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Tiotropium 18 Microgram Inhalation Powder Hard Capsule

Document: leaflet MAH BRAND_PLPI 08929-0276 change

SPIRIVA® 18 MICROGRAM INHALATION POWDER, HARD CAPSULES/ TIOTROPIUM 18 MICROGRAM INHALATION POWDER, HARD CAPSULE

_(tiotropium bromide)_


Common:

Uncommon:

Rare:

Not known:


POM


PACKAGE LEAFLET: INFORMATION FOR THE USER

Your medicine is available using the above names but will be referred to as Spiriva throughout this leaflet.

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 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.

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

What is in this leaflet:

1.    What Spiriva is and what it is used for

2.    What you need to know before you take Spiriva

3.    How to take Spiriva

4.    Possible side effects

5.    How to store Spiriva

6.    Contents of the pack and other information

1.    WHAT SPIRIVA IS AND WHAT IT IS USED FOR

Spiriva helps people who have chronic obstructive pulmonary disease (COPD) to breathe more easily. COPD is a chronic lung disease that causes shortness of breath and coughing. The term COPD is associated with the conditions chronic bronchitis and emphysema. As COPD is a chronic disease you should take Spiriva every day and not only when you have breathing problems or other symptoms of COPD.

Spiriva is a long-acting bronchodilator that helps to open your airways and makes it easier to get air in and out of the lungs. Regular use of Spiriva can also help you when you have on-going shortness of breath related to your disease and will help you to minimise the effects of the disease on your everyday life. It also helps you to be active longer. Daily use of Spiriva will also help to prevent sudden, shortterm worsening of your COPD symptoms which may last for several days. The effect of this medicine lasts for 24 hours, so you only need to take it once a day. For correct dosing of Spiriva please see section 3. How to take Spiriva and the instructions for use provided on the other side of the leaflet.

2.    WHAT YOU NEED TO KNOW BEFORE YOU TAKE SPIRIVA

Please read the following questions carefully. If you can answer any of these questions with "Yes" please discuss this with your doctor before taking Spiriva

•    are you allergic to tiotropium, atropine or similar drugs such as ipratropium or oxitropium or to milk protein?

•    are you taking any other medicinal products containing ipratropium or oxitropium?

•    are you pregnant, do you think you are pregnant, or are you breast-feeding?

•    are you suffering from narrow angle glaucoma, prostate problems or have difficulty passing urine?

•    do you have any kidney problems?

•    have you suffered from a myocardial infarction during the last 6 months or from any unstable or life threatening irregular heart beat or severe heart failure within the past year?

Do not take Spiriva

You should not use Spiriva if you are allergic (hypersensitive) to tiotropium, its active ingredient, or to lactose monohydrate which contains milk protein.

You should also not use Spiriva if you are allergic (hypersensitive) to atropine or substances related to it, e.g. ipratropium or oxitropium.

Warnings and precautions

•    Talk to your doctor if you suffer from narrow angle glaucoma, prostate problems or have difficulty passing urine.

•    If you have problems with your kidneys, please consult your doctor.

•    Spiriva is indicated for maintenance treatment of your chronic obstructive pulmonary disease, it should not be used to treat a sudden attack of breathlessness or wheezing.

•    Immediate allergic reactions such as rash, swelling, itching, wheezing or breathlessness may occur after administration of Spiriva. If this occurs, please consult your doctor immediately.

•    Inhaled medicines such as Spiriva may cause tightness of the chest, coughing, wheezing or breathlessness immediately after inhalation. If this occurs, please consult your doctor immediately.

•    Take care not to let the inhalation powder enter your eye as this may result in precipitation or worsening of narrow-angle glaucoma, which is a disease of the eyes. Eye pain or discomfort, blurred vision, seeing halos around lights or coloured images in association with red eyes may be signs of an acute attack of narrow-angle glaucoma. Eye symptoms may be accompanied by headache, nausea or vomiting. You should stop using tiotropium bromide and immediately consult your doctor, preferably an eye specialist, when signs and symptoms of narrow-angle glaucoma appear.

•    Dry mouth, which has been observed with anti-cholinergic treatment, may in the long term be associated with dental caries. Therefore, please remember to pay attention to oral hygiene.

•    In case you have suffered from a myocardial infarction during the last 6 months or from any unstable or life threatening irregular heart beat or severe heart failure within the past year, please, inform your doctor. This is important to decide if Spiriva is the right medicine for you to take.

•    Do not take Spiriva more frequently than once daily.

Children and adolescents

Spiriva is not recommended for children and adolescents under 18 years.

Other medicines and Spiriva

Please inform your doctor or pharmacist if you are taking, or have recently taken, any other medicines, even those not prescribed.

Please tell your doctor or pharmacist if you are taking/have taken similar medicines for your lung disease, such as ipratropium or oxitropium.

No specific side effects have been reported when Spiriva has been taken together with other products used to treat COPD such as reliever inhalers, e.g. salbutamol, methylxanthines, e.g. theophylline and/or oral and inhaled steroids e.g. prednisolone.

