Cyclobenzaprine side effects: what 49,555 FDA adverse event reports show
Drug class
Not stated in label
Brand names
Cyclobenzaprine Hydrochloride
Who reports
49,555 reports · 68% serious · 7,144 with death outcome · 72% female
Used for
Cyclobenzaprine hydrochloride tablets,USP are indicated as an adjunct to rest and physical therapy for relief of muscle spasm associated with acute, painful musculoskeletal conditions. Improvement is manifested by relief of muscle spasm and its associated signs and symptoms, namely, pain, tenderness, limitation of motion, and restriction in activities of daily living.
What it is
DESCRIPTION Cyclobenzaprine hydrochloride, USP is a white, crystalline tricyclic amine salt with the empirical formula C 20 H 21 N•HCl and a molecular weight of 311.9. It has a melting point of 217°C, and a pK a of 8.47 at 25°C.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- 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). 1,148 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 |
|---|---|---|---|---|---|---|
| Respiratory tract malformation | 36 | 161.1 109.7–236.7ROR 161.2 · calibrated p 9e-9 ✓ | 109.8 EB05 82.9 · IC025 +4.9 3/3 methods agree | Not in label — unassessed | serious n=36 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Sedation complication | 548 | 118.8 108.1–130.6ROR 120.1 · calibrated p 3e-8 ✓ | 92.4 EB05 86.0 · IC025 +6.3 3/3 methods agree | Reporting / coding artifact | serious n=546 · ♀ 100% (drug 72%) | no trial arm names this drug |
| Temperature regulation disorder | 461 | 113.1 102.1–125.4ROR 114.2 · calibrated p 4e-8 ✓ | 88.9 EB05 82.2 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=460 · ♀ 100% (drug 72%) | no trial arm names this drug |
| Vascular malformation | 43 | 107.2 76.7–149.8ROR 107.3 · calibrated p 1e-7 ✓ | 82.4 EB05 63.7 · IC025 +4.9 3/3 methods agree | Not in label — unassessed | serious n=43 · ♀ 100% (drug 72%) | no trial arm names this drug |
| Pulmonary malformation | 65 | 94.9 72.5–124.3ROR 95.1 · calibrated p 3e-7 ✓ | 75.8 EB05 61.6 · IC025 +5.2 3/3 methods agree | Not in label — unassessed | serious n=65 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Paranasal cyst | 43 | 92.3 66.3–128.4ROR 92.3 · calibrated p 4e-7 ✓ | 73.3 EB05 56.7 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious n=43 · ♀ 100% (drug 72%) | no trial arm names this drug |
| Hypocholesterolaemia | 43 | 68.6 49.7–94.7ROR 68.6 · calibrated p 3e-6 ✓ | 57.6 EB05 44.5 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=43 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Creatinine renal clearance decreased | 539 | 65.3 59.6–71.4ROR 66.0 · calibrated p 2e-6 ✓ | 56.4 EB05 52.6 · IC025 +5.6 3/3 methods agree | Lab value / disease marker | serious n=538 · ♀ 100% (drug 72%) | no trial arm names this drug |
| Overlap syndrome | 90 | 63.4 50.8–79.1ROR 63.5 · calibrated p 4e-6 ✓ | 54.5 EB05 45.7 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=90 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Multiple drug therapy | 90 | 62.5 50.1–78.0ROR 62.6 · calibrated p 4e-6 ✓ | 53.9 EB05 45.2 · IC025 +5.0 3/3 methods agree | Reporting / coding artifact | serious n=90 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Chronic kidney disease-mineral and bone disorder | 121 | 53.5 44.3–64.7ROR 53.6 · calibrated p 1e-5 ✓ | 47.2 EB05 40.6 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious n=121 | no trial arm names this drug |
| Lung cyst | 44 | 53.2 38.9–72.9ROR 53.3 · calibrated p 1e-5 ✓ | 46.4 EB05 36.0 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=43 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Nephrogenic anaemia | 439 | 43.8 39.7–48.3ROR 44.1 · calibrated p 3e-5 ✓ | 39.6 EB05 36.6 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=439 | no trial arm names this drug |
