Product image of Lidonostrum (Lidocaine) supplied by GNH India

Lidonostrum

Active Ingredient:
Lidocaine
Origin:
EU

Lidonostrum (Lidocaine)

Lidocaine, the active ingredient in Lidonostrum, is a local anesthetic presented as a topical preparation for cutaneous use. It provides temporary loss of sensation for skin anesthesia, pain relief, and relief of itching.
GNH India supplies Lidonostrum as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Sidefarma - Sociedade Industrial De Expansão Farmacêutica, S.A.

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Indications & Clinical Uses

Lidonostrum is a local anesthetic that acts on peripheral nerve sodium channels to provide surface analgesia.

  • Local anesthesia of skin: produces temporary numbness for minor surgical or diagnostic procedures.
  • Pain relief: reduces superficial pain associated with minor injuries or procedures.
  • Pruritus: alleviates itching by blocking sensory nerve transmission.

How It Works

  • Lidocaine blocks voltage‑gated sodium channels in neuronal membranes, stabilizing the neuronal membrane and preventing the initiation and propagation of action potentials. This inhibition of nerve impulse conduction results in loss of sensation in the area where the drug is applied.

Side Effects

Adverse reactions may occur following cutaneous application of lidocaine.

Common Side Effects

  • Mild skin irritation or burning sensation at the application site.
  • Redness or erythema.
  • Localized itching.
  • Swelling or edema.
  • Transient numbness extending beyond the intended area.
  • Dryness or peeling of the skin.

Serious or Rare Side Effects

  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Systemic toxicity manifesting as dizziness, tinnitus, or seizures.
  • Cardiac arrhythmias or conduction disturbances.
  • Methemoglobinemia.
  • Severe skin necrosis or ulceration.
  • Persistent numbness or motor weakness.

Precautions & Warnings

When using Lidonostrum, consider the following safety measures.

  • Allergy assessment: verify that the patient has no known hypersensitivity to lidocaine or amide‑type anesthetics.
  • Application area: avoid applying to broken skin, mucous membranes, or extensive open wounds.
  • Dose limitation: adhere strictly to the prescribed amount to prevent systemic absorption.
  • Concurrent anesthetics: do not combine with other topical anesthetics without medical guidance.
  • Pregnancy and lactation: consult a prescriber as safety data are limited.
  • Store below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Lidonostrum may interact with other medicines that affect cardiac or nervous system function.

Major Interactions (Avoid)

  • Other amide‑type local anesthetics: concurrent use can increase systemic toxicity.
  • Class I antiarrhythmics (e.g., quinidine, procainamide): may enhance cardiotoxic effects.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may reduce lidocaine metabolism.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask early signs of lidocaine toxicity.
  • Diuretics: can alter plasma concentrations of lidocaine.
  • General anesthetics: may potentiate central nervous system depression.

Frequently Asked Questions

Lidonostrum is a lidocaine‑based product applied to the skin to provide local anesthesia, relieve superficial pain, and reduce itching. It is commonly used before minor dermatologic procedures, for temporary pain control, and to alleviate pruritic skin conditions.

Lidocaine blocks voltage‑gated sodium channels in peripheral nerve membranes, preventing the initiation and propagation of nerve impulses. This interruption of signal transmission results in loss of sensation and analgesia at the site of application.

The appropriate amount of Lidonostrum is determined by the prescribing healthcare professional based on the treatment area, patient age, and clinical context. Patients should follow the prescriber's instructions and not exceed the recommended quantity.

Safety data for lidocaine topical use in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits and risks before prescribing Lidonostrum to pregnant or nursing individuals.

To request Lidonostrum, 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.

Lidonostrum contains lidocaine, an amide‑type anesthetic with a rapid onset and moderate duration of action. Compared with ester‑type agents such as benzocaine, lidocaine generally has a lower risk of allergic reactions and provides more consistent depth of anesthesia for skin procedures.

Lidonostrum should be stored below 25 °C in its original packaging, protected from moisture and direct light. Keep the container tightly closed and out of reach of children.

Lidonostrum is applied topically to intact skin. The prescribed amount is spread evenly over the target area using a sterile applicator or gloved finger, avoiding excessive use or application to damaged tissue.

Serious risks include systemic lidocaine toxicity, which can cause neurological symptoms such as seizures, and cardiac effects like arrhythmias. Rarely, severe allergic reactions or methemoglobinemia may occur, requiring immediate medical attention.

Individuals with known hypersensitivity to lidocaine or other amide‑type local anesthetics, those with extensive broken skin in the intended area, and patients taking medications that significantly increase lidocaine plasma levels should avoid using Lidonostrum unless directed by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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