Product image of Lidocaïne Hcl Baxter (Lidocaine Hydrochloride) supplied by GNH India

Lidocaïne Hcl Baxter

Active Ingredient:
Lidocaine Hydrochloride
Origin:
EU

Lidocaïne Hcl Baxter (Lidocaine Hydrochloride)

Lidocaine Hydrochloride, the active ingredient in Lidocaïne Hcl Baxter, is a local anesthetic (amide type) presented as an injection for intravenous use. It provides reversible loss of sensation for minor procedures and can be used to manage ventricular arrhythmias in appropriate patients.

GNH India supplies Lidocaïne Hcl Baxter as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Baxter B.V.

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Indications & Clinical Uses

Lidocaine Hydrochloride is used in clinical settings to provide local anesthesia and to treat certain cardiac rhythm disturbances.

  • Local anesthesia: produces reversible loss of sensation in the targeted area for dental, dermatologic or minor surgical procedures.
  • Ventricular arrhythmias: stabilizes cardiac membranes to suppress abnormal ventricular rhythms.
  • Procedural sedation: facilitates pain‑free performance of short, invasive interventions.

How It Works

  • Lidocaine Hydrochloride blocks voltage‑gated sodium channels on neuronal and cardiac cell membranes, preventing the rapid influx of sodium ions that initiates and propagates action potentials. This inhibition reduces nerve impulse conduction, producing local anesthesia, and stabilizes cardiac myocyte membranes, decreasing excitability and suppressing abnormal ventricular activity.

Side Effects

Lidocaine Hydrochloride may cause a range of adverse reactions, most of which are dose‑related and transient.

Common Side Effects

  • Tingling or numbness at the injection site
  • Light‑headedness or dizziness
  • Nausea or metallic taste
  • Mild hypotension

Serious or Rare Side Effects

  • Cardiac arrhythmias or conduction block
  • Seizures, especially with rapid intravascular injection
  • Methemoglobinemia
  • Severe allergic reactions including anaphylaxis
  • Respiratory depression or cardiovascular collapse

Precautions & Warnings

When using Lidocaine Hydrochloride, clinicians should observe several safety measures.

  • Cardiac assessment: evaluate history of heart block or ischemia before administration.
  • Blood pressure monitoring: watch for hypotension during and after injection.
  • Incremental dosing: administer slowly and titrate to effect to avoid toxicity.
  • Hypersensitivity: avoid in patients with known allergy to amide‑type local anesthetics.
  • Hepatic function: consider dose adjustment in severe liver impairment.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Lidocaine Hydrochloride can interact with other medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Class I anti‑arrhythmics (e.g., quinidine, procainamide): may increase lidocaine toxicity.
  • CYP3A4 inhibitors (e.g., amiodarone, ketoconazole): raise plasma concentrations.
  • Other local anesthetics: additive neuro‑cardiac toxicity.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may potentiate bradycardia.
  • Diuretics (e.g., furosemide): can enhance hypotensive effect.
  • Propofol or other sedatives: monitor for synergistic CNS depression.

Frequently Asked Questions

Lidocaïne Hcl Baxter contains lidocaine hydrochloride, which is employed to provide local anesthesia for dental, dermatologic and minor surgical procedures, and to manage ventricular arrhythmias by stabilizing cardiac membranes.

Lidocaine blocks voltage‑gated sodium channels on nerve and cardiac cells, preventing the rapid influx of sodium that initiates action potentials. This stops nerve impulse transmission for anesthesia and reduces cardiac excitability for arrhythmia control.

The specific dose and infusion rate are determined by the prescribing clinician based on the patient’s age, weight, clinical condition, and the intended procedure. Dosing guidelines are provided in the product’s prescribing information.

Safety data for lidocaine in pregnancy are limited, and the product is classified as pregnancy category unknown. It should be used only if the potential benefit justifies any potential risk to the fetus. Lidocaine is excreted in breast milk; caution is advised for nursing mothers.

Enquiries are submitted via the product page at gnhindia.com, where you specify the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and required import documentation.

Lidocaine is an amide‑type local anesthetic with a rapid onset and intermediate duration, making it suitable for many procedures. Compared with ester‑type agents such as procaine, lidocaine has a lower risk of allergic reactions and a more predictable pharmacokinetic profile.

The product should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Maintain the original packaging until use to preserve sterility.

Lidocaïne Hcl Baxter is supplied as a sterile solution for intravenous injection. It is administered by a qualified healthcare professional, typically as a slow bolus or continuous infusion, with careful monitoring of cardiovascular and neurological status.

Serious risks include cardiac arrhythmias, severe hypotension, seizures, methemoglobinemia, and anaphylactic reactions. Prompt recognition and supportive measures are essential if any of these events occur.

Patients with known hypersensitivity to amide‑type local anesthetics, severe hepatic impairment, or existing significant cardiac conduction abnormalities should not receive lidocaine unless the benefits outweigh the risks and close monitoring is ensured.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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