Propofol side effects: what 36,320 FDA adverse event reports show
Who reports
36,320 reports · 94% serious · 4,932 with death outcome · 51% female
Used for
Propofol injectable emulsion is an intravenous general anesthetic and sedation drug indicated for: • Induction of General Anesthesia for Patients Greater than or Equal to 3 Years of Age • Maintenance of General Anesthesia for Patients Greater than or E.
What it is
Propofol Injectable Emulsion, USP is an anesthetic available as a sterile, nonpyrogenic white to slight off-white homogeneous emulsion for intravenous administration.
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.
- 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). 1,188 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 |
|---|---|---|---|---|---|---|
| Propofol infusion syndrome | 618 | 4,449.0 3,520.9–5,621.7ROR 4,525.9 · calibrated p 2e-25 ✓ | 497.3 EB05 465.3 · IC025 +8.4 3/3 methods agree vs other General Anesthetics: PRR 221.9 (118.8–414.4) | Labeled adverse reaction exact term | serious n=613 · 96% clinician | no trial arm names this drug |
| Trigemino-cardiac reflex | 58 | 1,434.2 884.9–2,324.3ROR 1,436.4 · calibrated p 2e-17 ✓ | 359.5 EB05 288.3 · IC025 +6.1 3/3 methods agree vs other General Anesthetics: PRR 23.1 (11.5–46.7) | Not in label — unassessed | serious n=58 · ♀ 0% (drug 51%) · 100% clinician | no trial arm names this drug |
| Negative pressure pulmonary oedema | 63 | 1,235.5 795.9–1,917.8ROR 1,237.6 · calibrated p 5e-17 ✓ | 348.7 EB05 282.3 · IC025 +6.2 3/3 methods agree vs other General Anesthetics: PRR 6.0 (4.0–8.9) | Labeled (related wording) related wording | serious n=63 · ♀ 0% (drug 51%) · 100% clinician | no trial arm names this drug |
| Mitochondrial dna mutation | 38 | 459.8 299.9–705.1ROR 460.3 · calibrated p 1e-12 ✓ | 225.9 EB05 171.8 · IC025 +5.3 3/3 methods agree vs other General Anesthetics: only this drug | Not in label — unassessed | serious n=38 · ♀ 100% (drug 51%) | no trial arm names this drug |
| Neuromuscular block prolonged | 142 | 358.9 291.0–442.7ROR 360.3 · calibrated p 3e-12 ✓ | 214.1 EB05 186.1 · IC025 +6.7 3/3 methods agree vs other General Anesthetics: PRR 8.2 (6.1–11.1) | Not in label — unassessed | serious n=135 · 94% clinician | no trial arm names this drug |
| New onset refractory status epilepticus | 39 | 336.1 226.2–499.2ROR 336.4 · calibrated p 2e-11 ✓ | 191.8 EB05 146.4 · IC025 +5.3 3/3 methods agree vs other General Anesthetics: only this drug | Not in label — unassessed | serious n=39 · ♀ 0% (drug 51%) · 100% clinician | no trial arm names this drug |
| Delayed recovery from anaesthesia | 317 | 291.2 254.5–333.3ROR 293.8 · calibrated p 1e-11 ✓ | 190.7 EB05 173.8 · IC025 +7.0 3/3 methods agree vs other General Anesthetics: PRR 5.9 (5.0–7.1) | Labeled (related wording) related wording | serious n=301 · 95% clinician | no trial arm names this drug |
| Airway peak pressure increased | 49 | 275.9 196.2–388.1ROR 276.3 · calibrated p 7e-11 ✓ | 173.6 EB05 136.5 · IC025 +5.5 3/3 methods agree vs other General Anesthetics: PRR 6.8 (4.2–10.9) | Lab value / disease marker | serious n=49 · 94% clinician | no trial arm names this drug |
| Airway complication of anaesthesia | 81 | 263.2 202.3–342.5ROR 263.8 · calibrated p 7e-11 ✓ | 173.0 EB05 143.6 · IC025 +6.1 3/3 methods agree vs other General Anesthetics: PRR 16.2 (9.7–26.9) | Not in label — unassessed | serious n=76 · 95% clinician | no trial arm names this drug |
