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BRIMONIDINE TARTRATE 0.2% W/V EYE DROPS

Active substance(s): BRIMONIDINE TARTRATE / BRIMONIDINE TARTRATE / BRIMONIDINE TARTRATE

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SUMMARY OF PRODUCT CHARACTERISTICS

1

NAME OF THE MEDICINAL PRODUCT
Brimonidine Tartrate 0.2% w/v Eye Drops.

2

QUALITATIVE AND QUANTITATIVE COMPOSITION
Brimonidine tartrate 0.2% w/v (2.0 mg/ml). Excipients include Benzalkonium chloride 0.005% w/v. See section 6.1 for full list of excipients.

3

PHARMACEUTICAL FORM
Eye drops, solution. Clear, greenish-yellow solution.

4
4.1

CLINICAL PARTICULARS
Therapeutic indications
For reduction of elevated intraocular pressure (IOP) in patients with open angle glaucoma or ocular hypertension. - As monotherapy in patients in whom topical beta-blocker therapy is contraindicated. - As adjunctive therapy to other intraocular pressure lowering medications when the target intraocular pressure is not achieved with a single agent

4.2

Posology and method of administration
Adults including the elderly: One drop into the affected eye(s) twice daily, approximately 12 hours apart. No dosage adjustment is required in elderly patients. To reduce possible systemic absorption, it is recommended that the lachrymal sac be compressed at the medial canthus (punctul occlusion) for one minute immediately after the instillation of each drop. If more than one topical ophthalmic drug is to be administered, they should be instilled 5 to 15 minutes apart. Use in renal and hepatic impairment: Brimonidine eye drops have not been studied in patients with renal or hepatic impairment (see section 4.4). Use in paediatric subjects: No clinical studies have been performed in adolescents (12 to 17 years). Brimonidine eye drops are not recommended for use in children below 12 years and are contraindicated in neonates and infants (less than 2 years of age) (see sections 4.3, 4.4 & 4.9). It is known that severe adverse reactions can occur in neonates. The safety and efficacy of brimonidine has not been established in children.

4.3

Contraindications
Contraindicated in neonates and infants. Contraindicated in patients with known hypersensitivity to brimonidine tartrate or to any of the other ingredients. Contraindicated in patients receiving monoamine oxidase inhibitor (MAOI) therapy or those on antidepressants which affect noradrenergic transmission (eg. tricyclic antidepressants and mianserin).

4.4

Special warnings and precautions for use
Children of 2 years of age and above, especially those in the 2 to 7 age range and/or weighing less than 20 kg, should be treated with caution and closely monitored due to the high incidence of somnolence (see section 4.8). Caution is required in treating patients with: - severe or unstable and uncontrolled cardiovascular disease. - depression

- cerebral or coronary insufficiency - Raynauds phenomenon - orthostatic hypotension - thromboangiitis obliterans The use of Brimonidine Eye Drops has not been studied in patients with hepatic or renal impairment, therefore, caution should be exercised when treating such patients. It is reported that some patients (12.7%) in clinical trials experienced ocular allergic type reaction with brimonidine eye drops (see section 4.8); if allergic reactions are apparent, treatment should be discontinued. The eye drops contain benzalkonium chloride as preservative, which may cause eye irritation. Remove contact lenses prior to application and wait at least 15 minutes before reinserting. Known to discolour soft contact lenses.

4.5

Interaction with other medicinal products and other forms of interaction
Although specific drug interaction studies have not been conducted, the possibility of an additive or potentiating effect with CNS depressants (alcohol, barbiturates, opiates, sedatives or anaesthetics) should be considered. Although no actual data on the level of circulating catecholamines after administration of brimonidine eye drops are available, caution is advised when using the eye drops in patients who are taking medications which can affect the metabolism and uptake of circulating amines, eg. chlorpromazine, methylphenidate, reserpine. After application of bimonidine eye drops, clinically insignificant decreases in blood pressure have been reported in some patients. Caution is therefore advised when using drugs such as antihypertenstives and/or cardiac glycosides concomitantly with brimonidine eye drops. Caution is advised when initiating (or changing the dose of) a concomitant systemic agent (irrespective of pharmaceutical form) which may interact with -adrenergic agonists or interfere with their activity, ie. agonists or antagonists of the adrenergic receptor, eg. isoprenaline, prazosin.

