Soprobec 200 Micrograms/Inhalation Pressurized Solution For Inhalation

Contents of the leaflet

1. Introduction
2. What is Soprobec and what is it used for
3. What you need to know before you start using Soprobec
4. Warnings and precautions
5. Pregnancy and breastfeeding
6. Driving and using machines
7. How to use Soprobec
8. Possible side effects
9. Storage of Soprobec
10. Container Content and Additional Information

Introduction

Package Leaflet: Information for the Patient

Soprobec 200 micrograms/inhalation inhalation solution in a pressurized container

Beclometasone, dipropionate

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

• Keep this package 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 symptoms are the same as yours.
• If you experience any side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in this package leaflet. See section 4.

Contents of the package leaflet

1. What is Soprobec and what is it used for
2. What you need to know before you start using Soprobec
3. How to use Soprobec
4. Possible side effects
5. Storage of Soprobec
6. Contents of the pack and further information

1. What is Soprobec and what is it used for

Soprobec inhalation solution in a pressurized container is used to help preventasthma symptoms. The active ingredient, beclometasone dipropionate, belongs to a group of medicines known as corticosteroids, sometimes also called simply steroids. Steroids have an anti-inflammatory action, reducing swelling and irritation of the walls of the small airways in the lungs, making it easier to breathe.

2. What you need to know before you start using Soprobec

Do not use Soprobec:

• if you are allergic to beclometasone dipropionate or any of the other ingredients of this medicine (listed in section 6) or to any other medicine used to treat asthma.
• to treat a sudden attack of difficulty breathing. It will not help. Use a fast-acting inhaler for this purpose and carry it with you at all times.

Warnings and precautions

Talk to your doctor, pharmacist, or nurse before you start using Soprobec:

• if you have or have been treated for tuberculosis.
• if you have had thrush in your mouth.
• you should avoid drinking alcohol for any reason.

You should also talk to your doctor, pharmacist, or nurse:

• if your asthma seems to be getting worse. You may be getting more short of breath than usual, your rescue inhaler seems to be less effective, you need more puffs than usual from your rescue inhaler, or you do not seem to be getting better.
• when you are transferred from treatment with steroid tablets to an inhaler, you may find that, even if your chest is getting better, you feel unwell, develop a rash, itching, or runny nose and sneezing (rhinitis). Do not stoptreatment with your inhaler unless your doctor tells you to.

If you have been treated with high doses of inhaled steroids for a long time, you may need treatment with steroid tablets or possibly a steroid injection at times of stress. For example, during hospitalization after a serious accident, before an operation, during a severe asthma attack, or if you have a chest infection or other serious illness. Your doctor will consider whether you need extra steroid treatment and will tell you for how long you need to take the steroid tablets and how to reduce them as you get better.

Get in touch with your doctor if you experience blurred vision or other changes in your vision.

Children

Soprobec 200 micrograms/inhalation is not indicated for children.

Other medicines and Soprobec

Before you start treatment, tell your doctor if you are taking or have recently taken or might take any other medicines, including those obtained without a prescription.

Tell your doctor if you are taking disulfiram or metronidazole, as there is a potential risk of interaction in particularly sensitive individuals.

Remember to carry these medicines and your inhalers with you if you go to the hospital.

Some medicines may increase the effects of Soprobec, so your doctor will monitor you closely if you are taking these medicines (including some for HIV: ritonavir, cobicistat).

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before using this medicine.

Driving and using machines

Soprobec has no known effects on driving or using machines.

Soprobec contains alcohol

This medicine contains 8.05 mg of alcohol (ethanol) in each inhalation, which is equivalent to 14%. The amount of alcohol in each inhalation is equivalent to less than 4 ml of beer or 2 ml of wine. The small amount of alcohol in this medicine does not produce any noticeable effect.

3. How to use Soprobec

Soprobec is available in 4 different doses. Your doctor will decide which dose you need. Soprobec 200 micrograms/inhalation and Soprobec 250 micrograms/inhalation are not indicated for children.

Follow the instructions for administration of this medicine exactly as told by your doctor or pharmacist. If you are in doubt, consult your doctor or pharmacist again. The instructions for use of the inhaler are given after the dosage section. The inhaler takes a few days to start working. It is very important that you use it regularly.

Do not stoptreatment even if you feel better, unless your doctor tells you to. Do not stopusing the inhaler suddenly.

During your treatment with Soprobec, your doctor will regularly check your asthma with simple breathing tests and may need to do occasional blood tests.

Dosage:

The initial dose will depend on the severity of your asthma and will be decided by your doctor. It may be higher than those described below. Your doctor will prescribe the lowest dose of Soprobec that controls your symptoms.