| Postoperative delirium | 55 | 238.8 174.3–327.1ROR 239.1 · calibrated p 2e-10 ✓ | 159.2 EB05 126.9 · IC025 +5.6 3/3 methods agree vs other General Anesthetics: PRR 9.0 (5.5–14.7) | Labeled (related wording) related wording | serious n=55 · 100% clinician | no trial arm names this drug |
| Anaesthetic complication pulmonary | 26 | 238.5 150.9–377.0ROR 238.7 · calibrated p 6e-10 ✓ | 150.0 EB05 107.6 · IC025 +4.7 3/3 methods agree vs other General Anesthetics: PRR 8.5 (4.2–17.2) | Not in label — unassessed | serious n=26 · 100% clinician | no trial arm names this drug |
| Myoglobin urine present | 72 | 234.0 177.9–307.8ROR 234.4 · calibrated p 2e-10 ✓ | 159.1 EB05 130.6 · IC025 +5.9 3/3 methods agree vs other General Anesthetics: PRR 3.9 (2.8–5.5) | Lab value / disease marker | serious n=71 · ♀ 100% (drug 51%) · 100% clinician | no trial arm names this drug |
| Mechanical ventilation complication | 41 | 217.9 152.1–312.3ROR 218.2 · calibrated p 6e-10 ✓ | 147.1 EB05 113.1 · IC025 +5.3 3/3 methods agree vs other General Anesthetics: PRR 21.0 (9.4–46.9) | Reporting / coding artifact | serious n=41 · ♀ 0% (drug 51%) · 100% clinician | no trial arm names this drug |
| Tracheal deviation | 24 | 213.3 133.4–340.9ROR 213.4 · calibrated p 2e-9 ✓ | 138.5 EB05 97.9 · IC025 +4.5 3/3 methods agree vs other General Anesthetics: PRR 3.7 (2.1–6.6) | Not in label — unassessed | serious n=24 · ♀ 100% (drug 51%) · 100% clinician | no trial arm names this drug |
| Hyperthermia malignant | 397 | 212.8 189.7–238.7ROR 215.1 · calibrated p 2e-10 ✓ | 154.0 EB05 141.7 · IC025 +6.9 3/3 methods agree vs other General Anesthetics: PRR 5.0 (4.3–5.8) | Not in label — unassessed | serious n=392 · ♀ 30% (drug 51%) · 98% clinician | no trial arm names this drug |
| Allergy test negative | 40 | 199.5 139.2–286.0ROR 199.8 · calibrated p 1e-9 ✓ | 138.3 EB05 106.0 · IC025 +5.2 3/3 methods agree vs other General Anesthetics: PRR 28.7 (11.3–72.8) | Reporting / coding artifact | serious n=40 · 100% clinician | no trial arm names this drug |
| Recurrence of neuromuscular blockade | 42 | 185.2 130.7–262.2ROR 185.4 · calibrated p 2e-9 ✓ | 131.7 EB05 101.5 · IC025 +5.2 3/3 methods agree vs other General Anesthetics: PRR 3.7 (2.4–5.7) | Not in label — unassessed | serious n=42 | no trial arm names this drug |
| Unwanted awareness during anaesthesia | 78 | 180.3 139.8–232.6ROR 180.7 · calibrated p 2e-9 ✓ | 132.8 EB05 109.8 · IC025 +5.8 3/3 methods agree vs other General Anesthetics: PRR 3.1 (2.3–4.2) | Not in label — unassessed | serious n=73 · ♀ 83% (drug 51%) · 95% clinician | no trial arm names this drug |
| Burkholderia test positive | 28 | 167.6 110.0–255.5ROR 167.8 · calibrated p 8e-9 ✓ | 119.3 EB05 86.6 · IC025 +4.7 3/3 methods agree vs other General Anesthetics: only this drug | Lab value / disease marker | serious n=28 · ♀ 0% (drug 51%) · 100% clinician | no trial arm names this drug |
| Anaesthetic complication neurological | 203 | 165.6 141.7–193.6ROR 166.6 · calibrated p 2e-9 ✓ | 127.0 EB05 113.0 · IC025 +6.4 3/3 methods agree vs other General Anesthetics: PRR 1.4 (1.2–1.7) | Not in label — unassessed | serious n=200 · 100% clinician | no trial arm names this drug |
| Neuromuscular blockade | 47 | 150.2 108.9–207.1ROR 150.4 · calibrated p 1e-8 ✓ | 113.6 EB05 88.9 · IC025 +5.2 3/3 methods agree vs other General Anesthetics: PRR 6.8 (4.2–11.0) | Not in label — unassessed | serious n=45 · 100% clinician | no trial arm names this drug |
| Intensive care unit acquired weakness | 78 | 148.4 115.7–190.3ROR 148.7 · calibrated p 8e-9 ✓ | 114.6 EB05 94.8 · IC025 +5.7 3/3 methods agree vs other General Anesthetics: only this drug | Labeled (related wording) related wording | serious n=78 · ♀ 29% (drug 51%) · 95% clinician | no trial arm names this drug |
