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Latanoprost/Timolol 50 Micrograms/Ml And 5 Mg/Ml Eye Drops Solution

Informations for option: Latanoprost/Timolol 50 Micrograms/Ml And 5 Mg/Ml Eye Drops Solution, show other option

RPXP260BNA

PACKAGE LEAFLET: INFORMATION FOR THE USER

LATANOPROST/TIMOLOL 50 micrograms/ml and 5mg/ml eye drops, solution latanoprost/timolol

Read all of this leaflet carefully before you start using this medicine because it contains important information for you.

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-    If you have any further questions, ask your doctor or pharmacist.

-    This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.

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includes any side effects not listed in this leaflet. See section 4.

What is in this leaflet:

1.    What Latanoprost/Timolol is and what it is used for

2.    What you need to know before you use Latanoprost/Timolol

3.    How to use Latanoprost/Timolol

4.    Possible side effects

5.    How to store Latanoprost/Timolol

6.    Contents of the pack and other information

1.    WHAT LATANOPROST/TIMOLOL IS AND WHAT IT IS USED FOR

Latanoprost/Timolol is a medicine for the treatment of increased intraocular pressure (pressure inside the eye).

Latanoprost/Timolol is a drug combination containing two active substances: latanoprost (a prostaglandin derivative) and timolol maleate (a beta-blocker).

Fluid known as aqueous humour is produced inside the eye. This fluid is

then drained back into the bloodstream, thereby maintaining the required pressure within the eye. If this outflow is obstructed, pressure within the eye

increases.

Among other things, beta-blockers reduce pressure inside the eye, by reducing the production of aqueous humour. Prostaglandins promote the outflow of aqueous humour.

Latanoprost/Timolol is used:

-    to reduce inner eye pressure in patients with open-angle glaucoma (damage to the optic nerve, caused by excessive pressure within the eye).

-    to reduce inner eye pressure in patients for whom the effect of beta-blockers or prostaglandin derivaties alone is not sufficient

2.    WHAT YOU NEED TO KNOW BEFORE YOU USE LATANOPROST/TIMOLOL

Do not use Latanoprost/Timolol eye drops, solution

-    if you are allergic to latanoprost or timolol, beta-blockers or any of the other ingredients of Latanoprost/Timolol (listed in section 6)

-    if you have now or have had in past respiratory problems such as asthma, severe chronic obstructive bronchitis (severe lung disease which may cause wheeziness, difficulty in breathing and/or long-standing cough)

-    if you have serious heart problems or heart rhythm disorders

-    if you are pregnant (or trying to become pregnant)

-    if you are breast-feeding.

Warnings and precautions

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

-    disturbances of heart rate such as slow heart beat

-    breathing problems, asthma or chronic obstructive pulmonary disease

-    poor blood circulation disease (such as Raynaud's disease or Raynaud's syndrome)

-    diabetes as timolol may mask signs and symptoms of low blood sugar

-    overactivity of the thyroid gland as timolol may mask signs and symptoms

-    any kind of eye surgery (including cataract surgery)

-    eye problems (such as eye pain, eye irritation, eye inflammation or blurred vision)

-    dry eyes

-    wear contact lenses. You can still use Latanoprost/Timolol but follow the instructions for contact lens wearers in section "Latanoprost/Timolol contains”

-    angina (particularly a type known as Prinzmetal angina)

-    severe allergic reactions that would usually require hospital treatment

-    you have suffered or are currently suffering from a viral infection of the eye caused by the herpes simplex virus (HSV)

Tell your doctor before you have an operation that you are using Latanoprost/Timolol as latanoprost/timolol may change effects of some medicines used during anaesthesia.

Other medicines and Latanoprost/Timolol

Latanoprost/Timolol 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 or medicines to treat diabetes.

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines (including eye drops).

