Product image of Mydriasert (Phenylephrine Hydrochloride, Tropicamide) supplied by GNH India

Mydriasert

Active Ingredient:
Phenylephrine Hydrochloride, Tropicamide
Origin:
EU

Mydriasert (Phenylephrine Hydrochloride, Tropicamide)

Phenylephrine Hydrochloride, the active ingredient in Mydriasert, is an alpha‑adrenergic agonist presented as an ophthalmic solution for ocular (topical) use. Together with Tropicamide, it dilates the pupil and induces cycloplegia for diagnostic and surgical eye procedures.\n\nGNH India supplies Mydriasert as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Laboratoires Thea

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Indications & Clinical Uses

  • Mydriasert, a combination mydriatic/cycloplegic ophthalmic solution, acts on the iris muscles to produce pupil dilation.\n\nDiagnostic eye examinations: provides rapid pupil dilation to facilitate fundus evaluation.\nIntraocular surgery: creates adequate mydriasis for safe surgical access.\nCycloplegic testing: temporarily paralyzes accommodation for accurate refractive measurements.

How It Works

  • Phenylephrine hydrochloride activates alpha‑1 adrenergic receptors on the iris dilator muscle, causing contraction and pupil enlargement. Tropicamide competitively blocks muscarinic receptors in the iris sphincter muscle, preventing constriction and producing cycloplegia. The combined pharmacologic actions result in sustained mydriasis and loss of accommodation, facilitating ocular examination and surgery.

Side Effects

  • Adverse reactions may occur following ocular administration of Mydriasert.\n\nCommon Side Effects:\n- Transient ocular burning or stinging\n- Mild conjunctival hyperemia\n- Temporary blurred vision\n- Increased intraocular pressure in susceptible patients\n\nSerious or Rare Side Effects:\n- Acute angle‑closure glaucoma\n- Severe allergic reaction (anaphylaxis)\n- Systemic cardiovascular effects such as hypertension or tachycardia

Precautions & Warnings

  • Use Mydriasert only under professional supervision and consider patient‑specific factors.\n\nAssess intraocular pressure before use: avoid in patients with narrow‑angle glaucoma.\nScreen for hypersensitivity: discontinue if allergic reaction occurs.\nUse lowest effective dose: limit exposure to reduce systemic absorption.\nAvoid concurrent use with other mydriatics: may cause excessive dilation.\nMonitor in pediatric patients: increased sensitivity to anticholinergic effects.\nStore at room temperature: keep in original container, protect from light and moisture.

Avoid Interactions

  • Mydriasert may interact with other systemic or ocular agents; review patient medication lists.\n\nMajor Interactions (Avoid):\n- Systemic sympathomimetics (e.g., oral phenylephrine): additive hypertensive effects.\n- Other anticholinergic ophthalmic agents: risk of excessive cycloplegia.\n- Monoamine oxidase inhibitors: potential for hypertensive crisis.\n\nModerate Interactions (Monitor Closely):\n- Beta‑blocker eye drops: may blunt intraocular pressure reduction.\n- Topical anesthetics: may increase corneal absorption of active ingredients.\n- Systemic antihypertensives: monitor blood pressure during use.

Frequently Asked Questions

Mydriasert is an ophthalmic solution that combines phenylephrine hydrochloride and tropicamide to produce rapid pupil dilation (mydriasis) and temporary paralysis of accommodation (cycloplegia). It is used during diagnostic eye examinations, intraocular surgeries, and cycloplegic testing to improve visualization of intra‑ocular structures.

Phenylephrine hydrochloride is an alpha‑1 adrenergic agonist. When applied to the eye, it stimulates alpha‑1 receptors on the iris dilator muscle, causing the muscle to contract and the pupil to enlarge. This effect complements the antimuscarinic action of tropicamide, resulting in a pronounced mydriatic response.

The specific dosing regimen for Mydriasert is determined by the prescribing eye care professional based on the indication, patient age, and clinical circumstances. The prescriber will decide the number of drops, concentration, and frequency required for safe and effective pupil dilation.

Safety data for Mydriasert in pregnancy and lactation are limited. The product should only be used if the potential benefit justifies any potential risk to the fetus or infant. Healthcare providers should evaluate each case individually and discuss possible risks with the patient.

To request Mydriasert, 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.

Mydriasert combines an alpha‑adrenergic agonist (phenylephrine) with an antimuscarinic (tropicamide), offering both rapid dilator action and cycloplegia. Compared with single‑agent drops such as atropine or phenylephrine alone, Mydriasert provides a balanced, predictable dilation with a shorter duration, which can be advantageous for same‑day procedures.

Mydriasert should be stored at room temperature, below 25 °C, in its original container. Protect the solution from direct light, moisture, and extreme temperature fluctuations. Keep the vial tightly sealed when not in use to maintain sterility.

Mydriasert is applied topically to the eye as a sterile ophthalmic solution. The prescriber typically instills one or more drops into the conjunctival sac of the target eye(s) using aseptic technique. The onset of dilation usually occurs within minutes, and the effect lasts for the period required for the procedure.

The most serious risks include acute angle‑closure glaucoma, severe allergic reactions such as anaphylaxis, and systemic cardiovascular effects like hypertension or tachycardia. Patients with narrow‑angle glaucoma or known hypersensitivity should be evaluated carefully before use.

Mydriasert is contraindicated in patients with known hypersensitivity to phenylephrine, tropicamide, or any component of the formulation. It should also be avoided in individuals with narrow‑angle or acute angle‑closure glaucoma, and in patients where excessive pupil dilation could compromise ocular health.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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