| Csf oligoclonal band present | 25 | 148.1 95.4–230.0ROR 148.2 · calibrated p 2e-8 ✓ | 108.2 EB05 77.1 · IC025 +4.5 3/3 methods agree vs other General Anesthetics: only this drug | Lab value / disease marker | serious n=25 · ♀ 100% (drug 51%) | no trial arm names this drug |
| Intra-abdominal pressure increased | 32 | 148.0 100.3–218.3ROR 148.1 · calibrated p 2e-8 ✓ | 110.1 EB05 81.6 · IC025 +4.8 3/3 methods agree vs other General Anesthetics: only this drug | Lab value / disease marker | serious n=32 · ♀ 100% (drug 51%) | no trial arm names this drug |
| Confusion postoperative | 24 | 128.8 82.7–200.5ROR 128.9 · calibrated p 7e-8 ✓ | 97.2 EB05 68.8 · IC025 +4.4 3/3 methods agree vs other General Anesthetics: only this drug | Labeled (related wording) related wording | serious n=23 · 100% clinician | no trial arm names this drug |
| Procedural hypotension | 139 | 111.8 93.2–134.1ROR 112.2 · calibrated p 6e-8 ✓ | 92.4 EB05 80.3 · IC025 +5.9 3/3 methods agree vs other General Anesthetics: PRR 16.6 (11.2–24.7) | Not in label — unassessed | serious n=134 · 100% clinician | no trial arm names this drug |
| Myocardial depression | 37 | 105.2 74.1–149.4ROR 105.3 · calibrated p 2e-7 ✓ | 85.2 EB05 64.5 · IC025 +4.8 3/3 methods agree vs other General Anesthetics: only this drug | Labeled (related wording) related wording | serious n=37 · ♀ 100% (drug 51%) · 100% clinician | no trial arm names this drug |
| Phrenic nerve paralysis | 30 | 92.7 63.0–136.4ROR 92.8 · calibrated p 5e-7 ✓ | 76.1 EB05 55.9 · IC025 +4.5 3/3 methods agree vs other General Anesthetics: PRR 4.3 (2.5–7.3) | Not in label — unassessed | serious n=30 · ♀ 100% (drug 51%) · 100% clinician | no trial arm names this drug |
| Necrosis ischaemic | 56 | 79.4 60.1–105.0ROR 79.5 · calibrated p 1e-6 ✓ | 68.3 EB05 54.5 · IC025 +5.0 3/3 methods agree vs other General Anesthetics: only this drug | Not in label — unassessed | serious n=56 | no trial arm names this drug |
| Phaeochromocytoma crisis | 25 | 77.3 50.9–117.3ROR 77.3 · calibrated p 2e-6 ✓ | 64.9 EB05 46.2 · IC025 +4.2 3/3 methods agree vs other General Anesthetics: only this drug | Not in label — unassessed | serious n=25 · ♀ 100% (drug 51%) · 100% clinician | no trial arm names this drug |
| Anaphylactoid shock | 55 | 77.0 58.1–102.1ROR 77.2 · calibrated p 1e-6 ✓ | 66.5 EB05 53.0 · IC025 +5.0 3/3 methods agree vs other General Anesthetics: only this drug | Not in label — unassessed | serious n=54 · 92% clinician | no trial arm names this drug |
| Hepatic ischaemia | 36 | 75.3 53.2–106.5ROR 75.3 · calibrated p 2e-6 ✓ | 64.4 EB05 48.6 · IC025 +4.6 3/3 methods agree vs other General Anesthetics: only this drug | Not in label — unassessed | serious n=36 · ♀ 100% (drug 51%) · 100% clinician | no trial arm names this drug |
| Carcinoid crisis | 24 | 67.9 44.5–103.7ROR 68.0 · calibrated p 5e-6 ✓ | 58.1 EB05 41.1 · IC025 +4.1 3/3 methods agree vs other General Anesthetics: PRR 5.4 (2.9–10.1) | Not in label — unassessed | serious n=24 · 100% clinician | no trial arm names this drug |
| Tryptase increased | 71 | 64.7 50.6–82.7ROR 64.8 · calibrated p 3e-6 ✓ | 57.4 EB05 47.0 · IC025 +5.0 3/3 methods agree vs other General Anesthetics: PRR 28.3 (14.2–56.7) | Not in label — unassessed | serious n=70 | no trial arm names this drug |
| Spinal muscular atrophy | 26 | 61.6 41.1–92.3ROR 61.7 · calibrated p 8e-6 ✓ | 53.6 EB05 38.5 · IC025 +4.1 3/3 methods agree vs other General Anesthetics: only this drug | Not in label — unassessed | serious n=26 · ♀ 0% (drug 51%) · 100% clinician | no trial arm names this drug |
