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Understanding the Facts: Is Cyclobenzaprine a Controlled Substance?

3 min read

In 2011, over 25 million prescriptions were written for drugs containing cyclobenzaprine [1.5.1]. A common question among patients is, 'Is cyclobenzaprine a controlled substance?' The answer has important implications for its use and regulation.

Quick Summary

Cyclobenzaprine is not a federally controlled substance in the U.S., but it has the potential for misuse due to its sedative effects [1.2.1, 1.2.2]. This leads to careful monitoring and regulation at the state level.

Key Points

  • Not Federally Controlled: Cyclobenzaprine is not classified as a controlled substance under the U.S. Controlled Substances Act [1.2.1].

  • Potential for Misuse: Despite its non-controlled status, it has CNS depressant effects that lead to a potential for abuse, often with other substances like alcohol [1.3.1].

  • Short-Term Use Only: It is recommended for short-term treatment (2-3 weeks) for acute muscle spasms [1.4.2].

  • Significant Side Effects: Common side effects include drowsiness, dry mouth, and dizziness, and it can impair your ability to drive or operate machinery [1.9.4].

  • Dangerous Interactions: It can have life-threatening interactions with MAO inhibitors, alcohol, and other CNS depressants [1.9.1, 1.9.2].

  • State-Level Monitoring: Some states may monitor cyclobenzaprine prescriptions through PDMPs due to its misuse potential [1.3.2].

  • Not an Opioid: Cyclobenzaprine is a muscle relaxant and is not a narcotic or an opioid [1.4.4, 1.6.3].

In This Article

What is Cyclobenzaprine?

Cyclobenzaprine is a prescription muscle relaxant used to relieve skeletal muscle spasms and associated pain from acute, painful musculoskeletal conditions [1.2.2, 1.7.2]. Commonly known by brand names like Flexeril, Amrix, and Fexmid, it is typically prescribed for short-term use, often for two to three weeks, in conjunction with rest and physical therapy [1.3.2, 1.6.3].

Structurally related to tricyclic antidepressants, cyclobenzaprine works primarily within the central nervous system (CNS) at the brain stem level [1.7.1, 1.7.2]. It reduces tonic somatic motor activity, which helps to decrease muscle hyperactivity without interfering with overall muscle function [1.7.2]. This mechanism effectively blocks pain signals sent from the muscles to the brain, providing relief [1.4.2].

Is Cyclobenzaprine a Controlled Substance? The Official Answer

According to the U.S. Drug Enforcement Administration (DEA), cyclobenzaprine is not a controlled substance under the federal Controlled Substances Act (CSA) [1.2.1, 1.3.4]. This means it is not placed into one of the five schedules that categorize drugs based on their abuse potential and accepted medical use [1.3.1].

The reason for its non-controlled status is its relatively low risk for addiction and abuse compared to other substances like opioids or benzodiazepines [1.4.2, 1.4.4]. It doesn't activate the brain's reward centers in the same way that classic drugs of abuse do [1.4.1]. However, this does not mean the drug is without risks or potential for misuse.

Why is There Confusion? Potential for Misuse

Despite its non-controlled status, cyclobenzaprine has a known potential for misuse. Its CNS depressant effects can cause sedation, relaxation, and sometimes a feeling of euphoria, which can be sought by recreational users [1.2.2, 1.2.5]. The DEA acknowledges anecdotal reports of individuals taking cyclobenzaprine, sometimes in combination with other drugs like alcohol or benzodiazepines, to enhance these psychoactive effects [1.2.1, 1.3.1]. In 2011, there were over 11,000 emergency department visits related to the misuse of cyclobenzaprine [1.5.4].

The misuse may have seen an increase after carisoprodol (Soma), another muscle relaxant, was classified as a Schedule IV controlled substance in 2011, making cyclobenzaprine comparatively easier to obtain [1.3.1, 1.5.3]. Because of this potential for misuse, while not federally scheduled, some states may monitor its prescription through Prescription Drug Monitoring Programs (PDMPs) and may have specific regulations regarding its dispensing [1.3.2, 1.10.1].

Cyclobenzaprine vs. Other Muscle Relaxants: A Comparison

To understand cyclobenzaprine's status, it's helpful to compare it to another muscle relaxant, carisoprodol (Soma), which is a controlled substance.

