Product image of Mydrane (Lidocaine Hydrochloride Monohydrate, Phenylephrine Hydrochloride, Tropicamide) supplied by GNH India

Mydrane

Active Ingredient:
Lidocaine Hydrochloride Monohydrate, Phenylephrine Hydrochloride, Tropicamide
Origin:
EU

Mydrane (Lidocaine Hydrochloride Monohydrate, Phenylephrine Hydrochloride, Tropicamide)

Lidocaine Hydrochloride, Phenylephrine Hydrochloride and Tropicamide, the active ingredients in Mydrane, are local anesthetic, alpha‑adrenergic agonist and antimuscarinic agents, presented as an intracameral solution for intracameral use. They provide intraoperative pupil dilation and ocular anesthesia during cataract surgery in adult patients.

GNH India supplies Mydrane as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, surgical centres and ophthalmology clinics worldwide. The product complies with EU regulatory standards and is distributed under strict quality‑assured conditions to meet the needs of eye‑care providers.

Manufacturer / TM Owner

Laboratoires Thea

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Indications & Clinical Uses

Mydrane is employed in ophthalmic procedures to achieve rapid pupil dilation and intraocular anesthesia.

  • Cataract surgery: provides rapid pupil dilation and intraocular anesthesia for safe lens removal.
  • Intraocular lens implantation: facilitates adequate mydriasis and analgesia during lens placement.
  • Other ocular surgeries: enables pupil dilation and anesthesia for procedures such as trabeculectomy or vitrectomy.

How It Works

  • Mydrane combines three agents that act synergistically: lidocaine blocks voltage‑gated sodium channels, producing local anesthesia of intraocular tissues; phenylephrine stimulates α1‑adrenergic receptors on the iris dilator muscle, causing contraction and pupil dilation; tropicamide antagonizes muscarinic receptors in the iris sphincter, further relaxing the muscle and enhancing dilation. The combined effect yields prompt mydriasis and analgesia for intra‑ocular surgery.

Side Effects

Mydrane may cause a range of ocular and systemic reactions following intracameral administration.

Common Side Effects

  • Transient ocular pain or discomfort.
  • Mild conjunctival redness.
  • Temporary increase in intraocular pressure.
  • Blurred vision lasting a few minutes.
  • Headache.
  • Nausea.

Serious or Rare Side Effects

  • Allergic reaction (rash, swelling, anaphylaxis).
  • Persistent mydriasis leading to photophobia.
  • Corneal edema or endothelial damage.
  • Retinal toxicity.
  • Systemic lidocaine toxicity (central nervous system or cardiac effects).
  • Severe hypotension or hypertension from phenylephrine imbalance.

Precautions & Warnings

Prior to using Mydrane, clinicians should observe several safety measures.

  • Assess patient allergy: verify no known hypersensitivity to lidocaine, phenylephrine or tropicamide.
  • Monitor intraocular pressure: check IOP before and after injection.
  • Use appropriate dose: administer only by a qualified ophthalmic surgeon.
  • Avoid in patients with narrow‑angle glaucoma: risk of angle‑closure crisis.
  • Avoid in patients with severe cardiovascular disease: phenylephrine may raise blood pressure.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Mydrane can interact with other medications that affect ocular or systemic physiology.

Major Interactions (Avoid)

  • MAO inhibitors: phenylephrine may precipitate hypertensive crisis.
  • Beta‑blockers: may potentiate ocular hypotensive effects.
  • Systemic anesthetics: lidocaine may increase risk of toxicity.

Moderate Interactions (Monitor Closely)

  • Anticholinergic drugs: additive mydriasis.
  • Alpha‑adrenergic agonists: additive cardiovascular effects.
  • Other ocular vasoconstrictors: increased risk of ocular ischemia.

Frequently Asked Questions

Mydrane is an intracameral ophthalmic solution used to provide rapid pupil dilation and local anesthesia during intraocular procedures such as cataract surgery, intraocular lens implantation, and other eye surgeries that require a clear surgical field.

Lidocaine blocks sodium channels to numb intraocular tissues, phenylephrine activates α1‑adrenergic receptors causing the iris dilator muscle to contract, and tropicamide blocks muscarinic receptors, relaxing the iris sphincter. Together they produce quick, sustained mydriasis and analgesia.

The dose of Mydrane is determined by the operating ophthalmologist based on the specific surgical protocol and patient factors. It is administered as a single intracameral injection at the time of surgery.

Safety data for Mydrane 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 the prescribing physician.

To order Mydrane, 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 required import documentation.

Mydrane combines a local anesthetic with two mydriatic agents, offering both analgesia and rapid dilation in a single injection. Traditional regimens often require separate topical drops of phenylephrine or tropicamide, which may take longer to achieve adequate dilation and lack anesthetic effect.

Mydrane should be stored at ambient temperature, protected from light and moisture, and kept in its original sealed container until use. Do not freeze or expose the solution to extreme temperatures.

Mydrane is administered by a qualified ophthalmic surgeon as a sterile intracameral injection directly into the anterior chamber of the eye immediately before the surgical procedure.

Serious risks include allergic reactions, persistent mydriasis, corneal edema, retinal toxicity, and systemic lidocaine toxicity. Clinicians should monitor patients closely for any signs of these adverse events during and after the procedure.

Mydrane should not be used in patients with known hypersensitivity to any of its components, those with narrow‑angle glaucoma, severe cardiovascular disease, or in situations where intra‑ocular pressure cannot be safely monitored.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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