025 +6.1 3/3 methods agree vs other alpha-Adrenergic Agonists: only this drug | Labeled adverse reaction exact term | serious n=53 | no trial arm names this drug |
| Vascular access site complication | 95 | 204.8 158.2–265.0ROR 205.1 · calibrated p 6e-10 ✓ | 121.8 EB05 102.6 · IC025 +5.9 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.3 (5.5–9.6) | Reporting / coding artifact | 100% consumer | no trial arm names this drug |
| Coagulation factor deficiency | 39 | 102.1 71.2–146.5ROR 102.2 · calibrated p 2e-7 ✓ | 74.8 EB05 57.1 · IC025 +4.8 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.3 (4.7–11.3) | Not in label — unassessed | serious n=39 · ♀ 0% (drug 67%) · 100% consumer | no trial arm names this drug |
| Infusion site discharge | 333 | 77.9 69.1–87.8ROR 78.3 · calibrated p 7e-7 ✓ | 62.5 EB05 57.1 · IC025 +5.7 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.3 (6.3–8.5) | Labeled (related wording) related wording | serious n=297 · 84% consumer | no trial arm names this drug |
| Administration site swelling | 61 | 74.6 56.5–98.6ROR 74.7 · calibrated p 1e-6 ✓ | 59.5 EB05 48.0 · IC025 +4.9 3/3 methods agree vs other alpha-Adrenergic Agonists: only this drug | Labeled (related wording) related wording | ♀ 100% (drug 67%) · 100% clinician | no trial arm names this drug |
| Infusion site mass | 171 | 61.4 52.1–72.3ROR 61.5 · calibrated p 4e-6 ✓ | 51.3 EB05 45.2 · IC025 +5.2 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.7 (7.0–10.8) | Labeled (related wording) related wording | serious n=127 | no trial arm names this drug |
| Infusion site bruising | 320 | 57.0 50.6–64.2ROR 57.3 · calibrated p 6e-6 ✓ | 48.3 EB05 44.0 · IC025 +5.3 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.2 (7.0–9.6) | Labeled (related wording) related wording | serious n=238 | no trial arm names this drug |
| Infusion site pruritus | 450 | 54.3 49.1–60.0ROR 54.7 · calibrated p 8e-6 ✓ | 46.4 EB05 42.9 · IC025 +5.3 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.7 (7.6–10.0) | Likely indication confounding term in indications; also in warnings | serious n=297 | no trial arm names this drug |
| Infusion site urticaria | 91 | 51.6 41.3–64.4ROR 51.7 · calibrated p 1e-5 ✓ | 44.1 EB05 37.0 · IC025 +4.8 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.9 (6.6–12.1) | Likely indication confounding term in indications; also in warnings | serious n=60 · ♀ 100% (drug 67%) | no trial arm names this drug |
| Local anaesthetic systemic toxicity | 142 | 51.1 42.8–61.0ROR 51.2 · calibrated p 1e-5 ✓ | 43.9 EB05 38.2 · IC025 +5.0 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.3 (5.8–9.2) | Not in label — unassessed | serious n=142 · 100% clinician | no trial arm names this drug |
| Injection site anaesthesia | 44 | 50.0 36.4–68.7ROR 50.0 · calibrated p 2e-5 ✓ | 42.6 EB05 33.0 · IC025 +4.4 3/3 methods agree vs other alpha-Adrenergic Agonists: only this drug | Labeled (related wording) related wording | 100% consumer | no trial arm names this drug |
| Lagophthalmos | 55 | 49.8 37.5–66.2ROR 49.8 · calibrated p 2e-5 ✓ | 42.6 EB05 33.9 · IC025 +4.5 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.3 (5.0–10.5) | Not in label — unassessed | serious n=54 · 100% clinician | no trial arm names this drug |
| Hereditary angioedema | 1,387 | 49.0 46.3–51.8ROR 50.0 · calibrated p 1e-5 ✓ | 42.5 EB05 40.7 · IC025 +5.3 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 9.5 (8.8–10.3) | Likely indication confounding shares a disease stem with the indications wording | serious PRR 40.1 | no trial arm names this drug |
