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Home / Drugs / Starting with G / Gallamine Triethiodide
 
Gallamine Triethiodide
 

A synthetic nondepolarizing blocking drug. The actions of gallamine triethiodide are similar to those of tubocurarine, but this agent blocks the cardiac vagus and may cause sinus tachycardia and, occasionally, hypertension and increased cardiac output. It should be used cautiously in patients at risk from increased heart rate but may be preferred for patients with bradycardia. (From AMA Drug Evaluations Annual, 1992, p198)
BrandsFlaxedil
Fourneau 2559
Gallaflex
Miowas G
Parexyl
Pirolakson
Pyrolaxon
Relaxan
Remyolan
Retensin
Sincurarine
Syncurarine
Tricuran
CategoriesSkeletal Muscle Relaxants
Neuromuscular Nondepolarizing Agents
Nicotinic Antagonists
ManufacturersDavis and geck div american cyanamid co
SynonymsBenzcurine Iodide
Benzkurin
Gallamin Triethiodide
Gallamine Iodide
Gallamine Triethiiodide
Gallamine Triiodoethylate
Gallamone Triethiodide
Gallamonum
Triiodoethylate de Gallamine

indication

For use as adjuncts to anesthesia to induce skeletal muscle relaxation and to facilitate the management of patients undergoing mechanical ventilation

pharmacology

Gallamine Triethiodide is a nondepolarizing neuromuscular blocking drug (NDMRD) used as an adjunct to anesthesia to induce skeletal muscle relaxation. The actions of gallamine triethiodide are similar to those of tubocurarine, but this agent blocks the cardiac vagus and may cause sinus tachycardia and, occasionally, hypertension and increased cardiac output. Muscle groups differ in their sensitivity to these types of relaxants with ocular muscles (controlling eyelids) being most sensitive, followed by the muscles of the neck, jaw, limbs and then abdomen. The diaphragm is the least sensitive muscle to NDMRDs. Although the nondepolarizing neuromuscular blocking drugs do not have the same adverse effects as succinylcholine, their onset of action is slower. They also have a longer duration of action, making them more suitable for maintaining neuromuscular relaxation during major surgical procedures.

mechanism of action

It competes with acetylcholine (ACh) molecules and binds to muscarinic acetylcholine receptors on the post-synaptic membrane of the motor endplate. It acts by combining with the cholinergic receptor sites in muscle and competitively blocking the transmitter action of acetylcholine. It blocks the action of ACh and prevents activation of the muscle contraction process. It can also act on nicotinic presynaptic acetylcholine receptors which inhibits the release of ACh.