Product image of Lidocaïne/Adrenaline Aguettant (Epinephrine, Lidocaine Hydrochloride) supplied by GNH India

Lidocaïne/Adrenaline Aguettant

Active Ingredient:
Epinephrine, Lidocaine Hydrochloride
Origin:
EU

Lidocaïne/Adrenaline Aguettant (Epinephrine, Lidocaine Hydrochloride)

Lidocaine Hydrochloride, the active ingredient in Lidocaïne/Adrenaline Aguettant, is a local anesthetic presented as a sterile solution for injection for epidural, infiltration, intravenous and peripheral use. It provides rapid, localized numbness for minor surgical or diagnostic procedures and supports regional anesthesia techniques.

GNH India supplies Lidocaïne/Adrenaline Aguettant as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution, ensuring timely delivery.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Lidocaïne/Adrenaline is a local anesthetic combination used in procedures requiring regional or infiltration anesthesia.

  • Minor surgical procedures: provides rapid onset local anesthesia with prolonged duration due to vasoconstriction.
  • Epidural anesthesia: extends the sensory block while limiting systemic absorption.
  • Infiltration anesthesia: enhances depth and duration of numbness for tissue infiltration.
  • Intravenous regional (Bier) block: reduces systemic toxicity by limiting lidocaine spread.

How It Works

  • Lidocaine blocks voltage‑gated sodium channels in neuronal membranes, preventing the initiation and propagation of action potentials, which produces loss of sensation. Epinephrine activates α‑ and β‑adrenergic receptors, causing vasoconstriction at the injection site, which reduces local blood flow, delays systemic absorption of lidocaine, and thereby prolongs and intensifies the anesthetic effect. The combined effect allows clinicians to use lower concentrations of lidocaine while achieving adequate analgesia.

Side Effects

Adverse reactions to Lidocaïne/Adrenaline may vary in frequency and severity.

Common Side Effects

  • Injection site pain or burning sensation.
  • Transient tingling or numbness beyond the target area.
  • Light‑headedness or dizziness.
  • Nausea or mild vomiting.
  • Temporary increase in heart rate.

Serious or Rare Side Effects

  • Severe hypertension or hypertensive crisis.
  • Cardiac arrhythmias, including ventricular tachycardia.
  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Methemoglobinemia.
  • Central nervous system toxicity manifesting as seizures or loss of consciousness.

Precautions & Warnings

Before using Lidocaïne/Adrenaline, clinicians should consider several safety precautions.

  • Cardiovascular assessment: evaluate blood pressure and heart rhythm due to epinephrine’s sympathomimetic effects.
  • Use caution in patients with uncontrolled hypertension or coronary artery disease.
  • Avoid in individuals with known hypersensitivity to lidocaine, epinephrine, or any excipients.
  • Monitor for signs of systemic toxicity, especially when large volumes are administered.
  • Adjust dosage in pediatric or geriatric patients as recommended by the prescriber.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Lidocaïne/Adrenaline can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Non‑selective β‑blockers (e.g., propranolol): may potentiate epinephrine‑induced hypertension and bradycardia.
  • Monoamine oxidase inhibitors (MAOIs): increase risk of hypertensive crisis when combined with epinephrine.
  • Tricyclic antidepressants: can enhance lidocaine’s cardiotoxic potential.
  • Class I antiarrhythmic agents (e.g., quinidine): may exacerbate cardiac conduction disturbances.

Moderate Interactions (Monitor Closely)

  • Other local anesthetics: cumulative toxicity risk if used concurrently.
  • Vasoconstrictors (e.g., phenylephrine): may augment local vasoconstriction and systemic blood pressure.
  • Sympathomimetic drugs (e.g., dopamine): additive cardiovascular effects.
  • Calcium channel blockers: may alter vascular response to epinephrine.

Frequently Asked Questions

Lidocaïne/Adrenaline is a sterile injectable solution that combines lidocaine, a local anesthetic, with epinephrine, a vasoconstrictor. It is used to provide rapid, localized numbness for minor surgical procedures, epidural blocks, infiltration anesthesia, and intravenous regional (Bier) blocks, helping to prolong the anesthetic effect and reduce bleeding at the injection site.

Lidocaine blocks voltage‑gated sodium channels on neuronal membranes, stopping the initiation and propagation of nerve impulses. This interruption of signal transmission results in loss of sensation in the targeted area, producing the anesthetic effect required for surgical or diagnostic procedures.

The dose of Lidocaïne/Adrenaline is determined by the prescribing clinician based on the specific procedure, patient age, weight, health status, and the intended route of administration. Healthcare professionals calculate the appropriate volume and concentration to achieve effective anesthesia while minimizing the risk of systemic toxicity.

The pregnancy safety category for this combination is not definitively established. It should only be used during pregnancy or lactation when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and after careful evaluation by the treating physician.

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

Compared with plain lidocaine, the addition of epinephrine in Lidocaïne/Adrenaline causes local vasoconstriction, which reduces systemic absorption, prolongs the duration of anesthesia, and decreases intra‑operative bleeding. This allows clinicians to use lower total doses of lidocaine while achieving comparable or superior analgesic outcomes.

Lidocaïne/Adrenaline should be stored at room temperature, below 25 °C, in its original sealed container. Protect the product from direct sunlight, moisture, and extreme temperature fluctuations. Do not freeze the solution, and inspect the vial for any particulate matter or discoloration before use.

The product is administered by injection. Accepted routes include epidural, infiltration, peripheral nerve block, and intravenous regional (Bier) block. The healthcare professional selects the appropriate technique, prepares the injection site aseptically, and injects the calculated volume slowly while monitoring the patient for any immediate reactions.

Serious risks include severe hypertension, cardiac arrhythmias (such as ventricular tachycardia), allergic reactions ranging from urticaria to anaphylaxis, methemoglobinemia, and central nervous system toxicity that can lead to seizures or loss of consciousness. Prompt recognition and management of these events are essential.

The product should be avoided in patients with known hypersensitivity to lidocaine, epinephrine, or any formulation excipients. It is also contraindicated in individuals with uncontrolled severe hypertension, certain cardiac conduction disorders, or those taking non‑selective β‑blockers without appropriate medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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