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	<title>Vecuronium bromide - Revision history</title>
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	<updated>2026-04-24T12:44:39Z</updated>
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		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[File:Vecuronium_bromide.svg|Vecuronium bromide|thumb]] &amp;#039;&amp;#039;&amp;#039;Vecuronium bromide&amp;#039;&amp;#039;&amp;#039; is a [[muscle relaxant]] used in [[anesthesia]] to facilitate [[endotracheal intubation]] and to provide skeletal muscle relaxation during surgery or mechanical ventilation. It is a non-depolarizing neuromuscular blocking agent of intermediate duration. Vecuronium bromide works by competing with [[acetylcholine]] for receptors at the [[neuromuscular junction]], leading to muscle relaxation. It is often preferred in patients with cardiovascular problems due to its minimal effects on heart rate and blood pressure.&lt;br /&gt;
&lt;br /&gt;
== Pharmacology ==&lt;br /&gt;
Vecuronium bromide acts by binding competitively to the nicotinic [[acetylcholine receptor]]s at the neuromuscular junction, inhibiting acetylcholine from binding and thus preventing muscle contraction. Its action is reversed by acetylcholinesterase inhibitors, such as [[neostigmine]], which increase the concentration of acetylcholine at the neuromuscular junction.&lt;br /&gt;
&lt;br /&gt;
== Indications ==&lt;br /&gt;
Vecuronium bromide is indicated for use as an adjunct to general [[anesthesia]] to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation. It is also used in the ICU setting for managing patients requiring mechanical ventilation.&lt;br /&gt;
&lt;br /&gt;
== Dosage and Administration ==&lt;br /&gt;
The dosage of vecuronium bromide varies based on the patient&amp;#039;s weight, the desired degree of muscle relaxation, and the method of administration. It is typically administered intravenously, and its effects are seen within 2 to 3 minutes of administration.&lt;br /&gt;
&lt;br /&gt;
== Side Effects ==&lt;br /&gt;
Common side effects of vecuronium bromide include:&lt;br /&gt;
* Skin flushing&lt;br /&gt;
* Hypotension&lt;br /&gt;
* Tachycardia&lt;br /&gt;
* Bronchospasm&lt;br /&gt;
* Anaphylaxis (rare)&lt;br /&gt;
&lt;br /&gt;
Prolonged use of vecuronium bromide can lead to muscle weakness and myopathy, especially in critically ill patients.&lt;br /&gt;
&lt;br /&gt;
== Contraindications ==&lt;br /&gt;
Vecuronium bromide is contraindicated in patients with known hypersensitivity to the drug. Caution is advised in patients with neuromuscular diseases such as [[myasthenia gravis]], as the effects of vecuronium may be profoundly increased in these individuals.&lt;br /&gt;
&lt;br /&gt;
== Pharmacokinetics ==&lt;br /&gt;
Vecuronium bromide is metabolized in the liver and excreted by the kidneys. Its elimination half-life is approximately 65 to 75 minutes, but this can be prolonged in patients with hepatic or renal impairment.&lt;br /&gt;
&lt;br /&gt;
== History ==&lt;br /&gt;
Vecuronium bromide was introduced in the 1980s as a safer alternative to older neuromuscular blocking agents. It quickly gained popularity due to its favorable pharmacokinetic profile and minimal cardiovascular effects.&lt;br /&gt;
&lt;br /&gt;
== See Also ==&lt;br /&gt;
* [[Neuromuscular-blocking drug]]&lt;br /&gt;
* [[Anesthesia]]&lt;br /&gt;
* [[Acetylcholine receptor]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Muscle relaxants]]&lt;br /&gt;
[[Category:Anesthesia]]&lt;br /&gt;
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		<author><name>Prab</name></author>
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