Product image of Mofecet (Bupivacaine Hydrochloride Monohydrate) supplied by GNH India

Mofecet

Active Ingredient:
Bupivacaine Hydrochloride Monohydrate
Origin:
EU

Mofecet (Bupivacaine Hydrochloride Monohydrate)

Bupivacaine Hydrochloride Monohydrate, the active ingredient in Mofecet, is an amide‑type local anesthetic presented as a sterile injectable solution for intrathecal use. It provides regional nerve block for spinal, surgical and obstetric anesthesia. Mofecet is marketed in the European Union and is supplied in compliance with Good Distribution Practice.

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

Manufacturer / TM Owner

Grindeks

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Indications & Clinical Uses

Mofecet is an amide‑type local anesthetic used in regional anesthesia and pain management.

  • Spinal anesthesia: produces dense sensory and motor block for procedures requiring a regional block.
  • Surgical analgesia: offers prolonged postoperative pain relief after various surgical interventions.
  • Obstetric anesthesia: enables safe pain control during labor and cesarean delivery.

How It Works

  • Bupivacaine reversibly blocks voltage‑gated sodium channels on neuronal membranes, preventing the initiation and propagation of nerve impulses. By stabilising the neuronal membrane, it inhibits depolarisation and thus produces a reversible loss of sensation and motor function in the targeted area.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Hypotension: transient drop in blood pressure.
  • Bradycardia: slowed heart rate.
  • Nausea: mild to moderate upset stomach.
  • Dizziness: feeling of light‑headedness.
  • Headache: post‑dural puncture headache.
  • Transient motor weakness: temporary reduced muscle strength.

Serious or Rare Side Effects

  • Cardiac arrhythmia: potentially life‑threatening rhythm disturbances.
  • Respiratory depression: reduced breathing effort.
  • Seizures: central nervous system excitation.
  • Prolonged nerve block: extended loss of sensation beyond intended duration.
  • Allergic reaction: rash, itching, or anaphylaxis.
  • Toxic plasma concentrations: systemic toxicity with neurological and cardiovascular signs.

Precautions & Warnings

Careful patient assessment and monitoring are essential when using intrathecal bupivacaine.

  • Patient assessment: evaluate cardiac, hepatic and renal function before administration.
  • Dose calculation: ensure dose is individualized based on weight, age and clinical context.
  • Monitoring: continuously observe blood pressure, heart rate and respiratory status during and after injection.
  • Contraindications: avoid in patients with known hypersensitivity to amide‑type anesthetics.
  • Caution in cardiac disease: use reduced doses in patients with conduction abnormalities or heart failure.
  • Store at controlled room temperature: keep in original packaging, protect from light and moisture.

Avoid Interactions

Bupivacaine may interact with other drugs that affect cardiac conduction or share metabolic pathways.

Major Interactions (Avoid)

  • Other local anesthetics: additive neuro‑ and cardiotoxicity.
  • Class I antiarrhythmics (e.g., quinidine): increased risk of arrhythmias.
  • Beta‑blockers: may exacerbate bradycardia and hypotension.

Moderate Interactions (Monitor Closely)

  • Calcium channel blockers: potential additive hypotensive effect.
  • Epinephrine: may potentiate systemic toxicity.
  • CYP3A4 inhibitors (e.g., ketoconazole): possible increased plasma levels.
  • Vasodilators: enhanced hypotensive response.

Frequently Asked Questions

Mofecet contains bupivacaine, an amide‑type local anesthetic used for spinal anesthesia, surgical analgesia, and obstetric anesthesia. It is administered intrathecally to provide regional nerve block for procedures requiring loss of sensation and muscle relaxation.

Bupivacaine blocks voltage‑gated sodium channels on nerve membranes, preventing depolarisation and the propagation of action potentials. This reversible blockade stops nerve impulse transmission, resulting in loss of sensation and motor function in the targeted area.

The appropriate dose of Mofecet is determined by the prescribing clinician based on the patient’s age, weight, clinical condition and the specific procedure. Dosage should always follow the prescriber’s instructions and local guidelines.

Safety data for bupivacaine in pregnancy and lactation are limited. Use only if the potential benefit justifies the potential risk to the fetus or infant, and always under the guidance of a qualified healthcare professional.

To order Mofecet, 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.

Bupivacaine, the active ingredient in Mofecet, has a longer duration of action than lidocaine or mepivacaine, making it suitable for procedures requiring prolonged anesthesia. However, its higher cardiotoxic potential necessitates careful dosing and monitoring compared with shorter‑acting agents.

Mofecet should be stored at controlled room temperature, protected from light and moisture, and kept in its original sealed container. Do not freeze the product, and ensure it is handled using aseptic techniques to maintain sterility.

Mofecet is administered by a trained healthcare professional via intrathecal injection into the cerebrospinal fluid. The procedure is performed under sterile conditions, typically in an operating theatre or dedicated anesthesia suite.

Serious risks include cardiac arrhythmias, respiratory depression, seizures, and systemic toxicity leading to neurologic or cardiovascular collapse. Immediate recognition and supportive management are essential if these events occur.

Mofecet should be avoided in patients with known hypersensitivity to bupivacaine or other amide‑type local anesthetics, those with severe cardiac conduction disorders, and individuals with uncontrolled epilepsy. Contra‑indications must be confirmed by the prescribing clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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