It may be given at a dose not more than 500 mg initially and 750 mg/day. Liver function tests should be checked Selleckchem Ponatinib regularly during obidoxime therapy to avoid severe hepatotoxicity. Adverse effects of PAM-2 iodide include dizziness, blurred vision, occasional diplopia, impaired accommodation,

nausea and headache. The use of PAM-2 iodide in conjunction with atropine and diazepam has been shown to be very useful. However, PAM-2 lacks the efficacy against tabun and soman and hence, can’t be considered as the drug of choice in nerve agent poisoning.106 Benzodiazepines Benzodiazepines (BDZ) have several effects. Most importantly, they are CNS depressants, anxiolytics and muscle relaxants through action at the gamma-aminobutyric Inhibitors,research,lifescience,medical acid (GABA) receptors.72 The receptor for GABA, a major inhibitory neurotransmitter, is a ligand gated chloride ion channel, and contribute to nicotinic acetylcholine and glycine receptors. In a study on rat cerebral cortex, it was demonstrated Inhibitors,research,lifescience,medical that organophosphates in high dose inhibited GABA metabolism in synaptosomal preparations.107 Inhibitors,research,lifescience,medical The main effect of benzodiazepines in CNS is hyperpolarization of neurons resulting in less susceptibility to cholinergic depolarization. Benzodiazepines such as diazepam, alter GABA binding to its receptor allosterictly, but do not directly activate the receptors. Administration of atropine and diazepam at the same time

is more efficient in decreasing mortality in soman poisoning than atropine or oxime alone. Diazepam enhances the efficacy of low doses of atropine, and decreases the synaptic release of ACh in the cholinergic nervous system.108 On the other Inhibitors,research,lifescience,medical hand, benzodiazepines have favorable effects on anxiety, restlessness, muscle fasciculation, seizures, apprehension and agitation, and Inhibitors,research,lifescience,medical decrease morbidity and mortality when used together with atropine and an oxime in nerve agents poisoning.109 Diazepam should be administered when convulsions or pronounced muscle fasciculation are present. In severe poisoning, it should be considered even before the occurrence of these complications.110

The dose of diazepam in OP poisoning is 5–10 mg intravenously in the absence of convulsions, and 10–20 mg intravenous bolus in its presence. Its use should be continued as required.111,112 The recommended dose of diazepam by World Health Organization (WHO) is 5–10 mg intravenously over a period secondly of 3 min that can be repeated every 10–15 min in adult patients up to a maximum of 30 mg. For children, it is 0.2–0.3 mg/kg given intravenously over 3 minutes. The maximum dose for children up to 5 years old is 5 mg, while up to 10 mg can be used for children who are older than 5 years. Several authors have reported that compared with other benzodiazepines midazolam may stop the seizures faster and at lower blood concentrations when applied intramuscularly.