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WebPhenytoin hepatic metabolism becomes saturated, which causes Michaelis-Menten pharmacokinetics to take place. As a result, when phenytoin doses are increased, total and unbound steady-state concentrations increase more than a proportional amount (e.g., when the dose is doubled, serum concentrations may increase three- to five-fold or more). WebPhenytoin suspension is very viscous and hyperosmolartherefore dilution with equal amounts of water is recommended. Phenytoin interacts with feed therefore feed must be stopped for 2 hours before and after giving phenytoin via enteral feeding tubes. Flush the feeding tubes with saline before and after phenytoin administration. chipping norton stakes day
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Web18. jan 2016 · Despite strong overall correlation between the total pheny toin serum and free serum concentrations, there is excessive variability in phenytoin protein binding and monitoring of total serum concentrations is unreliable and free phenYtoin serum … WebPhenytoin is highly protein bound (mainly to albumin; 85-95%) and only the free (unbound) fraction is pharmacologically active. Differences in formulation between brand names and generic equivalents can result in altered bioavailability, causing toxicity or the development of subtherapeutic levels. Web3. nov 2024 · Phenytoin is a sodium channel blocker, this is why you should never give it as an intravenous bolus. It would cause acute sodium channel blockade like a tricyclic antidepressant causing widening of the QRS with risk of dysrhythmias including VT. Specifically it suppresses membrane post-titanic potentiation and hyper excitability. … chipping norton surgery doctors