| Infusion site haemorrhage | 381 | 42.8 38.5–47.7ROR 43.1 · calibrated p 3e-5 ✓ | 37.8 EB05 34.7 · IC025 +5.0 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.8 (6.8–9.0) | Labeled (related wording) related wording | serious n=294 | no trial arm names this drug |
| Infusion site scar | 50 | 41.4 30.8–55.5ROR 41.4 · calibrated p 6e-5 ✓ | 36.2 EB05 28.6 · IC025 +4.3 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.7 (5.2–11.5) | Labeled (related wording) related wording | serious n=40 · ♀ 100% (drug 67%) · 100% consumer | no trial arm names this drug |
| Infusion site swelling | 653 | 38.2 35.2–41.4ROR 38.5 · calibrated p 7e-5 ✓ | 34.1 EB05 32.0 · IC025 +4.9 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.8 (7.8–9.8) | Likely indication confounding term in indications; also in warnings | serious n=408 | no trial arm names this drug |
| Infusion site rash | 144 | 38.0 32.0–45.2ROR 38.1 · calibrated p 8e-5 ✓ | 33.9 EB05 29.5 · IC025 +4.7 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.8 (6.9–11.2) | Labeled (related wording) related wording | serious n=93 | no trial arm names this drug |
| Injection site laceration | 67 | 37.6 29.2–48.5ROR 37.7 · calibrated p 9e-5 ✓ | 33.5 EB05 27.3 · IC025 +4.4 3/3 methods agree vs other alpha-Adrenergic Agonists: only this drug | Labeled (related wording) related wording | serious n=45 · ♀ 0% (drug 67%) | no trial arm names this drug |
| Infusion site discomfort | 98 | 34.1 27.7–42.0ROR 34.1 · calibrated p 2e-4 ✓ | 30.7 EB05 25.9 · IC025 +4.4 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.1 (6.1–10.8) | Labeled (related wording) related wording | serious n=69 | no trial arm names this drug |
| Infusion site nodule | 86 | 33.9 27.2–42.4ROR 34.0 · calibrated p 2e-4 ✓ | 30.6 EB05 25.5 · IC025 +4.4 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 16.9 (11.5–24.8) | Labeled (related wording) related wording | serious n=32 | no trial arm names this drug |
| Accidental exposure | 389 | 32.6 29.4–36.2ROR 32.8 · calibrated p 2e-4 ✓ | 29.6 EB05 27.2 · IC025 +4.7 3/3 methods agree vs other alpha-Adrenergic Agonists: only this drug | Reporting / coding artifact | serious n=99 | no trial arm names this drug |
| Steroid dependence | 78 | 32.5 25.7–41.0ROR 32.5 · calibrated p 2e-4 ✓ | 29.4 EB05 24.3 · IC025 +4.3 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.3 (5.3–9.9) | Not in label — unassessed | serious n=78 · ♀ 0% (drug 67%) · 100% clinician | no trial arm names this drug |
| Liquid product physical issue | 646 | 32.4 29.9–35.1ROR 32.7 · calibrated p 2e-4 ✓ | 29.4 EB05 27.6 · IC025 +4.7 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 11.2 (9.9–12.6) | Not in label — unassessed | serious n=43 | no trial arm names this drug |
| Toxic anterior segment syndrome | 97 | 31.4 25.5–38.7ROR 31.5 · calibrated p 2e-4 ✓ | 28.5 EB05 24.1 · IC025 +4.3 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.0 (6.0–10.7) | Not in label — unassessed | serious n=97 · 100% clinician | no trial arm names this drug |
| Device failure | 1,338 | 31.1 29.4–32.9ROR 31.7 · calibrated p 2e-4 ✓ | 28.4 EB05 27.1 · IC025 +4.7 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 29.2 (26.0–33.0) | Reporting / coding artifact | age-adj. PRR 19.6 · serious PRR 44.9 | no trial arm names this drug |