| Inspiratory capacity decreased | 26 | 60.1 40.1–90.0ROR 60.2 · calibrated p 9e-6 ✓ | 52.5 EB05 37.6 · IC025 +4.1 3/3 methods agree vs other General Anesthetics: only this drug | Not in label — unassessed | serious n=26 · ♀ 0% (drug 51%) · 100% clinician | no trial arm names this drug |
| Postoperative fever | 25 | 55.5 36.8–83.7ROR 55.6 · calibrated p 2e-5 ✓ | 48.9 EB05 34.8 · IC025 +4.0 3/3 methods agree vs other General Anesthetics: only this drug | Labeled (related wording) related wording | 100% clinician | no trial arm names this drug |
| Anaesthetic complication | 220 | 51.7 45.1–59.4ROR 52.1 · calibrated p 1e-5 ✓ | 47.3 EB05 42.3 · IC025 +5.2 3/3 methods agree vs other General Anesthetics: PRR 5.3 (4.3–6.6) | Reporting / coding artifact | serious n=185 | no trial arm names this drug |
| Anaphylactic shock | 2,106 | 51.7 49.5–54.0ROR 54.8 · calibrated p 8e-6 ✓ | 47.4 EB05 45.7 · IC025 +5.5 3/3 methods agree vs other General Anesthetics: PRR 14.6 (13.3–16.1) | Not in label — unassessed | serious PRR 29.2 · 92% clinician | no trial arm names this drug |
| Pco2 increased | 58 | 50.7 38.8–66.4ROR 50.8 · calibrated p 2e-5 ✓ | 46.0 EB05 36.9 · IC025 +4.6 3/3 methods agree vs other General Anesthetics: PRR 8.0 (5.0–12.7) | Not in label — unassessed | serious n=56 | no trial arm names this drug |
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 |
|---|---|---|---|---|---|---|
| Hypotension (low blood pressure) | 2,923 | 8.5 8.2–8.8ROR 9.2 · calibrated p 0.043 ✓ | 8.4 EB05 8.2 · IC025 +3.0 3/3 methods agree vs other General Anesthetics: PRR 8.3 (7.8–8.9) | Labeled adverse reaction exact term | serious PRR 5.9 · 91% clinician | no trial arm names this drug |
| Drug ineffective (drug did not work) | 2,805 | 1.2 1.2–1.3ROR 1.2 · calibrated p 0.474 | 1.2 EB05 1.2 · IC025 +0.2 vs other General Anesthetics: PRR 34.1 (30.3–38.5) | Reporting / coding artifact | serious PRR 1.8 · 93% clinician | no trial arm names this drug |
| Anaphylactic shock | 2,106 | 51.7 49.5–54.0ROR 54.8 · calibrated p 8e-6 ✓ | 47.4 EB05 45.7 · IC025 +5.5 3/3 methods agree vs other General Anesthetics: PRR 14.6 (13.3–16.1) | Not in label — unassessed | serious PRR 29.2 · 92% clinician | no trial arm names this drug |
| Cardiac arrest (heart stopping) | 1,822 | 13.0 12.4–13.6ROR 13.6 · calibrated p 0.010 ✓ | 12.7 EB05 12.2 · IC025 +3.6 3/3 methods agree vs other General Anesthetics: PRR 7.3 (6.8–7.9) | Labeled adverse reaction exact term | serious PRR 7.8 · 93% clinician | no trial arm names this drug |
| Anaphylactic reaction (severe allergic reaction) | 1,721 | 18.6 17.8–19.5ROR 19.5 · calibrated p 0.002 ✓ | 18.1 EB05 17.4 · IC025 +4.1 3/3 methods agree vs other General Anesthetics: PRR 15.8 (14.2–17.7) | Labeled (related wording) related wording | serious PRR 11.3 · 92% clinician | no trial arm names this drug |
| Off label use (used outside approved label) | 1,698 | 1.1 1.1–1.2ROR 1.1 · calibrated p 0.397 | 1.1 EB05 1.1 · IC025 +0.1 vs other General Anesthetics: PRR 27.7 (24.1–31.9) | Reporting / coding artifact | serious PRR 1.2 · 93% clinician | no trial arm names this drug |
| Drug interaction | 1,562 | 5.7 5.5–6.0ROR 5.9 · calibrated p 0.154 | 5.7 EB05 5.4 · IC025 +2.4 3/3 methods agree vs other General Anesthetics: PRR 6.3 (5.8–6.8) | Reporting / coding artifact | serious PRR 3.9 · 94% clinician | no trial arm names this drug |
