Patient leaflet - Betoptic suspension single dose 0.25% w/v eye drops
1. WHAT BETOPTIC SUSPENSION SINGLE DOSE
IS AND WHAT IT IS USED FOR
BETOPTIC Suspension Single Dose belongs to a group of medicines known as beta blockers.
It is used to treat glaucoma or ocular hypertension (high pressure in the eye) by reducing the fluid pressure in your eye(s).
2. BEFORE YOU USE BETOPTIC SUSPENSION SINGLE DOSE
Do not use BETOPTIC Suspension Single Dose eye drops, suspension...
If you are allergic to betaxolol, beta-blockers or any of the other
ingredients listed in section 6.
If you have now or have had in the past, respiratory problems such
as severe asthma, severe chronic obstructive bronchitis (severe lung condition which may cause wheeziness, difficulty in breathing and/or long-standing cough).
If you have a slow heart beat, heart failure or disorders of heart
rhythm (irregular heartbeats).
Ask your doctor for advice.
Take special care...
Before you use this medicine, tell your doctor if you have now or have had in the past
coronary heart disease (symptoms can include chest pain or
tightness, breathlessness or choking), heart failure, low blood pressure (hypotension)
- disturbances of heart rate such as slow heart beat (bradycardia)
breathing problems, asthma or chronic obstructive pulmonary
disease (lung disease which may cause wheeziness, difficulty in breathing and/or long-standing cough)
poor blood circulation disease (such as Raynaud’s disease or
Raynaud’s syndrome)
diabetes, as betaxolol may mask the signs and symptoms of low
blood sugar
overactivity of the thyroid gland as betaxolol may mask the signs
and symptoms
muscle weakening disease such as myasthenia gravis. Your
symptoms may get worse
- angle-closure glaucoma
- dry eyes (Sicca Syndrome)
Tell your doctor before you have an operation that you are using Betoptic as betaxolol may change the effects of some medicines used during anaesthesia.
If any of these apply you may still be able to use BETOPTIC Suspension Single Dose, but discuss it with your doctor first.
Using other medicines
BETOPTIC Suspension Single Dose can affect or be affected by other medicines you are using including other eye drops for the treatment of glaucoma. Tell your doctor if you are using or intend to use medicines to lower blood pressure, heart medicine, medicines to treat diabetes or medicines to treat emotional, behavioural or mental disorders such as anxiety or depression.
BETOPTIC Suspension Single Dose may reduce the effectiveness of adrenaline, which can be used to treat serious allergic reactions
(anaphylaxis). Tell your doctor if you have a history of anaphylaxis or allergic reactions.
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.
If you are using more than one type of eye drop, wait 5 minutes between using each one. Eye ointments should be administered last.
Pregnancy and breast-feeding
Do not use BETOPTIC Suspension Single Dose if you are pregnant unless your doctor considers it necessary.
Do not use BETOPTIC Suspension Single Dose if you are breast- feeding. Betaxolol may get into your breast milk.
Ask your doctor for advice before taking any medicine during breast- feeding.
Driving and using machines
If your sight is affected in any way following the use of BETOPTIC Suspension Single Dose, you should not drive or operate machinery.
Important information if you wear Contact Lenses
Do not use the drops while wearing contact lenses. Wait at least 15 minutes after use before putting your lenses back in.
3. HOW TO USE BETOPTIC SUSPENSION SINGLE DOSE
BETOPTIC Suspension Single Dose should only be used in the eye(s).
The usual dose is...
The usual dose is 1 drop in the affected eye(s) twice daily.
Not recommended for use in CHILDREN.
Always use BETOPTIC Suspension Single Dose exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.
How to use
- Wash your hands before you start.
Open the foil pouch, remove the
plastic vial and shake well (picture 1)
Twist off the cap of the plastic vial
(picture 2)
- Hold the vial upside down.
- Tilt your head back.
Pull down your lower eyelid with a
finger, until there is a 'pocket'
between the eyelid and your eye.
The drop will go in here.
- Bring the tip of the vial close to the eye. Do this in front of a mirror if it helps.
Do not touch your eye or eyelid,
surrounding areas or other surfaces
with the tip of the vial. It could infect
the drops.
Gently squeeze the vial so that one
drop falls into the gap between the
eye and the lower lid (picture 3).
437871GB 330PIL01
2841
2841
Product name: Betoptic S
Strength: 0.25%
Formulation: Eyedrops
Countries: UK
Braille: N/A
Component: Leaflet
Printing colours:
Dimensions: 178x274 mm
Internal article no.: 0330PIL01
External article no.: 437871 GB
Version: 01
Data changed: 2022-12-05
Release the lower eyelid. After using BETOPTIC Suspension Single
Dose, press a finger into the corner of your eye by the nose (picture 4) for 2 minutes. This helps to stop betaxolol getting into the rest of the body.
If you use drops in both eyes, repeat
the steps for your other eye.
Dispose of the vial after use. Do not keep
to use again.
If a drop misses your eye,
try again.
If you miss a dose, just take it
as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule.
Do not use a double dose to make up for a missed dose.
If you use more BETOPTIC Suspension Single Dose than you
should it can be washed out of your eye with warm water. If you have any further questions on the use of BETOPTIC Suspension Single Dose, ask your doctor or pharmacist.
4. POSSIBLE SIDE EFFECTS
Like all medicines, BETOPTIC Suspension Single Dose can cause side effects, although not everybody gets them.
You can usually carry on taking the drops, unless the effects are serious. If you are worried, talk to a doctor or pharmacist. Do not stop using BETOPTIC Suspension Single Dose without speaking to your doctor.