Medicines can affect each other and interactions may occur. You must bear this in mind if you are taking or using any of the following types of medicine: Calcium antagonists (e.g. in coronary heart disease or for high blood pressure)

Guanethidine (for high blood pressure)

Beta-blockers (for high blood pressure)

Antiarrhythmics (medications that normalise the heart rhythm)

Digitalis glycosides (for heart failure)

Parasympathomimetic agents (e.g. for the treatment of glaucoma) Taking/using Latanoprost/Timolol together with the above medicines can cause low blood pressure and/or slow down the heart rate.

Medicines that act in a similar way to Latanoprost/Timolol If used at the same time as Latanoprost/Timolol, the effect of other medicines with a similar action to Latanoprost/Timolol may be increased.

For this reason, ophthalmic use (i.e. in the eye) of two beta-blockers or two prostaglandin derivatives is not recommended.

Clonidine

If you are using the active substance clonidine to reduce inner eye pressure together with Latanoprost/Timolol and you suddenly stop using clonidine, your blood pressure may rise. If you are also using beta-blockers at the same time to lower your blood pressure, your blood pressure may - due to this reverse effect - rise even further.

Quinidine (used to treat heart conditions and some types of malaria) Antidepressants known as fluoxetine and paroxetine

Children and adolescents

Latanoprost/Timolol is not recommended for children or adolescents.

Elderly patients

Latanoprost/Timolol is also suitable for the treatment of elderly patients.

Pregnancy and breast-feeding and fertility

Pregnancy

Do not use Latanoprost/Timolol if you are pregnant unless your doctor considers it necessary.

Breast-feeding

Do not use Latanoprost/Timolol if you are breast-feeding. Latanoprost/ Timolol may get into your milk.

Ask your doctor or pharmacist for advice before taking any medicine during pregnancy or breast-feeding.

Driving and using machines

After putting in Latanoprost/Timolol eye drops, your vision may become temporarily impaired.

If you should experience blurred vision - particularly after just putting in Latanoprost/Timolol eye drops - you should

-    not drive any vehicles.

-    not use any tools or machines.

Latanoprost/Timolol contains

This medicinal product contains benzalkonium chloride which may cause eye irritation. Avoid contact with soft contact lenses. Remove contact lenses prior to application and wait at least 15 minutes before putting them back in. Benzalkonium chloride is known to discolour soft contact lenses.

3.    HOW TO USE LATANOPROST/TIMOLOL

Always use this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure.

Unless otherwise prescribed by the doctor, the usual dose is:

Adults, including elderly patients: insert one drop once a day into each affected eye.

If you are using other eye drops in addition to Latanoprost/Timolol, these should be used at least 5 minutes apart.

Directions for use

1.    Wash your hands and sit or stand in a comfortable position.

2.    Remove the outer protective cap from the bottle.

3.    Use your fingertip to gently pull down the lower lid of the affected eye.

4.    Place the tip of the bottle close to, but not touching the eye. Carefully squeeze the bottle until one drop falls into your eye. Please make sure that you do not squeeze the bottle too hard, so that no more than one drop falls into the affected eye.

5.    Let go of your eyelid.

6.    After using Latanoprost/Timolol press a finger into the corner of your eye, by the nose for 2 minutes.

This helps to stop latanoprost/timolol getting into the rest of the body.

If prescribed by your doctor, repeat the procedure in your other eye. If the drop should miss your eye, apply another drop.

7.    Close the bottle.

If you use more Latanoprost/Timolol than you should

If too many drops have gone into your eye, irritation and redness may occur. Tell a doctor immediately if you or anyone else has swallowed the eye drops by mistake, or if you have been using the drops more often than prescribed.

Keep the pack of this medicine ready, so that the doctor can find out more

about the medication. He/she will then decide what to do next.

If you forget to use Latanoprost/Timolol

If you have forgotten to use your eye drops, continue your treatment as normal at the next dose. The daily dose of one drop into the affected eye

should not be exceeded.

Do not use a double dose to make up for a forgotten dose.

If you stop using Latanoprost/Timolol

Do not interrupt or stop your treatment with Latanoprost/Timolol without talking to your doctor first.

