Trade Names:Enlon-Plus- Injection, solution edrophonium chloride 10 mg and atropine sulfate 0.14 mg per mL
Antagonizes the effect of nondepolarizing neuromuscular blocking agents primarily by inhibiting or inactivating acetylcholinesterase.Atropine
Inhibits action of acetylcholine or other cholinergic stimuli at postganglionic cholinergic receptors, including smooth muscles, secretory glands, and CNS sites.
Used as a reversal agent or antagonist of nondepolarizing neuromuscular blocking agents; adjunct in treating respiratory depression caused by curare overdosage.
Patients with intestinal or urinary obstruction of mechanical type; presence of acute glaucoma; adhesions between the iris and the lens of the eye; pyloric stenosis; hypersensitivity to any component of the product.
IV 0.05 to 0.1 mL/kg (edrophonium 0.5 to 1 mg/kg in combination with atropine 0.007 to 0.014 mg/kg) administered slowly over 45 to 60 sec at a point of at least 5% recovery of twitch response to neuromuscular stimulation (95% block). A total dose of edrophonium 1 mg/kg should rarely be exceeded.
Store between 59° and 78°F.
The risk of excessive bradycardia from unopposed parasympathetic vagal tone may be increased.Corticosteroids (eg, prednisolone)
Effects of edrophonium in myasthenia gravis may be antagonized, resulting in profound muscular depression refractory to anticholinesterases.Muscle relaxants with no vagolytic effects (eg, vecuronium)
Compared with muscle relaxants with vagolytic effects, there may be a slightly higher incidence of vagotonic effects such as bradycardia and first-degree heart block when reversed with edrophonium/atropine.Narcotic analgesics
Except when combined with potent inhaled anesthetics, narcotic analgesics appear to potentiate the effect of edrophonium on the sinus node and conduction system, increasing both the frequency and duration of bradycardia.Nondepolarizing muscle relaxants
Do not administer prior to nondepolarizing muscle relaxants.Phenothiazines (eg, chlorpromazine)
Therapeutic effects may be decreased by atropine.
None well documented.
Bradycardia, junctional rhythm, tachycardia (more than 10%); atrial premature contractions, first- and second-degree AV block, P-wave changes (3% to 10%); third-degree AV block, ventricular premature contractions (1% to 3%).Edrophonium
Fall in cardiac output resulting in hypotension; nonspecific ECG changes.
Restlessness with asthenia; speech disturbances.Edrophonium
Convulsions; dysarthria; dysphagia; dysphonia.
Flushed dry skin; formation of scarlatiniform rashEdrophonium
Blurred vision, dry nose, photophobia, slight mydriasis.Edrophonium
Conjunctival hyperemia, diplopia, increased lacrimation, papillary constriction.
Abdominal cramps, diarrhea, nausea, increased gastric and intestinal secretions, increased peristalsis, vomiting.
Increased urinary frequency.
Bronchiolar constriction, increased tracheobronchial secretions, laryngospasm, respiratory muscle paralysis.
Monitor response to therapy carefully and secure assisted or controlled ventilation.
Category C .
Safety and efficacy not established.
Use with caution, usually starting at the low end of the dosage range, because of the greater frequency of decreased hepatic, renal, or cardiac function, and concomitant diseases or other drug therapy.
Contains sodium sulfite, which may cause allergic-type reactions, including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in susceptible individuals.
Atropine may slow gastric emptying and GI motility, which may interfere with absorption of other medications.
Use with caution in patients with myasthenic weakness who are receiving anticholinesterase drugs. Anticholinesterase overdosage symptoms may mimic underdosage (myasthenic symptoms), which may worsen the condition of these patients.
Use with caution in patients with bronchial asthma, cardiac arrhythmias, or prostatic hypertrophy, and in debilitated patients with chronic lung disease.
Muscarinic symptoms, including bradycardia, diarrhea, increased bronchial and salivary secretions, nausea, sweating, and vomiting. Airway obstruction may result from increased bronchial secretions.
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