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Lidocaine


Generic Medicine Info
Indications and Dosage
Intramuscular
Ventricular arrhythmias
Adult: For cases that occur after MI or during cardiac manipulation (e.g. cardiac surgery): 50-100 mg or 1-1.5 mg/kg via IV bolus inj given at a rate of approx 25-50 mg/min. If the desired effect is not achieved, a 2nd dose may be given 5 minutes after completion of the 1st dose. Max: 200-300 mg during a 1-hour period. For prevention of recurrent arrhythmia, if oral antiarrhythmic therapy is not feasible: 1-4 mg/min (20-50 mcg/kg/min) as continuous IV infusion following initial bolus inj. Discontinue infusion as soon as there is a stable cardiac rhythm or at the earliest signs of toxicity. For patients with heart failure, dosage reduction may be necessary. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.
Child: For cases that occur after MI or during cardiac manipulation (e.g. cardiac surgery): Loading dose: 0.5-1 mg/kg via IV bolus inj; may be repeated as necessary according to patient's response (Max total dose: 3-5 mg/kg). Maintenance dose: 10-50 mcg/kg/min as IV infusion via infusion pump. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).

Intravenous
Intravenous regional anaesthesia
Adult: Individualise dosage based on the procedure, degree or duration of anaesthesia required, vascularity of tissue, and the patient's weight and physical condition. As 0.5% solution: 10-60 mL (50-300 mg). Max: 4 mg/kg/dose. Use the lowest dose and concentration that will produce the desired effect. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.

Mouth/Throat, Nasal
Surface anaesthesia
Adult: For the prevention of pain associated with various procedures: As 10 mg/actuation (10%) metered-dose spray: For dentistry: 1-5 actuations (10-50 mg) to the oral mucous membranes. For otorhinolaryngology: 3 actuations (30 mg) for puncture of the maxillary sinus or other minor procedures. For the introduction of instruments into the respiratory and gastrointestinal tracts: Up to 20 actuations (200 mg) for procedures in pharynx, larynx, and trachea. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.
Child: Dosage recommendations may vary according to age, weight, and physical condition (refer to local or specific product guidelines).

Mouth/Throat
Topical anaesthesia
Adult: For painful conditions (irritated or inflamed mucous membranes) of the mouth and pharynx: As 2% viscous solution: Usual dose: 15 mL (Max: 120 mL or 2.4 g within 24 hours). Dose intervals must not be less than 3 hours. If used in the mouth, the solution can be swished around and then spat out. If used in the pharynx, the solution can be gargled and slowly swallowed. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.
Child: Dosage recommendations may vary according to age, weight, and physical condition (refer to local or specific product guidelines).

Ophthalmic
Ocular anaesthesia
Adult: As 3.5% ophthalmic gel: Apply 2 drops to the ocular surface in the area of the planned procedure. Doses may be re-applied to maintain the anaesthetic effect. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).

Otic/Aural
Otic pain
Adult: As 4% otic drops: Instil 2-3 drops to the affected ear not more than 3-4 times daily. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).

Parenteral
Percutaneous infiltration anaesthesia
Adult: Individualise dosage based on the procedure, degree or duration of anaesthesia required, vascularity of tissue, and the patient's weight and physical condition. As 0.5% solution: 1-60 mL. As 1% solution: 0.5-30 mL. Alternative recommendation as 0.5% or 1% solution: 1-60 mL (5-300 mg). Use the lowest dose and concentration that will produce the desired effect. Recommendations may vary among countries and between individual products (refer to local or specific produce guidelines).
Elderly: Dosage reduction may be necessary.

Parenteral
Epidural anaesthesia
Adult: Individualise dosage based on the procedure, degree or duration of anaesthesia required, vascularity of tissue, and the patient's weight and physical condition. Administer a test dose of 2-3 mL at least 5 minutes before giving the total dose. Usual dose: 2-3 mL of the indicated concentration for each dermatome. For thoracic epidural anaesthesia: As 1% solution (preservative free): 20-30 mL (200-300 mg). For lumbar epidural analgesia: As 1% solution (preservative free): 25-30 mL (225-300 mg). For lumbar epidural anaesthesia: As 1.5% solution (preservative free): 15-20 mL (225-300 mg). As 2% solution (preservative free): 10-15 mL (200-300 mg). Use the lowest dose and concentration that will produce the desired effect. The Max recommended dose must not be administered at intervals of <1.5 hours. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.