| Hyperparathyroidism secondary | 235 | 43.2 37.8–49.4ROR 43.4 · calibrated p 3e-5 ✓ | 39.1 EB05 35.1 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | serious n=235 | no trial arm names this drug |
| Food allergy | 620 | 37.8 34.8–41.0ROR 38.2 · calibrated p 7e-5 ✓ | 34.7 EB05 32.4 · IC025 +4.9 3/3 methods agree | Not in label — unassessed | serious n=612 · ♀ 100% (drug 72%) | no trial arm names this drug |
| Rebound acid hypersecretion | 241 | 36.0 31.6–41.1ROR 36.2 · calibrated p 1e-4 ✓ | 33.1 EB05 29.8 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=241 | no trial arm names this drug |
| Infusion site reaction | 228 | 35.9 31.4–41.1ROR 36.1 · calibrated p 1e-4 ✓ | 33.1 EB05 29.6 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=226 · ♀ 100% (drug 72%) · 94% clinician | no trial arm names this drug |
| Creatinine renal clearance increased | 58 | 35.3 27.0–46.1ROR 35.3 · calibrated p 1e-4 ✓ | 32.3 EB05 25.9 · IC025 +4.2 3/3 methods agree | Lab value / disease marker | serious n=58 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Facet joint syndrome | 226 | 32.6 28.5–37.3ROR 32.7 · calibrated p 2e-4 ✓ | 30.2 EB05 27.1 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=226 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Post-traumatic neck syndrome | 58 | 32.4 24.8–42.3ROR 32.4 · calibrated p 2e-4 ✓ | 29.9 EB05 24.0 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=56 · ♀ 100% (drug 72%) | no trial arm names this drug |
| Asthma-chronic obstructive pulmonary disease overlap syndrome | 37 | 32.3 23.1–45.1ROR 32.3 · calibrated p 3e-4 ✓ | 29.6 EB05 22.4 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=36 · ♀ 0% (drug 72%) · 100% clinician | no trial arm names this drug |
| Peripheral venous disease | 264 | 29.9 26.4–33.8ROR 30.0 · calibrated p 3e-4 ✓ | 27.9 EB05 25.2 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=263 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Bursitis | 788 | 29.5 27.5–31.7ROR 30.0 · calibrated p 3e-4 ✓ | 27.6 EB05 26.0 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious PRR 27.1 · ♀ 98% (drug 72%) | no trial arm names this drug |
| Blepharospasm | 392 | 28.5 25.7–31.5ROR 28.7 · calibrated p 3e-4 ✓ | 26.7 EB05 24.5 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=385 · ♀ 100% (drug 72%) · 91% clinician | no trial arm names this drug |
| Lupus vulgaris | 75 | 28.4 22.5–35.9ROR 28.4 · calibrated p 4e-4 ✓ | 26.5 EB05 21.8 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=75 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Soft tissue injury | 47 | 27.9 20.8–37.5ROR 27.9 · calibrated p 5e-4 ✓ | 26.0 EB05 20.3 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=47 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Bone demineralisation | 57 | 23.9 18.3–31.3ROR 24.0 · calibrated p 0.001 ✓ | 22.5 EB05 18.0 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=47 · ♀ 0% (drug 72%) | no trial arm names this drug |
| Blood calcium decreased | 580 | 22.9 21.0–24.9ROR 23.1 · calibrated p 0.001 ✓ | 21.7 EB05 20.3 · IC025 +4.3 3/3 methods agree | Lab value / disease marker | serious PRR 22.7 · ♀ 97% (drug 72%) | no trial arm names this drug |
| Mastoiditis | 50 | 22.9 17.2–30.4ROR 22.9 · calibrated p 0.001 ✓ | 21.6 EB05 17.0 · IC025 +3.7 3/3 methods agree | Not in label — unassessed | serious n=50 · ♀ 100% (drug 72%) | no trial arm names this drug |
| Foetal death | 253 | 21.6 19.1–24.6ROR 21.8 · calibrated p 0.001 ✓ | 20.6 EB05 18.6 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=253 · ♀ 100% (drug 72%) · 93% clinician | no trial arm names this drug |
