Xylocaine 2% Viscous – Product Information
|Ingredients:||lignocaine hydrochloride, methyl hydroxybenzoate, propy hydroxybenzoate, sodium hydroxide, saccharin sodium, cherry extract|
Name of the medicine
Xylocaine 2% Viscous contains lignocaine hydrochloride as the active ingredient.
Australian Approved Name: Lignocaine hydrochloride
Molecular Formula: C14H22N2O,HCl,H2O
Molecular Weight: 288.8
Xylocaine 2% Viscous is an aqueous topical anaesthetic for use on mucous embranes.
Each mL of Xylocaine Viscous contains lignocaine hydrochloride monohydrate 21.3 mg (equivalent to lignocaine hydrochloride 20 mg), methyl hydroxybenzoate, propy hydroxybenzoate, sodium hydroxide, saccharin sodium, cherry extract
FACHE 59130 (PI: 2395), carmellose sodium and purified water.
Lignocaine, the active ingredient of Xylocaine Viscous, stabilises the neuronal membrane and prevents the initiation and conduction of nerve impulses, thereby effecting local anaesthetic action.
The onset of action of Xylocaine Viscous occurs within 3-5 minutes on mucous membranes. Its low surface tension ensures an even film over the surface of the mucous membrane so that the Xylocaine comes into intimate contact with the total surface. High viscosity ensures sufficiently prolonged contact with the mucous membrane. It is ineffective when applied to intact skin.
Lignocaine may be absorbed following topical administration to mucous membranes, its rate of absorption and amount of dose absorbed depending upon concentration and total dose administered, the specific site of application and duration of exposure. In general, the rate of absorption occurs most rapidly after intratracheal administration.
Lignocaine is well absorbed from the gastrointestinal tract, but little intact drug appears in the circulation because of bio transformation in the liver. Lignocaine is metabolised rapidly by the liver, and metabolites and unchanged drug are excreted by the kidney.
Excessive blood levels may cause changes in cardiac output, total peripheral resistance and mean arterial pressure. These changes may be attributable to a direct depressant effect of the anaesthetic agent on various components of the cardiovascular system.
Biotransformation includes oxidative N-dealkylation, ring hydroxylation, cleavage of the amide linkage and conjugation. The pharmacological / toxicological actions of the metabolites are similar to, but not less potent than, those of lignocaine.
Approximately 90% of lignocaine is excreted in the form of various metabolites, and less than 10% is excreted unchanged. The primary metabolite in urine is a conjugate of 4-hydroxy-2,6-dimethylaniline.
The plasma binding of lignocaine is dependent on drug concentration, and the fraction bound decreases with increasing concentration. At concentrations of 1 to 4 μg of free base/mL, 60 to 80% of lignocaine is protein bound. Binding is also dependent on the plasma concentrations of the alpha-1-acid glycoprotein.
Lignocaine crosses the blood-brain and placental barriers, presumably by passive diffusion.
Studies of lignocaine metabolism following IV bolus injection have shown that the elimination half-life is usually 1.5 to 2 hours. The half-life may be prolonged 2-fold or more in patients with liver dysfunction. Renal dysfunction does not affect lignocaine kinetics, but may increase the accumulation of metabolites.
Factors such as acidosis and the use of CNS stimulants and depressants affect the CNS levels of lignocaine required to produce overt systemic effects. Objective adverse manifestations become increasingly apparent with increasing venous plasma levels above 6.0 μg free base/mL. In the rhesus monkey arterial blood levels of 18 to 21 μg/mL have been shown to be the threshold for convulsive activity.
Xylocaine 2% Viscous Solution is indicated for the relief of pain and discomfort associated with:
- irritated or inflamed mucous membranes of the mouth, pharynx and upper gastrointestinal tract, e.g. post-tonsillectomy sore throat, dumping syndrome;
- introduction of instruments and catheters into the respiratory and gastrointestinal tract.
Known history of hypersensitivity to lignocaine or other local anaesthetics of the amide type or to other components of the viscous solution.
Hypersensitivity to methyl and/or propyl hyroxybenzoate or to their metabolite para aminobenzoic acid.