Pregnancy and breast-feeding

If you are pregnant or believe you are pregnant, or if you are breast-feeding, consult with your doctor. You should not use this medicine unless specifically recommended by your doctor.

Driving and using machines

The occurrence of dizziness, blurred vision, or headache may influence the ability to drive and use machinery.

Spiriva contains lactose monohydrate

When taken according to dosage recommendations, one capsule once a day, each dose supplies up to 5.5mg lactose monohydrate.

3.    HOW TO TAKE SPIRIVA

Follow your doctor's instructions about when and how to take your medicine. If you are unsure ask your doctor or pharmacist.

The recommended dose is to inhale the contents of 1 capsule (18 micrograms of tiotropium) once a day. Do not take more than the recommended dose.

Spiriva is not recommended for children and adolescents under 18 years.

You should try to take the capsule at the same time every day. This is important because Spiriva is effective over 24 hours.

The capsules are only for inhalation and not for oral intake. Do not swallow the capsules.

The HandiHaler device, which you should put the Spiriva capsule into, makes holes in the capsule and allows you to breathe in the powder.

Make sure that you have a HandiHaler and that you can use it properly. The instructions for use of the HandiHaler are provided on the other side of this leaflet.

Make sure that you do not blow into the HandiHaler.

If you have any problems using the HandiHaler, ask your doctor, nurse or pharmacist to show you how it works.

You should clean your HandiHaler once a month. Cleaning instructions for the HandiHaler are provided on the other side of this leaflet.

When taking Spiriva, take care not to let any of the powder enter your eyes. If any powder does get into your eyes you may get blurred vision, eye pain and/or red eyes, you should wash your eyes in warm water immediately. Then talk to your doctor immediately for further advice.

If you feel that your breathing is worsening, you should tell your doctor as soon as possible.

If you take more Spiriva than you should

If you inhale from more than 1 capsule of Spiriva in a day, you should talk to your doctor immediately. You may be at a higher risk of experiencing a side effect such as dry mouth, constipation, difficulties passing urine, increased heart beat, or blurred vision.

If you forget to take Spiriva

If you forget to take a dose, take one as soon as you remember but do not take two doses at the same time or on the same day. Then take your next dose as usual.

If you stop taking Spiriva

Before you stop taking Spiriva, you should talk to your doctor or your pharmacist. If you stop taking Spiriva the signs and symptoms of COPD may worsen.

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

4. POSSIBLE SIDE EFFECTS

Like all medicines, this medicine can cause side effects, although not everybody gets them. Evaluation of the side effects is based on the following frequencies:

may affect up to 1 in 10 people

may affect up to 1 in 100 people

may affect up to 1 in 1,000 people

frequency cannot be estimated from the available data

The side effects described below have been experienced by people taking this medicine and they are listed according to frequency as either common, uncommon, rare or not known.

Common:

•    Dry mouth: this is usually mild

Uncommon:

•    Dizziness

•    Headache

•    Taste disorders

•    Blurred vision

•    Irregular heart beat (atrial fibrillation)

•    Sore throat (pharyngitis)

•    Hoarseness (dysphonia)

•    Cough

•    Heart burn (gastrooesophageal reflux disease)

•    Constipation

•    Fungal infections of the oral cavity and throat (oropharyngeal candidiasis)

•    Rash

•    Difficulty passing urine (urinary retention)

•    Painful urination (dysuria)

Rare:

•    Difficulty in sleeping (insomnia)

•    Seeing halos around lights or coloured images in association with red eyes (glaucoma)

•    Increase of the measured eye pressure

•    Irregular heart beat (supraventricular tachycardia)

•    Faster heart beat (tachycardia)

•    Feeling your heart beat (palpitations)

•    Tightness of the chest, associated with coughing, wheezing or breathlessness immediately after inhalation (bronchospasm)

•    Nosebleed (epistaxis)

•    Inflammation of the larynx (laryngitis)

•    Inflammation of the sinuses (sinusitis)

•    Blockage of intestines or absence of bowel movements (intestinal obstruction including ileus paralytic)

•    Inflammation of the gums (gingivitis)

•    Inflammation of the tongue (glossitis)

•    Difficulties swallowing (dysphagia)

•    Inflammation of the mouth (stomatitis)

•    Feeling sick (nausea)

•    Allergic reactions (hypersensitivity), including immediate reactions

•    Serious allergic reaction which causes swelling of the face or throat (angioedema)

•    Nettle rash (urticaria)

•    Itching (pruritus)

•    Infections of the urinary tract

Not known:

• Depletion of body water (dehydration)

• Tooth decay (dental caries)

•    Severe allergic reaction (anaphylactic reaction)

•    Infections or ulcerations of the skin

•    Dryness of the skin

•    Swelling of joints

Serious side effects include allergic reactions which cause swelling of the face or throat (angioedema) or other hypersensitivity reactions (such as sudden reduction of your blood pressure or dizziness) may occur individually or as part of severe allergic reaction (anaphylactic reaction) after administration of Spiriva. In addition, in common with all inhaled medicines, some patients may experience an unexpected tightness of the chest, coughing, wheezing or breathlessness immediately after inhalation (bronchospasm). If any of these occur, please consult your doctor immediately.

