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Neuromuscular blocking drugs toxicity

Neuromuscular blocking drugs (ie, succinylcholine) are occasionally used to attenuate the peripheral (motor) manifestations of convulsions associated with status epilepticus or local anesthetic toxicity. Although this approach is effective in eliminating the muscular manifestations of the seizures, it has no effect on the central processes because neuromuscular blocking drugs do not cross the blood-brain barrier. [Pg.590]

Nigrovic V. New insights into the toxicity of neuromuscular-blocking drugs and their metabolites. Curr Opin Anaesthesiol 1991 4 603. [Pg.373]

Treatment of toxicity Severe toxicity is best treated symptomatically. Convulsions are often treated with intravenous diazepam or a short-acting barbiturate such as thiopental. Hyperventilation with oxygen is helpful. Occasionally, a neuromuscular blocking drug may be used to control violent convulsive activity. The cardiovascular toxicity of bupivacaine overdose is difficult to treat and has caused fatalities in healthy young adults. [Pg.240]

AGEP acute generalized exanthematous pustulosis, DRESS drug reaction with eosinophilia and systemic symptoms, EM erythema multiforme, FDE fixed drug eruption, niAbs monoclonal antibodies, NMBDs neuromuscular blocking drugs, NSAIDs nonsteroidal anti-inflammatory drugs, SJS Stevens-Johnson syndrome, TEN toxic epidermal necrolysis... [Pg.27]

Emetine [EM e teen] and dehydroemetine [de hye dro EM e teen] are alternate agents for the treatment of amebiasis. They inhibit protein synthesis by blocking chain elongation1. Intramuscular injection is the preferred route. Emetine is concentrated in the liver where it persists for a month after a single dose. It is slowly metabolized and excreted and can accumulate. Its ty2 is 5 days. The use of these ipecac alkaloids is limited by their toxicities. Dehydroemetine is probably less toxic than emetine. Close clinical observation is necessary when these drugs are used. Among the untoward effects are pain at the site of injection, transient nausea, cardiotoxicity (e.g., arrhythmias, congestive heart failure), neuromuscular weakness, dizziness, and rashes. [Pg.359]


See other pages where Neuromuscular blocking drugs toxicity is mentioned: [Pg.155]    [Pg.300]    [Pg.300]    [Pg.185]    [Pg.693]    [Pg.300]    [Pg.82]    [Pg.259]    [Pg.34]    [Pg.207]    [Pg.447]    [Pg.112]    [Pg.249]    [Pg.650]    [Pg.104]    [Pg.352]    [Pg.123]    [Pg.131]    [Pg.123]    [Pg.2076]    [Pg.154]    [Pg.119]    [Pg.166]   
See also in sourсe #XX -- [ Pg.246 , Pg.247 ]




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