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BRINZOLAMIDE/BRIMONIDINE is a brand name for Brimonidine. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Decrease of elevated intraocular pressure (IOP) in adult patients with open-angle glaucoma or ocular hypertension for whom monotherapy provides insufficient IOP reduction (see section 5.1).
Verbatim from this product's MHRA label. Tap a section to expand.
Posology Use in adults, including the elderly The recommended dose is one drop of Brinzolamide/Brimonidine in the affected eye(s) two times daily. Missed dose If a dose is missed, treatment should be continued with the next dose as planned.
4). Brinzolamide + brimonidine has not been studied in patients with severe renal impairment (CrCl < 30 mL/min) or in patients with hyperchloraemic acidosis. 3). Paediatric population The safety and efficacy of brinzolamide + brimonidine in children and adolescents aged 2 to 17 years have not been established.
No data are available. 3). Method of administration For ocular use. Patients should be instructed to shake the bottle well before use. When nasolacrimal occlusion is used and the eyelids are closed for 2 minutes, systemic absorption is reduced.
4). To prevent contamination of the dropper tip and solution, care must be taken not to touch the eyelids, surrounding areas or other surfaces with the dropper tip of the bottle. Patients should be instructed to keep the bottle tightly closed when not in use.
Brinzolamide/Brimonidine may be used concomitantly with other topical ophthalmic medicinal products to lower intraocular pressure. If more than one topical ophthalmic medicinal product is being used, the medicinal products must be administered at least 5 minutes apart.
Summary of the safety profile In clinical trials involving Brinzolamide/Brimonidine 10 mg/mL + 2 mg/mL eye drops, suspension dosed twice daily the most common adverse reactions were ocular hyperaemia and ocular allergic type reactions occurring in approximately 6-7 % of patients, and dysgeusia (bitter or unusual taste in the mouth following instillation) occurring in approximately 3 % of patients.
Tabulated summary of adverse reactions The following adverse reactions have been reported during clinical studies with Brinzolamide/Brimonidine 10 mg/mL + 2 mg/mL eye drops, suspension twice-daily dosing and during clinical studies and post-marketing surveillance with the individual components brinzolamide and brimonidine.
They are classified according to the subsequent convention: very common (≥ 1/10), common (≥ 1/100 to < 1/10), uncommon (≥ 1/1 000 to < 1/100), rare (≥ 1/10 000 to < 1/1 000), very rare (< 1/10 000) or not known (cannot be estimated from the available data).
Within each frequency-grouping, adverse reactions are presented in order of decreasing seriousness. 4), face oedema3, dermatitis2,3, erythema2,3 Musculoskeletal and connective tissue disorders Uncommon: back pain2, muscle spasms2, myalgia2 Not known: arthralgia2, pain in extremity2 Renal and urinary disorders Uncommon: renal pain2 Not known: pollakiuria2 Reproductive system and breast disorders Uncommon: erectile dysfunction2 General disorders and administration site conditions Uncommon: pain2, chest discomfort2, feeling abnormal2, feeling jittery2, irritability2, medication residue1 Not known: chest pain2, peripheral oedema2,3 1 adverse reaction observed with brinzolamide/brimonidine.
2 additional adverse reaction observed with brinzolamide monotherapy. 4 %). It is likely to be caused by passage of the eye drops in the nasopharynx via the nasolacrimal canal and is mainly attributable to the brinzolamide component of Brinzolamide/Brimonidine.
The medicinal product should not be injected. Patients should be instructed not to swallow Brinzolamide/Brimonidine. Ocular effects Brinzolamide + brimonidine has not been studied in patients with narrow-angle glaucoma and its use is not recommended in these patients.
The possible effect of brinzolamide on corneal endothelial function has not been investigated in patients with compromised corneas (particularly in patients with low endothelial cell count). Specifically, patients wearing contact lenses have not been studied and careful monitoring of these patients when using brinzolamide is recommended, since carbonic anhydrase inhibitors may affect corneal hydration and wearing contact lenses might increase the risk for the cornea (for further instructions on wearing contact lenses, see below under “Benzalkonium chloride”).
