Product image of Lidoposterin (Lidocaine) supplied by GNH India

Lidoposterin

Active Ingredient:
Lidocaine
Origin:
EU

Lidoposterin (Lidocaine)

Lidocaine, the active ingredient in Lidoposterin, is a local anesthetic presented as a topical preparation for cutaneous and rectal use. It provides temporary numbness and pain relief for minor skin procedures and superficial irritations in adult patients.

GNH India supplies Lidoposterin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, adhering to EU GMP standards and providing reliable batch‑to‑batch consistency for global procurement. Our distribution network ensures timely delivery across Europe, Asia and the Americas.

Manufacturer / TM Owner

Dr. Kade Pharmazeutische Fabrik Gmbh

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Indications & Clinical Uses

Lidoposterin, a lidocaine‑based local anesthetic, is used to provide analgesia in superficial tissue procedures.

  • Minor skin procedures: provides rapid surface anesthesia to facilitate incision or removal of lesions.
  • Superficial wound pain: reduces discomfort from cuts, abrasions, or burns.
  • Irritation relief: alleviates pain associated with minor dermatologic irritations.

How It Works

  • Lidocaine acts by reversibly binding to voltage‑gated sodium channels in neuronal membranes, stabilizing the inactive state of the channel. This blocks the influx of sodium ions required for depolarization, thereby inhibiting initiation and propagation of nerve impulses. The resulting loss of sensory transmission produces localized numbness without affecting motor function when applied to intact skin or mucous membranes.

Side Effects

Topical lidocaine can be associated with a range of adverse reactions, ranging from mild to severe.

Common Side Effects

  • Localized burning or stinging at the application site.
  • Redness or mild erythema.
  • Pruritus or itching.
  • Swelling or edema of the treated area.

Serious or Rare Side Effects

  • Allergic contact dermatitis with vesiculation.
  • Systemic toxicity manifesting as dizziness, tinnitus, or visual disturbances.
  • Cardiac arrhythmias in cases of excessive absorption.
  • Seizures secondary to high plasma concentrations.

Precautions & Warnings

When using Lidoposterin, consider the following safety measures.

  • Patient assessment: verify no known hypersensitivity to amide‑type local anesthetics before use.
  • Application area: avoid use on broken skin, mucous membranes, or large surface areas to limit systemic absorption.
  • Concomitant agents: do not combine with other topical anesthetics containing lidocaine or similar agents without professional guidance.
  • Medical conditions: exercise caution in patients with cardiac conduction disorders or severe hepatic impairment.
  • Pediatric use: limit exposure in children; dosing and area should be determined by a qualified clinician.
  • Store at below 25°C: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lidoposterin may interact with other medicines; awareness of the level of interaction helps manage risk.

Major Interactions (Avoid)

  • Concurrent use with Class I antiarrhythmic drugs (e.g., quinidine, procainamide) may potentiate cardiotoxic effects.
  • Co‑administration with other potent sodium‑channel blockers (e.g., bupivacaine) can increase risk of systemic toxicity.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole) may reduce lidocaine metabolism, raising plasma levels.
  • Beta‑blockers may enhance lidocaine’s cardiac effects, requiring ECG monitoring.
  • High‑dose epinephrine may alter lidocaine absorption, affecting duration of action.

Frequently Asked Questions

Lidoposterin is a lidocaine‑based topical formulation indicated for local anesthesia during minor skin procedures, for pain relief of superficial wounds such as cuts or abrasions, and for alleviating discomfort associated with mild dermatologic irritations.

Lidocaine blocks voltage‑gated sodium channels on neuronal membranes, preventing sodium influx needed for depolarisation. This inhibition stops the generation and conduction of nerve impulses, resulting in temporary loss of sensation in the area where the drug is applied.

The appropriate dose of Lidoposterin is determined by the prescribing clinician based on the size of the treatment area, patient age, and clinical context. Healthcare professionals should follow local guidelines and product labeling when establishing the regimen.

Safety data for Lidoposterin in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

To request Lidoposterin, 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.

Lidoposterin contains lidocaine, an amide‑type anesthetic known for rapid onset and moderate duration. Compared with ester‑type agents such as procaine, lidocaine generally offers a lower risk of allergic reactions and a longer period of analgesia, making it a common choice for minor procedural anesthesia.

Lidoposterin should be stored at temperatures below 25 °C, in its original container, protected from moisture and direct sunlight. Keep the product out of reach of children and avoid exposing it to extreme heat or freezing conditions.

Lidoposterin is applied topically to intact skin or rectal mucosa. The recommended amount is spread thinly over the target area using a sterile applicator or gloved finger, avoiding excessive coverage that could increase systemic absorption.

Serious adverse events include systemic toxicity such as dizziness, visual disturbances, cardiac arrhythmias, and seizures, particularly when large amounts are absorbed. Allergic contact dermatitis with blistering is also a rare but important risk that requires immediate medical attention.

Lidoposterin should be avoided in individuals with a known hypersensitivity to lidocaine or other amide‑type local anesthetics, in patients with severe cardiac conduction disorders, and in those with extensive broken skin where uncontrolled systemic absorption could occur.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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