Product image of Lidocaina E Prilocaina Teva (Lidocaine, Prilocaine) supplied by GNH India

Lidocaina E Prilocaina Teva

Active Ingredient:
Lidocaine, Prilocaine
Origin:
EU

Lidocaina E Prilocaina Teva (Lidocaine, Prilocaine)

Lidocaine, the active ingredient in Lidocaina E Prilocaina, is a local anesthetic presented as a topical formulation for skin application. It is combined with prilocaine to provide surface anesthesia for minor procedures, superficial wound pain relief, and pre‑operative skin preparation in patients of various ages.
GNH India supplies Lidocaina E Prilocaina as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Italia S.R.L.

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Indications & Clinical Uses

Lidocaina E Prilocaina acts on peripheral nerve sodium channels to provide topical anesthesia for skin‑related procedures.

  • Minor skin procedures: produces rapid, reversible loss of sensation for biopsies, laser treatments, or minor excisions.
  • Superficial wound pain relief: reduces discomfort from cuts, abrasions, or burns.
  • Pre‑operative skin anesthesia: numbs the skin before surgical incision or injection.
  • Dermatologic procedures: facilitates painless application of topical agents during cosmetic or therapeutic treatments.
  • Cosmetic injections: provides local numbness for filler or toxin administration.

How It Works

  • Lidocaine and prilocaine block neuronal voltage‑gated sodium channels in a reversible manner, preventing depolarization and the propagation of nerve impulses. By stabilizing the neuronal membrane, they inhibit the initiation and conduction of pain signals in the peripheral nerves at the site of topical application, resulting in localized loss of sensation without systemic anesthetic effects when used as directed.

Side Effects

Common Side Effects

  • Transient erythema: mild redness at the application site.
  • Burning sensation: brief feeling of warmth or stinging.
  • Pruritus: occasional itching of the treated area.
  • Localized swelling: mild edema limited to the site.
  • Tingling: temporary pins‑and‑needles feeling.

Serious or Rare Side Effects

  • Allergic contact dermatitis: severe skin reaction with rash and itching.
  • Systemic toxicity: signs such as seizures, cardiac arrhythmia, or altered mental status if excessive absorption occurs.
  • Severe skin necrosis: rare tissue death at the application site.
  • Methemoglobinemia: uncommon blood disorder causing cyanosis.
  • Anaphylaxis: rare life‑threatening allergic response.

Precautions & Warnings

Before using Lidocaina E Prilocaina, consider the following precautions.

  • Allergy assessment: avoid in patients with known hypersensitivity to lidocaine, prilocaine, or other amide anesthetics.
  • Application area: limit use to intact, non‑inflamed skin and avoid mucous membranes.
  • Duration of exposure: do not exceed the recommended contact time to reduce systemic absorption.
  • Concomitant anesthetics: avoid simultaneous use of other topical anesthetic products to prevent additive toxicity.
  • Pediatric use: apply with caution in children and follow prescriber guidance regarding dose and area.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lidocaina E Prilocaina may interact with other medications that affect cardiac or nervous system function.

Major Interactions (Avoid)

  • Systemic local anesthetics: concurrent use of injectable lidocaine can increase total anesthetic load and risk of toxicity.
  • Class I antiarrhythmics (e.g., quinidine): may enhance cardiotoxic effects of absorbed anesthetic.
  • Strong CYP3A4 inhibitors: can raise systemic levels of prilocaine, increasing adverse effect risk.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may potentiate cardiac depression if systemic absorption occurs.
  • Diuretics: can alter plasma concentration of local anesthetics, requiring observation.

Frequently Asked Questions

Lidocaina E Prilocaina is a topical combination of lidocaine and prilocaine used to provide local anesthesia for minor skin procedures, relieve pain from superficial wounds, and numb the skin before surgical or cosmetic interventions. It works by temporarily blocking nerve signal transmission at the site of application.

Lidocaine, together with prilocaine, reversibly inhibits voltage‑gated sodium channels on peripheral nerves. This prevents the rapid influx of sodium ions required for depolarization, thereby halting the generation and conduction of pain impulses. The effect is localized to the area where the cream or gel is applied.

The appropriate amount and frequency of application are determined by the prescribing healthcare professional based on the specific procedure, patient age, and treatment area. The prescriber will provide instructions on how much product to apply and how long to leave it on the skin.

Safety data for the combination in pregnancy and lactation are limited. It 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 after evaluating the individual situation.

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, and will request trade or institutional credentials. The sales team will then respond with pricing, availability, shipping details (including any cold‑chain requirements), and necessary import documentation.

Lidocaina E Prilocaina combines two amide‑type anesthetics, offering broader coverage and potentially longer duration of action compared with single‑agent products such as lidocaine‑only creams. The dual formulation may provide more effective anesthesia for larger or more painful areas while maintaining a similar safety profile when used as directed.

Store the product at ambient temperature, preferably below 25 °C, in its original packaging. Protect it from moisture, direct sunlight, and extreme temperatures. Ensure the container is tightly closed when not in use to maintain product stability.

The medication is applied topically to clean, dry, intact skin. A thin layer is spread over the intended area and covered with an occlusive dressing if required. After the prescribed exposure time, the excess product is removed, and the area is cleaned before proceeding with the planned procedure.

Serious risks include systemic toxicity leading to seizures or cardiac arrhythmias, severe allergic reactions such as anaphylaxis or contact dermatitis, and rare cases of methemoglobinemia. These events are uncommon when the product is used according to prescribing information, but patients should be monitored for any signs of systemic absorption or hypersensitivity.

Individuals with a known hypersensitivity to lidocaine, prilocaine, or any amide‑type local anesthetic should avoid this product. It is also contraindicated in patients with certain cardiac conduction disorders or severe liver disease where systemic absorption could pose additional risk. The prescriber will assess suitability for each patient.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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