Enoxaparin side effects: what 57,199 FDA adverse event reports show
Drug class
Low molecular weight heparin (lmwh)
Label matched
Enoxaparin Sodium (Enoxaparin Sodium)
Who reports
57,199 reports · 87% serious · 8,879 with death outcome · 53% female
Used for
Enoxaparin Sodium Injection is a low molecular weight heparin (LMWH) indicated for: Prophylaxis of deep vein thrombosis (DVT) in abdominal surgery, hip replacement surgery, knee replacement surgery, or medical patients with severely restricted mobility.
What it is
Enoxaparin Sodium Injection, USP is a sterile aqueous solution containing enoxaparin sodium, a low molecular weight heparin. The pH of the injection is 5.5 to 7.5. Enoxaparin sodium is obtained by alkaline depolymerization of heparin benzyl ester derived from porcine intestinal mucosa.
Boxed warning
SPINAL/EPIDURAL HEMATOMAS Epidural or spinal hematomas may occur in patients who are anticoagulated with low molecular weight heparins (LMWH) or heparinoids and are receiving neuraxial anesthesia or undergoing spinal puncture. These hematomas may result in long-term or permanent paralysis. Consider these risks when scheduling patients for spinal procedures.
Causality screen of the 40 strongest signals
What the badges mean
- Labeled — boxed warning The term (or its clinical synonym) appears in the FDA boxed warning: causality is regulator-recognised and considered serious.
- 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). 1,229 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 |
|---|---|---|---|---|---|---|
| Abdominal haematoma | 47 | 136.7 97.8–191.3ROR 136.9 · calibrated p 2e-8 ✓ | 95.7 EB05 74.8 · IC025 +5.1 3/3 methods agree | Labeled (related wording) related wording | serious n=47 · 100% clinician | NCT01583218: 1/3,716 (0.0%) on Enoxaparin (serious AE) |
| Truncus arteriosus persistent | 41 | 93.6 66.4–132.0ROR 93.7 · calibrated p 4e-7 ✓ | 72.1 EB05 55.4 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious n=41 · 100% clinician | not reported in cached trials |
| Amaurosis fugax | 213 | 91.2 78.4–105.9ROR 91.5 · calibrated p 3e-7 ✓ | 72.5 EB05 64.7 · IC025 +5.7 3/3 methods agree | Not in label — unassessed | serious n=213 · 94% clinician | not reported in cached trials |
| Pelvic haematoma | 70 | 70.1 54.3–90.6ROR 70.2 · calibrated p 2e-6 ✓ | 58.0 EB05 47.5 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious n=70 · ♀ 100% (drug 53%) · 100% clinician | not reported in cached trials |
| Retroperitoneal haemorrhage | 341 | 58.6 52.3–65.7ROR 59.0 · calibrated p 5e-6 ✓ | 50.4 EB05 46.1 · IC025 +5.4 3/3 methods agree | Labeled (related wording) related wording | serious n=335 | NCT00571649: 1/3,997 (0.0%) on Enoxaparin (serious AE) |
| Haematoma muscle | 159 | 57.2 48.4–67.6ROR 57.3 · calibrated p 6e-6 ✓ | 49.2 EB05 43.1 · IC025 +5.2 3/3 methods agree | Not in label — unassessed | serious n=158 · 100% clinician | not reported in cached trials |
| Abdominal wall haematoma | 258 | 56.0 49.1–63.8ROR 56.2 · calibrated p 7e-6 ✓ | 48.4 EB05 43.7 · IC025 +5.3 3/3 methods agree | Labeled (related wording) related wording | serious n=249 · 90% clinician | NCT01583218: 1/3,716 (0.0%) on Enoxaparin (serious AE) |
| Retroperitoneal haematoma | 286 | 54.8 48.4–62.1ROR 55.1 · calibrated p 8e-6 ✓ | 47.6 EB05 43.1 · IC025 +5.3 3/3 methods agree | Labeled (related wording) related wording | serious n=284 | NCT00571649: 1/4,001 (0.0%) on Enoxaparin (serious AE) |