The Volumatic spacer chamber must always be used when:

• adults, elderly patients, and adolescents over 16 years inhale total daily doses of Soprobec equal to or greater than 1,000 micrograms.

Soprobec 200 micrograms/inhalation

The standard initial dose is:

Only for adults and elderly patients: 200 micrograms (1 puff) twice a day.

Normally, the maximum you will inhale in a day is: 800 micrograms (4 puffs).

The total daily dose can be divided into 2, 3, or 4 daily doses.

This dose is not suitable for children.

If you use more Soprobec than you should:

Tell your doctor as soon as possible. Your doctor may want to check your cortisol levels in your blood, so you will need to have a blood test (cortisol is a human steroid hormone that is naturally present in the body).

It is important that you take your dose as your doctor has told you. Do not increase or reduce your dose without medical supervision.

In case of overdose or accidental ingestion, consult the Toxicological Information Service. Phone: 91 562 04 20, consult your doctor or pharmacist.

If you forget to use Soprobec:

Do not take a double dose to make up for forgotten doses, just wait until the next dose. Do not take more puffs than prescribed.

Method of administration

Soprobec is for inhalation use only.

Instructions for use:

It is important that you know how to use your inhaler correctly. Your doctor, nurse, or pharmacist will teach you how to use your inhaler correctly and will check periodically that you are using it correctly. You must follow the instructions carefully, so that you know how, when, and how manypuffs you should inhale and how often you should use your inhaler. If you are not sure what to do or have problems inhaling, consult your doctor, nurse, or pharmacist.

1. To remove the protective cap, hold it between your index finger and thumb, squeeze gently, and pull the cap off as shown. Check that the mouthpiece is clean inside and outside and that there are no foreign objects.

Checking the inhaler:If the inhaler is new or has not been used for 3 or more days, take a puff into the air to make sure it is working.

1. Hold the inhaler in the upright position as shown, with your thumb on the base, below the mouthpiece. Breathe out as much as you can.

1. Put the mouthpiece in your mouth between your teeth and close your lips around it, but do not bite.

1. Just after you start breathing in through your mouth, press the top of the inhaler to release a puff while continuing to breathe in slowly and deeply.

1. Hold your breath; remove the inhaler from your mouth and your finger from the top of the inhaler. Continue holding your breath for a few seconds or as long as you can. Breathe out slowly.
2. If you need to take another puff, keep the inhaler upright and wait for half a minute before repeating steps 2 to 5.

1. After use, always replace the protective cap to prevent dust and fluff. Replace it firmly and insert it into its position.

Important: Do not perform steps 2, 3, 4, and 5 quickly.

It is important that you start breathing in as slowly as possible before operating the inhaler. Practice in front of a mirror the first few times.

If you see ‘mist’ coming out of the top of the inhaler or the sides of your mouth, the beclometasone will not reach your lungs properly. Take another puff, following the instructions carefully from step 2 onwards.

People with weak hands may find it easier to hold the inhaler with both hands. Put both index fingers on the top of the inhaler and both thumbs below the mouthpiece.

If you find it difficult to manage the inhaler while inhaling, use the Volumatic spacer chamber. Consult your doctor, nurse, or pharmacist about this device.

The Volumatic spacer chamber must always be used when:

• you are an adult, elderly patient, or adolescent over 16 years who takes a total daily dose of Soprobec equal to or greater than 1,000 micrograms.

Tell your doctor, nurse, or pharmacist if you have difficulties.

Cleaning:

It is important to clean the inhaler at least once a week to prevent it from becoming blocked.

• Remove the metal canister from the plastic casing and take off the protective cap.
• Wash the plastic casing and protective cap with warm water. If you use a mild detergent, rinse carefully with clean water before drying. Do not put the metal canister in water.
• Let it dry well in a warm place. Avoid excessive heat.
• Replace the canister and protective cap.

It is important that you read the package leaflet that comes with the Volumatic spacer chamber and follow the instructions for use and cleaning of the Volumatic.

4. Possible side effects

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

Stop taking Soprobec and talk to your doctor if:

• you have an allergic reaction, such as a skin rash, urticaria, itching, or redness, or swelling of the face, eyes, lips, or throat.
• you notice a sudden increase in wheezing, difficulty breathing, or coughing after using your inhaler, stopusing Soprobec and use a fast-acting rescue inhaler immediately. Contact your doctor immediately. Your doctor will assess your asthma and may change your treatment and prescribe a different inhaler for your asthma.

The following side effects have been reported. Tell your doctor as soon as possibleif you experience any of these side effects, but do not stop treatmentunless your doctor tells you to. Your doctor will try to prevent these effects by prescribing Soprobec at the lowest possible dose to control your asthma.