| Allergy to plants | 40 | 30.9 22.3–42.8ROR 30.9 · calibrated p 3e-4 ✓ | 27.9 EB05 21.4 · IC025 +3.9 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.5 (5.4–13.5) | Likely indication confounding shares a disease stem with the indications wording | serious n=38 · ♀ 100% (drug 67%) · 100% consumer | no trial arm names this drug |
| Catarrh | 78 | 30.9 24.5–39.0ROR 30.9 · calibrated p 3e-4 ✓ | 28.1 EB05 23.2 · IC025 +4.2 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.3 (5.3–9.9) | Not in label — unassessed | serious n=78 · ♀ 0% (drug 67%) · 100% clinician | no trial arm names this drug |
| Multiple allergies | 633 | 28.2 26.0–30.6ROR 28.5 · calibrated p 4e-4 ✓ | 26.0 EB05 24.3 · IC025 +4.5 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.6 (6.8–8.5) | Likely indication confounding shares a disease stem with the indications wording | serious n=579 · 77% consumer | no trial arm names this drug |
| Administration site pain | 86 | 26.4 21.2–32.8ROR 26.4 · calibrated p 6e-4 ✓ | 24.3 EB05 20.3 · IC025 +4.1 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 15.2 (10.5–22.1) | Labeled (related wording) related wording | serious n=38 | no trial arm names this drug |
| Infusion site extravasation | 467 | 26.1 23.7–28.7ROR 26.3 · calibrated p 5e-4 ✓ | 24.2 EB05 22.4 · IC025 +4.4 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.4 (7.3–9.6) | Labeled (related wording) related wording | serious n=260 | no trial arm names this drug |
| Infusion site erythema | 618 | 25.9 23.9–28.1ROR 26.1 · calibrated p 5e-4 ✓ | 24.0 EB05 22.4 · IC025 +4.4 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.8 (7.9–9.9) | Labeled (related wording) related wording | serious n=382 | no trial arm names this drug |
| Maternal exposure during delivery | 72 | 25.7 20.2–32.7ROR 25.8 · calibrated p 7e-4 ✓ | 23.7 EB05 19.5 · IC025 +4.0 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.6 (5.4–10.5) | Reporting / coding artifact | serious n=66 · ♀ 100% (drug 67%) · 100% clinician | no trial arm names this drug |
| Injection site coldness | 61 | 25.3 19.5–32.9ROR 25.4 · calibrated p 8e-4 ✓ | 23.4 EB05 18.9 · IC025 +3.9 3/3 methods agree vs other alpha-Adrenergic Agonists: only this drug | Labeled (related wording) related wording | – | no trial arm names this drug |
| Bronchopulmonary aspergillosis allergic | 66 | 24.9 19.4–32.0ROR 25.0 · calibrated p 8e-4 ✓ | 23.1 EB05 18.7 · IC025 +3.9 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.5 (5.3–10.6) | Likely indication confounding shares a disease stem with the indications wording | serious n=66 · ♀ 0% (drug 67%) | no trial arm names this drug |
| Infusion site pain | 901 | 24.4 22.8–26.1ROR 24.7 · calibrated p 7e-4 ✓ | 22.7 EB05 21.5 · IC025 +4.4 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.3 (7.5–9.1) | Labeled (related wording) related wording | age-adj. PRR 21.2 · serious n=580 | no trial arm names this drug |
| Stress cardiomyopathy | 391 | 23.3 21.0–25.8ROR 23.4 · calibrated p 1e-3 ✓ | 21.7 EB05 20.0 · IC025 +4.2 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.1 (7.0–9.4) | Not in label — unassessed | serious n=389 · 100% clinician | no trial arm names this drug |
| Infusion site irritation | 84 | 23.3 18.7–29.1ROR 23.3 · calibrated p 0.001 ✓ | 21.7 EB05 18.0 · IC025 +3.9 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.8 (6.4–12.1) | Labeled (related wording) related wording | serious n=52 | no trial arm names this drug |
