Product image of Instillagel (Lidocaine Hydrochloride) supplied by GNH India

Instillagel

Active Ingredient:
Lidocaine Hydrochloride
Origin:
EU

Instillagel (Lidocaine Hydrochloride)

Lidocaine Hydrochloride, the active ingredient in Instillagel, is a local anesthetic presented as a gel for urethral use. It provides topical anesthesia for diagnostic or therapeutic procedures involving the urethra and helps relieve discomfort during catheterization.

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

Manufacturer / TM Owner

Farco-Pharma Gmbh

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Indications & Clinical Uses

  • Instillagel, a lidocaine‑based local anesthetic, is used for urogenital procedures that require urethral anesthesia.
  • Urethral anesthesia for diagnostic procedures: provides pain relief during cystoscopy or uroflowmetry.
  • Therapeutic urethral procedures: facilitates comfortable performance of urethral dilatation or surgery.
  • Catheterization discomfort relief: reduces pain and spasm when inserting urinary catheters.
  • Post‑procedure urethral care: helps manage pain after urological interventions.

How It Works

  • Lidocaine hydrochloride reversibly blocks voltage‑gated sodium channels on neuronal membranes, preventing depolarisation and the transmission of pain signals. By stabilising the neuronal membrane, it produces a rapid, temporary loss of sensation in the area where the gel is applied, allowing painless urethral manipulation.

Side Effects

Instillagel may cause local and systemic adverse reactions.

Common Side Effects

  • Burning or stinging sensation at the application site.
  • Mild irritation or redness of the urethral mucosa.
  • Transient numbness that resolves after the gel is cleared.

Serious or Rare Side Effects

  • Allergic reactions such as rash, urticaria, or angioedema.
  • Systemic lidocaine toxicity presenting as dizziness, seizures, or cardiac arrhythmia.
  • Severe local tissue necrosis if applied excessively or left in situ for prolonged periods.

Precautions & Warnings

  • Before using Instillagel, consider the following safety measures.
  • Allergy assessment: confirm no known hypersensitivity to lidocaine or amide‑type anesthetics.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk; data are limited.
  • Age considerations: exercise caution in paediatric or geriatric patients due to altered absorption.
  • Concurrent local anesthetics: avoid exceeding the total recommended lidocaine dose.
  • Urethral pathology: do not use in the presence of severe infection, ulceration, or trauma.
  • Store at room temperature below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Instillagel can interact with other medicines; monitor the following.

Major Interactions (Avoid)

  • Class I antiarrhythmic agents (e.g., quinidine, procainamide): may increase systemic lidocaine levels.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): can raise lidocaine exposure.
  • Concurrent use of other local anesthetics: risk of cumulative toxicity.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may enhance cardiac depressant effects of lidocaine.
  • Diuretics such as furosemide: may alter lidocaine clearance.
  • Anticonvulsants: may affect seizure threshold when lidocaine systemic absorption occurs.

Frequently Asked Questions

Instillagel is a lidocaine‑hydrochloride gel applied to the urethra to provide local anaesthesia for diagnostic or therapeutic urological procedures and to reduce discomfort during urinary catheterisation.

Lidocaine hydrochloride blocks voltage‑gated sodium channels on nerve cells, preventing depolarisation and the transmission of pain signals. This reversible blockade creates a temporary loss of sensation in the urethral mucosa where the gel is applied.

The prescribed amount of Instillagel is determined by the treating clinician based on the specific procedure, patient characteristics and institutional protocols. No fixed dosing regimen is provided in the product information.

Safety data for Instillagel in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and after a careful risk‑benefit assessment by the prescriber.

Enquiries for Instillagel can be submitted on the product page at gnhindia.com by entering the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Instillagel delivers lidocaine in a gel formulation, offering rapid onset and localized effect. Compared with liquid solutions, the gel may provide longer mucosal contact time and reduced runoff, potentially improving patient comfort during procedures.

Instillagel should be stored at room temperature below 25 °C, in its original packaging, protected from moisture and direct sunlight. Keep the container tightly closed and avoid freezing the product.

Instillagel is applied directly into the urethra using a sterile applicator or catheter as directed by the healthcare professional. The gel is allowed to dwell for the recommended time before proceeding with the intended urological procedure.

Serious risks include allergic reactions such as rash, urticaria or angioedema, and systemic lidocaine toxicity that may manifest as dizziness, seizures or cardiac arrhythmias, especially if excessive amounts are absorbed.

Instillagel should be avoided in patients with a known hypersensitivity to lidocaine or other amide‑type local anaesthetics, and in those with severe urethral infection, ulceration or trauma where the gel could exacerbate tissue damage.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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