Product image of Lidocaine/Prilocaine Aguettant (Lidocaine, Prilocaine) supplied by GNH India

Lidocaine/Prilocaine Aguettant

Active Ingredient:
Lidocaine, Prilocaine
Origin:
EU

Lidocaine/Prilocaine Aguettant (Lidocaine, Prilocaine)

Lidocaine, the active ingredient in Lidocaine/Prilocaine Aguettant, is a local anesthetic presented as a topical formulation for cutaneous use. It provides surface anesthesia for minor skin procedures, mucosal surfaces and superficial wounds.

GNH India supplies Lidocaine/Prilocaine Aguettant as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Lidocaine/Prilocaine is a local anesthetic used on the skin and mucous membranes to achieve temporary loss of sensation.

  • Minor skin procedures: provides rapid surface anesthesia for biopsies, suturing or laser treatment.
  • Mucous membrane anesthesia: numbs oral, nasal or genital mucosa during diagnostic or therapeutic procedures.
  • Superficial wound or burn pain relief: reduces pain and discomfort from shallow injuries or first‑degree burns.

How It Works

  • Lidocaine and prilocaine reversibly block voltage‑gated sodium channels in peripheral nerve membranes, preventing the initiation and propagation of action potentials. This inhibition stops the transmission of pain signals from the site of application, resulting in localized loss of sensation without affecting central nervous system function when used as directed.

Side Effects

Adverse reactions are generally limited to the application site, but systemic absorption can produce rare serious events.

Common Side Effects

  • Mild skin irritation or erythema
  • Itching or burning sensation at the site
  • Localized edema or swelling
  • Allergic contact dermatitis
  • Transient numbness lasting longer than expected
  • Dryness or peeling of the treated skin

Serious or Rare Side Effects

  • Systemic toxicity (e.g., dizziness, seizures, CNS depression)
  • Methemoglobinemia leading to cyanosis
  • Severe allergic reaction or anaphylaxis
  • Cardiac arrhythmias or conduction disturbances
  • Persistent numbness or paresthesia
  • Tissue necrosis with prolonged occlusive use

Precautions & Warnings

Before applying Lidocaine/Prilocaine, consider patient history and proper usage to minimise risk.

  • Allergy assessment: confirm no known hypersensitivity to amide‑type local anesthetics.
  • Application area: avoid use on broken, infected or inflamed skin unless directed.
  • Surface area limit: restrict total treated area to the amount recommended by the prescriber.
  • Patient monitoring: observe for signs of systemic toxicity, especially in children or the elderly.
  • Special populations: use with caution in infants, pregnant or lactating women when benefits outweigh risks.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lidocaine/Prilocaine may interact with other agents that affect sodium channels or metabolic pathways.

Major Interactions (Avoid)

  • Concurrent use of other amide‑type local anesthetics (risk of cumulative toxicity).
  • Class I antiarrhythmic drugs such as quinidine or procainamide (enhanced cardiac effects).
  • High‑dose epinephrine formulations (increased systemic absorption).

Moderate Interactions (Monitor Closely)

  • Strong CYP3A4 inhibitors (e.g., erythromycin, ketoconazole) that may raise plasma levels.
  • Methemoglobin‑inducing agents such as dapsone or nitrites (additive risk of methemoglobinemia).
  • Other medications that lower seizure threshold (e.g., tramadol, bupropion).

Frequently Asked Questions

Lidocaine/Prilocaine Aguettant is a topical local anesthetic applied to the skin or mucous membranes to provide temporary numbness. It is commonly used for minor dermatological procedures, mucosal anesthesia during examinations, and to relieve pain from superficial wounds or first‑degree burns.

Both lidocaine and prilocaine act by reversibly blocking voltage‑gated sodium channels on peripheral nerves. This blockade prevents the initiation and spread of nerve impulses, thereby interrupting pain signal transmission and producing localized anesthesia at the site of application.

The appropriate amount and frequency of application are determined by the prescribing healthcare professional based on the size of the treatment area, patient age, and specific procedure. Users should follow the prescriber’s instructions and not exceed the recommended quantity.

Safety data for use in pregnancy and lactation are limited. The product should only be used if the potential benefit justifies any possible risk to the fetus or infant, and this decision must be made by a qualified healthcare provider.

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 and any necessary import documentation.

Lidocaine/Prilocaine combines two amide‑type anesthetics, offering a broader spectrum of nerve blockade than single‑agent products. This can result in faster onset and longer duration of anesthesia compared with lidocaine‑only preparations, while maintaining a similar safety profile when used as directed.

Store the cream at room temperature, preferably below 25 °C, in its original packaging. Keep it away from moisture, direct sunlight and sources of heat. Ensure the container is tightly closed to maintain product stability.

The product is applied topically to clean, dry skin or mucous membrane. A thin layer is spread over the intended area and covered with an occlusive dressing if required. The duration of contact is determined by the prescriber, typically ranging from a few minutes to up to an hour before the procedure.

Serious adverse events, although rare, include systemic toxicity such as central nervous system symptoms (dizziness, seizures), methemoglobinemia, severe allergic reactions (anaphylaxis) and cardiac arrhythmias. Immediate medical attention is required if any of these symptoms develop.

Patients with a known hypersensitivity to lidocaine, prilocaine, or other amide‑type local anesthetics should avoid this product. It is also contraindicated on severely damaged or infected skin unless directed by a clinician, and caution is advised in infants, the elderly and patients taking interacting medications.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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