Feature Cyclobenzaprine (Flexeril) Carisoprodol (Soma)
DEA Schedule Not a controlled substance [1.6.1] Schedule IV controlled substance [1.6.1]
Abuse Potential Lower, but potential for misuse exists, often with other CNS depressants [1.4.3] Higher potential for misuse and dependence [1.6.1]
Mechanism Acts on the brain stem to reduce muscle hyperactivity [1.7.2] Changes nerve activity in the central nervous system [1.6.2]
Primary Use Short-term relief of muscle spasms from acute painful conditions [1.9.4] Short-term relief of muscle pain and discomfort [1.6.2]
Common Side Effects Drowsiness, dry mouth, dizziness [1.9.4] Drowsiness, dizziness, headache [1.6.2]

Side Effects and Important Safety Information

Even when used as prescribed, cyclobenzaprine can cause a range of side effects. The most common include:

  • Drowsiness [1.9.4]
  • Dry mouth [1.9.4]
  • Dizziness [1.9.4]
  • Fatigue [1.9.4]
  • Headache [1.9.4]
  • Constipation [1.8.2]

Drug Interactions

Cyclobenzaprine can have dangerous interactions with other substances:

  • CNS Depressants: Combining it with alcohol, barbiturates, benzodiazepines, or opioids can lead to extreme sedation, impaired coordination, slowed breathing, and potentially coma or death [1.9.1, 1.9.2, 1.9.3].
  • MAO Inhibitors: Taking cyclobenzaprine with or within 14 days of using a monoamine oxidase inhibitor (MAOI) is contraindicated and can cause life-threatening reactions, including high fever and seizures [1.9.1, 1.9.2].
  • Serotonergic Drugs: When taken with other drugs that increase serotonin levels (like SSRIs, SNRIs, and tramadol), there is a risk of developing serotonin syndrome, a potentially fatal condition with symptoms like agitation, hallucinations, rapid heart rate, and fever [1.9.1, 1.9.2].

Long-Term Use Risks

Cyclobenzaprine is intended for short-term use (2-3 weeks) [1.4.2]. Prolonged use is not recommended and can lead to tolerance, physical dependence, and withdrawal symptoms upon cessation, such as nausea, headache, and malaise [1.4.4, 1.8.1]. Long-term use may also increase the risk for cognitive impairment and liver damage [1.8.1, 1.8.3].

Conclusion

In summary, is cyclobenzaprine a controlled substance? No, it is not federally classified as a controlled substance by the DEA [1.2.1]. However, its status as a prescription-only medication reflects its potential for causing significant side effects and its known potential for misuse and abuse [1.2.2]. Its sedative properties, especially when combined with other CNS depressants, create serious health risks [1.9.1]. Patients should only use cyclobenzaprine under the strict guidance of a healthcare provider, adhere to the prescribed dosage and duration, and be fully aware of the potential drug interactions.

For more detailed information from a primary source, you can review the DEA's drug fact sheet on Cyclobenzaprine.

Frequently Asked Questions

No, cyclobenzaprine is not a federally controlled substance in the United States according to the DEA [1.2.1, 1.3.4].

No, cyclobenzaprine is a muscle relaxant and is not an opioid or a narcotic [1.4.4, 1.6.3].

People may misuse cyclobenzaprine for its sedative, relaxing, and potentially euphoric effects, which can be enhanced when mixed with other substances like alcohol [1.2.5].

It is not recommended. Cyclobenzaprine can cause drowsiness, dizziness, and may impair your coordination and reaction time, making it unsafe to drive or operate heavy machinery [1.7.4].

Long-term use, which is not recommended, can lead to tolerance, dependence, cognitive impairment, and potential liver damage. Abruptly stopping after prolonged use can cause withdrawal symptoms like headache and nausea [1.8.1, 1.4.4].

Cyclobenzaprine has a long half-life of about 18 hours. It can be detectable in urine for up to 8 days, in blood for 3-4 days, and in hair for up to 90 days after the last dose [1.11.3].

No. Combining alcohol with cyclobenzaprine can dangerously enhance its CNS depressant effects, leading to extreme drowsiness, impaired motor skills, slowed breathing, and in severe cases, coma or death [1.9.2, 1.9.3].

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.