| Incorrect drug administration rate | 276 | 22.4 19.9–25.4ROR 22.5 · calibrated p 0.001 ✓ | 21.0 EB05 19.0 · IC025 +4.1 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.6 (6.4–8.9) | Reporting / coding artifact | serious n=217 | no trial arm names this drug |
| Mast cell activation syndrome | 86 | 22.3 17.9–27.8ROR 22.3 · calibrated p 0.001 ✓ | 20.8 EB05 17.4 · IC025 +3.9 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 12.0 (8.5–16.9) | Not in label — unassessed | serious n=84 · ♀ 100% (drug 67%) | no trial arm names this drug |
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 |
|---|---|---|---|
| Anaphylaxis / angioedema | 2,309 | 6.05.8–6.3 | signal |
| Serious infection | 5,920 | 2.52.4–2.5 | signal |
| Opportunistic infection | 837 | 2.01.9–2.1 | raised |
| Arrhythmia / qt | 1,155 | 1.91.8–2.0 | raised |
| Fall / fracture | 2,017 | 1.71.6–1.8 | raised |
| Venous thromboembolism | 924 | 1.41.3–1.5 | raised |
| Seizure | 786 | 1.31.2–1.4 | raised |
| Kidney injury | 1,668 | 1.21.1–1.2 | raised |
| Depression | 980 | 1.11.1–1.2 | raised |
| Heart failure | 521 | 0.90.9–1.0 | no difference |
| Myocardial infarction | 588 | 0.90.9–1.0 | no difference |
| Tendon disorder | 106 | 0.90.7–1.1 | no difference |
| Anaemia | 800 | 0.90.8–0.9 | lower than other drugs |
| Gi bleeding | 479 | 0.80.8–0.9 | lower than other drugs |
| Rhabdomyolysis / myopathy | 212 | 0.80.7–1.0 | lower than other drugs |
| Stroke | 649 | 0.80.8–0.9 | lower than other drugs |
Trial evidence (ClinicalTrials.gov)
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 |
|---|---|---|---|---|---|---|
| Drug ineffective (drug did not work) | 5,928 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.640 | 1.5 EB05 1.4 · IC025 +0.5 vs other alpha-Adrenergic Agonists: PRR 9.7 (9.4–10.1) | Reporting / coding artifact | age-adj. PRR 2.2 · serious PRR 3.3 | no trial arm names this drug |
| Headache | 4,392 | 2.3 2.2–2.3ROR 2.4 · calibrated p 0.875 | 2.3 EB05 2.2 · IC025 +1.1 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 10.6 (10.1–11.0) | Labeled adverse reaction exact term | age-adj. PRR 2.1 · serious PRR 2.8 | no trial arm names this drug |
| Sinusitis | 4,030 | 13.1 12.7–13.5ROR 13.9 · calibrated p 0.009 ✓ | 12.6 EB05 12.3 · IC025 +3.6 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 10.1 (9.7–10.6) | Not in label — unassessed | age-adj. PRR 10.8 · serious PRR 14.3 | no trial arm names this drug |
| Fatigue (tiredness) | 4,005 | 1.7 1.6–1.7ROR 1.7 · calibrated p 0.774 | 1.7 EB05 1.6 · IC025 +0.7 vs other alpha-Adrenergic Agonists: PRR 8.2 (7.8–8.5) | Not in label — unassessed | age-adj. PRR 1.8 · serious PRR 2.1 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 3,448 | 2.0 1.9–2.0ROR 2.0 · calibrated p 0.957 | 2.0 EB05 1.9 · IC025 +0.9 vs other alpha-Adrenergic Agonists: PRR 11.3 (10.7–11.9) | Not in label — unassessed | age-adj. PRR 2.3 · serious PRR 2.2 | no trial arm names this drug |
| Nausea | 3,351 | 1.4 1.3–1.4ROR 1.4 · calibrated p 0.569 | 1.4 EB05 1.3 · IC025 +0.4 vs other alpha-Adrenergic Agonists: PRR 11.2 (10.6–11.8) | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 1.7 | no trial arm names this drug |
| Pain | 3,335 | 1.8 1.7–1.8ROR 1.8 · calibrated p 0.824 | 1.7 EB05 1.7 · IC025 +0.7 vs other alpha-Adrenergic Agonists: PRR 9.9 (9.4–10.4) | Labeled adverse reaction exact term | age-adj. PRR 2.3 · serious PRR 2.0 | no trial arm names this drug |