| Tachycardia (fast heart rate) | 1,221 | 8.0 7.6–8.5ROR 8.3 · calibrated p 0.060 | 7.9 EB05 7.6 · IC025 +2.9 3/3 methods agree vs other General Anesthetics: PRR 11.1 (9.9–12.4) | Labeled adverse reaction exact term | serious PRR 5.3 · 90% clinician | no trial arm names this drug |
| Bradycardia (slow heart rate) | 1,187 | 13.2 12.4–13.9ROR 13.6 · calibrated p 0.010 ✓ | 12.9 EB05 12.3 · IC025 +3.6 3/3 methods agree vs other General Anesthetics: PRR 5.9 (5.4–6.5) | Labeled adverse reaction exact term | serious PRR 8.0 · 93% clinician | no trial arm names this drug |
| Pyrexia (fever) | 1,009 | 1.7 1.6–1.8ROR 1.7 · calibrated p 0.772 | 1.7 EB05 1.6 · IC025 +0.6 vs other General Anesthetics: PRR 33.9 (27.8–41.3) | Labeled (related wording) related wording | serious PRR 1.2 | no trial arm names this drug |
| Acute kidney injury (sudden kidney damage) | 993 | 3.8 3.6–4.0ROR 3.9 · calibrated p 0.405 | 3.8 EB05 3.6 · IC025 +1.8 3/3 methods agree vs other General Anesthetics: PRR 16.6 (14.3–19.2) | Labeled (related wording) related wording | serious PRR 2.3 · 94% clinician | no trial arm names this drug |
| Rhabdomyolysis (muscle breakdown) | 910 | 12.9 12.1–13.7ROR 13.2 · calibrated p 0.012 ✓ | 12.6 EB05 11.9 · IC025 +3.5 3/3 methods agree vs other General Anesthetics: PRR 9.0 (8.0–10.2) | Labeled adverse reaction exact term | serious PRR 7.8 · ♀ 27% (drug 51%) · 97% clinician | no trial arm names this drug |
| Bronchospasm (airway tightening) | 827 | 35.4 33.0–37.9ROR 36.2 · calibrated p 9e-5 ✓ | 33.3 EB05 31.5 · IC025 +4.9 3/3 methods agree vs other General Anesthetics: PRR 9.7 (8.5–11.1) | Labeled adverse reaction exact term | serious PRR 22.2 | no trial arm names this drug |
| Renal failure (kidney failure) | 813 | 3.5 3.3–3.8ROR 3.6 · calibrated p 0.465 | 3.5 EB05 3.3 · IC025 +1.7 3/3 methods agree vs other General Anesthetics: PRR 4.2 (3.8–4.6) | Labeled adverse reaction exact term | serious PRR 2.2 | no trial arm names this drug |
| Oxygen saturation decreased | 811 | 8.5 7.9–9.1ROR 8.7 · calibrated p 0.052 | 8.4 EB05 7.9 · IC025 +2.9 3/3 methods agree vs other General Anesthetics: PRR 8.2 (7.3–9.3) | Lab value / disease marker | serious PRR 5.5 · 91% clinician | 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.
- Trigemino-cardiac reflex — n=58, PRR 1,434.2
- Mitochondrial dna mutation — n=38, PRR 459.8
- Neuromuscular block prolonged — n=142, PRR 358.9
- New onset refractory status epilepticus — n=39, PRR 336.1
- Airway complication of anaesthesia — n=81, PRR 263.2
- Anaesthetic complication pulmonary — n=26, PRR 238.5
- Tracheal deviation — n=24, PRR 213.3
- Hyperthermia malignant — n=397, PRR 212.8
- Recurrence of neuromuscular blockade — n=42, PRR 185.2
- Unwanted awareness during anaesthesia — n=78, PRR 180.3
✓ A hand-written Bradford Hill causality assessment exists for this drug: Propofol ↔ Infusion syndrome.
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 Propofol?
In FDA FAERS, the most frequently co-reported reaction terms for Propofol are hypotension, anaphylactic shock, cardiac arrest, anaphylactic reaction, tachycardia, bradycardia. 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 Propofol have an FDA boxed warning?
No. The FDA label retrieved for Propofol has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Propofol 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 28d7ba00-f824-4e55-139a-03f509c099db, effective 20260813; matched on
openfda.generic_name.exact:"PROPOFOL") - 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, 1,228 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
PROPOFOL, 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.