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 vitamin B complex combined with a local anesthetic presented as an injectable for intramuscular use. It is employed to correct vitamin deficiencies and to provide local anesthesia in clinical settings.

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 combines vitamins and a local anesthetic, addressing nutritional deficiencies and providing short‑term anesthesia.

  • Vitamin B1 deficiency: restores thiamine levels and supports carbohydrate metabolism.
  • Vitamin B12 deficiency: replenishes cyanocobalamin for red blood cell formation and neurological health.
  • Vitamin B6 deficiency: supplies pyridoxine for amino‑acid metabolism and neurotransmitter synthesis.
  • Minor surgical or diagnostic procedures: provides local anesthesia through lidocaine to reduce pain.

How It Works

  • Thiamine acts as a cofactor for enzymes in carbohydrate metabolism, cyanocobalamin participates in DNA synthesis and neurologic function, and pyridoxine supports amino‑acid metabolism and neurotransmitter production. Lidocaine blocks voltage‑gated sodium channels in neuronal membranes, preventing depolarization and producing reversible local anesthesia.

Side Effects

Neiratax may cause a range of adverse reactions.

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the site.
  • Nausea: transient feeling of queasiness.
  • Headache: mild headache following administration.
  • Dizziness: temporary light‑headedness.
  • Local irritation: redness or swelling.
  • Transient numbness: temporary loss of sensation.

Serious or Rare Side Effects

  • Anaphylactic reaction: severe allergy requiring immediate medical attention.
  • Cardiovascular instability: hypotension or arrhythmia.
  • Seizures: rare central nervous system excitation.
  • Stevens‑Johnson syndrome: severe skin reaction.
  • Respiratory depression: difficulty breathing.
  • Persistent neurological deficits: prolonged numbness or weakness.

Precautions & Warnings

Before using Neiratax, consider the following safety measures.

  • Assess vitamin status: evaluate patient’s B‑vitamin levels prior to therapy.
  • Monitor hypersensitivity: observe for signs of allergic reaction during and after injection.
  • Cardiac caution: use carefully in patients with conduction disorders or arrhythmias.
  • Lidocaine allergy: avoid in individuals with known hypersensitivity to amide‑type local anesthetics.
  • Renal/hepatic impairment: adjust use in patients with significant organ dysfunction.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Neiratax may interact with other medicines.

Major Interactions (Avoid)

  • Other local anesthetics: combined use can increase systemic toxicity.
  • MAO inhibitors: concurrent use may potentiate cardiovascular effects of lidocaine.
  • High‑dose vitamin B supplements: risk of hypervitaminosis.

Moderate Interactions (Monitor Closely)

  • Anticoagulants: monitor bleeding risk due to injection trauma.
  • Anticonvulsants: observe for additive CNS effects.
  • Beta‑blockers: may enhance bradycardic effects of lidocaine.

Frequently Asked Questions

Neiratax is an injectable combination of thiamine, cyanocobalamin, pyridoxine and lidocaine. It is used to correct deficiencies of vitamins B1, B12 and B6, and to provide local anesthesia for minor surgical or diagnostic procedures.

The vitamin components act as essential cofactors in metabolic pathways: thiamine supports carbohydrate metabolism, cyanocobalamin is required for DNA synthesis and nerve health, and pyridoxine aids amino‑acid metabolism. Lidocaine blocks sodium channels in nerve cells, producing reversible local numbness.

The dose of Neiratax is determined by the prescribing healthcare professional based on the patient’s clinical condition, vitamin status and the required anesthetic effect. Specific dosing regimens are not disclosed here.

Safety of Neiratax in pregnancy or lactation has not been fully established. Prescribers should weigh potential benefits against possible risks and consider alternative therapies when appropriate.

To order Neiratax, 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 necessary import documentation.

Neiratax combines three B‑vitamins with a local anesthetic in a single intramuscular formulation, offering both deficiency correction and immediate analgesia. Other products may contain only one vitamin or lack an anesthetic component, requiring separate administrations for supplementation and pain control.

Neiratax should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight and extreme temperature fluctuations to maintain stability.

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

Serious risks include anaphylactic reactions, severe cardiovascular effects such as hypotension or arrhythmia, seizures, and rare dermatologic conditions like Stevens‑Johnson syndrome. Immediate medical attention is required if any of these occur.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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