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

• Oral candidiasis (thrush). This is more likely if the dose is greater than 400 micrograms. Thrush can be treated with antifungals while you continue to use Soprobec. Brushing your teeth or rinsing your mouth with water immediately after each dose may help prevent thrush.

Common (may affect up to 1 in 10 people)

• Hoarseness or throat irritation. Using a Volumatic spacer chamber for inhalation or rinsing your mouth with water immediately after each dose may help.

Rare (may affect up to 1 in 100 people)

• Rashes, urticaria, itching, and/or redness.

Very rare (may affect up to 1 in 10,000 people)

• Allergic reactions, which can cause swelling of the eyelids, face, lips, and/or throat (angioedema).
• Respiratory problems, such as dyspnea (feeling of lack of air or difficulty breathing) and/or bronchospasm (narrowing of the airways with decreased air intake).
• Anaphylactic or anaphylactoid reactions (severe allergic reactions that can make breathing difficult and affect your level of consciousness).
• Delayed growth in children and adolescents, they may need to have their height checked periodically by their doctor. This occurs particularly after treatment with Soprobec at high doses for a long time. Rounded face (moon face) (Cushing's syndrome).
• Loss of bone density (thinning and weakening of the bones).
• Eye problems, such as cataracts or glaucoma (increased pressure in the eye).
• Paradoxical bronchospasm.

Frequency not known:

• Sleep problems, depression, or feelings of worry, anxiety, nervousness, overexcitement, or irritability.
• These effects are more likely to occur in children.
• Blurred vision.
• Headache.
• Nausea.

If you become unwellor develop symptoms such as loss of appetite, abdominal pain, weight loss, tiredness, nausea (feeling unwell), vomiting, feeling faint, sweating, and possible convulsions (seizures), you should talk to your doctor. This is particularly important if you have been exposed to stressful situations, such as surgery, infection, a severe asthma attack, or other serious illness. Your doctor may do a blood test to monitor the levels of steroids in your body.

Reporting of side effects

If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this package leaflet. You can also report side effects directly through the Spanish Pharmacovigilance System for Human Use Medicines: http://www.notificaRAM.es. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storage of Soprobec

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 outer packaging and label, after EXP. The expiry date is the last day of the month shown.

Do not freeze.

Store in the original packaging to protect from light.

If the inhaler becomes very cold, take the metal canister out of the plastic casing and warm it in your handsfor a few minutes before use. Neveruse anything else to warm it up.

Medicines should not be disposed of via wastewater or household waste. Return any unused medicine to a pharmacy for disposal. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.

Warning:The container contains a pressurized liquid. Keep away from heat and direct sunlight, do not expose to high temperatures (above 50°C), and do not pierce or burn (incinerate), even when empty.

6. Container Content and Additional Information

Soprobec Composition

• The active ingredient in your inhaler is beclometasone dipropionate. Each actuation contains 200 micrograms of beclometasone dipropionate.
• The other excipients are glycerol, anhydrous ethanol, and norflurane (HFC-134a).

This medication contains fluorinated greenhouse gases.

Each inhaler contains 11,634 g of HFC-134a, which corresponds to 0.017 tons of CO2 equivalent (global warming potential = 1430).

Appearance of Soprobec and Container Content

Soprobec 200 micrograms/inhalation:

Soprobec is an inhalation solution in a pressurized aluminum container with a pink plastic actuator and a red protective cap. Each container contains a single inhaler or two inhalers. Each container contains 200 actuations.

Not all pack sizes may be marketed.

Marketing Authorization Holder and Manufacturer

Marketing Authorization Holder:

Glenmark Arzneimittel GmbH

Industriestr. 31

82194 Grobenzell

Germany

Manufacturer:

Glenmark Pharmaceuticals s.r.o.

Fibichova 143

56617 Vysoke Myto

Czech Republic

Glenmark Pharmaceuticals Europe Limited

Building 2, Croxley Green Business Park, Croxley Green

Hertfordshire WD18 8YA

United Kingdom

Synoptis Industrial Sp. z.o.o.

Ul. Rabowicka 15

62-020 Swarzedz

Poland

Further information about this medication can be obtained by contacting the local representative of the Marketing Authorization Holder:

Glenmark Farmacéutica, S.L.U.

C/ Retama 7, 7th floor

28045 Madrid

Spain

This medication is authorized in the Member States of the European Economic Area under the following names:

Date of the last revision of this leaflet:January 2021.

Detailed information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://aemps.gob.es/.

Volumatic™ is a trademark of GlaxoSmithKline Group of Companies