Parenteral
Obstetric analgesia
Adult: Individualise dosage based on the procedure, degree or duration of anaesthesia required, vascularity of tissue, and the patient's weight and physical condition. As 1% solution: For paracervical nerve block (each side): 10 mL (100 mg). Use the lowest dose and concentration that will produce the desired effect. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.

Parenteral
Caudal anaesthesia
Adult: Individualise dosage based on the procedure, degree or duration of anaesthesia required, vascularity of tissue, and the patient's weight and physical condition. Administer a test dose of 2-3 mL at least 5 minutes before giving the total dose. For obstetrical analgesia: As 1% solution (preservative free): 20-30 mL (200-300 mg). For surgical anaesthesia: As 1.5% solution: 15-20 mL (225-300 mg). Use the lowest dose and concentration that will produce the desired effect. The Max recommended dose must not be administered at intervals of <1.5 hours. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.

Parenteral
Peripheral nerve block
Adult: Individualise dosage based on the procedure, degree or duration of anaesthesia required, vascularity of tissue, and the patient's weight and physical condition. As 1% solution: For intercostal nerve block: 3 mL (30 mg). For paravertebral nerve block: 3-5 mL (30-50 mg). For pudendal (each side) nerve block: 10 mL (100 mg). As 1.5% solution: For brachial plexus block: 15-20 mL (225-300 mg). As 2% solution: For dental nerve block: 1-5 mL (20-100 mg). Use the lowest dose and concentration that will produce the desired effect. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.

Parenteral
Sympathetic nerve block
Adult: Individualise dosage based on the procedure, degree or duration of anaesthesia required, vascularity of tissue, and the patient's weight and physical condition. As 1% solution: For cervical nerve block: 5 mL (50 mg). For lumbar nerve block: 5-10 mL (50-100 mg). Use the lowest dose and concentration that will produce the desired effect. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.

Rectal
Anorectal pain and itching
Adult: As 5% w/w cream: Apply to the affected area up to 6 times daily. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Child: ≥12 years As 5% w/w cream: Same as adult dose. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).

Topical/Cutaneous
Topical anaesthesia
Adult: For temporary relief of pain or skin irritation: As 3.88% or 4.12% cream: Apply thinly to the affected area 2-3 times daily. As 4% w/w cream (LMX4): Apply to the affected area up to 3-4 times daily. As 4% cream (Aspercreme): Apply thinly to the affected area every 6-8 hours (Max: 3-4 applications in 24 hours). As 4% spray: Spray to the affected area every 6-8 hours (Max: 3-4 applications in 24 hours). Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Child: Dosage recommendations may vary according to age, weight, and physical condition (refer to local or specific product guidelines).

Topical/Cutaneous
Surface anaesthesia
Adult: As local anaesthesia prior to superficial skin procedures (including venous cannulation or venepuncture): As 4% w/w cream (LMX4): Apply a thick layer (1-2.5 g) of cream to the small area (2.5 cm × 2.5 cm) of intact skin where the procedure will occur. Max application time: 5 hours. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Child: As local anaesthesia prior to superficial skin procedures (including venous cannulation or venepuncture): As 4% w/w cream (LMX4): <1 year Apply a thick layer (up to 1 g) of cream to the small area (2.5 cm × 2.5 cm) of intact skin where the procedure will occur. Max application time: 1-2 months 1 hour; 3-11 months 4 hours. ≥1 year Same as adult dose. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).

Transdermal
Postherpetic neuralgia
Adult: For pain relief: As 1.8% patch (ZTlido) or 5% patch: Apply to intact skin covering the most painful area (Max: 3 patches in a single application) for up to 12 hours within a 24-hour period. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.

