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Desloratadine 5 Mg Film-Coated Tablets

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Document: leaflet MAH GENERIC_PL 24837-0035 change

1. WHAT DESLORATADINE IS AND WHAT IT IS USED FOR


2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE DESLORATADINE


3. HOW TO TAKE DESLORATADINE


3fp    PACKAGE LEAFLET:

INFORMATION FOR THE USER

CONSILIENT HEALTH u

Desloratadine 5 mg

film-coated tablets

desloratadine

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

•    Keep this leaflet. You may need to read it again.

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

•    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.

•    If you getany side effects, talk to your doctor, pharmacist or nurse.This includes any possible side effects not listed in this leaflet. See section 4.

What is in this leaflet

1.    What Desloratadine is and what it is used for

2.    What you need to know before you take Desloratadine

3.    Howto take Desloratadine

4.    Possible side effects

5.    Howto store Desloratadine

6.    Contents of the pack and other information

What Desloratadine is

Desloratadine is an antihistamine.

How Desloratadine works

Desloratadine is an anti-allergy medicine that does not

make you drowsy. It helps control your allergic reaction and its symptoms.

When Desloratadine should be used

Desloratadine relieves symptoms associated with allergic rhinitis (inflammation of the nasal passages caused by an allergy, for example, hay fever or allergy to dust mites) in adults and adolescents 12 years of age or older. These symptoms include sneezing, runny or itchy nose, itchy palate, and itchy, red or watery eyes.

Desloratadine is also used to relieve the symptoms associated with urticaria (a skin condition caused by an allergy).These symptoms include itching and hives.

Relief of these symptoms lasts a full day and helps you to resume your normal daily activities and sleep.

Do not take Desloratadine

•    if you are allergic to desloratadine, to any of the other ingredients of this medicine (listed in section 6) or to loratadine.

Warnings and precautions

Talkto your doctor or pharmacist before taking Desloratadine

•    if you have poor kidney function.

Use in children and adolescents

Do not give this medicine to children less than 12 years of age.

Other medicines and Desloratadine

There are no known interactions of Desloratadine with other medicines.

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.

Desloratadine with food, drink and alcohol

Desloratadine may be taken with or without a meal.

Use in caution when taking desloratadine with alcohol.

Pregnancy, breast feeding and fertility

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine

Taking Desloratadine is not recommended if you are pregnant or nursing a baby.

Fertility

There is no data available on male/female fertility. Driving and using machines

At the recommended dose, this medicine is not expected to affect your ability to drive or use machines. Although most people do not experience drowsiness, it is recommended not to engage in activities requiring mental alertness, such as driving a car or operating machinery until you have established your own response to the medicinal product.

Desloratadine contains lactose

Desloratadine tablets contain lactose. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

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

Adults and adolescents 12 years of age and over

The recommended dose is one tablet once a day with water, with or without food.

This medicine is for oral use.

Swallow the tablet whole.

Regarding the duration of treatment, your physician will determine the type of allergic rhintisyou are suffering from and will determine for how long you should take Desloratadine.

If your allergic rhinitis is intermittent (presence of symptoms for less than 4 days per week or for less than 4 weeks), your physician will recommend you a treatment schedule that will depend on the evaluation of the history of your disease.

If your allergic rhinitis is persistent (presence of symptoms for 4 days or more per week and for more than 4 weeks), your physician may recommend you a longer term treatment.

For urticaria, the duration of treatment may be variable from patient to patient and therefore you should follow the instructions of your physician.

If you take more Desloratadine than you should

Take Desloratadine only as it is prescribed for you. No serious problems are expected with accidental overdose. However, if you take more Desloratadine than you were told to, contact your doctor pharmacist, or nurse immediately.

If you forget to take Desloratadine

If you forget to take your dose on time, take it as soon as possible, then go back to your regular dosing schedule. Do not take a double dose to make up for a forgotten dose.

If you stop taking Desloratadine

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

4. POSSIBLE SIDE EFFECTS


5. HOWTO STORE DESLORATADINE


6. CONTENTS OF THE PACK AND OTHER INFORMATION


Like all medicines, this medicine can cause side effects, although not everybody gets them.

During the marketing of Desloratadine, cases of severe allergic reactions (difficulty in breathing, wheezing, itching, hives and swelling) have been reported very rarely. If you notice any of these serious side effects, stop taking the medicine and seek urgent medical advice straight away.

In clinical studies in adults, side effects were about the same as with a dummy tablet. However, fatigue, dry mouth and headache were reported more often than with a dummy tablet. In adolescents, headache was the most commonly reported side effect.

In clinical studies with desloratadine, the following side effects were reported as:

Common: the following may affect up to 1 in 10 people

•    fatigue • dry mouth • headache

Adults

During the marketing of Desloratadine, the following side effects were reported as:

Very rare: the following may affect upto 1 in 10,000 people:

•    severe allergic reactions • pounding or irregular heatbeat • fast heartbeat • stomach ache • feeling sick (nausea) • vomiting • upset stomach • diarrhoea

•    dizziness • drowsiness • inability to sleep • muscle pain

•    hallucinations • seizures • restlessness with increased body movement • rash • liver inflammation

•    abnormal liver function tests.

Not known: frequency cannot be estimated from the available data

•    unusual weakness • yellowing of the skin and/or eyes

•    increased sensitivity of the skin to the sun, even in case of hazy sun, and to UV light, for instance to UV lights of a solarium • change in the way the heart beats

Children

Not known: frequency cannot be estimated from the available data

•    slow heartbeat • change in the way the heart beats

Reporting of side effects

If you get any side effects, talk to your doctor 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.

Keep this medicine out of the sight and reach of children.

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

Store in the original package in order to protect from moisture.

After first opening of the tablet container, the medicinal product should be used within 3 months.

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

What Desloratadine contains

•    The active substance is desloratadine. Each film-coated tablet contains 5 mg desloratadine.

•    The other ingredients in the tablet core are: microcrystalline cellulose (E460), hypromellose (E464), hydrochloric acid (E507), sodium hydroxide (E524), maize starch, lactose monohydrate and talc (E553b).

•    The other ingredients in the film coating are: hypromellose (E464), macrogol, lactose monohydrate, titanium dioxide (El71) and indigo carminealuminium lake (El 32).

What Desloratadine looks like and contents of the pack

Light blue, round, film-coated tablets with bevelled edges (diameter 6.5 mm).

Desloratadine is available in carton boxes of 7,10,20,30, 50,90 and 100 film-coated tablets in blisters and in plastic tablet containers of 250 film-coated tablets.

Not all pack sizes may be marketed.

Marketing Authorisation Holder

Consilient Health Ltd., 5th floor. Beaux Lane House, Mercer Street Lower, Dublin 2, Ireland

Manufacturers

KRKA, d.d.. Novo mesto, Smarjeska cesta 6,

8501 Novo mesto, Slovenia

TAD Pharma GmbH, Heinz-Lohmann-StraBe 5,

27472 Cuxhaven, Germany

This leaflet was last revised in October 2015.

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