Product image of Levobupivacaine Kabi (Levobupivacaine Hydrochloride) supplied by GNH India

Levobupivacaine Kabi

Active Ingredient:
Levobupivacaine Hydrochloride
Origin:
EU

Levobupivacaine Kabi (Levobupivacaine Hydrochloride)

Levobupivacaine Hydrochloride, the active ingredient in Levobupivacaine Kabi, is a local anesthetic presented as a sterile solution for epidural, infiltration, intrathecal and peripheral nerve block use. It provides surgical anesthesia and postoperative or labor analgesia in adult patients.

GNH India supplies Levobupivacaine Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Fresenius Kabi France S.A.S.

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Indications & Clinical Uses

  • Levobupivacaine is a long‑acting amide local anesthetic used in the management of pain associated with surgical and obstetric procedures.
  • Surgical anesthesia: provides dense sensory block for operative procedures.
  • Postoperative analgesia: extends pain relief after surgery, reducing opioid requirement.
  • Labor analgesia: offers effective neuraxial analgesia during childbirth.

How It Works

  • Levobupivacaine blocks voltage‑gated sodium channels on neuronal membranes, inhibiting the initiation and propagation of nerve impulses. By preferentially affecting sensory fibers and exhibiting high protein binding, it produces prolonged loss of sensation with limited motor block, resulting in effective anesthesia and analgesia for the duration of the procedure.

Side Effects

Adverse reactions may occur following administration of levobupivacaine.

Common Side Effects

  • Hypotension: transient drop in blood pressure.
  • Bradycardia: slowed heart rate.
  • Dizziness or light‑headedness.
  • Nausea or vomiting.
  • Metallic taste or oral paraesthesia.
  • Injection site pain or irritation.

Serious or Rare Side Effects

  • Cardiac arrhythmias or conduction disturbances.
  • Seizures, especially with high plasma concentrations.
  • Respiratory depression or apnea.
  • Allergic reactions including rash, urticaria, or anaphylaxis.
  • Methemoglobinemia.
  • Central nervous system toxicity presenting as tinnitus or visual disturbances.

Precautions & Warnings

Careful patient assessment and monitoring are essential when using levobupivacaine.

  • Hepatic impairment: reduce dose and monitor plasma levels.
  • Known hypersensitivity: avoid use in patients with documented allergy to amide local anesthetics.
  • Cardiovascular status: monitor heart rate and blood pressure during administration.
  • Obstetric patients: use the lowest effective dose for labor analgesia.
  • Concomitant CNS depressants: observe for enhanced sedation.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Levobupivacaine may interact with other drugs, influencing safety and efficacy.

Major Interactions (Avoid)

  • Other local anesthetics: risk of cumulative toxicity.
  • Potent CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): increase plasma concentrations.
  • Drugs lowering seizure threshold (e.g., bupropion, tramadol): heighten risk of seizures.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may exacerbate bradycardia.
  • Vasodilators: can enhance hypotensive effects.
  • Anticoagulants/antiplatelet agents: increase bleeding risk with neuraxial techniques.
  • Diuretics: may affect plasma protein binding.
  • General anesthetics: monitor for additive CNS depression.

Frequently Asked Questions

Levobupivacaine Kabi is used to provide surgical anesthesia, postoperative analgesia, and labor analgesia. It is administered via epidural, infiltration, intrathecal, or peripheral nerve block techniques to achieve effective pain control during and after procedures.

Levobupivacaine works by blocking voltage‑gated sodium channels on nerve membranes, preventing the initiation and propagation of action potentials. This inhibition stops pain signal transmission, resulting in loss of sensation in the targeted area while preserving motor function to a lesser extent.

The appropriate dose of Levobupivacaine Kabi is determined by the prescribing clinician based on the specific procedure, patient characteristics, and route of administration. Dosage adjustments may be required for factors such as age, weight, and hepatic function.

Safety data for Levobupivacaine in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. Use during pregnancy or breastfeeding should only occur when clearly needed and after careful risk‑benefit assessment by the healthcare provider.

To order Levobupivacaine Kabi, 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.

Levobupivacaine is the S‑enantiomer of bupivacaine and offers a similar duration of action with a lower risk of cardiotoxicity and central nervous system toxicity. Both are amide‑type local anesthetics, but levobupivacaine is often preferred when a safer cardiac profile is desired.

Levobupivacaine Kabi should be stored at 2‑8 °C in a refrigerator, protected from light and moisture. Do not freeze the product, and keep it in the original packaging until use to maintain sterility and potency.

Levobupivacaine is administered by a qualified healthcare professional via epidural, intrathecal, infiltration, or peripheral nerve block injection. The specific technique and volume depend on the clinical indication and the anatomical site requiring anesthesia.

Serious risks include cardiovascular toxicity such as arrhythmias, severe hypotension, central nervous system toxicity leading to seizures, and rare allergic reactions. Prompt recognition and supportive management are essential if these events occur.

Levobupivacaine should be avoided in patients with known hypersensitivity to amide local anesthetics, severe hepatic impairment without dose adjustment, or those with pre‑existing significant cardiac conduction abnormalities unless benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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