Product image of Lidocaína Aurovitas (Lidocaine Hydrochloride) supplied by GNH India

Lidocaína Aurovitas

Active Ingredient:
Lidocaine Hydrochloride
Origin:
EU

Lidocaína Aurovitas (Lidocaine Hydrochloride)

Lidocaine Hydrochloride, the active ingredient in Lidocaína Aurovitas, is a local anesthetic (amide type) presented as a sterile solution for epidural, intramuscular and intravenous use. It provides reversible nerve block for surgical and pain‑management procedures in adult patients.
GNH India supplies Lidocaína Aurovitas as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Eugia Pharma (Malta) Ltd

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Indications & Clinical Uses

Lidocaína Aurovitas is a local anesthetic used in procedures that require temporary nerve blockade.

  • Epidural procedures: provides localized anesthesia for obstetric or surgical interventions performed via the epidural space.
  • Intramuscular injections: produces rapid, site‑specific numbness to facilitate painful intramuscular drug administration.
  • Intravenous regional anesthesia (Bier block): enables safe, reversible anesthesia of a limb during minor orthopedic surgeries.
  • Pain management: offers short‑term analgesia for acute procedural pain when administered by qualified clinicians.

How It Works

  • Lidocaine Hydrochloride exerts its effect by reversibly binding to voltage‑gated sodium channels on neuronal membranes, stabilizing the inactive state of the channel. This blockade prevents the influx of sodium ions required for depolarization, thereby inhibiting the initiation and propagation of nerve impulses and producing localized loss of sensation.

Side Effects

Lidocaína Aurovitas may cause a range of adverse reactions, most of which are related to its local anesthetic properties.

Common Side Effects

  • Transient numbness or tingling at the injection site
  • Mild hypotension or dizziness
  • Nausea or metallic taste
  • Localized swelling or erythema
  • Headache
  • Mild pruritus

Serious or Rare Side Effects

  • Allergic reactions including rash, urticaria or anaphylaxis
  • Central nervous system toxicity such as seizures or loss of consciousness
  • Cardiac arrhythmias or conduction disturbances
  • Methemoglobinemia
  • Respiratory depression
  • Systemic toxicity with CNS and cardiovascular collapse

Precautions & Warnings

When using Lidocaína Aurovitas, clinicians should observe several safety measures.

  • Assess patient allergy: verify no known hypersensitivity to lidocaine or amide‑type anesthetics.
  • Monitor cardiovascular status: watch for hypotension, bradycardia or arrhythmias during administration.
  • Use the lowest effective dose: limit systemic exposure to reduce toxicity risk.
  • Avoid concurrent use with other local anesthetics: prevents additive toxic effects.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Lidocaína Aurovitas can interact with other medicines, altering its safety profile.

Major Interactions (Avoid)

  • Class I antiarrhythmics (e.g., quinidine, procainamide): may cause severe cardiotoxicity.
  • Beta‑blockers: can enhance hypotensive effects.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): increase plasma lidocaine concentrations.

Moderate Interactions (Monitor Closely)

  • Other local anesthetics: additive risk of systemic toxicity.
  • General anesthetics (e.g., propofol, volatile agents): may potentiate central nervous system depression.
  • Diuretics: may affect lidocaine plasma levels and renal clearance.

Frequently Asked Questions

Lidocaína Aurovitas is a sterile lidocaine hydrochloride solution used to provide local anesthesia for epidural procedures, intramuscular injections, intravenous regional (Bier) blocks, and short‑term pain management during minor surgical or diagnostic interventions.

Lidocaine hydrochloride blocks voltage‑gated sodium channels on nerve membranes, stabilising them in an inactive state. This prevents sodium influx, halting depolarisation and stopping the transmission of pain signals, resulting in a reversible loss of sensation in the targeted area.

The dose of Lidocaína Aurovitas is determined by the prescribing clinician based on the specific procedure, patient weight, and clinical setting. Healthcare professionals calculate the appropriate volume and concentration to achieve effective anesthesia while minimising systemic exposure.

Safety data for lidocaine hydrochloride 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 it must be prescribed by a qualified healthcare provider.

To 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.

Both lidocaine and bupivacaine are amide‑type local anesthetics, but lidocaine has a faster onset and shorter duration of action, making it suitable for procedures requiring rapid, temporary anesthesia. Bupivacaine provides a longer block but carries a higher risk of cardiotoxicity at equivalent doses.

Lidocaína Aurovitas should be stored at ambient temperature, below 25 °C, in its original sealed container. Protect the solution from moisture, direct sunlight and extreme temperatures to maintain sterility and potency.

The product is administered by qualified healthcare professionals via epidural, intramuscular or intravenous routes, depending on the clinical indication. Injection techniques follow standard aseptic procedures, and dosing is adjusted to achieve the desired level of anesthesia.

Serious risks include systemic toxicity leading to seizures, cardiac arrhythmias, severe hypotension, allergic reactions such as anaphylaxis, and rare cases of methemoglobinemia. Immediate medical attention is required if any of these symptoms appear.

Patients with a known hypersensitivity to lidocaine or other amide‑type local anesthetics, those with severe cardiac conduction disorders, and individuals with significant hepatic impairment should avoid using Lidocaína Aurovitas unless a clinician determines that benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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