Product image of Lidocaïne/Prilocaïne Teva (Lidocaine, Prilocaine) supplied by GNH India

Lidocaïne/Prilocaïne Teva

Active Ingredient:
Lidocaine, Prilocaine
Origin:
EU

Lidocaïne/Prilocaïne Teva (Lidocaine, Prilocaine)

Lidocaine and Prilocaine, the active ingredients in Lidocaïne/Prilocaïne Teva, are local anesthetics presented as a topical formulation for cutaneous use. They provide surface anesthesia to reduce pain during minor skin procedures, venipuncture, cannulation, and superficial burns, offering rapid onset and short‑duration relief for patients of all ages.

GNH India supplies Lidocaïne/Prilocaïne Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality, regulatory compliance, and reliable global distribution to meet diverse clinical needs through established logistics networks.

Manufacturer / TM Owner

Teva Nederland B.V.

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Indications & Clinical Uses

Lidocaine/Prilocaine is a topical local anesthetic that works by reversibly blocking sodium channels in peripheral nerves, providing surface numbness for a variety of minor dermatologic and procedural applications.

  • Minor skin procedures: provides localized anesthesia to facilitate biopsies, suturing or minor excisions.
  • Venipuncture or cannulation: reduces pain and discomfort during blood draws or intravenous line placement.
  • Superficial burns or abrasions: alleviates discomfort from minor thermal or mechanical skin injuries.
  • Dermatologic laser or cosmetic procedures: offers temporary anesthesia to improve patient tolerance.

How It Works

  • Lidocaine and prilocaine act by reversibly binding to the intracellular portion of voltage‑gated sodium channels on neuronal membranes. This binding stabilizes the inactive state of the channel, preventing the influx of sodium ions during depolarization. Consequently, the generation and propagation of action potentials are inhibited, resulting in loss of sensation in the applied area without affecting surrounding tissues.

Side Effects

Topical application of lidocaine/prilocaine may be associated with local and systemic adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Mild skin irritation: redness or itching at the application site.
  • Transient burning sensation: brief warmth during onset.
  • Erythema: localized redness without swelling.
  • Edema: slight swelling of the treated area.
  • Contact dermatitis: allergic skin reaction with rash.
  • Dryness or flaking: mild desquamation of the skin.

Serious or Rare Side Effects

  • Methemoglobinemia: reduced oxygen‑carrying capacity, presenting with cyanosis.
  • Systemic toxicity: dizziness, seizures, or cardiac arrhythmias after excessive absorption.
  • Severe allergic reaction: anaphylaxis with airway compromise.

Precautions & Warnings

When using lidocaine/prilocaine topical products, clinicians should observe several precautionary measures to minimize risk and ensure optimal efficacy.

  • Assess allergy history: verify patient has no known hypersensitivity to amide‑type local anesthetics.
  • Limit application area: avoid covering large skin surfaces to prevent systemic absorption.
  • Avoid use on compromised skin: do not apply to open wounds, mucous membranes, or infected areas unless directed.
  • Monitor cardiovascular status: use cautiously in patients with heart disease or arrhythmias.
  • Pregnancy and lactation: consider risk‑benefit ratio and consult prescribing information.
  • Store at ambient temperature: keep below 25 °C, protect from moisture and direct sunlight, retain in original packaging.

Avoid Interactions

Lidocaine/prilocaine may interact with other agents that affect cardiac conduction or alter drug metabolism, requiring careful assessment.

Major Interactions (Avoid)

  • Class I antiarrhythmics (e.g., quinidine, procainamide): increased risk of cardiac toxicity and conduction disturbances.
  • Concurrent use of other local anesthetics: additive systemic toxicity, especially with high total dose.
  • Monoamine oxidase inhibitors (MAOIs): potential enhancement of central nervous system effects, including seizures.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask early signs of systemic toxicity such as tachycardia.
  • CYP450 inhibitors (e.g., cimetidine, erythromycin): can raise plasma levels of lidocaine, necessitating dose adjustment.
  • Alcohol: may potentiate CNS depression when combined with high topical doses.

Frequently Asked Questions

Lidocaïne/Prilocaïne Teva is a topical formulation that combines lidocaine and prilocaine to provide local skin anesthesia. It is commonly applied to numb the surface of the skin before minor dermatologic procedures, venipuncture, cannulation, or to relieve discomfort from superficial burns and abrasions.

Lidocaine, together with prilocaine, blocks voltage‑gated sodium channels on peripheral nerves. By stabilizing the inactive state of these channels, the drug prevents sodium influx during depolarisation, thereby inhibiting the generation and propagation of nerve impulses and producing a loss of sensation in the treated area.

The appropriate dose is determined by the prescribing clinician based on the size of the area to be treated, patient age, and clinical context. The product is applied as a thin layer to the intended skin surface, and the prescriber decides the exact amount and duration of exposure.

Safety data for topical lidocaine/prilocaine in pregnancy and lactation are limited. The product should be used only if the expected benefit justifies any potential risk to the fetus or infant, and the decision should be made in consultation with a qualified healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and the necessary import documentation.

Lidocaine/prilocaine offers a balanced 1:1 mixture that provides rapid onset and a slightly longer duration than lidocaine alone, and it is comparable to other eutectic mixtures such as EMLA® cream. The combination can achieve effective surface anesthesia with a lower total dose of each individual agent, potentially reducing the risk of systemic toxicity.

Lidocaïne/Prilocaïne Teva should be stored at ambient temperature, preferably below 25 °C. Keep the container tightly closed, protect it from moisture and direct sunlight, and retain the product in its original packaging until use to maintain stability and potency.

The product is applied topically to intact skin in a thin, even layer covering the intended area. It may be covered with an occlusive dressing if required by the clinical protocol. The duration of exposure is defined by the prescriber, after which the medication is removed and the area is cleaned.

Serious adverse events, although rare, include methemoglobinemia, systemic toxicity manifesting as central nervous system depression, seizures or cardiac arrhythmias, and severe allergic reactions such as anaphylaxis. Patients should be monitored for signs of these reactions, especially when large skin areas are treated or when used in conjunction with interacting drugs.

The product should be avoided in individuals with a known hypersensitivity to lidocaine, prilocaine, or any amide‑type local anesthetic. It is also contraindicated in patients with severe liver disease, certain cardiac conduction disorders, or when applied to broken, infected or mucosal surfaces unless specifically directed by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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