Product image of Lidoject (Lidocaine Hydrochloride) supplied by GNH India

Lidoject

Active Ingredient:
Lidocaine Hydrochloride
Origin:
EU

Lidoject (Lidocaine Hydrochloride)

Lidocaine Hydrochloride, the active ingredient in Lidoject, is a local anesthetic presented as an injectable solution for intravenous and subcutaneous use. It provides temporary loss of sensation for minor surgical or diagnostic procedures and for acute pain relief in adult patients.

GNH India supplies Lidoject as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides regulatory documentation for global distribution. Customers benefit from reliable lead times, temperature‑controlled logistics, and dedicated technical support throughout the procurement process.

Manufacturer / TM Owner

Labesfal Laboratorios Almiro, S.A.

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Indications & Clinical Uses

Lidoject is used as a local anesthetic for procedures involving the peripheral nervous system.

  • Minor surgical procedures: provides localized numbness to facilitate incision and suturing
  • Diagnostic interventions (e.g., endoscopy, catheter placement): reduces patient discomfort during the procedure
  • Acute pain management: offers short‑term analgesia for severe pain episodes

How It Works

  • Lidocaine Hydrochloride blocks voltage‑gated sodium channels on neuronal membranes, preventing the initiation and propagation of action potentials. By stabilizing the neuronal membrane, it inhibits the rapid influx of sodium ions required for depolarization, resulting in reversible loss of sensation in the targeted area without affecting surrounding tissues.

Side Effects

Adverse reactions may occur following administration of Lidoject.

Common Side Effects

  • Injection site pain
  • Transient tingling or numbness
  • Mild hypotension
  • Bradycardia
  • Nausea

Serious or Rare Side Effects

  • Severe allergic reaction (anaphylaxis)
  • Cardiac arrhythmias
  • Methemoglobinemia
  • Central nervous system toxicity (e.g., seizures)

Precautions & Warnings

Before using Lidoject, consider the following safety measures.

  • Allergy assessment: verify no known hypersensitivity to lidocaine or amide‑type anesthetics
  • Cardiovascular status: monitor patients with heart block or severe conduction disorders
  • Dosage limits: adhere to maximum recommended dose to avoid toxicity
  • Concurrent CNS depressants: use caution when combined with other agents that lower seizure threshold
  • Pregnancy and lactation: evaluate risk‑benefit, limited data available
  • Store at controlled room temperature: keep in original container, protect from light and moisture

Avoid Interactions

Lidoject may interact with other medicines; review the following categories.

Major Interactions (Avoid)

  • Class I antiarrhythmics (e.g., quinidine, procainamide): may potentiate cardiotoxicity
  • Beta‑blockers (e.g., propranolol): increase risk of bradycardia and hypotension
  • CYP3A4 inhibitors (e.g., ketoconazole): raise plasma lidocaine levels

Moderate Interactions (Monitor Closely)

  • Other local anesthetics: cumulative toxicity risk
  • Diuretics (e.g., furosemide): may lower seizure threshold
  • General anesthetics (e.g., propofol): additive CNS depression

Frequently Asked Questions

Lidoject is a lidocaine hydrochloride injection used to provide local anesthesia during minor surgical or diagnostic procedures and to deliver short‑term analgesia for acute pain episodes in adult patients.

Lidocaine blocks voltage‑gated sodium channels on nerve membranes, stopping the rapid influx of sodium ions needed for depolarisation. This stabilises the neuronal membrane and prevents the transmission of pain signals, producing a reversible loss of sensation.

The appropriate dose of Lidoject is determined by the prescribing clinician based on the specific procedure, patient weight, and clinical context. Dosing guidelines are provided in the product’s prescribing information and must be followed by the healthcare professional.

Safety data for lidocaine during pregnancy and lactation are limited. Use of Lidoject in pregnant or nursing women should only occur when the potential benefit justifies any potential risk to the fetus or infant, and after careful evaluation by the prescriber.

To order Lidoject, 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 any cold‑chain requirements) and import documentation.

Lidoject (lidocaine) is an amide‑type local anesthetic with a rapid onset and moderate duration, making it suitable for short procedures. Compared with ester‑type agents such as procaine, lidocaine has a lower incidence of allergic reactions and a more predictable pharmacokinetic profile.

Lidoject should be stored at controlled room temperature, protected from light and moisture, and kept in its original packaging. Do not freeze the product. Follow standard aseptic techniques when preparing the injection to maintain sterility.

Lidoject is administered by a qualified healthcare professional via intravenous or subcutaneous injection. The injection site is selected based on the intended area of anesthesia, and the dose is injected slowly while monitoring the patient for any adverse reactions.

Serious risks include severe allergic reactions (anaphylaxis), cardiac arrhythmias, methemoglobinemia, and central nervous system toxicity such as seizures. Immediate medical attention is required if any of these events occur during or after administration.

Lidoject should be avoided in patients with known hypersensitivity to lidocaine or other amide‑type local anesthetics, those with severe heart block, uncontrolled epilepsy, or significant hepatic impairment that could increase drug accumulation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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