Loperamide toxicity: Difference between revisions

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*[[Loperamide]] is widely used nonprescription anti-diarrheal medication
*[[Loperamide]] is widely used nonprescription anti-diarrheal medication
*Increasing reports of intentional overdose at very high doses either for euphoric effects or to attenuate symptoms of [[opioid withdrawal]]<ref>Wu PE, et al. "Clinical Review: Loperamide Toxicity." Annals of EM. August 2017. 70(2):245-252</ref>
*Increasing reports of intentional overdose at very high doses either for euphoric effects or to attenuate symptoms of [[opioid withdrawal]]<ref>Wu PE, et al. "Clinical Review: Loperamide Toxicity." Annals of EM. August 2017. 70(2):245-252</ref>
*Has a wide margin of safety, largely due to extremely low bioavailability (0.3%)<ref>Wu PE, et al. "Clinical Review: Loperamide Toxicity." Annals of EM. August 2017. 70(2):245-252</ref>


==Clinical Features==
==Clinical Features==

Revision as of 07:32, 14 August 2017

Background

  • Loperamide is widely used nonprescription anti-diarrheal medication
  • Increasing reports of intentional overdose at very high doses either for euphoric effects or to attenuate symptoms of opioid withdrawal[1]
  • Has a wide margin of safety, largely due to extremely low bioavailability (0.3%)[2]

Clinical Features

Loperamide-induced cardiac toxicity[3]

  • Often young
  • May present in cardiac arrest or with recurrent syncope in conjunction with ECG agnormalities

Differential Diagnosis

Sedative/hypnotic toxicity

Evaluation

ECG Findings

Management

Disposition

See Also

External Links

References

  1. Wu PE, et al. "Clinical Review: Loperamide Toxicity." Annals of EM. August 2017. 70(2):245-252
  2. Wu PE, et al. "Clinical Review: Loperamide Toxicity." Annals of EM. August 2017. 70(2):245-252
  3. Wu PE, et al. "Clinical Review: Loperamide Toxicity." Annals of EM. August 2017. 70(2):245-252