Carbacholine
Carbacholine Uses, Dosage, Side Effects, Food Interaction and all others data.
Carbacholine, also known as carbachol, is a muscarinic agonist discovered in 1932. Carbacholine was initially used as a treatment for migraines, induction of diuresis, and other parasympathetic effects.
Carbacholine was granted FDA approval on 28 September 1972.
Carbacholine is a parasympathomimetic that acts as an agonist of muscarinic and nicotinic receptors. It is more resistant to hydrolysis by acetylcholinesterase than other choline esters leading to a longer duration of action, with significant effects 24 hours after administration. Data regarding the therapeutic index of carbamoylcholine is not readily available. Patients should be counselled regarding the risk of administering the drug to patients with acute cardiac failure, bronchial asthma, peptic ulcer, hyperthyroidism, gastrointestinal spasm, urinary tract obstruction, or Parkinson's disease.
Trade Name | Carbacholine |
Generic | Carbamoylcholine |
Carbamoylcholine Other Names | Carbacholine, carbacol, Carbamylcholine, Choline carbamate, Carbachol |
Type | |
Formula | C6H15N2O2 |
Weight | Average: 147.1955 Monoisotopic: 147.113352734 |
Protein binding | Data regarding protein binding of carbamoylcholine is not readily available. |
Groups | Approved |
Therapeutic Class | |
Manufacturer | |
Available Country | |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Carbachol is a direct acting miotic agent administered ophthalmically to decrease intraocular pressure after cataract surgery, and to induce miosis during surgery.
Carbacholine is indicated to induce miosis for surgery and to reduce intraocular pressure elevations in the first 24 hours after cataract surgery.
Carbacholine is also used to associated treatment for these conditions: Increased Intra Ocular Pressure (IOP), Open Angle Glaucoma (OAG), Acute Angle closure glaucoma
How Carbacholine works
Carbacholine is a parasympathomimetic that acts as an agonist of muscarinic and nicotinic receptors. Intraocular administration leads to miosis and decreases intraocular pressure via increased aqueous humour outflow.
Toxicity
Patients experiencing an overdose of carbamoylcholine may experience nausea, sweating, hypotension, hypersalivation, bronchorrhea, miosis, and dyspnea. Patients should be treated with symptomatic and supportive treatment. Treatment may include atropine, furosemide, epinephrine, and/or dopamine. Some patients may require intubation.
The oral LD50 in mice is 15 mg/kg and in rats is 40 mg/kg.
Food Interaction
No interactions found.Volume of Distribution
Data regarding the volume of distribution of carbamoylcholine is not readily available.
Elimination Route
Choline esters in general are hydrophilic and therefore poorly absorbed through the gastrointestinal tract and are unlikely to cross the blood brain barrier. Data regarding the absorption of carbamoylcholine are not readily available.
Half Life
Data regarding the half life of carbamoylcholine is not readily available.
Clearance
Data regarding the clearance of carbamoylcholine is not readily available.
Elimination Route
Data regarding the route of elimination of carbamoylcholine is not readily available.
Innovators Monograph
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