If you do not use Latanoprost/Timolol regularly or if you frequently forget to use it, the success of your treatment may be at risk.

Increased intraocular pressure (pressure within the eye) can damage the optic nerve and worsen your eyesight. Blindness may occur. Normally, you can barely feel increased intraocular pressure. The disorder can only be diagnosed via an examination by an eye specialist. If you suffer from increased intraocular pressure, regular eye tests are necessary, together with measurements of inner eye pressure. Pressure within the eye should be measured at least every 3 months. Visual field measurements and optic nerve examinations should be performed at least once a year.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

4.    POSSIBLE SIDE EFFECTS

Like all medicines, this medicine can cause side effects, although not

everybody gets them.

You can usually carry on taking the eye drops, unless the effects are

serious. If you are worried, talk to a doctor or pharmacist. Do not stop using Latanoprost/Timolol without speaking to your doctor.

Listed below are the known side effects of using eye drops containing the active substances latanoprost and timolol. The most important side effect is the possibility of a gradual, permanent change in your eye colour. It is also possible that eye drops containing the active substances latanoprost and timolol might cause serious changes in the way your heart works. If you notice changes in your heart rate or heart function you should speak to a doctor and tell them you have been using Latanoprost/Timolol.

The frequency of possible side effects listed below is defined using the following convention:

Very common (may affect more than 1 in 10 people):

•    A gradual change in your eye colour by increasing the amount of brown pigment in the coloured part of the eye known as the iris. If you have mixed-colour eyes (blue-brown, grey-brown, yellow-brown or green-brown) you are more likely to see this change than if you have eyes of one colour (blue, grey, green or brown eyes). Any changes in your eye colour may take years to develop. The colour change may be permanent and may be more noticeable if you use Latanoprost/Timolol in only one eye. There appears to be no problems associated with the change in eye colour. The eye colour change does not continue after Latanoprost/Timolol treatment is stopped.

Common (may affect up to 1 in 10 people):

•    Eye irritation (a feeling of burning, grittiness, itching, stinging or the sensation of a foreign body in the eye) and eye pain.

Uncommon (may affect up to 1 in 100 people):

•    Headache.

•    Redness of the eye, eye infection (conjunctivitis), blurred vision, watery eyes, inflammation of the eyelids, irritation or disruption of the surface of

the eye

•    Skin rashes or itching (pruritus)

Other side effects

The following side effects have been seen with latanoprost:

Infections and Infestations:

•    Developing a viral infection of the eye caused by the herpes simplex virus (HSV)

Immune System Disorders:

•    Symptoms of allergic reaction (swelling and redness of the skin and rash). Psychiatric Disorders:

•    Depression, memory loss, decreased sex drive, inability to sleep, nightmares.

Nervous System Disorders:

•    Dizziness, tingling or numbness in the skin, changes in blood flow to the brain, worsening of symptoms of myasthenia gravis (if you already suffer

from this condition), sudden fainting or feeling you may faint (syncope).

Eye Disorders:

•    Changes to the eyelashes and fine hairs around the eye (increased

number, length, thickness and darkening), changes to the direction of eyelash growth, swelling around the eye, swelling of the coloured part of the eye (iritis/uveitus), swelling at the back of the eye (macular oedema), inflammation/irritation of the surface of the eye (keratitis), dry eyes, fluid filled cyst within the coloured part of the eye (iris cyst), light sensitivity (photophobia), sunken eye appearance (deepening of the eye sulcus).

Ear Disorders:

•    Whistling/ringing in the ears (tinnitus).

Heart (Cardiac) Disorders:

•    Worsening of angina, awareness of heart rhythm (palpitations).

Breathing (Respiratory) Disorders:

•    Asthma, worsening of asthma, shortness of breath.

Skin Disorders:

•    Darkening of the skin around the eyes.

Muscle and Skeletal Disorders:

•    Joint pain, muscle pain General Disorders:

•    Chest pain.