Excessive dosage, or short intervals between doses, can result in high levels of lignocaine or its metabolites and serious adverse effects. Patients should be instructed to strictly adhere to the recommended dosage and administration guidelines. The management of serious adverse reactions may require the use of resuscitative equipment, oxygen and other resuscitative drugs. Patients should not exceed the recommended dose or use Xylocaine 2% Viscous for prolonged periods except on the advice of their physician.
The lowest dose that results in effective anaesthesia should be used to avoid high plasma levels and serious adverse effects. Tolerance to elevated blood levels varies with the status of the patient.
Excessive dosage or short intervals between doses may result in high plasma levels and serious adverse effects. Following too high or repeated doses of viscous lignocaine in children under the age of three, serious side effects have been reported. Patients should be instructed to adhere strictly to the recommended dosage. This is especially important in children where the doses vary with weight.
Debilitated, elderly patients or patients with partial or complete heart block and/or acutely ill patients, and children should be given reduced doses commensurate with their age and physical status.
Absorption from wound surfaces and mucous membranes is relatively high, especially in the bronchial tree. Because of the possibility of significant systemic absorption, Xylocaine Viscous should be used with caution in patients with traumatised mucosa and/or sepsis in the region of the proposed application.
If the dose or site of administration is likely to result in high blood levels, lignocaine, in common with other local anaesthetics, should be used with caution in patients with epilepsy, impaired cardiac conduction, bradycardia, impaired hepatic function, in severe shock, the elderly, patients in poor general health and patients with severe renal dysfunction.
Patients treated with anti-arrhythmic drugs class III (eg, amiodarone) should be kept under close surveillance and ECG monitoring considered, since cardiac effects may be additive.
Eating and drinking
The use of topical anaesthetic agents in the oral cavity may interfere with swallowing and thus enhance the danger of aspiration of food or drink. For this reason, food or drink should not be ingested within 60 minutes of using local anaesthetics in the mouth or throat area. Numbness of the tongue or buccal mucosa may increase the danger of biting or heat trauma. Food, chewing gum or hot drinks should not be taken while the mouth or throat area is anaesthetised.
Many drugs used during the conduct of anaesthesia are considered potential triggering agents for familial malignant hyperthermia. It has been shown that the use of amide local anaesthetics in malignant hypothermia patients is generally safe, but cases of malignant hyperthermia have occasionally documented after use.
Endotracheal tube lubrication
When used for endotracheal tube lubrication care should be taken to avoid introduction of the viscous solution into the lumen of the tube. The solution may dry on the inner surface leaving residue which tend to clump with flexion, narrowing the lumen. There have been rare reports in which this residue has caused the lumen to occlude.
Xylocaine 2% Viscous is probably porphyrinogenic and should only be used on patients with acute porphyria where there are strong or urgent indications.Appropriate precautions should be taken for all porphyric patients.
Carcinogenic and Mutagenic Potentia
Genotoxicity tests with lignocaine are inconclusive. In genotoxicity studies, a metabolite of lignocaine, 2,6-xylidine, showed evidence of activity in some tests but not in other tests. This metabolite has been shown to have carcinogenic potential (nasal and subcutaneous tumours) in preclinical toxicological studies evaluating chronic exposure.
Use in pregnancy - Category A
Lignocaine crosses the placental barrier and may be taken up by foetal tissues.When used for surface anaesthesia, lignocaine blood levels after normal doses are low so little drug is available for placental transfer.
There are, however, no adequate and well-controlled studies in pregnant women.Reproduction studies have been performed in rats at doses of 500 mg/kg/day and have revealed no evidence of harm to the foetus caused by lignocaine.
It is reasonable to assume that a large number of pregnant women and women of child-bearing age have used lignocaine. No specific disturbances to the reproduction process have so far been reported.
Labour and delivery
Lignocaine is not contraindicated in labour and delivery.
Use in lactation
Lignocaine enters the breast milk, but in such small quantities that there is generally no risk of affecting the child at therapeutic dose levels.
Effects on ability to drive and operate machines
Depending on the dose, local anaesthetics may have a very mild effect on mental function and may temporarily impair locomotion and co-ordination.
Interaction with other medicines
Lignocaine should be used with caution in patients receiving other local anaesthetics or agents structurally related to amide-type local anaesthetics, e.g. antiarrhythmic drugs such as mexiletine, since the toxic effects are additive.
Specific interaction studies with lidocaine and anti-arrhythmic drugs class III (e.g. amiodarone) have not been performed, but caution is advised.
