Product image of Neiratax (Thiamine Hydrochloride, Cyanocobalamin, Pyridoxine Hydrochloride, Lidocaine Hydrochloride) supplied by GNH India

Neiratax

Active Ingredient:
Thiamine Hydrochloride, Cyanocobalamin, Pyridoxine Hydrochloride, Lidocaine Hydrochloride
Origin:
EU

Neiratax (Thiamine Hydrochloride, Cyanocobalamin, Pyridoxine Hydrochloride, Lidocaine Hydrochloride)

Thiamine Hydrochloride, Cyanocobalamin, Pyridoxine Hydrochloride, and Lidocaine Hydrochloride, the active ingredients in Neiratax, are a combination presented for intramuscular use. They address vitamin B1, B12 and B6 deficiencies while providing local anesthesia for procedural pain control.

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

Manufacturer / TM Owner

Kalceks

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Indications & Clinical Uses

Neiratax is indicated for conditions related to vitamin B deficiencies and for procedural pain management.

  • Vitamin B1 deficiency: restores thiamine levels to support carbohydrate metabolism.
  • Vitamin B12 deficiency: supplies cobalamin needed for DNA synthesis and red blood cell formation.
  • Vitamin B6 deficiency: provides pyridoxine for amino‑acid metabolism and neurotransmitter synthesis.
  • Local anesthesia: delivers lidocaine to block nerve transmission and reduce pain during minor procedures.

How It Works

  • Thiamine Hydrochloride acts as a cofactor for enzymes in carbohydrate metabolism, facilitating energy production. Cyanocobalamin (Vitamin B12) serves as a cofactor for methionine synthase, supporting DNA synthesis and red blood cell formation. Pyridoxine Hydrochloride (Vitamin B6) functions as a cofactor for transamination reactions in amino‑acid metabolism. Lidocaine Hydrochloride blocks voltage‑gated sodium channels in neuronal membranes, preventing depolarization and providing local anesthetic effect.

Side Effects

Neiratax may cause a range of adverse reactions following intramuscular administration.

Common Side Effects

  • Injection site pain or tenderness.
  • Mild erythema or swelling at the injection site.
  • Transient numbness or tingling in the area.
  • Headache.
  • Nausea.
  • Dizziness.

Serious or Rare Side Effects

  • Allergic reaction including rash, itching or swelling.
  • Anaphylaxis, a severe, potentially life‑threatening reaction.
  • Severe hypotension or cardiovascular collapse.
  • Cardiac arrhythmias.
  • Seizures.
  • Persistent or prolonged numbness beyond the expected duration.

Precautions & Warnings

Before using Neiratax, consider the following safety measures.

  • Assess deficiency status: confirm vitamin B1, B12 or B6 deficiency before administration.
  • Monitor for allergic reactions: observe patients for signs of hypersensitivity during and after injection.
  • Cardiac caution: use with care in patients with known conduction disorders or severe cardiac disease.
  • Avoid in lidocaine hypersensitivity: do not administer to individuals with documented lidocaine allergy.
  • Adjust in organ impairment: consider renal or hepatic dysfunction when determining dose.
  • Store at ambient temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

Neiratax can interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Concurrent use of other local anesthetics: may increase risk of systemic toxicity.
  • High‑dose beta‑blockers: can potentiate lidocaine‑induced bradycardia.
  • MAO inhibitors: may enhance hypotensive effects of lidocaine.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin): increased bleeding risk at injection site.
  • CYP450 substrates (e.g., certain antiepileptics): vitamins may alter metabolism of some drugs.
  • Diuretics: may affect electrolyte balance, influencing lidocaine activity.

Frequently Asked Questions

Neiratax is a combination injectable that supplies the vitamins thiamine (B1), cyanocobalamin (B12) and pyridoxine (B6) to correct specific vitamin deficiencies, and it contains lidocaine to provide local anesthesia for minor surgical or diagnostic procedures.

Thiamine hydrochloride acts as a cofactor for enzymes involved in carbohydrate metabolism, such as pyruvate dehydrogenase, helping convert glucose into usable energy and supporting normal nervous system function.

The dosage of Neiratax is determined by the prescribing healthcare professional based on the patient’s specific deficiency, weight, age and clinical situation. The prescriber will set the appropriate amount and frequency.

Safety of Neiratax in pregnancy or lactation has not been fully established. Healthcare providers should weigh the potential benefits against any possible risks and consider alternative treatments when appropriate.

To order Neiratax, submit an enquiry on the product page at gnhindia.com with 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.

Neiratax combines three B‑vitamins (B1, B12, B6) with lidocaine in a single intramuscular formulation, offering both deficiency correction and local anesthesia. Other products may provide individual vitamins without anesthetic, requiring separate administrations for pain control.

Neiratax should be stored at ambient temperature, below 25 °C, in its original container. Protect it from moisture, direct sunlight and extreme temperature fluctuations to maintain potency.

Neiratax is given by intramuscular injection, typically into a large muscle such as the gluteus or deltoid. Administration should be performed by a qualified healthcare professional following aseptic technique.

Serious risks include severe allergic reactions (anaphylaxis), profound hypotension, cardiac arrhythmias, seizures, and prolonged numbness. Immediate medical attention is required if any of these symptoms occur after injection.

Neiratax should not be used in individuals with known hypersensitivity to any of its components, especially lidocaine, or in patients with severe cardiac conduction disorders without close monitoring. Contraindications should be confirmed by the prescribing clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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