| Heparin-induced thrombocytopenia | 637 | 54.1 49.8–58.8ROR 54.7 · calibrated p 8e-6 ✓ | 47.1 EB05 44.1 · IC025 +5.4 3/3 methods agree | Labeled — boxed warning exact term | serious n=626 · 95% clinician | NCT00571649: 1/4,001 (0.0%) on Enoxaparin (serious AE) |
| Device safety feature issue | 118 | 51.6 42.6–62.6ROR 51.7 · calibrated p 1e-5 ✓ | 45.0 EB05 38.6 · IC025 +4.9 3/3 methods agree | Reporting / coding artifact | ♀ 100% (drug 53%) | not reported in cached trials |
| Intra-abdominal haematoma | 153 | 51.4 43.4–60.9ROR 51.5 · calibrated p 1e-5 ✓ | 44.9 EB05 39.2 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious n=153 | NCT01583218: 1/3,716 (0.0%) on Enoxaparin (serious AE) |
| Thrombocythaemia | 63 | 46.5 35.8–60.4ROR 46.5 · calibrated p 3e-5 ✓ | 40.8 EB05 33.0 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=59 · 100% clinician | not reported in cached trials |
| Mixed liver injury | 205 | 27.7 24.1–31.9ROR 27.8 · calibrated p 4e-4 ✓ | 25.8 EB05 22.9 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=205 · 100% clinician | not reported in cached trials |
| Shock haemorrhagic | 549 | 26.5 24.3–28.9ROR 26.8 · calibrated p 5e-4 ✓ | 24.7 EB05 23.1 · IC025 +4.5 3/3 methods agree | Labeled (related wording) related wording | serious PRR 16.4 | NCT00571649: 1/4,001 (0.0%) on Enoxaparin (serious AE) |
| Muscle haemorrhage | 268 | 26.2 23.2–29.7ROR 26.3 · calibrated p 5e-4 ✓ | 24.5 EB05 22.1 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=264 | NCT00571649: 1/4,001 (0.0%) on Enoxaparin (serious AE) |
| Cardiac septal defect | 41 | 21.9 16.0–30.1ROR 22.0 · calibrated p 0.002 ✓ | 20.6 EB05 15.8 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=41 · 100% clinician | not reported in cached trials |
| Spontaneous haematoma | 42 | 21.9 16.0–29.9ROR 21.9 · calibrated p 0.002 ✓ | 20.5 EB05 15.8 · IC025 +3.6 3/3 methods agree | Labeled (related wording) related wording | serious n=42 · ♀ 100% (drug 53%) · 100% clinician | NCT01583218: 1/3,716 (0.0%) on Enoxaparin (serious AE) |
| Extradural haematoma | 73 | 21.3 16.8–26.9ROR 21.3 · calibrated p 0.002 ✓ | 20.0 EB05 16.5 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=72 · 100% clinician | not reported in cached trials |
| Vascular purpura | 73 | 20.3 16.0–25.6ROR 20.3 · calibrated p 0.002 ✓ | 19.1 EB05 15.7 · IC025 +3.7 3/3 methods agree | Labeled (related wording) related wording | serious n=73 · ♀ 0% (drug 53%) · 100% clinician | not reported in cached trials |
| Haemorrhagic stroke | 405 | 19.9 18.0–22.0ROR 20.0 · calibrated p 0.002 ✓ | 18.9 EB05 17.4 · IC025 +4.0 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 12.5 | NCT00571649: 1/3,997 (0.0%) on Enoxaparin (serious AE) |
| Hepatic cytolysis | 628 | 19.8 18.3–21.5ROR 20.0 · calibrated p 0.002 ✓ | 18.8 EB05 17.6 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious PRR 12.5 · 97% clinician | not reported in cached trials |
| International normalised ratio decreased | 204 | 19.2 16.7–22.1ROR 19.3 · calibrated p 0.002 ✓ | 18.3 EB05 16.3 · IC025 +3.9 3/3 methods agree | Lab value / disease marker | serious n=151 | not reported in cached trials |
| Peritoneal haemorrhage | 68 | 18.6 14.6–23.7ROR 18.6 · calibrated p 0.003 ✓ | 17.6 EB05 14.4 · IC025 +3.6 3/3 methods agree | Labeled (related wording) related wording | serious n=68 · 100% clinician | NCT00571649: 2/3,997 (0.1%) on Enoxaparin (serious AE) |
| Hepatocellular injury | 656 | 17.7 16.4–19.1ROR 17.9 · calibrated p 0.003 ✓ | 16.9 EB05 15.8 · IC025 +3.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 11.2 · 94% clinician | NCT01583218: 1/3,716 (0.0%) on Enoxaparin (serious AE) |