4.6

Pregnancy and lactation
The safety of use during human pregnancy has not been established. In animal studies, brimonidine tartrate did not cause any teratogenic effects. In rabbits, brimonidine tartrate at plasma levels higher than are achieved during therapy in humans, has been shown to cause increased preimplantation loss and postnatal growth



reduction. Brimonidine eye drops should only be used during pregnancy if the potential benefit to the mother outweighs the potential risk to the foetus. It is not known if brimonidine is excreted in human milk. The compound is excreted in the milk of the lactating rat. Brimonidine eye drops should not be used by women nursing infants.

4.7

Effects on ability to drive and use machines
Brimonidine eye drops may cause fatigue and/or drowsiness which may impair the ability to drive or to use machinery. They may also cause blurred and/or abnormal vision, which may impair the ability to drive or to use machinery, especially at night or in reduced lighting. The patient should wait until these symptoms have cleared before driving or operating machinery.

4.8

Undesirable effects
The most commonly reported ADRs are oral dryness, ocular hyperaemia and burning/stinging, all occurring in 22 to 25% of patients. They are usually transient and not commonly of a nature serious enough to require discontinuation of treatment. Symptoms of ocular allergic reactions have been reported to have occurred in 12.7% of subjects in clinical trials (causing withdrawal in 11.5% of subjects), with onset being between 3 and 9 months in the majority of patients. The following convention has been used for classification of frequency of undesirable effects: Uncommon : Very rare : 1 in 1,000 and <1 in 100. Rare : 1 in 10,000 and <1 in 1,000.

< 1 in 10,000.

Within each frequency grouping, undesired effects are presented in order of decreasing seriousness. Cardiac disorders: Uncommon: Palpitations/arrhythmias (including bradycardia and tachycardia). Nervous system disorders: Very common: Headache, drowsiness. Common: Dizziness, abnormal taste. Very rare: Syncope







Very common :

1 in 10.

Common : 1 in 100 and <1 in 10.

Eye disorders: Very common : Ocular irritation including allergic reactions (hyperaemia, burning, stinging, pruritis, foreign body sensation, conjunctival follicles); blurred vision. Common : Local irritation (eyelid hyperaemia and oedema, blepharitis, conjunctival oedema and discharge, ocular pain and tearing); photophobia; corneal erosion and staining; ocular dryness; conjunctival blanching; abnormal vision; conjunctivitis. Very rare : Iritis (anterior uveitis); miosis. Respiratory, thoracic and mediastinal disorders: Common: Upper respiratory symptoms. Uncommon: Nasal dryness. Rare: Dyspnoea Gastrointestinal disorders: Very common: Oral dryness. Common: Gastrointestinal symptoms. Vascular disorders: Very rare: Hypertension, hypotension. General disorders and administration site conditions: Very common: Fatigue. Common: Asthenia. Immune system disorders: Uncommon: Systemic allergic reactions. Psychiatric disorders: Uncommon: Depression. Very rare: Insomnia. In cases where brimonidine has been used as part of the medical treatment of congenital glaucoma, symptoms of brimonidine overdose such as loss of consciousness, hypotension, hypotonia, bradycardia, hypothermia, cyanosis and apnoea have been reported in neonates and infants receiving brimonidine (see section 4.3). In a 3 month, phase 3 study in children aged 2 to 7 years with glaucoma, inadequately controlled by beta-blockers, a high prevalence of somnolence (55%) was reported with brimonidine eye drops as adjunctive treatment. In 8% of children, this was severe and led to discontinuation of treatment in 13%. The incidence of somnolence decreased with increasing age, being least in the 7-year-old age group (25%), but was

more affected by weight, occurring more frequently in those children weighing 20 kg (63%) compared to those weighing >20 kg (25%) (see section 4.4).

4.9

Overdose
Ophthalmic overdose: There is no experience in adults, as it is unlikely that overdose would be experienced via the ophthalmic route. However, 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. Systemic overdose resulting from accidental ingestion: Two cases of adverse effects following inadvertent ingestion of 9-10 drops of a brimonidine eye drop by adults have been reported; the subjects experienced a hypotensive episode, followed in one instance by rebound hypertension approximately 8 hours after ingestion. Both subjects were reported to have made a full recovery within 24 hours. No adverse effects were noted in a third subject who also ingested an unknown amount of brimonidine eye drops orally. Reports of serious adverse effects following inadvertent ingestion of brimonidine eye drops have been published/reported. The subjects experienced symptoms of CNS depression, typically temporary coma or low level of consciousness, hypotonia, bradycardia, hypothermia and apnoea, and required admission to intensive care with intubation if indicated. All subjects were reported to have made a full recovery, usually within 6-24 hours. Oral overdoses of other alpha-2-agonists have been reported to cause symptoms such as hypotension, asthenia, vomiting, lethargy, sedation, bradycardia, arrhythmias, miosis, apnoea, hypotonia, hypothermia, respiratory depression and seizure.

