Camphor toxicity: Difference between revisions

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==Clinical Features==
==Clinical Features==
*Nausea, vomiting, abdominal pain
*[[Nausea/vomiting]], [[abdominal pain]]
*Oral burning, headache
*Oral burning
*Vertigo, confusion, agitation
*[[Headache]]
*Seizure, respiratory depression, coma
*[[Vertigo]], [[confusion]], [[agitation]]
*Hepatitis and liver failure
*[[Seizure]], respiratory depression, [[coma]]
*[[Hepatitis]] and [[liver failure]]


==Differential Diagnosis==
==Differential Diagnosis==
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==Management==
==Management==
*Aggressive supportive care<ref>American Academy of Pediatrics Policy Statement. Camphor Revisited: Focus on Toxicity (RE9422). Pediatrics 1994;94:127-128</ref>
*Aggressive supportive care<ref>American Academy of Pediatrics Policy Statement. Camphor Revisited: Focus on Toxicity (RE9422). Pediatrics 1994;94:127-128</ref>
*Benzodiazepines for seizure
*[[Benzodiazepines]] for seizure
*Intubation and mechanical ventilation as needed
*[[Intubation]] and [[mechanical ventilation]] as needed
*Charcoal not likely effective
*[[Charcoal]] not likely effective


==Disposition==
==Disposition==

Latest revision as of 02:14, 27 January 2019

Background

  • Common topical agent for pain relief, wart removal, osteoarthritis, cold sores, cough suppression, nasal decongestion
  • FDA limits over the counter preparations to 11%[1]
  • Highly lipophilic, widely and rapidly distributed, symptom onset 5-15 minutes
  • CNS stimulant when ingested

Clinical Features

Differential Diagnosis

Evaluation

Management

Disposition

See Also

References

  1. United States Food and Drug Administration. Proposed rules: external analgesic drug products for over-the-counter human use; tentative final monograph. Fed Reg 1983
  2. American Academy of Pediatrics Policy Statement. Camphor Revisited: Focus on Toxicity (RE9422). Pediatrics 1994;94:127-128