Product image of Lidokainklorid Galenika (Lidocaine Hydrochloride) supplied by GNH India

Lidokainklorid Galenika

Active Ingredient:
Lidocaine Hydrochloride
Origin:
EU

Lidokainklorid Galenika (Lidocaine Hydrochloride)

Lidocaine Hydrochloride, the active ingredient in Lidokainklorid, is a local anesthetic presented as a sterile solution for epidural, infiltration, and intradermal use. It provides reversible loss of sensation in targeted tissues for minor surgical procedures and pain‑management interventions.
GNH India supplies Lidokainklorid as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Galenika International Kft.

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Indications & Clinical Uses

Lidokainklorid is a local anesthetic used in procedures that require regional nerve blockade.

  • Minor surgical procedures: provides local anesthesia to reduce pain during the operation.
  • Epidural analgesia: delivers regional pain relief during labor or surgical procedures.
  • Infiltration anesthesia: numbs targeted tissue for diagnostic or therapeutic interventions.
  • Intradermal testing: used as a reagent for skin allergy testing.

How It Works

  • Lidocaine Hydrochloride blocks voltage‑gated sodium channels in neuronal membranes, preventing the initiation and propagation of nerve impulses. By stabilizing the neuronal membrane, it inhibits depolarization, resulting in reversible loss of sensation in the area where it is administered.

Side Effects

Lidokainklorid may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Transient burning or stinging at the injection site
  • Mild dizziness or light‑headedness
  • Nausea or metallic taste
  • Localized swelling or erythema

Serious or Rare Side Effects

  • Allergic reactions such as rash, angioedema, or anaphylaxis
  • Cardiac arrhythmias, including ventricular tachycardia
  • Central nervous system toxicity (seizures, loss of consciousness)
  • Methemoglobinemia, a rare blood disorder affecting oxygen transport

Precautions & Warnings

Before using Lidokainklorid, consider the following safety measures.

  • Allergy assessment: verify no known hypersensitivity to amide‑type local anesthetics.
  • Cardiovascular status: avoid in patients with severe heart block or conduction disorders.
  • Dosage limits: adhere to recommended maximum dose to prevent systemic toxicity.
  • Concurrent CNS depressants: monitor for enhanced sedation when combined with other depressants.
  • Pregnancy and lactation: use only if the benefit outweighs the potential risk (category unknown).
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Lidokainklorid can interact with other medicines, altering its safety profile.

Major Interactions (Avoid)

  • Class I antiarrhythmics (e.g., quinidine, procainamide): may increase lidocaine plasma levels.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): can raise systemic exposure.
  • Concurrent use of other local anesthetics: additive risk of toxicity.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may potentiate cardiac effects of lidocaine.
  • Diuretics such as furosemide: may reduce plasma protein binding, increasing free drug.
  • General anesthetics (e.g., propofol): may enhance central nervous system depression.

Frequently Asked Questions

Lidokainklorid contains lidocaine hydrochloride, a local anesthetic employed to provide regional numbness for minor surgical procedures, epidural analgesia during labor or surgery, infiltration anesthesia for targeted tissue, and as a reagent in intradermal allergy testing.

Lidocaine hydrochloride blocks voltage‑gated sodium channels on neuronal membranes, preventing the initiation and spread of nerve impulses. This stabilises the membrane and produces a reversible loss of sensation in the area where the drug is administered.

The specific dose of Lidokainklorid is determined by the prescribing clinician based on the procedure, patient weight, and clinical context. Healthcare professionals calculate the appropriate amount to stay within safe maximum limits.

Safety data for lidocaine hydrochloride in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. Use is permitted only when the potential benefit justifies any potential risk to the fetus or infant.

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 and any necessary import documentation.

Lidokainklorid (lidocaine) is an amide‑type local anesthetic with a rapid onset and moderate duration, making it suitable for many short‑ to medium‑duration procedures. Compared with ester‑type agents, lidocaine has a lower risk of allergic reactions and a well‑established safety profile.

Lidokainklorid should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight and extreme temperature fluctuations to maintain sterility and potency.

The drug is supplied as a sterile solution and is administered by a qualified healthcare professional via epidural, infiltration, or intradermal injection, depending on the intended clinical use and anatomical site.

Serious risks include allergic reactions such as anaphylaxis, cardiac arrhythmias, central nervous system toxicity (e.g., seizures), and rare methemoglobinemia. Prompt recognition and management of these events are essential.

Patients with a known hypersensitivity to lidocaine or other amide‑type local anesthetics, those with severe heart block, uncontrolled cardiac conduction disorders, or individuals for whom the risk outweighs the benefit should avoid using Lidokainklorid.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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