Enzyme inducing drugs
Cimetidine or betablockers have been shown to cause potentially toxic plasma concentrations when lignocaine is given in repeated high doses over a long period of time. Therefore, caution should be taken if lignocaine was administered at higher than recommended doses over extended period of time.
Phenytoin and other antiepileptic drugs such as phenobarbitone, primidone and carbamazepine appear to enhance the metabolism of lignocaine but the significance of this effect is not known. Phenytoin and lignocaine have additive cardiac depressant effects.
Systemic adverse reactions are rare and may result from high plasma levels caused by excessive dosage or rapid absorption, or may result from a hypersensitivity, idiosyncrasy or reduced tolerance on the part of the patient. Such reactions are systemic in nature and involve the central nervous system and/or the cardiovascular system.
Central Nervous System
CNS reactions are excitatory and/or depressant and may be characterised by lightheadedness, nervousness, apprehension, euphoria, confusion, dizziness, drowsiness, tinnitus, blurred vision, vomiting, sensations of heat, cold or numbness, twitching, tremors, convulsions, unconsciousness and possibly respiratory arrest. The excitatory reactions may be brief or may not occur at all, in which case the first manifestations of toxicity may be drowsiness, progressing to unconsciousness and respiratory arrest.
Drowsiness following administration of lignocaine is usually an early sign of a high blood level of the drug and may occur as a result of rapid absorption.
Cardiovascular reactions are usually depressant and may be characterised by hypotension, myocardial depression, bradycardia and possibly cardiac arrest.
Allergic reactions may occur as a result of sensitivity either to the local anaesthetic agent or to other ingredients in the formulation. Allergic reactions as a result of sensitivity to lignocaine are rare (<0.1%). The detection of sensitivity by skin testing is of doubtful value.
The extremely rare cases of allergy to local anaesthetic preparations have included bronchospasm, chest pain, dyspnoea, pruritus, rash, rhinitis, increased sweating, urticaria, sleepiness, dizziness, paraesthesia, oedema, and in the most severe instances anaphylactic shock. Several cases of contact dermatitis have been reported with the use of lignocaine.
Dosage and administration
With any local anaesthetic, reactions and complications are best averted by employing the minimal effective dosage. Debilitated, acutely ill or elderly patients and children should be given doses commensurate with their age and physical condition.
Shake the bottle well before use.
For symptomatic treatment of irritated or inflamed mucous membranes of the mouth and pharynx, the usual adult dose is 15 mL undiluted. For use in the mouth, the solution should be swished around the mouth for approximately 30 seconds and spat out. For use on the pharynx, the solution should be gargled and may be swallowed. This dose should not be administered at intervals of less than three hours.
Although the incidence of adverse effects with lignocaine is quite low, caution should be exercised when using large amounts.
Adults: No more than 15 mL (300 mg lignocaine HCl) every 3 hours or 120 mL in a 24 hour period.
Children over 3 years of age: No more than 4.5 mg/kg of bodyweight or 5 mL (100 mg lignocaine HCl) every 3 hours or 40 mL in a 24 hour period.
Children under 3 years of age: No more than 1.25 mL applied with a cotton swab every 3 hours or 10 mL in a 24 hour period.
For information on the management of overdose, contact the Poisons Information Centre on 13 11 26 (Australia).
Management of Local Anaesthetic Emergencies
The first consideration is prevention, best accomplished by careful and constant monitoring of cardiovascular and respiratory vital signs and the patient's state of consciousness after each local anaesthetic administration. At the first sign of change, oxygen should be administered.
Should symptoms of systemic toxicity occur, the signs are anticipated to be similar in nature to those following the administration of local anaesthetics by other routes. Local anaesthetic toxicity is manifested by symptoms of nervous system excitation and, in severe cases, central nervous and cardiovascular depression.
Severe neurological symptoms (convulsions, CNS depression) must be treated symptomatically by respiratory support and the administration of anti-convulsive drugs.
If circulatory arrest should occur, immediate cardiopulmonary resuscitation should be instituted. Optimal oxygenation and ventilation and circulatory support as well as treatment of acidosis are of vital importance.
Presentation and storage conditions
Xylocaine 2% Viscous Solution is a red viscous liquid packed in 200 mL bottle.
Store below 25°C.