Does clonazepam have anticholinergic (antimuscarinic) properties?

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Last updated: March 11, 2026 • View editorial policy

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Does Clonazepam Have Anticholinergic Properties?

No, clonazepam does not have significant anticholinergic (antimuscarinic) properties—it is a benzodiazepine that acts primarily through GABA-A receptor enhancement, not muscarinic receptor blockade.

Mechanism of Action

Clonazepam works by enhancing the activity of gamma-aminobutyric acid (GABA), the major inhibitory neurotransmitter in the central nervous system 1. This is fundamentally different from anticholinergic medications, which block muscarinic receptors.

Evidence from Guidelines

The 2021 Mayo Clinic polypharmacy guideline explicitly distinguishes between anticholinergic medications and benzodiazepines in their deprescribing recommendations 2:

  • Anticholinergic medications (like diphenhydramine, cyclobenzaprine, oxybutynin) cause "broad muscarinic receptor blockade" resulting in impaired vision, urinary retention, constipation, and cognitive impairment
  • Benzodiazepines (including clonazepam) are listed separately with different side effects: sedation, cognitive impairment, falls, and withdrawal syndromes—but not anticholinergic effects

The guideline specifically states that opioids have "anticholinergic properties" but makes no such claim about benzodiazepines like clonazepam 2.

Clinical Side Effect Profile

Multiple sleep medicine guidelines 3, 4, 5 consistently describe clonazepam's side effects as:

  • Morning sedation
  • Gait imbalance and falls
  • Cognitive disturbances (delirium, amnesia)
  • Respiratory depression
  • Depression

Notably absent from these comprehensive lists are classic anticholinergic effects such as:

  • Dry mouth
  • Urinary retention
  • Constipation
  • Blurred vision
  • Tachycardia

Important Clinical Caveat

One case report 6 described a patient taking multiple medications including clonazepam who developed severe hyperthermia attributed to "excessive anticholinergic effects." However, this patient was simultaneously taking amitriptyline, cyclobenzaprine, and benztropine—all of which are strongly anticholinergic medications. The hyperthermia was caused by the combination of truly anticholinergic drugs, not by clonazepam itself.

Practical Implications

  • Do not count clonazepam when calculating anticholinergic burden scales or Drug Burden Index scores
  • Clonazepam does not contribute to anticholinergic side effects like urinary retention, constipation, or dry mouth
  • However, clonazepam does carry significant risks in older adults through its sedative and cognitive effects, warranting caution per Beers Criteria 3
  • When a patient on clonazepam develops anticholinergic symptoms, look for other culprit medications

The distinction matters clinically: while both anticholinergics and benzodiazepines can impair cognition in older adults, they do so through entirely different mechanisms and require different management strategies.

References

Guideline

polypharmacy management in older patients.

Mayo Clinic Proceedings, 2021

Guideline

management of rem sleep behavior disorder: an american academy of sleep medicine clinical practice guideline.

Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine, 2023

Guideline

best practice guide for the treatment of rem sleep behavior disorder (rbd).

Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine, 2010

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.