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.

5.    HOW TO STORE SPIRIVA

•    Keep out of the sight and reach of children.

•    Do not use Spiriva after the expiry date which is stated on the carton and blister foil or 9 days after opening the blister strip. The expiry date refers to the last day of that month.

•    Once you have taken your first capsule from the blister strip, you must continue to take the capsules for the next 9 days, one capsule a day, from the same strip.

•    Do not store above 25°C. Do not freeze. Protect from direct sunlight and heat.

•    Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

•    If your doctor decides to stop treatment, return any left over capsules to your pharmacist. Only keep them if your doctor tells you to.

•    If your capsules appear to be discoloured or show any other signs of deterioration, please return to your pharmacist who will advise you.

6.    CONTENTS OF THE PACK AND OTHER INFORMATION

What Spiriva contains

Each inhalation capsule contains 18 micrograms of the active ingredient tiotropium (as bromide monohydrate).

The capsule also contains the inactive ingredient Lactose monohydrate.

The capsules contain powder, which should be breathed in using the HandiHaler device.

What Spiriva looks like and contents of the pack

The capsules are light green hard capsules, containing a white or yellowish white powder, with 'TI 01' and company logo printed on the capsules.

The HandiHaler device is light grey with 'HandiHaler' & 'Boehringer Ingelheim Logo' printed on the front. Lot/number & Boehringer address printed on the back. The HandiHaler device comprises of a dust cap, mouthpiece, piercing button and clear plastic centre chamber.

The HandiHaler is the device, which must be used with Spiriva.

Your medicine is available in packs of 30 capsules or 30 capsules with a HandiHaler device.

Manufacturer

The manufacturer of Spiriva is:

Boehringer Ingelheim Pharma GmbH & Co. KG, Ingelheim am Rhein, Germany. Procured from within the EU and repackaged by:

Doncaster Pharmaceuticals Group Ltd, Kirk Sandall, Doncaster, DN3 1QR.

Product Licence holder: BR Lewis Pharmaceuticals Ltd, Kirk Sandall, Doncaster, DN3 1QR.

PL No: 08929/0276

Leaflet revision and issue date (Ref): 10.03.16

Spiriva® and HandiHaler® are registered trademarks of Boehringer Ingelheim Pharma GmbH & Co. KG.

HandiHaler® Instructions for use


Dear Patient,

The HandiHaler® enables you to inhale the medicine contained in the Spiriva capsule -that your physician has prescribed for your breathing problems.



Remember to carefully follow your doctor's instructions for using Spiriva. The HandiHaler® is especially designed for Spiriva. You must not use it to take any other medication. You can use your HandiHaler® for up to one year to take your medication.



Raise the HandiHaler® to your mouth and close your lips tightly around the mouthpiece. Keep your head in an upright position and breathe in slowly and deeply but at a rate sufficient to hear or feel the capsule vibrate. Breathe until your lungs are full; then hold your breath as long as comfortable and at the same time take the HandiHaler® out of your mouth. Resume normal breathing. Repeat steps 6 and 7 once, in order to empty the capsule completely.



The HandiHaler®

1.    Dust cap

2.    Mouthpiece

3.    Base

4.    Piercing button

5.    Centre chamber


Open the mouthpiece again. Tip out the used capsule and dispose. Close the mouthpiece and dust cap for storage of your HandiHaler® device.


To release the dust cap press the piercing button completely in and let go.


Cleaning your HandiHaler®:


Clean the HandiHaler® once a month. Open the dust cap and mouthpiece. Then open the base by lifting the piercing button. Rinse the complete inhaler with warm water to remove any powder. Dry the HandiHaler® thoroughly by tipping excess of water out on a paper towel and air-dry afterwards, leaving the dust cap, mouthpiece and base open. It takes 24 hours to air dry, so clean it right after you have used it and it will be ready for your next dose. If needed the outside of the mouthpiece may be cleaned with a moist but not wet tissue.


Open the dust cap completely by pulling it upwards. Then open the mouthpiece by pulling it upwards.


Blister handling

Separate the blister strips by tearing along the perforation.


Remove a Spiriva capsule from the blister (only immediately before use, see blister handling) and place it in the centre chamber (5), as illustrated. It does not matter which way the capsule is placed in the chamber.


Peel back foil (only immediately before use) using the tab until one capsule is fully visible.

In case a second capsule is exposed to air inadvertently this capsule has to be discarded.


Close the mouthpiece firmly until you hear a click, leaving the dust cap open.


Remove capsule.

Spiriva capsules contain only a small amount of powder so that the capsule is only partially filled.


Hold the HandiHaler® device with the mouthpiece upwards and press the piercing button completely in only once, and release. This makes holes in the capsule and allows the medication to be released when you breathe in.


Leaflet revision and issue date (Ref): 10.03.16

Spiriva® and HandiHaler® are registered trademarks of Boehringer Ingelheim Pharma GmbH & Co. KG.


Breathe out completely.

Important:

Please avoid breathing into the mouthpiece at any time.


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