Product image of Lidocain-Egis (Lidocaine Hydrochloride) supplied by GNH India

Lidocain-Egis

Active Ingredient:
Lidocaine Hydrochloride
Origin:
EU

Lidocain-Egis (Lidocaine Hydrochloride)

Lidocaine Hydrochloride, the active ingredient in Lidocain-Egis, is a local anesthetic (amide) presented as an injection solution for intravenous use. It provides rapid onset of nerve block for minor surgical or diagnostic procedures and is also employed in the management of certain ventricular arrhythmias.

GNH India supplies Lidocain-Egis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU GMP standards and provides regulatory documentation for cross‑border procurement. This ensures product integrity and timely delivery to end‑users.

Manufacturer / TM Owner

Egis Pharmaceuticals Plc

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Indications & Clinical Uses

Lidocain-Egis, a local anesthetic acting on voltage‑gated sodium channels, is indicated for the following clinical situations:

  • Minor surgical procedures: provides rapid, reversible loss of sensation to facilitate pain‑free operation.
  • Diagnostic procedures: enables comfortable performance of endoscopic or catheter‑based examinations.
  • Ventricular arrhythmias: stabilizes cardiac electrical activity to suppress life‑threatening rhythm disturbances.

How It Works

  • Lidocaine hydrochloride exerts its effect by binding to the intracellular portion of voltage‑gated sodium channels in neuronal and cardiac membranes. This blockade prevents the rapid influx of sodium ions during the depolarization phase, thereby inhibiting the initiation and propagation of action potentials. In cardiac tissue, the reduced excitability diminishes abnormal automaticity and re‑entry circuits, while in peripheral nerves it produces a reversible loss of sensory and motor conduction.

Side Effects

Lidocain-Egis may be associated with adverse reactions that vary in frequency and severity.

Common Side Effects

  • Tingling or numbness at the injection site.
  • Transient dizziness or light‑headedness.
  • Mild hypotension.

Serious or Rare Side Effects

  • Anaphylaxis with rash, bronchospasm or angioedema.
  • Cardiac conduction disturbances such as bradycardia or heart block.
  • Central nervous system toxicity, including seizures.

Precautions & Warnings

When using Lidocain-Egis, clinicians should observe specific precautions to minimize risk.

  • Patient assessment: evaluate cardiac history and existing conduction abnormalities before administration.
  • Dose titration: adjust dosage based on age, weight and hepatic function, especially in elderly patients.
  • Monitoring: continuously monitor ECG and blood pressure during intravenous infusion.
  • Drug interactions: avoid concurrent use with other class I anti‑arrhythmics or potent CYP450 inhibitors without supervision.
  • Allergic history: confirm no prior hypersensitivity to amide‑type local anesthetics.
  • Store at ambient temperature: keep the solution below 25 °C, protect from light, and retain in original packaging.

Avoid Interactions

Lidocain-Egis can interact with several medicines that affect its plasma levels or cardiac effects.

Major Interactions (Avoid)

  • Class I anti‑arrhythmic agents (e.g., quinidine, procainamide) – additive cardiotoxicity.
  • Beta‑blockers (e.g., propranolol) – enhanced bradycardia and hypotension.
  • CYP3A4 inhibitors (e.g., ketoconazole) – increased lidocaine concentrations.

Moderate Interactions (Monitor Closely)

  • CYP1A2 inducers (e.g., carbamazepine) – reduced efficacy.
  • Diuretics (e.g., furosemide) – may potentiate hypotensive effects.
  • General anesthetics (e.g., propofol) – may require dosage adjustment.

Frequently Asked Questions

Lidocain-Egis is employed as an intravenous local anesthetic to provide rapid, reversible numbness during minor surgical or diagnostic procedures. It is also used in the acute management of ventricular arrhythmias to stabilize cardiac electrical activity.

Lidocaine blocks voltage‑gated sodium channels on neuronal and cardiac cell membranes, preventing sodium influx during depolarisation. This inhibition stops the initiation and propagation of action potentials, producing loss of sensation in peripheral nerves and reducing abnormal electrical activity in the heart.

The dosage of Lidocain-Egis is determined by the prescribing clinician based on the specific procedure, patient characteristics and clinical setting. Healthcare professionals calculate the appropriate amount and rate of intravenous administration according to established guidelines.

Lidocain-Egis falls under an unknown pregnancy category, and limited data exist on its use during pregnancy or lactation. Clinicians should weigh potential benefits against risks and consider alternative therapies when treating pregnant or nursing patients.

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 import documentation.

Compared with other amide‑type local anesthetics such as bupivacaine, lidocaine has a faster onset and shorter duration of action, making it suitable for brief procedures and acute arrhythmia control. Bupivacaine provides longer analgesia but carries a higher risk of cardiotoxicity at comparable plasma levels.

Lidocain-Egis should be stored at ambient temperature, preferably below 25 °C, protected from light, and kept in its original sealed container. Avoid freezing the solution and ensure that the vial is not shaken vigorously before use.

The product is supplied as a sterile injection solution for intravenous use. It is administered by a qualified healthcare professional, typically as a bolus or controlled infusion, depending on the clinical indication and patient monitoring requirements.

Serious adverse events include anaphylactic reactions, severe cardiac conduction disturbances such as bradycardia or heart block, and central nervous system toxicity that may manifest as seizures or loss of consciousness. Immediate medical intervention is required if any of these occur.

Lidocain-Egis is contraindicated in patients with known hypersensitivity to lidocaine or other amide‑type local anesthetics, those with severe heart block or uncontrolled ventricular arrhythmias, and individuals with significant hepatic impairment without appropriate dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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