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OTC
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EQ 0.5% BASE, Solution/drops
INN: APRACLONIDINE HYDROCHLORIDE
Available in:
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Form
SOLUTION/DROPS
Dosage
EQ 0.5% BASE
Route
OPHTHALMIC
Storage
—
About This Product
User Reviews
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
Manufacturer
HARROW EYE LLC
ATC Code
C02AC01
Source
FDA_OB · 020258
(
ARTG
)
To control intraocular pressure in glaucoma patients on maximally tolerated glaucoma therapy for a period of 3 months. In clinical studies the drop in intraocular pressure (IOP) appeared to decrease after Day 60 which may be associated with a progression of the disease or loss of effect of the drug. This phenomenon appears to be an individual occurence with a variable time of onset. As with any patient on maximally tolerated therapy (See Dosage & Administration), patients using apraclonidine 0.5% eye drops to delay surgery should have frequent follow-up examinations and treatment should be discontinued if IOP rises significantly. In patients who have maintained a response to apraclonidine 0.5% eye drops for 3 months and a decision is made to continue treatment, safety aspects, including any evidence of corneal changes (see Warnings and Precautions), and IOP control should be closely monitored.
⚠️ Warnings
• Caution should be exercised in patients with history of depression, sugar, high blood pressure, stroke, Raynaud's disease, inflammation of the blood vessels, fainting, heart, liver, or kidney disease, who are taking other medications, children, during pregnancy and breastfeeding.
• It may cause drowsiness, dizziness, or blurred vision, do not drive a car or operate machinery while taking this medication.
• Avoid alcohol consumption.