| Coeliac disease | 476 | 21.5 19.6–23.6ROR 21.7 · calibrated p 0.001 ✓ | 20.5 EB05 19.0 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious PRR 21.0 · ♀ 100% (drug 72%) | no trial arm names this drug |
| Immunodeficiency | 691 | 20.8 19.3–22.4ROR 21.1 · calibrated p 0.002 ✓ | 19.8 EB05 18.6 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | age-adj. PRR 18.7 · serious PRR 18.0 · ♀ 97% (drug 72%) | no trial arm names this drug |
| Onychomadesis | 179 | 19.0 16.4–22.1ROR 19.1 · calibrated p 0.003 ✓ | 18.2 EB05 16.0 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=174 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Sternal fracture | 52 | 18.6 14.1–24.5ROR 18.6 · calibrated p 0.003 ✓ | 17.7 EB05 14.0 · IC025 +3.5 3/3 methods agree | Not in label — unassessed | serious n=52 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Rheumatic fever | 175 | 17.6 15.1–20.5ROR 17.7 · calibrated p 0.004 ✓ | 16.9 EB05 14.9 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=175 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| End stage renal disease | 725 | 17.3 16.1–18.6ROR 17.5 · calibrated p 0.004 ✓ | 16.6 EB05 15.6 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious PRR 14.0 | no trial arm names this drug |
| Orthostatic hypotension (dizziness on standing) | 686 | 17.3 16.0–18.6ROR 17.5 · calibrated p 0.004 ✓ | 16.6 EB05 15.6 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious PRR 15.8 · ♀ 96% (drug 72%) | no trial arm names this drug |
| Dislocation of vertebra | 86 | 17.0 13.7–21.0ROR 17.0 · calibrated p 0.005 ✓ | 16.3 EB05 13.6 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | serious n=86 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| X-ray abnormal | 67 | 16.5 12.9–21.0ROR 16.5 · calibrated p 0.005 ✓ | 15.8 EB05 12.8 · IC025 +3.4 3/3 methods agree | Lab value / disease marker | serious n=67 · ♀ 100% (drug 72%) · 100% clinician | no trial arm names this drug |
| Breast cancer stage iii | 241 | 16.4 14.4–18.7ROR 16.5 · calibrated p 0.005 ✓ | 15.8 EB05 14.2 · IC025 +3.7 3/3 methods agree | Not in label — unassessed | serious n=241 · ♀ 100% (drug 72%) · 100% clinician | 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 |
|---|---|---|---|
| Suicidality | 2,619 | 4.54.4–4.7 | signal |
| Kidney injury | 3,252 | 3.02.9–3.1 | signal |
| Depression | 1,946 | 2.92.8–3.1 | signal |
| Fall / fracture | 2,588 | 2.92.8–3.0 | signal |
| Serious infection | 3,753 | 2.12.0–2.1 | raised |
| Liver injury | 1,433 | 2.01.9–2.1 | raised |
| Venous thromboembolism | 960 | 1.91.8–2.0 | raised |
| Tendon disorder | 153 | 1.71.5–2.0 | raised |
| Opportunistic infection | 505 | 1.61.4–1.7 | raised |
| Thrombocytopenia | 800 | 1.51.4–1.6 | raised |
| Pancreatitis | 273 | 1.41.3–1.6 | raised |
| Hyperglycaemia / diabetes | 1,159 | 1.41.3–1.5 | raised |
| Anaemia | 884 | 1.21.2–1.3 | raised |
| Extrapyramidal | 289 | 1.21.0–1.3 | raised |
| Anaphylaxis / angioedema | 337 | 1.11.0–1.3 | raised |
| Myocardial infarction | 547 | 1.11.0–1.2 | raised |
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 |
|---|---|---|---|---|---|---|
| Pain | 5,095 | 3.5 3.4–3.6ROR 3.8 · calibrated p 0.415 | 3.5 EB05 3.4 · IC025 +1.8 3/3 methods agree | Likely indication confounding term in indications; also in warnings | age-adj. PRR 3.6 · serious PRR 3.8 | no trial arm names this drug |
| Fatigue (tiredness) | 4,026 | 2.2 2.1–2.3ROR 2.3 · calibrated p 0.901 | 2.2 EB05 2.1 · IC025 +1.1 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 2.0 · serious PRR 2.4 | no trial arm names this drug |
| Drug ineffective (drug did not work) | 3,602 | 1.2 1.1–1.2ROR 1.2 · calibrated p 0.419 | 1.2 EB05 1.1 · IC025 +0.2 | Reporting / coding artifact | age-adj. PRR 1.3 · serious PRR 1.7 | no trial arm names this drug |
