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, Lidocaine Hydrochloride, the active ingredient in Neiratax, is a vitamin B complex and local anesthetic presented as an injectable solution for intramuscular use. It is employed to correct vitamin B deficiencies and to provide local anesthesia for minor procedures.

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 addresses vitamin B deficiency disorders and provides local anesthesia for minor interventions.

  • Thiamine (vitamin B1) deficiency: restores normal carbohydrate metabolism and prevents neurological complications.
  • Cyanocobalamin (vitamin B12) deficiency: supports red blood cell formation and neurological function.
  • Pyridoxine (vitamin B6) deficiency: aids amino‑acid metabolism and hemoglobin synthesis.
  • Minor procedural anesthesia: produces temporary loss of sensation for short, superficial surgeries or diagnostic procedures.

How It Works

  • The thiamine, cyanocobalamin and pyridoxine components act as essential co‑enzymes in carbohydrate metabolism, hematopoiesis and amino‑acid processing, facilitating energy production and red blood cell formation. Lidocaine binds to voltage‑gated sodium channels on neuronal membranes, stabilising the inactive state and preventing depolarisation, thereby blocking nerve impulse transmission and producing local anaesthesia.

Side Effects

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

Common Side Effects

  • Injection site pain or tenderness.
  • Redness or mild swelling at the injection site.
  • Transient dizziness or light‑headedness.
  • Nausea or mild gastrointestinal upset.
  • Headache.
  • Temporary tingling or numbness near the injection area.

Serious or Rare Side Effects

  • Anaphylactic or severe allergic reaction.
  • Marked hypotension or cardiovascular collapse.
  • Cardiac arrhythmias or conduction disturbances.
  • Seizures or central nervous system depression.
  • Persistent numbness or motor weakness.
  • Severe skin reactions such as Stevens‑Johnson syndrome.

Precautions & Warnings

Before administering Neiratax, consider the following safety measures.

  • Assess vitamin B status: evaluate baseline levels to avoid unnecessary supplementation.
  • Monitor for hypersensitivity: observe patients for signs of allergic reaction during and after injection.
  • Use with caution in cardiac conduction disorders: lidocaine may exacerbate arrhythmias.
  • Avoid in patients with known lidocaine allergy: substitute with an alternative anesthetic.
  • Adjust dose in renal or hepatic impairment: impaired metabolism may increase systemic exposure.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Neiratax can interact with several medicines; awareness of major and moderate interactions helps minimise risk.

Major Interactions (Avoid)

  • Concurrent other local anesthetics: cumulative toxicity risk.
  • Monoamine oxidase inhibitors: may enhance hypotensive effect.
  • Class I antiarrhythmic agents (e.g., quinidine): increase lidocaine plasma levels.
  • High‑dose vitamin B supplements: potential masking of deficiency symptoms.
  • Strong CYP450 inhibitors: reduce lidocaine metabolism, raising toxicity.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may potentiate bradycardia.
  • Diuretics: can alter electrolyte balance affecting lidocaine action.
  • Alcohol: may increase central nervous system depression.
  • Anticonvulsants: may modify pyridoxine metabolism.
  • NSAIDs: possible increased bleeding tendency.

Frequently Asked Questions

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

The vitamin B components act as essential co‑enzymes in carbohydrate metabolism, red‑blood‑cell formation and amino‑acid processing, while lidocaine blocks voltage‑gated sodium channels on nerves, preventing impulse transmission and producing a temporary loss of sensation.

The appropriate dose of Neiratax is determined by the prescribing healthcare professional based on the patient’s clinical condition, vitamin status and the required depth of local anesthesia. Dosage details are provided on the prescription.

Safety data for Neiratax in pregnancy and lactation are limited. Prescribers should weigh potential benefits against possible risks and consider alternative therapies if uncertainty exists. Consultation with a specialist is recommended.

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

Neiratax combines three B‑vitamins with a local anesthetic in a single injectable formulation, offering both deficiency correction and procedural anesthesia. Stand‑alone oral B‑vitamin supplements lack the rapid correction and anesthetic effect provided by Neiratax, making it suitable for acute clinical settings.

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 potency and sterility.

Neiratax is administered by intramuscular injection. The healthcare professional selects an appropriate injection site, follows aseptic technique, and injects the prescribed volume slowly to minimize discomfort and ensure proper absorption.

Serious risks include severe allergic reactions such as anaphylaxis, marked hypotension, cardiac arrhythmias, seizures, and rare skin reactions like Stevens‑Johnson syndrome. Immediate medical attention is required if any of these symptoms occur.

Neiratax should be avoided in individuals with a known allergy to lidocaine or any of its components, patients with severe cardiac conduction disorders, and those with uncontrolled hepatic or renal impairment unless dosage adjustments are made by a qualified clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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