Ambenonium chloride
(Redirected from Ambenonium)
Overview of the drug Ambenonium chloride
Ambenonium chloride is a medication used in the management of myasthenia gravis, a chronic autoimmune neuromuscular disease characterized by varying degrees of weakness of the skeletal muscles. It is classified as a cholinesterase inhibitor, which works by increasing the levels of acetylcholine at the neuromuscular junction, thereby improving muscle contraction.
Mechanism of Action
Ambenonium chloride functions by inhibiting the enzyme acetylcholinesterase, which is responsible for breaking down acetylcholine in the synaptic cleft. By preventing the degradation of acetylcholine, ambenonium chloride enhances neuromuscular transmission and improves muscle strength in patients with myasthenia gravis.
Pharmacokinetics
Ambenonium chloride is administered orally and is absorbed through the gastrointestinal tract. The onset of action typically occurs within 30 to 60 minutes, and the duration of effect can last from 3 to 8 hours, depending on the individual patient's response and the severity of the condition.
Clinical Use
Ambenonium chloride is primarily used in the treatment of myasthenia gravis. It is often prescribed when patients do not respond adequately to other cholinesterase inhibitors such as pyridostigmine or neostigmine. The dosage of ambenonium chloride must be carefully adjusted to achieve optimal therapeutic effects while minimizing side effects.
Side Effects
Common side effects of ambenonium chloride include nausea, diarrhea, abdominal cramps, and increased salivation. In some cases, patients may experience muscle cramps, sweating, and bradycardia. Overdosage can lead to a cholinergic crisis, characterized by severe muscle weakness, respiratory distress, and potentially life-threatening symptoms.
Contraindications
Ambenonium chloride is contraindicated in patients with mechanical intestinal obstruction or urinary tract obstruction. Caution is advised in patients with asthma, epilepsy, cardiovascular disease, and peptic ulcer disease.
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Contributors: Prab R. Tumpati, MD