| Congenital cardiovascular anomaly | 39 | 17.6 12.8–24.3ROR 17.6 · calibrated p 0.004 ✓ | 16.6 EB05 12.6 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=39 · 100% clinician | not reported in cached trials |
| Acute generalised exanthematous pustulosis | 350 | 17.3 15.6–19.3ROR 17.4 · calibrated p 0.004 ✓ | 16.6 EB05 15.2 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious PRR 11.0 · 93% clinician | NCT01583218: 1/3,716 (0.0%) on Enoxaparin (serious AE) |
| Streptococcal sepsis | 51 | 16.3 12.3–21.6ROR 16.3 · calibrated p 0.006 ✓ | 15.5 EB05 12.2 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=51 · ♀ 100% (drug 53%) | not reported in cached trials |
| Arterial haemorrhage | 49 | 16.3 12.2–21.7ROR 16.3 · calibrated p 0.006 ✓ | 15.5 EB05 12.1 · IC025 +3.3 3/3 methods agree | Labeled (related wording) related wording | serious n=49 · 100% clinician | not reported in cached trials |
| Haematoma | 1,109 | 16.3 15.3–17.3ROR 16.6 · calibrated p 0.005 ✓ | 15.6 EB05 14.9 · IC025 +3.9 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 10.8 | NCT00571649: 1/4,001 (0.0%) on Enoxaparin (serious AE) |
| Post procedural haematoma | 72 | 16.2 12.8–20.5ROR 16.2 · calibrated p 0.006 ✓ | 15.5 EB05 12.6 · IC025 +3.4 3/3 methods agree | Reporting / coding artifact | serious n=70 · 100% clinician | not reported in cached trials |
| Urinary tract disorder | 189 | 16.0 13.9–18.6ROR 16.1 · calibrated p 0.005 ✓ | 15.4 EB05 13.6 · IC025 +3.7 3/3 methods agree | Not in label — unassessed | serious n=187 · 94% clinician | NCT00571649: 13/4,001 (0.3%) on Enoxaparin (serious AE) |
| Intra-abdominal haemorrhage | 97 | 15.5 12.6–19.0ROR 15.5 · calibrated p 0.007 ✓ | 14.8 EB05 12.5 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=97 | not reported in cached trials |
| Cholestasis (bile flow blockage) | 767 | 15.3 14.2–16.4ROR 15.5 · calibrated p 0.006 ✓ | 14.7 EB05 13.9 · IC025 +3.7 3/3 methods agree | Not in label — unassessed | serious PRR 9.8 · 95% clinician | NCT00571649: 2/3,997 (0.1%) on Enoxaparin (serious AE) |
| Vascular pseudoaneurysm | 67 | 14.6 11.4–18.6ROR 14.6 · calibrated p 0.009 ✓ | 13.9 EB05 11.3 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=65 · 100% clinician | not reported in cached trials |
| Rash morbilliform | 106 | 14.5 12.0–17.6ROR 14.6 · calibrated p 0.008 ✓ | 13.9 EB05 11.8 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=104 · 100% clinician | not reported in cached trials |
| Subcutaneous haematoma | 46 | 13.6 10.1–18.3ROR 13.6 · calibrated p 0.012 ✓ | 12.9 EB05 9.9 · IC025 +3.0 3/3 methods agree | Labeled (related wording) related wording | serious n=45 · ♀ 100% (drug 53%) · 100% clinician | not reported in cached trials |
| Jugular vein thrombosis | 63 | 13.5 10.5–17.4ROR 13.6 · calibrated p 0.012 ✓ | 12.9 EB05 10.4 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=59 | not reported in cached trials |
| Eosinophilia | 621 | 13.5 12.4–14.6ROR 13.6 · calibrated p 0.010 ✓ | 13.0 EB05 12.2 · IC025 +3.6 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 9.0 · 95% clinician | not reported in cached trials |
| Cytolytic hepatitis | 119 | 13.4 11.2–16.1ROR 13.4 · calibrated p 0.012 ✓ | 12.9 EB05 11.0 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | serious n=118 | NCT00571649: 1/4,001 (0.0%) on Enoxaparin (serious AE) |
| Hypercoagulation | 67 | 13.3 10.4–16.9ROR 13.3 · calibrated p 0.013 ✓ | 12.7 EB05 10.2 · IC025 +3.2 3/3 methods agree | Not in label — unassessed | serious n=63 | 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 Enoxaparin 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 (17 of 40 signal terms matched).