Careful monitoring of patients with compromised corneas, such as patients with diabetes mellitus or corneal dystrophies, is recommended. Brimonidine tartrate may cause ocular allergic reactions. If allergic reactions are observed, treatment should be discontinued.
Delayed ocular hypersensitivity reactions have been reported with brimonidine tartrate, with some reported to be associated with an increase in IOP. The potential effects following cessation of treatment with brinzolamide + brimonidine have not been studied.
While the duration of IOP-lowering effect for brinzolamide + brimonidine has not been studied, the IOP-lowering effect of brinzolamide is expected to last for 5-7 days. The IOP-lowering effect of brimonidine may be longer. Systemic effects Brinzolamide/Brimonidine contains brinzolamide, a sulphonamide inhibitor of carbonic anhydrase and, although administered topically, is absorbed systemically.
The same types of adverse drug reactions that are attributable to sulphonamides may occur with topical administration, including Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN). At the time of prescription, patients should be advised of the signs and symptoms and monitored closely for skin reactions.
1. 4). 5). g. 5). 4). Patients with hyperchloraemic acidosis. 4).
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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2). Brinzolamide/Brimonidine contains brinzolamide, which is a sulphonamide inhibitor of carbonic anhydrase with systemic absorption. Gastrointestinal, nervous system, haematological, renal and metabolic effects are generally associated with systemic carbonic anhydrase inhibitors.
The same type of adverse reactions attributable to oral carbonic anhydrase inhibitors may occur with topical administration. Adverse reactions commonly associated with the brimonidine component of Brinzolamide/Brimonidine include the development of ocular allergic type reactions, fatigue and/or drowsiness, and dry mouth.
The use of brimonidine has been associated with minimal decreases in blood pressure. Some patients who dosed with brinzolamide + brimonidine experienced decreases in blood pressure similar to those observed with the use of brimonidine as monotherapy.
Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. uk/yellowcard or search for MHRA Yellow Card in […]
If signs of serious reactions or hypersensitivity occur, brinzolamide should be withdrawn immediately. Cardiac disorders Following administration of brinzolamide + brimonidine, small decreases in blood pressure were observed in some patients.
5). Brinzolamide/Brimonidine should be used with caution in patients with depression, cerebral or coronary insufficiency, Raynaud's phenomenon, orthostatic hypotension or thromboangiitis obliterans. Acid/base disturbances Acid-base disturbances have been reported with oral carbonic anhydrase inhibitors.
Brinzolamide/Brimonidine contains brinzolamide, an inhibitor of carbonic anhydrase, and although administered topically, is absorbed systemically. e. 5). Brinzolamide/Brimonidine should be used with caution in patients with risk of renal impairment because of the possible risk of metabolic acidosis.
3). 2). Mental alertness Oral carbonic anhydrase inhibitors may impair the ability to perform tasks requiring mental alertness and/or physical coordination in elderly patients. 7). Paediatric population The safety and efficacy of brinzolamide + brimonidine in children and adolescents aged 2 to 17 years have not been established.
Symptoms of brimonidine overdose (including loss of consciousness, hypotension, hypotonia, bradycardia, hypothermia, cyanosis and apnoea) have been reported in neonates and infants receiving brimonidine eye drops as part of medical treatment of congenital glaucoma.
3). 9). Excipients Benzalkonium chloride Brinzolamide/Brimonidine contains benzalkonium chloride which may cause eye irritation and is known to discolour soft contact lenses. Contact with soft contact lenses should be avoided. Patients must be instructed to remove contact lens prior to application of Brinzolamide/Brimonidine and wait at least 15 minutes before reinsertion.
Benzalkonium chloride has been reported to cause eye irritation and symptoms of dry eyes and may affect the tear film and corneal surface. It should be used with caution in dry eye patients and in patients whose cornea may be compromised.
Patients should be monitored in case of prolonged use. This medicinal product should not be given to a child younger than 2 years old without medical advice, as it contains boron and may impair fertility in the future.