Like other medicines applied into eyes, betaxolol is absorbed into the blood. This may cause similar side effects as seen with beta-blockers given by injection or taken by mouth. Incidence of side effects after beta-blockers are used in the treatment of eye conditions is lower than when medicines are, for example, taken by mouth or injected. Listed side effects include reactions seen following treatment with Betaxolol eye drops and within the class of other beta-blockers used for treating eye conditions.
Side effects experienced by patients during clinical trials with BETOPTIC Suspension Single Dose are:
Very common: may affect more than 1 in 10 users
- Eye discomfort (includes a feeling of something in the eye)
Common (affects 1 to 10 users in 100):
- Blurred vision, watery eyes
- Headache
Uncommon (affects 1 to 10 users in 1000):
Inflammation of the eye surface, conjunctivitis or symptoms
of conjunctivitis, visual impairment, sensitivity to light, painful, dry or tired eyes, excessive blinking, irritated, red or swollen eyes, a feeling of something in the eye, eye itchiness eye discharge, weeping eyelids, bloodshot eyes
- Slow heart beat or unusually rapid heart beat
- Asthma, difficulty breathing, blocked nose
- Nausea
Rare (affects 1 to 10 users in 10,000):
Cataract formation, decreased sensitivity of the eye, inflammation
of the eyelid
- Anxiety, difficulty sleeping (insomnia), depression
- Fainting
- Low blood pressure
- Cough, runny nose
- Taste disturbances
- Inflamed, itchy skin or rash, hair loss
- Libido decreased
The following side effects have also been reported by people using BETOPTIC Suspension Single Dose. The frequency cannot be estimated from the available data:
- Hypersensitivity reaction
- Dizziness
- Changes in the rhythm or speed of the heartbeat
- Loss or lack of strength
Additional side effects have been seen with other ophthalmic beta-blockers and could potentially occur with BETOPTIC Suspension Single Dose. The frequency is unknown:
Generalised allergic reactions including swelling beneath the skin
(that can occur in areas such as the face and limbs, and can obstruct the airway which may cause difficulty swallowing or breathing), hives (or itchy rash), localised and generalised rash, itchiness, severe sudden life-threatening allergic reaction.
- Low blood glucose levels.
- Nightmares, memory loss, hallucinations, delusions and confusion.
- Stroke, reduced blood supply to the brain, increases in signs and symptoms of myasthenia gravis (muscle disorder), unusual sensations (like pins and needles).
- Detachment of the layer below the retina that contains blood vessels following filtration surgery which may cause visual disturbances, corneal erosion (damage to the front layer of the eyeball), drooping of the upper eyelid (making the eye stay half closed), double vision.
Chest pain, palpitations, oedema
(fluid build-up), congestive heart
failure (heart disease with
shortness of breath and swelling
of the feet and legs due to fluid
build-up), a type of heart rhythm
disorder, heart attack, heart
failure.
Raynaud's phenomenon, cold
hands and feet with a blue
colour, leg pains (especially if
you have a history of poor
circulation).
Constriction of the airways in the
lungs (predominantly in patients with pre-existing disease).
- Indigestion, diarrhoea, dry mouth, abdominal pain, vomiting.
Skin rash with white silvery coloured appearance (psoriasiform rash)
or worsening of psoriasis.
- Muscle pain not caused by exercise.
- Sexual dysfunction, impotence.
- Tiredness.
An increased in Anti Nuclear Antibodies has also been seen in patients taking ophthalmic beta blockers.
Reporting of side effects
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system listed below. By reporting side effects, you can help provide more information on the safety of this medicine.
United Kingdom - Yellow Card Scheme
Website: www.mhra.gov.uk/yellowcard
Ireland - HPRA Pharmacovigilance
Earlsfort Terrace, IRL - Dublin 2; Tel: +353 1 6764971
Fax: +353 1 6762517. Website: www.hpra.ie; E-mail: medsafety@hpra.ie.
5. HOW TO STORE BETOPTIC SUSPENSION SINGLE DOSE
- Keep out of the reach and sight of children.
- Do not store above 25°C.
- Do not freeze.
- Store in the original package in order to protect from light.
- Do not use the drops after the expiry date (marked 'Exp') on the sachet and the carton. The expiry date refers to the last day of that month.
- Once opened, use immediately.
- Dispose of the vial after use. Do not keep an open vial to use again.
- Medicines should not be disposed of via waste water or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.
- Do not pass this medicine on to others. It may harm them even if their symptoms are the same as yours.
6. FURTHER INFORMATION
What BETOPTIC Suspension Single Dose contains
- The active substance is betaxolol 0.25% w/v (2.5 mg/ml) (as the hydrochloride). Each single dose dispenser contains 625 micrograms of betaxolol (as the hydrochloride).
The other ingredients are amberlite (Poly (styrene divinyl benzene)
sulphonic acid), carbomer, mannitol, hydrochloric acid and/or sodium hydroxide (to adjust pH) and purified water.
What BETOPTIC Suspension Single Dose looks like and contents of the pack
BETOPTIC Suspension Single Dose is a white to off-white liquid supplied in a plastic single-dose dispenser containing 0.25 ml. Five dispensers are enclosed in a foil overwrap. Each pack contains 50 single dose dispensers.
Suitable for people who are sensitive to preservatives. Marketing authorisation holder:
Immedica Pharma AB
SE-113 63 Stockholm, Sweden
Manufacturer:
Kaysersberg Pharmaceuticals, 23 avenue Georges Ferrenbach, F-68240 Kaysersberg, France
This leaflet was last revised in 10/2022
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