| Nausea | 3,539 | 1.9 1.8–2.0ROR 2.0 · calibrated p 0.927 | 1.9 EB05 1.8 · IC025 +0.9 | Labeled adverse reaction exact term | age-adj. PRR 1.7 · serious PRR 2.1 | no trial arm names this drug |
| Headache | 3,517 | 2.4 2.3–2.5ROR 2.5 · calibrated p 0.818 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 2.0 · serious PRR 2.9 | no trial arm names this drug |
| Off label use (used outside approved label) | 2,975 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.628 | 1.4 EB05 1.4 · IC025 +0.5 | Reporting / coding artifact | age-adj. PRR 1.5 · serious PRR 1.8 | no trial arm names this drug |
| Chronic kidney disease | 2,750 | 15.7 15.1–16.3ROR 16.6 · calibrated p 0.005 ✓ | 15.2 EB05 14.7 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | age-adj. PRR 12.0 · serious PRR 13.0 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 2,632 | 1.7 1.7–1.8ROR 1.8 · calibrated p 0.814 | 1.7 EB05 1.7 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.7 · serious PRR 1.7 | no trial arm names this drug |
| Arthralgia (joint pain) | 2,462 | 2.5 2.4–2.6ROR 2.6 · calibrated p 0.771 | 2.5 EB05 2.4 · IC025 +1.3 3/3 methods agree | Not in label — unassessed | age-adj. PRR 2.2 · serious PRR 2.8 | no trial arm names this drug |
| Fall | 2,430 | 3.1 3.0–3.2ROR 3.2 · calibrated p 0.561 | 3.1 EB05 3.0 · IC025 +1.6 3/3 methods agree | Not in label — unassessed | age-adj. PRR 3.2 · serious PRR 2.8 | no trial arm names this drug |
| Toxicity to various agents | 2,336 | 6.0 5.7–6.2ROR 6.2 · calibrated p 0.138 | 5.9 EB05 5.7 · IC025 +2.5 3/3 methods agree | Not in label — unassessed | age-adj. PRR 5.8 · serious PRR 5.1 · 91% clinician | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 2,224 | 1.7 1.6–1.7ROR 1.7 · calibrated p 0.767 | 1.7 EB05 1.6 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.6 | no trial arm names this drug |
| Constipation | 2,165 | 4.3 4.1–4.4ROR 4.4 · calibrated p 0.309 | 4.2 EB05 4.1 · IC025 +2.0 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 4.9 · serious PRR 5.5 | no trial arm names this drug |
| Back pain | 2,135 | 3.9 3.8–4.1ROR 4.0 · calibrated p 0.370 | 3.9 EB05 3.7 · IC025 +1.9 3/3 methods agree | Not in label — unassessed | age-adj. PRR 3.7 · serious PRR 4.4 | no trial arm names this drug |
| Dizziness | 2,090 | 1.8 1.7–1.9ROR 1.8 · calibrated p 0.837 | 1.8 EB05 1.7 · IC025 +0.8 | Labeled adverse reaction exact term | 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.
- Respiratory tract malformation — n=36, PRR 161.1
- Temperature regulation disorder — n=461, PRR 113.1
- Vascular malformation — n=43, PRR 107.2
- Pulmonary malformation — n=65, PRR 94.9
- Paranasal cyst — n=43, PRR 92.3
- Hypocholesterolaemia — n=43, PRR 68.6
- Overlap syndrome — n=90, PRR 63.4
- Chronic kidney disease-mineral and bone disorder — n=121, PRR 53.5
- Lung cyst — n=44, PRR 53.2
- Nephrogenic anaemia — n=439, PRR 43.8
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 Cyclobenzaprine?
In FDA FAERS, the most frequently co-reported reaction terms for Cyclobenzaprine are pain, fatigue, nausea, headache, chronic kidney disease, diarrhoea. 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 Cyclobenzaprine have an FDA boxed warning?
No. The FDA label retrieved for Cyclobenzaprine has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Cyclobenzaprine 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 3bc7e2b4-e1a0-66e3-e063-6294a90a676a, effective 20250807; matched on
openfda.generic_name.exact:"CYCLOBENZAPRINE") - 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, 1,188 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
CYCLOBENZAPRINE, 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.