- NCT00571649 — Venous Thromboembolic Event (VTE) Prophylaxis in Medically Ill Patients (N=8101, PHASE3; 854 AE terms posted; arms: Rivaroxaban (Xarelto, BAY59-7939); Enoxaparin)
- NCT01583218 — Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study) (N=7513, PHASE3; 459 AE terms posted; arms: Betrixaban; Enoxaparin)
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 |
|---|---|---|---|---|---|---|
| Off label use (used outside approved label) | 2,566 | 1.1 1.0–1.1ROR 1.1 · calibrated p 0.365 | 1.1 EB05 1.0 · IC025 +0.1 | Reporting / coding artifact | serious PRR 0.9 | not reported in cached trials |
| Dyspnoea (shortness of breath) | 2,429 | 1.6 1.5–1.6ROR 1.6 · calibrated p 0.708 | 1.6 EB05 1.5 · IC025 +0.6 | Labeled adverse reaction exact term | serious PRR 1.4 | NCT00571649: 17/4,001 (0.4%) on Enoxaparin (serious AE) |
| Nausea | 2,420 | 1.1 1.1–1.2ROR 1.1 · calibrated p 0.393 | 1.1 EB05 1.1 · IC025 +0.1 | Labeled adverse reaction exact term | serious PRR 1.3 | NCT00571649: 5/4,001 (0.1%) on Enoxaparin (serious AE) |
| Diarrhoea (diarrhea) | 2,304 | 1.3 1.3–1.4ROR 1.3 · calibrated p 0.527 | 1.3 EB05 1.3 · IC025 +0.3 | Labeled adverse reaction exact term | serious PRR 1.4 | NCT00571649: 10/4,001 (0.2%) on Enoxaparin (serious AE) |
| Anaemia (low red blood cells) | 2,233 | 4.3 4.2–4.5ROR 4.5 · calibrated p 0.302 | 4.3 EB05 4.1 · IC025 +2.0 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 3.1 | NCT00571649: 13/4,001 (0.3%) on Enoxaparin (serious AE) |
| Thrombocytopenia (low platelets) | 2,106 | 7.0 6.7–7.3ROR 7.3 · calibrated p 0.089 | 6.9 EB05 6.7 · IC025 +2.7 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 4.7 | NCT00571649: 9/4,001 (0.2%) on Enoxaparin (serious AE) |
| Pyrexia (fever) | 2,080 | 2.2 2.1–2.3ROR 2.3 · calibrated p 0.924 | 2.2 EB05 2.1 · IC025 +1.1 3/3 methods agree | Labeled (related wording) related wording | serious PRR 1.8 | NCT00571649: 9/4,001 (0.2%) on Enoxaparin (serious AE) |
| Fatigue (tiredness) | 2,015 | 1.0 0.9–1.0ROR 0.9 · calibrated p 0.274 | 1.0 EB05 0.9 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Not in label — unassessed | serious PRR 1.0 | NCT00571649: 3/4,001 (0.1%) on Enoxaparin (serious AE) |
| Vomiting | 1,892 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.640 | 1.5 EB05 1.4 · IC025 +0.5 | Not in label — unassessed | serious PRR 1.4 | NCT00571649: 4/4,001 (0.1%) on Enoxaparin (serious AE) |
| Pulmonary embolism (lung blood clot) | 1,809 | 7.1 6.7–7.4ROR 7.3 · calibrated p 0.089 | 6.9 EB05 6.7 · IC025 +2.7 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 4.6 | NCT00571649: 4/4,001 (0.1%) on Enoxaparin (serious AE) |
