Product image of Lidocaína Adrenalina Labesfal (Epinephrine Bitartrate, Lidocaine Hydrochloride) supplied by GNH India

Lidocaína Adrenalina Labesfal

Active Ingredient:
Epinephrine Bitartrate, Lidocaine Hydrochloride
Origin:
EU

Lidocaína Adrenalina Labesfal (Epinephrine Bitartrate, Lidocaine Hydrochloride)

Lidocaine hydrochloride and epinephrine bitartrate, the active ingredient in Lidocaína Adrenalina Labesfal, is a local anesthetic with vasoconstrictor presented as a sterile solution for subcutaneous administration. It is used to achieve rapid, reversible loss of sensation in minor surgical, dental and dermatologic procedures for adult patients.

GNH India supplies Lidocaína Adrenalina Labesfal as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, including procurement teams in transplant and oncology centres.

Manufacturer / TM Owner

Labesfal Laboratorios Almiro, S.A.

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Indications & Clinical Uses

Lidocaína Adrenalina Labesfal, a combination local anesthetic with vasoconstrictor, is indicated for procedures requiring soft‑tissue anesthesia.

  • Minor surgical procedures: provides localized numbness to facilitate incision, excision and suturing.
  • Dental procedures: enables painless soft‑tissue work such as extractions, root canal access and periodontal surgery.
  • Dermatologic or cosmetic interventions: allows infiltration anesthesia for skin lesion removal, laser therapy or minor cosmetic surgery.

How It Works

  • Lidocaine blocks voltage‑gated sodium channels in neuronal membranes, preventing initiation and propagation of nerve impulses and thereby producing loss of sensation. Epinephrine stimulates α‑adrenergic receptors on vascular smooth muscle, causing vasoconstriction that limits systemic absorption of lidocaine, prolongs its local effect and reduces bleeding at the injection site.

Side Effects

Adverse reactions to Lidocaína Adrenalina Labesfal may vary in frequency and severity.

Common Side Effects

  • Tingling or numbness at the injection site
  • Mild swelling or erythema
  • Transient dizziness
  • Headache
  • Nausea
  • Elevated heart rate (palpitations)

Serious or Rare Side Effects

  • Severe allergic reaction (anaphylaxis)
  • Cardiac arrhythmias
  • Seizures
  • Methemoglobinemia
  • Persistent hypotension
  • Tissue necrosis at the injection site

Precautions & Warnings

When using Lidocaína Adrenalina Labesfal, clinicians should observe several safety measures.

  • Assess patient allergy: verify no known hypersensitivity to lidocaine, epinephrine or amide anesthetics.
  • Review cardiovascular status: avoid in patients with uncontrolled hypertension, arrhythmias, or recent myocardial infarction.
  • Limit dosage: adhere to the recommended maximum dose based on patient weight and injection site.
  • Use caution with MAO inhibitors or tricyclic antidepressants: these may increase systemic toxicity.
  • Monitor for signs of systemic toxicity: watch for CNS or cardiovascular symptoms.
  • Store at room temperature: keep in the original container, protect from light and moisture.

Avoid Interactions

Lidocaína Adrenalina Labesfal can interact with several drug classes; clinicians should review patient medication lists.

Major Interactions (Avoid)

  • MAO inhibitors: increased risk of hypertensive crisis with epinephrine.
  • β‑blockers: may potentiate epinephrine‑induced tachycardia.
  • Class I antiarrhythmics (e.g., quinidine): can exacerbate lidocaine toxicity.
  • Tricyclic antidepressants: raise lidocaine plasma levels.
  • Non‑selective α‑adrenergic antagonists: reduce vasoconstrictive effect of epinephrine.

Moderate Interactions (Monitor Closely)

  • Antihistamines: may mask early signs of allergic reaction.
  • Diuretics: alter plasma volume affecting drug distribution.
  • CYP3A4 inhibitors (e.g., erythromycin): modestly increase lidocaine levels.
  • Sympathomimetic drugs (e.g., phenylephrine): additive vasoconstriction.
  • Alcohol: may enhance central nervous system depression.

Frequently Asked Questions

Lidocaína Adrenalina Labesfal is a combination of lidocaine and epinephrine formulated to provide local anesthesia. It is employed in minor surgical, dental and dermatologic procedures where rapid, reversible loss of sensation is required, helping to reduce pain and bleeding at the treatment site.

Lidocaine blocks voltage‑gated sodium channels in nerve membranes, preventing the transmission of pain signals. Epinephrine activates α‑adrenergic receptors on blood vessels, causing vasoconstriction. This constriction limits systemic absorption of lidocaine, prolongs its anesthetic effect, and reduces intra‑procedural bleeding.

The dose is determined by the prescribing clinician based on the patient’s weight, the specific procedure, and the maximum recommended limits for lidocaine and epinephrine. Healthcare professionals calculate the appropriate volume to achieve effective anesthesia while staying within safety guidelines.

Safety data for this product in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the 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 (including cold‑chain if needed) and the necessary import documentation.

The addition of epinephrine to lidocaine creates a vasoconstrictive effect that prolongs the duration of anesthesia, reduces systemic absorption, and minimizes bleeding at the injection site. Plain lidocaine lacks these benefits, often requiring higher volumes or repeat dosing for comparable duration.

Lidocaína Adrenalina Labesfal should be stored at room temperature, below 25 °C, in its original sealed container. Protect the solution from direct light and moisture, and avoid freezing. Inspect the vial for particulate matter before use.

The product is administered by subcutaneous or intradermal injection, typically as an infiltration technique. The clinician injects the solution directly into the tissue surrounding the procedural area, allowing rapid onset of anesthesia within minutes.

Serious risks include severe allergic reactions (anaphylaxis), cardiac arrhythmias, seizures, methemoglobinemia, persistent hypotension, and tissue necrosis at the injection site. Immediate medical attention is required if any of these events occur.

Patients with known hypersensitivity to lidocaine, epinephrine, or any amide‑type local anesthetic should avoid this product. It is also contraindicated in individuals with uncontrolled hypertension, severe cardiac disease, recent myocardial infarction, or those taking MAO inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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