5
5.1

Pharmacodynamic properties
ATC code, S01E A 05. Sympathomimetics in glaucoma therapy. Brimondine is an alpha-2 adrenergic receptor agonist that is 1000-fold more selective for the alpha-2 adrenoceptor than the alpha-1 adrenoceptor. This selectivity results in no mydriasis and the absence of vasoconstriction in microvessels associated with human retinal xenografts. Topical administration of brimonidine tartrate decreases intraocular pressure in humans with minimal effect on cardiovascular or pulmonary parameters.



PHARMACOLOGICAL PROPERTIES

Limited data are available for patients with bronchial asthma showing no adverse effects. Brimonidine has a rapid onset of action, with peak ocular hypotensive effect seen at 2 hours post-dosing. In two 1 year studies, brimonidine has been shown to lower intraocular pressure by mean values of approximately 4-6 mmHg. Flourophotometric studies in animals and humans suggest that brimonidine tartrate has a dual mechanism of action. It is thought that it may lower intraocular pressure by reducing aqueous humour formation and enhancing uveoscleral outflow. Clinical trials show that brimonidine eye drops are effective in combination with topical beta-blockers. Shorter term studies also suggest that brimonidine eye drops have a clinically additive effect in combination with travoprost (6 weeks) and latanoprost (3 months).

5.2

Pharmacokinetic properties
a) General characteristics: It is reported that after ocular administration of a 0.2% solution twice daily for 10 days, plasma concentrations are low (mean Cmax 0.06 ng/ml). There is a slight accumulation in the blood after multiple instillations (twice daily for 10 days). AUC0-12h at steady stated is reported as 0.31 nghr/ml, compared to 0.23 nghr/ml after the initial dose. The mean apparent half-life in the systemic circulation was approximately 3 hours in humans after topical dosing. Plasma protein binding of brimonidine after topical dosing in humans is approximately 29%. Brimonidine binds reversibly to melanin in ocular tissues, in vitro and in vivo. It is reported that following 2 weeks of ocular instillation, the concentrations of brimonidine in iris, ciliary body and choroid-retina were 3- to 17-fold higher than those after a single dose. Accumulation does not occur in the absence of melanin. The significance of melanin binding in humans is unclear, however, no significant ocular adverse reaction was found during biomicroscopic examination of eyes in patients treated with brimonidine eye drops for up to one year, nor was significant ocular toxicity found during a one year ocular safety study in monkeys given approximately 4 times the recommended dose. Following oral administration to man, brimonidine is well absorbed and rapidly eliminated. The major part of the dose (around 75%) is excreted as metabolites in urine within 5 days; no unchanged drug was detected in urine. In-vitro studies, using animal and human liver, indicate that the metabolism is mediated largely by aldehyde oxidase and cytochrome P450. Hence, the systemic elimination seems to be primarily hepatic metabolism. Kinetics profile: No great deviation from dose proportionality for plasma Cmax and AUC has been observed following a single topical dose of 0.08%, 0.2% and 0.5%. b) Characteristics in patients:

The Cmax, AUC, and apparent half-life of brimonidine are similar in the elderly (subjects 65 years or older) after a single dose compared with young adults, indicating that its systemic absorption and elimination are not affected by age. Based on data from a 3 months clinical study, which included elderly patients, it is reported that systemic exposure to brimonidine was very low.

5.3

Preclinical safety data
Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, genotoxicty, carcinogenic potential, toxicity to reproduction.

6
6.1

PHARMACEUTICAL PARTICULARS
List of excipients
Benzalkonium chloride Polyvinyl alcohol Sodium citrate Citric acid anhydrous Sodium chloride Sodium hydroxide (to adjust pH) Purified Water (water for injection)

6.2

Incompatibilities
Not applicable

6.3

Shelf life
Before first opening : 2 years. After first opening : 28 days.

6.4

Special precautions for storage
Before and after first opening (see section 6.3): Do not store above 25C. Do not refrigerate.

6.5

Nature and contents of container
5 ml low density polyethylene dropper bottle with polystyrene cap.

6.6

Special precautions for disposal
None.

7

MARKETING AUTHORISATION HOLDER
FDC International Ltd Unit 6, Fulcrum 1 Solent Way, Whiteley Fareham Hampshire PO15 7FE

8

MARKETING AUTHORISATION NUMBER(S)
PL 15872/0018

9

DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
26/03/2010

10

DATE OF REVISION OF THE TEXT
26/03/2010

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Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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