Urethral
Surface anaesthesia
Adult: As 2% Jelly: For procedures involving the female urethra: Insert 3-5 mL (60-100 mg) slowly into the urethra several minutes before the procedure. For procedures involving the male urethra: 5-10 mL (100-200 mg) prior to catheterisation or a total dose of 30 mL (600 mg) prior to sounding or cystoscopy. Recommendations may vary among countries and between individual products (refer to local or specific product guidelines).
Elderly: Dosage reduction may be necessary.
Other Known Brands
  • Lakan
  • Lidocain
  • Lidocaine B Braun
  • Lignocaine 1% Pfizer
  • Lignocaine 10%-Bodene
  • Lignocaine 2% Pfizer
  • Lignocaine 2%-Bodene
  • Lignopad
  • Trachisan
See more
Special Patient Group
Intravenous/Parenteral/Transdermal/Mouth/Throat/Nasal/Urethral:
Debilitated patients: Dosage reduction may be necessary.
Reconstitution
IV infusion: Recommendations for reconstitution may vary between individual products (refer to specific product guidelines).
Incompatibility
Amphotericin B, sulfadiazine sodium in glucose inj, methohexital sodium, and glyceryl trinitrate.
Contraindications
When used for ventricular arrhythmias: Severe degree of sinoatrial, AV, or intraventricular heart block (in the absence of a functioning artificial pacemaker), Stokes-Adams syndrome. Otic: Perforation or injury of the eardrum, including tubes in the ear. Contraindications may vary among countries and between individual products (refer to specific product guidelines).
Special Precautions
Patient with G6PD deficiency, epilepsy, myasthenia gravis, cardiac conduction disturbances, CHF, bradycardia, severe shock, impaired respiratory function, congenital or idiopathic methaemoglobinaemia, exposure to oxidising agents or their metabolites, hypovolaemia, porphyria, history of malignant hyperthermia; pseudocholinesterase deficiency, sepsis, severely traumatised mucosa. Debilitated patients. Injection into infected tissues or application to broken or inflamed skin and damaged mucosa may increase absorption and risk for potential systemic adverse effects. Avoid intravascular inj. Not approved for continuous intra-articular infusion of local anaesthetics after arthroscopic or other surgical procedures. Lidocaine is available in multiple formulations with varying concentrations; refer to specific product guidelines before administration. Hepatic and renal impairment. Children and elderly. Pregnancy and lactation.
Adverse Reactions
Significant: Serious adverse effects (e.g. seizures, breathing difficulties, irregular heartbeat, coma) may occur when topical anaesthetics are applied in excessive amounts, at short dose intervals, and to large areas of the skin, particularly on broken or irritated skin. Methaemoglobinaemia; chondrolysis (particularly in the shoulder joint following intra-articular infusion); CV depression, hypotension, bradycardia. Familial malignant hyperthermia, application site reactions such as sensitivity, infection, or irritation (topical); may impair swallowing, resulting in increased risk of aspiration, numbness of buccal mucosa or tongue that may increase risk of biting trauma (oropharyngeal). Permanent corneal ulceration and/or opacification with loss of vision during prolonged use (ophthalmic).
Ear and labyrinth disorders: Tinnitus.
Eye disorders: Blurred vision; conjunctival hyperaemia, epithelial keratopathy, burning sensation of the eyes (ophthalmic).
Gastrointestinal disorders: Nausea, vomiting.
General disorders and administration site conditions: Oedema.
Immune system disorders: Hypersensitivity reactions.
Nervous system disorders: Dizziness, drowsiness, tremor; headache (ophthalmic).
Respiratory, thoracic and mediastinal disorders: Dyspnoea, bronchospasm, respiratory depression, respiratory arrest.
Skin and subcutaneous tissue disorders: Rash, urticaria.
Vascular disorders: Hypertension.
Buccal/Dental/Endotracheal/Epidural/IM/Intradermal/IV/Mouth/Throat/Ophth/Parenteral/Perineural/Rectal/SC/Topical/Transdermal/Urethral: B
Patient Counseling Information
Transdermal patch: Avoid exposure to external heat sources (e.g. electric blanket, heat lamp, heating pad, hot tub).
Monitoring Parameters
Correct hypoxia, hypokalaemia, and acid‐base balance disorder prior to IV administration. Monitor LFTs; ECG, blood pressure, and respirations (during IV administration); lidocaine serum concentrations (in patients requiring continuous infusions or therapy >24 hours). Assess for signs and symptoms of methaemoglobinaemia (e.g. cyanosis, rapid pulse, shortness of breath, headache, lightheadedness, fatigue), neurologic signs and symptoms of toxicity (e.g. perioral tingling, light-headedness, restlessness), and severe skin irritation.
Overdosage
Symptoms: Circumoral paraesthesia, numbness of the tongue, lightheadedness, hyperacusis, tinnitus, visual disturbances, muscular tremors or twitching, unconsciousness, grand mal seizures, hypoxia, hypercapnia. In severe cases, apnoea, hypotension, bradycardia, arrhythmia, and cardiac arrest may occur. Management: Symptomatic and supportive treatment. Ensure appropriate airway/respiratory support, oxygenation and ventilation and circulatory support. Administer anticonvulsants to treat seizures. Employ standard cardiopulmonary resuscitation if cardiac arrest occurs.
Drug Interactions
May cause additive systemic effects with other local anaesthetics or agents structurally related to amide-type local anaesthetics (e.g. mexiletine). May increase the risk of potentiated and prolonged neuromuscular blockade with muscle relaxants (e.g. suxamethonium). Increased plasma concentration with β-blockers (e.g. propranolol) and cimetidine. Antiviral agents (e.g. saquinavir, atazanavir, lopinavir) may increase the serum concentration of lidocaine. Increased risk of methaemoglobinaemia with other agents associated with methaemoglobinaemia (e.g. nitric oxide, prilocaine, dapsone).
Action
Description:
Mechanism of Action: Lidocaine is an amide-type local anaesthetic agent. It inhibits the initiation and conduction of nerve impulses through a reduction in the permeability of neuronal membrane to sodium ions, resulting in inhibition of depolarisation with resultant conduction blockade.
Synonym(s): Lignocaine.
Onset: Systemic administration: 45-90 seconds (single IV bolus dose). Ophthalmic: 20 seconds to 5 minutes (median: 40 seconds). Topical: 3-5 minutes. Transdermal: Approx 4 hours.
Duration: Systemic administration: 10-20 minutes (single IV bolus dose). Ophthalmic: 5-30 minutes (median: 15 minutes).
Pharmacokinetics:
Absorption: Rapidly absorbed from the inj site, mucous membranes, and through damaged skin; extent and rate of absorption varies, depending on the concentration, dose, application site, and duration of exposure (transdermal).
Distribution: Rapidly and widely distributed into highly perfused tissues, then redistributed into skeletal muscle and adipose tissue; crosses the blood-brain barrier. Crosses the placenta and enters breast milk. Plasma protein binding: 60-80% to α1-acid glycoprotein.
Metabolism: Metabolised in the liver by CYP1A2 and CYP3A4 isoenzymes into the active metabolites, monoethylglycinexylidide and glycinexylidide. Undergoes extensive first-pass metabolism.
Excretion: Via urine (approx 90% as metabolites, <10% as unchanged drug). Elimination half-life: 1.5-2 hours.
Chemical Structure

