Product image of Mepivacaína B. Braun (Mepivacaine Hydrochloride) supplied by GNH India

Mepivacaína B. Braun

Active Ingredient:
Mepivacaine Hydrochloride
Origin:
EU

Mepivacaína B. Braun (Mepivacaine Hydrochloride)

Mepivacaine, the active ingredient in Mepivacaína B. Braun, is a local anesthetic presented as a sterile solution for epidural, intradermal and perineural use. It provides reversible loss of sensation in targeted nerve regions for surgical and diagnostic procedures.
GNH India supplies Mepivacaína B. Braun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

B.Braun Medical, S.A.

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Indications & Clinical Uses

Mepivacaine is used in clinical settings to achieve local anesthesia through various administration routes.

  • Epidural anesthesia: produces a dense block of sensation for obstetric or lower‑body surgeries.
  • Intradermal anesthesia: provides rapid, superficial numbness for minor skin procedures and diagnostic testing.
  • Perineural anesthesia: creates targeted nerve block to facilitate orthopedic or dental surgeries.

How It Works

  • Mepivacaine blocks voltage‑gated sodium channels on neuronal membranes, preventing the influx of sodium ions required for depolarization. This inhibition stops the initiation and propagation of nerve impulses, resulting in a reversible loss of sensory and motor function in the area where the drug is administered.

Side Effects

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

Common Side Effects

  • Mild hypotension: temporary drop in blood pressure after injection.
  • Dizziness or light‑headedness: sensation of unsteadiness during onset.
  • Nausea or vomiting: gastrointestinal upset in some patients.
  • Transient metallic taste: brief alteration in taste perception.
  • Injection site pain or burning: local discomfort at the puncture site.
  • Tingling or numbness beyond the intended area: mild paresthesia.

Serious or Rare Side Effects

  • Cardiovascular collapse: severe drop in heart function requiring emergency care.
  • Anaphylaxis: life‑threatening allergic reaction with rash, swelling, and airway compromise.
  • Seizures: central nervous system excitation in overdose situations.
  • Prolonged nerve block: extended loss of motor function beyond expected duration.
  • Methemoglobinemia: abnormal hemoglobin causing reduced oxygen delivery.
  • Cardiac arrhythmia: irregular heart rhythm potentially leading to hemodynamic instability.

Precautions & Warnings

When using Mepivacaína B. Braun, clinicians should observe several safety measures.

  • Patient assessment: evaluate cardiovascular and hepatic status before administration.
  • Dose adjustment: reduce dose in patients with impaired liver function.
  • Allergy screening: avoid use in individuals with known hypersensitivity to amide‑type anesthetics.
  • Cardiovascular monitoring: observe heart rate and blood pressure during and after injection.
  • Concomitant anesthetics: limit simultaneous use of other local anesthetics to prevent toxicity.
  • Store at ambient temperature: keep in original packaging, protect from moisture and direct light.

Avoid Interactions

Mepivacaine can interact with other drugs, altering its safety profile.

Major Interactions (Avoid)

  • Class I antiarrhythmics (e.g., quinidine, procainamide): increase risk of cardiac toxicity.
  • High‑dose epinephrine: may exacerbate cardiovascular effects.
  • Other amide local anesthetics: additive neuro‑ and cardiotoxicity.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., erythromycin, ketoconazole): may raise plasma levels.
  • Beta‑blockers: enhance bradycardia and hypotension.
  • Diuretics: potentiate hypotensive response.

Frequently Asked Questions

Mepivacaína B. Braun is a sterile solution of the local anesthetic mepivacaine hydrochloride. It is employed to produce temporary loss of sensation for epidural, intradermal and perineural anesthesia during surgical, obstetric and diagnostic procedures.

Mepivacaine blocks voltage‑gated sodium channels on nerve membranes, preventing sodium influx that is essential for depolarization. By inhibiting nerve impulse generation and propagation, it creates a reversible loss of sensory and motor function in the targeted area.

The specific dose of Mepivacaína B. Braun is determined by the prescribing clinician based on the procedure, patient characteristics, and route of administration. Healthcare professionals calculate the appropriate volume and concentration to achieve the desired anesthetic effect.

Safety data for mepivacaine in pregnancy and lactation are limited. It should only be used when clearly needed and after a risk‑benefit assessment by the treating physician. Breastfeeding mothers should consult their healthcare provider before use.

To 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.

Both mepivacaine and lidocaine are amide‑type local anesthetics, but mepivacaine has a slightly longer duration of action and less vasodilatory effect, which can reduce the need for added vasoconstrictors. Choice depends on the clinical context and provider preference.

Mepivacaína B. Braun should be stored at ambient temperature, below 25 °C. Keep the vial in its original packaging, protect it from moisture and direct sunlight, and avoid freezing to maintain solution stability.

The product is administered by a qualified healthcare professional via injection. Depending on the intended block, it may be delivered epidurally, intradermally or perineurally using aseptic technique and appropriate needle size.

Serious risks include cardiovascular collapse, severe allergic reactions (anaphylaxis), seizures, prolonged nerve block, methemoglobinemia, and life‑threatening cardiac arrhythmias. Immediate medical attention is required if any of these events occur.

Patients with known hypersensitivity to mepivacaine or other amide‑type local anesthetics, those with severe hepatic impairment, and individuals taking interacting Class I antiarrhythmics or high‑dose epinephrine should avoid this medication unless a specialist determines that benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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