Product image of Marcain Heavy Steripack (Bupivacaine Hydrochloride, Anhydrous) supplied by GNH India

Marcain Heavy Steripack

Active Ingredient:
Bupivacaine Hydrochloride, Anhydrous
Origin:
EU

Marcain Heavy Steripack (Bupivacaine Hydrochloride, Anhydrous)

Bupivacaine Hydrochloride, the active ingredient in Marcain Heavy Steripack, is a local anesthetic presented as a sterile solution for injection for intrathecal use. It provides long‑lasting nerve block for surgical procedures, spinal anesthesia and postoperative pain control in adult patients, and is commonly employed in operating rooms and obstetric suites.

GNH India supplies Marcain Heavy Steripack as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide, with full regulatory documentation, temperature‑controlled logistics and a commitment to quality assurance for global markets.

Manufacturer / TM Owner

Aspen Pharma Trading Limited

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Indications & Clinical Uses

Bupivacaine is used in the central nervous system pathway to achieve regional anesthesia and analgesia.

  • Surgical anesthesia: provides dense sensory and motor block for intra‑operative pain control.
  • Spinal anesthesia: produces rapid onset spinal cord blockade for procedures below the waist.
  • Postoperative analgesia: extends pain relief after surgery, reducing the need for systemic opioids.

How It Works

  • Bupivacaine exerts its effect by reversibly binding to the intracellular portion of voltage‑gated sodium channels on neuronal membranes. This binding stabilizes the channel in its inactivated state, preventing the influx of sodium ions during depolarisation and thereby blocking the generation and propagation of nerve impulses. The result is a prolonged loss of sensation and motor function in the targeted area.

Side Effects

Bupivacaine may be associated with a range of adverse reactions following intrathecal administration.

Common Side Effects

  • Hypotension: transient drop in blood pressure due to sympathetic blockade.
  • Nausea and vomiting: mild to moderate gastrointestinal upset.
  • Pruritus: localized itching, often at the injection site.
  • Back pain: mild discomfort at the lumbar injection site.
  • Headache: post‑dural puncture headache that may respond to conservative measures.

Serious or Rare Side Effects

  • Cardiac arrhythmia: irregular heart rhythm that may be life‑threatening.
  • Central nervous system toxicity: seizures, confusion or loss of consciousness.
  • Persistent motor block: prolonged paralysis beyond the expected duration.

Precautions & Warnings

When using Marcain Heavy Steripack, clinicians should observe specific safety measures to minimise risk.

  • Patient assessment: evaluate cardiovascular and neurological status before administration.
  • Dose calculation: base the volume on patient weight and procedure length as directed by the prescriber.
  • Monitoring: continuously observe blood pressure, heart rate and respiratory function during and after injection.
  • Contraindications: avoid use in patients with known hypersensitivity to bupivacaine or other amide anesthetics.
  • Emergency preparedness: have resuscitation equipment and lipid emulsion therapy readily available.
  • Store at ambient temperature: keep the vial below 25 °C, protected from light and moisture, and do not freeze.

Avoid Interactions

Bupivacaine can interact with other agents, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Local anesthetic systemic toxicity (LAST) agents: concurrent use of other amide anesthetics may increase toxicity risk.
  • Class I antiarrhythmic drugs (e.g., quinidine, procainamide): can potentiate cardiac conduction disturbances.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may enhance bradycardia and hypotension.
  • Calcium channel blockers: can augment the depressant effects on cardiac contractility.
  • Opioids: combined use may increase the depth of analgesia but requires careful respiratory monitoring.

Frequently Asked Questions

Marcain Heavy Steripack is a sterile injectable solution of bupivacaine hydrochloride used to provide regional anaesthesia for surgical procedures, spinal anaesthesia for operations below the waist, and extended postoperative analgesia to reduce the need for systemic pain medication.

Bupivacaine blocks voltage‑gated sodium channels on nerve membranes, stabilising them in an inactivated state. This prevents sodium influx during depolarisation, halting the propagation of nerve impulses and resulting in loss of sensation and motor function in the targeted area.

The dose is determined by the prescribing clinician based on the patient’s weight, the type and duration of the surgical procedure, and the desired depth of anaesthesia. Exact dosing regimens are individualized and should follow the prescriber’s instructions.

Safety data for intrathecal bupivacaine during pregnancy and lactation are limited. It should be used only if the potential benefit justifies any potential risk to the fetus or infant, and the decision should be made by the treating physician.

Enquiries are submitted via the product page on gnhindia.com, where you specify 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 required) and import documentation.

Bupivacaine provides a longer duration of action than shorter‑acting agents such as lidocaine, making it suitable for prolonged procedures and postoperative pain control. Compared with ropivacaine, it has a similar potency but a slightly higher risk of cardiotoxicity, so the choice depends on the clinical context and safety considerations.

The product should be stored at ambient temperature, preferably below 25 °C, protected from light and moisture, and must not be frozen. Vials should remain in their original packaging until use and be handled with aseptic technique to maintain sterility.

It is administered by a qualified healthcare professional via intrathecal injection into the cerebrospinal fluid, typically in the lumbar region. The injection is performed under strict aseptic conditions, and the patient is monitored continuously for haemodynamic and neurological responses.

The most serious risks include local anaesthetic systemic toxicity (LAST), which can manifest as cardiac arrhythmias, seizures, or central nervous system depression, and profound hypotension. Prompt recognition and treatment, including lipid emulsion therapy, are essential to mitigate these life‑threatening events.

Patients with known hypersensitivity to bupivacaine or other amide‑type local anaesthetics, those with severe cardiac conduction disorders, and individuals with uncontrolled epilepsy should avoid this product. Contraindications must be confirmed by the prescribing clinician before administration.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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