Like other medicines applied into eyes, Latanoprost/Timolol is absorbed into the blood. The timolol portion of this combination may cause similar side effects as seen with'intraveneous'and/or'oral'as applicable beta-blocking agents. Incidence of side effects after topical ophthalmic administration is lower than when medicines are, for example, taken by mouth or injected.

Listed side effects include reactions seen within the class of beta-blockers when used for treating eye conditions:

•    Generalized 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, localized and generalized rash, itchiness, severe sudden life-threatening allergic reaction.

•    Low blood glucose levels.

•    Difficulty sleeping (insomnia), depression, nightmares, memory loss.

•    Fainting, stroke, reduced blood supply to the brain, increases in signs and symptoms of myasthenia gravis (muscle disorder), dizziness, unusual sensations like pins and needles, and headache.

•    Signs and symptoms of eye irritation (e.g. burning, stinging, itching, tearing, redness), inflammation of the eyelid, inflammation in the cornea, blurred vision and detachment of the layer below the retina that contains blood vessels following filtration surgery which may cause visual disturbances, decreased corneal sensitivity, dry eyes, corneal erosion (damage to the front layer of the eyeball), drooping of the upper eyelid (making the eye stay half closed), double vision.

•    Slow heart rate, chest pain, palpitations, oedema (fluid build up), changes in the rhythm or speed of the heartbeat, 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.

•    Low blood pressure, Raynaud's phenomenon, cold hands and feet.

•    Constriction of the airways in the lungs (predominantly in patients with pre-existing disease), difficulty breathing, cough.

•    Taste disturbances, nausea, indigestion, diarrhoea, dry mouth, abdominal pain, vomiting.

•    Hair loss, skin rash with white silvery coloured appearance (psoriasiform rash) or worsening of psoriasis, skin rash.

•    Muscle pain not caused by exercise.

•    Sexual dysfunction, decreased libido.

•    Muscle weakness/tiredness.

In very rare cases, some patients with severe damage to the clear layer at the front of the eye (the cornea) have developed cloudy patches on the cornea due to calcium build-up during treatment.

Reporting of side effects

If you get any side effects, talk to your doctor, nurse or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.

By reporting side effects you can help provide more information on the safety of this medicine.

5.    HOW TO STORE LATANOPROST/TIMOLOL

Keep out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the bottle label and carton after "EXP”. The expiry date refers to the last day of that month.

Please note the following storage instructions:

Unopened bottles: Store in a refrigerator at 2°C - 8°C.

After the first opening of the bottle: Do not store above 25°C.

Once opened, you must discard the bottle - with any remaining contents -after 4 weeks. Otherwise, there is a risk of eye infection.

Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6.    CONTENTS OF THE PACK AND OTHER INFORMATION

What Latanoprost/Timolol contains

The active substances are: latanoprost and timolol maleate.

1 ml eye drops contains 50 micrograms of latanoprost and 6.8 mg of timolol maleate, equivalent to 5.0 mg timolol.

The other ingredients are:

Sodium chloride, benzalkonium chloride, sodium dihydrogen phosphate dihydrate, disodium hydrogen phosphate dodecahydrate, purified water, sodium hydroxide for pH adjustment and hydrochloric acid for pH adjustment.

What Latanoprost/Timolol looks like and contents of the pack

Latanoprost/Timolol is a clear, colourless liquid packed in a transparent dropper bottle with a screw cap.

Latanoprost/Timolol is available in the following pack sizes:

1 dropper bottle containing 2.5 ml eye drops,

3 dropper bottles, each containing 2.5 ml eye drops,

6 dropper bottles, each containing 2.5 ml eye drops.

Not all pack sizes may be marketed.

Marketing Authorisation Holder

Beacon Pharmaceuticals Ltd., 85 High Street, Tunbridge Wells, TN1 1YG, UK. Manufacturer

S.C. ROMPHARM COMPANY S.R.L., Eroilor Street, no. 1A, Otopeni 075100, IIfov., Romania

This leaflet was last revised 07/2015.

RPXP260BNA

PHARMACEUTICALS