Chemical Structure Image
Lidocaine

Source: National Center for Biotechnology Information. PubChem Compound Summary for CID 3676, Lidocaine. https://pubchem.ncbi.nlm.nih.gov/compound/Lidocaine. Accessed Apr. 30, 2025.

Storage
Store at controlled room temperature. Storage recommendations may vary among individual products. Refer to specific product guidelines.
MIMS Class
Anaesthetics - Local & General / Cardiac Drugs
ATC Classification
R02AD02 - lidocaine ; Belongs to the class of local anesthetics used in throat preparations.
D04AB01 - lidocaine ; Belongs to the class of topical anesthetics used in the treatment of pruritus.
C05AD01 - lidocaine ; Belongs to the class of local anesthetics. Used in the topical treatment of hemorrhoids and anal fissures.
S02DA01 - lidocaine ; Belongs to the class of analgesic and anesthetic agents used as otologicals.
S01HA07 - lidocaine ; Belongs to the class of local ophthalmologic anesthetics.
N01BB02 - lidocaine ; Belongs to the class of amides. Used as local anesthetics.
C01BB01 - lidocaine ; Belongs to class Ib antiarrhythmics.
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Disclaimer: This information is independently developed by MIMS based on Lidocaine from various references and is provided for your reference only. Therapeutic uses, prescribing information and product availability may vary between countries. Please refer to MIMS Product Monographs for specific and locally approved prescribing information. Although great effort has been made to ensure content accuracy, MIMS shall not be held responsible or liable for any claims or damages arising from the use or misuse of the information contained herein, its contents or omissions, or otherwise. Copyright © 2025 MIMS. All rights reserved. Powered by MIMS.com
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