| Death | 1,761 | 0.7 0.7–0.8ROR 0.7 · calibrated p 0.152 | 0.7 EB05 0.7 · IC025 -0.5 PRR-only: not supported by EBGM or IC | Outcome field, not a reaction | serious PRR 0.5 | NCT00571649: 9/4,001 (0.2%) on Enoxaparin (serious AE) |
| Pneumonia (lung infection) | 1,694 | 1.9 1.8–2.0ROR 2.0 · calibrated p 0.919 | 1.9 EB05 1.8 · IC025 +0.9 | Labeled adverse reaction exact term | serious PRR 1.3 | NCT00571649: 10/4,001 (0.2%) on Enoxaparin (serious AE) |
| Asthenia (weakness) | 1,629 | 1.6 1.5–1.7ROR 1.6 · calibrated p 0.711 | 1.6 EB05 1.5 · IC025 +0.6 | Not in label — unassessed | serious PRR 1.4 | NCT00571649: 1/4,001 (0.0%) on Enoxaparin (serious AE) |
| Acute kidney injury (sudden kidney damage) | 1,600 | 3.9 3.7–4.1ROR 4.0 · calibrated p 0.384 | 3.8 EB05 3.7 · IC025 +1.9 3/3 methods agree | Not in label — unassessed | serious PRR 2.5 · 90% clinician | not reported in cached trials |
| Fall | 1,540 | 1.7 1.6–1.8ROR 1.7 · calibrated p 0.782 | 1.7 EB05 1.6 · IC025 +0.7 | Labeled adverse reaction exact term | serious PRR 1.3 | NCT00571649: 3/4,001 (0.1%) on Enoxaparin (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.
- Truncus arteriosus persistent — n=41, PRR 93.6
- Amaurosis fugax — n=213, PRR 91.2
- Pelvic haematoma — n=70, PRR 70.1
- Haematoma muscle — n=159, PRR 57.2
- Intra-abdominal haematoma — n=153, PRR 51.4 (also seen in trial arm)
- Thrombocythaemia — n=63, PRR 46.5
- Mixed liver injury — n=205, PRR 27.7
- Muscle haemorrhage — n=268, PRR 26.2 (also seen in trial arm)
- Cardiac septal defect — n=41, PRR 21.9
- Extradural haematoma — n=73, PRR 21.3
✓ A hand-written Bradford Hill causality assessment exists for this drug: Enoxaparin (low-molecular-weight heparins) ↔ Heparin-induced thrombocytopenia (HIT).
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 Enoxaparin?
In FDA FAERS, the most frequently co-reported reaction terms for Enoxaparin are dyspnoea, nausea, diarrhoea, anaemia, thrombocytopenia, pyrexia. 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 Enoxaparin have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: SPINAL/EPIDURAL HEMATOMAS Epidural or spinal hematomas may occur in patients who are anticoagulated with low molecular weight heparins (LMWH) or heparinoids and are receiving neuraxial anesthesia or undergoing spinal puncture. These hematomas may result in long-term or permanent paralysis. Consider these risks when scheduling patients for spinal procedures.
Do FAERS signals prove that Enoxaparin 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 32f8d292-0dda-4931-81ea-ba47e23edf61, effective 20241206; matched on
openfda.generic_name.exact:"ENOXAPARIN SODIUM") - 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, 1,269 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
ENOXAPARIN, 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.