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Atropine/pralidoxime nerve

Johnson, D.D., Stewart, W.C. (1970). The effects of atropine, pralidoxime and lidocaine on nerve-muscle and respiratory function in organophosphate-treated rabbits. Can. J. Physiol. [Pg.994]

The three therapeutic drugs for treatment of nerve agent intoxication are atropine, pralidoxime chloride, and diazepam. [Pg.2352]

Table 2. Effect of delaying therapy (IV atropine, pralidoxime, diazepam) on protection ratios in guinea pigs given pyridostigmine 30 min before nerve agent (Green et al., 1983)... Table 2. Effect of delaying therapy (IV atropine, pralidoxime, diazepam) on protection ratios in guinea pigs given pyridostigmine 30 min before nerve agent (Green et al., 1983)...
Nerve Agent Antidote Kit (NAAK or MARK I) consists of an atropine auto-injector (2 mg), a pralidoxime chloride auto-injector (2-Pam-Cl, 600 mg), the plastic clip joining the two injectors, and a foam case. The kit serve as a countermeasure to nerve agents, including tabun (GA), sarin (GB), soman (GD), GF, and VX. Military personnel can receive three MARK I for self/buddy aid. Possible side effects of atropine and/or 2-PAM-C1 are deemed insignificant in a nerve agent casualty. Intravenous atropine and 2-PAM-C1 can also be made available. The MARK I kit is manufactured by Survival Technology, Inc., Rockville, Maryland. [Pg.67]

General supportive care should be provided as outlined above. Extra precautions should be taken to ensure that rescuers and health care providers are not poisoned by exposure to contaminated clothing or skin. This is especially critical for the most potent substances such as parathion or nerve gas agents. Antidotal treatment consists of atropine and pralidoxime (see Table 58-4). Atropine is an effective competitive inhibitor at muscarinic sites but has no effect at nicotinic sites. Pralidoxime given early enough is capable of restoring the cholinesterase activity and is active at both muscarinic and nicotinic sites. [Pg.1259]

The standard treatment of nerve agent-induced muscle toxicity calls for (1) reactivation of the phosphorylated AChE with an oxime, and (2) blockage of the nicotinic ACh receptor sites from the stimulating action of ACh with fii-tubocurarine. Oximes such as obidoxime, pralidoxime (2-pyridine aldoxime methochloride, 2-PAM) and a few others have been found very effective when given in combination with other drugs such as atropine, pretreatment with oximes varies with the ehemieal structures of the nerve agents and depends on the time after exposure. For example, it has been... [Pg.524]


See other pages where Atropine/pralidoxime nerve is mentioned: [Pg.10]    [Pg.11]    [Pg.8]    [Pg.26]    [Pg.2849]    [Pg.113]    [Pg.705]    [Pg.8]    [Pg.26]    [Pg.113]    [Pg.361]    [Pg.258]    [Pg.260]    [Pg.264]    [Pg.266]    [Pg.270]    [Pg.272]    [Pg.276]    [Pg.277]    [Pg.279]    [Pg.284]    [Pg.286]    [Pg.110]    [Pg.263]    [Pg.11]    [Pg.84]    [Pg.397]    [Pg.9]    [Pg.9]    [Pg.84]    [Pg.1412]    [Pg.210]    [Pg.361]    [Pg.294]    [Pg.294]    [Pg.488]    [Pg.27]    [Pg.59]   


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Atropine/pralidoxime (nerve agent antidote kit-NAAK Mark

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