| Product dose omission issue | 3,223 | 3.7 3.6–3.8ROR 3.8 · calibrated p 0.413 | 3.6 EB05 3.5 · IC025 +1.8 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.9 (7.6–8.3) | Reporting / coding artifact | age-adj. PRR 4.2 · serious PRR 10.4 | no trial arm names this drug |
| Off label use (used outside approved label) | 2,916 | 1.1 1.0–1.1ROR 1.1 · calibrated p 0.364 | 1.1 EB05 1.0 · IC025 +0.1 vs other alpha-Adrenergic Agonists: PRR 10.5 (10.0–11.1) | Reporting / coding artifact | age-adj. PRR 1.2 · serious PRR 1.4 | no trial arm names this drug |
| Pneumonia (lung infection) | 2,644 | 2.6 2.6–2.7ROR 2.7 · calibrated p 0.725 | 2.6 EB05 2.6 · IC025 +1.3 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 9.3 (8.8–9.9) | Labeled (related wording) related wording | age-adj. PRR 2.8 · serious PRR 2.8 | no trial arm names this drug |
| Covid-19 | 2,629 | 4.8 4.7–5.0ROR 5.0 · calibrated p 0.234 | 4.8 EB05 4.6 · IC025 +2.2 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 7.7 (7.3–8.1) | Not in label — unassessed | age-adj. PRR 5.4 · serious PRR 6.8 | no trial arm names this drug |
| Cough | 2,261 | 2.6 2.5–2.7ROR 2.7 · calibrated p 0.742 | 2.6 EB05 2.5 · IC025 +1.3 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 10.6 (10.0–11.3) | Not in label — unassessed | age-adj. PRR 2.8 · serious PRR 3.1 | no trial arm names this drug |
| Pyrexia (fever) | 2,215 | 2.1 2.0–2.2ROR 2.1 · calibrated p 1.000 | 2.1 EB05 2.0 · IC025 +1.0 vs other alpha-Adrenergic Agonists: PRR 9.9 (9.3–10.5) | Not in label — unassessed | age-adj. PRR 1.9 · serious PRR 1.8 | no trial arm names this drug |
| Nasopharyngitis (common cold) | 2,191 | 3.9 3.7–4.0ROR 4.0 · calibrated p 0.386 | 3.8 EB05 3.7 · IC025 +1.9 3/3 methods agree vs other alpha-Adrenergic Agonists: PRR 8.7 (8.1–9.2) | Not in label — unassessed | age-adj. PRR 3.6 · serious PRR 5.3 | no trial arm names this drug |
| Rash | 2,145 | 1.6 1.5–1.7ROR 1.6 · calibrated p 0.717 | 1.6 EB05 1.5 · IC025 +0.6 vs other alpha-Adrenergic Agonists: PRR 11.4 (10.7–12.2) | Not in label — unassessed | age-adj. PRR 1.7 · serious PRR 1.9 | no trial arm names this drug |
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.
- No device malfunction — n=60, PRR 19,013.4
- Coagulation factor deficiency — n=39, PRR 102.1
- Local anaesthetic systemic toxicity — n=142, PRR 51.1
- Lagophthalmos — n=55, PRR 49.8
- Steroid dependence — n=78, PRR 32.5
- Liquid product physical issue — n=646, PRR 32.4
- Toxic anterior segment syndrome — n=97, PRR 31.4
- Catarrh — n=78, PRR 30.9
- Stress cardiomyopathy — n=391, PRR 23.3
- Mast cell activation syndrome — n=86, PRR 22.3
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 Epinephrine?
In FDA FAERS, the most frequently co-reported reaction terms for Epinephrine are headache, sinusitis, fatigue, dyspnoea, nausea, pain. 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 Epinephrine have an FDA boxed warning?
No. The FDA label retrieved for Epinephrine has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Epinephrine 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 01fd19cd-190c-4989-b733-60ba95941297, effective 20251218; matched on
openfda.generic_name.exact:"EPINEPHRINE") - 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, 1,230 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
EPINEPHRINE, 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.