Methocarbamol vs Cyclobenzaprine for Lower Back Pain
Neither methocarbamol nor cyclobenzaprine (Flexeril) demonstrates superior efficacy for lower back pain, and both should be used cautiously for short-term treatment (≤2 weeks) of acute low back pain only—not for chronic pain—with cyclobenzaprine having slightly more robust evidence supporting its use. 1, 2
Evidence Quality and Direct Comparisons
The American College of Physicians/American Pain Society guidelines found insufficient evidence to conclude that any specific muscle relaxant is superior to others for benefits or harms in low back pain treatment. 1
Head-to-head comparison data is extremely limited:
- One lower-quality trial found no efficacy difference between cyclobenzaprine and diazepam for chronic low back pain. 1
- No direct randomized trials comparing methocarbamol versus cyclobenzaprine exist in the evidence base. 1
Individual Agent Evidence
Cyclobenzaprine
- Has the most recent and largest clinical trials demonstrating benefit for acute low back pain. 3
- Efficacy is independent of sedative effects, though sedation is dose-related. 3
- Included in multiple systematic reviews showing moderate superiority to placebo for short-term (2-4 days) pain relief. 1
- Pooled data from 20 trials (n=1553) showed cyclobenzaprine superior to placebo for short-term global improvement. 1
Methocarbamol
- A 2015 randomized controlled trial showed 44% of methocarbamol patients achieved complete pain relief versus 18% with placebo (p<0.0001). 4
- However, a 2018 high-quality ED trial found adding methocarbamol to naproxen provided no functional improvement over naproxen alone on the Roland-Morris Disability Questionnaire (improvement 8.1 points vs 10.9 points with placebo, not clinically significant). 5
- A 2021 trial showed methocarbamol plus indomethacin reduced pain more than indomethacin alone, but this contradicts the 2018 findings. 6
Critical Limitations for Both Agents
The American Geriatrics Society explicitly states that methocarbamol, cyclobenzaprine, and other "muscle relaxants" do not directly relax skeletal muscle and have no evidence of efficacy in chronic pain. 1 Given potential adverse effects in older adults, these drugs are not favored for chronic pain. 1
Duration of Evidence
- All trials of skeletal muscle relaxants were ≤2 weeks duration (except one 3-week trial). 1
- There is only one trial of cyclobenzapine for chronic low back pain available in the United States, and it was lower-quality and did not report pain intensity or global efficacy. 1
Adverse Effects
Both agents cause central nervous system effects:
- Drowsiness/sedation, fatigue, dizziness, and lightheadedness are common. 1, 3
- In the 2018 trial, adverse events occurred in 19% of methocarbamol patients versus 17% with placebo. 5
- Cyclobenzaprine's sedation is dose-related but efficacy is independent of sedative effects. 3
Clinical Algorithm for Selection
For acute low back pain (<4 weeks):
- Start with acetaminophen or NSAIDs as first-line therapy. 1, 2
- If severe pain persists after 2-3 days and functional impairment is significant, consider adding a muscle relaxant for short-term use (≤1-2 weeks). 1, 2
- Choose cyclobenzaprine over methocarbamol based on larger body of evidence, though expect similar efficacy. 3
- Use lowest effective dose and discontinue as soon as pain-free state is achieved. 4
For chronic low back pain (>12 weeks):
- Avoid both agents entirely. 1, 2
- Consider tricyclic antidepressants (amitriptyline) or duloxetine instead, which have moderate evidence for chronic pain. 2
- For radicular component, use gabapentin as first-choice for neuropathic pain. 2
Key Pitfalls to Avoid
- Do not prescribe either agent for chronic low back pain—no evidence supports efficacy beyond 2 weeks. 1
- Do not use in elderly patients without careful consideration of fall risk and cognitive impairment from sedation. 1, 7
- Do not expect muscle relaxants to work alone—they should be combined with NSAIDs or acetaminophen and patient education about remaining active. 1, 5
- Avoid carisoprodol due to abuse potential if considering alternatives. 3