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Verquvo 5 mg comprimidos recubiertos con pelicula

О препарате

Introduction

Prospect: information for the patient

Verquvo 2.5mg film-coated tablets

Verquvo 5mg film-coated tablets

Verquvo 10mg film-coated tablets

vericiguat

This medicine is subject to additional monitoring, which will speed up the detection of new information about its safety. You can contribute by reporting any adverse effects you may experience. The final part of section4 includes information on how to report these adverse effects.

Read this prospect carefully before starting to take this medicine, because it contains important information for you.

  • Keep this prospect, as you may need to read it again.
  • If you have any doubts, consult your doctor or pharmacist.
  • This medicine has been prescribed only for you, and you should not give it to other people even if they have the same symptoms as you, as it may harm them.
  • If you experience adverse effects, consult your doctor or pharmacist, even if they do not appear in this prospect. See section4.

1.What is Verquvo and for what it is used

2.What you need to know before starting to take Verquvo

3.How to take Verquvo

4.Possible adverse effects

5.Storage of Verquvo

6.Contents of the package and additional information

1. What is Verquvo and how is it used

Verquvo contains the active ingredient vericiguat, which is a type of heart medication called a soluble guanylate cyclase stimulator.

Verquvo is used to treat adults with long-standing heart failure who have recently experienced an increase in heart failure symptoms. You may have been hospitalized and/or received a medication (diuretic) administered through a vein to help you urinate more frequently.

Heart failure occurs when the heart is weak and cannot pump enough blood to the body. Common symptoms of heart failure include difficulty breathing, fatigue, or swelling caused by fluid accumulation.

2. What you need to know before starting Verquvo

Do not take Verquvo

  • if you areallergicto vericiguat or any of the other components of this medication (listed in section6),
  • if you are taking any medication that contains anothersoluble guanylate cyclase stimulator, for example, riociguat, which is used to treat high blood pressure in the lungs.

If you apply to any of these circumstances,talk to your doctor firstand do not take this medication.

Warnings and precautions

Consult your doctor or pharmacist before starting to take Verquvo if you have

  • low blood pressurewith symptoms such as dizziness or lightheadedness,
  • serious kidney problemsor are undergoinghemodialysis,
  • serious liver problems.

Children and adolescents

Do not administer this medication to children or adolescents under 18years of age, as it has not yet been studied in this age group.

Other medications and Verquvo

Inform your doctor or pharmacist if you are taking, have taken recently or may need to take any other medication, particularly medications that

  • pertain to the group of soluble guanylate cyclase stimulators (for example, riociguat). Do not take Verquvo during treatment with these medications. See “Do not take Verquvo”.
  • are used to treat high blood pressure in the lungs, or medications to achieve or maintain an erection, known as PDE5 inhibitors (for example, sildenafilo, tadalafilo, vardenafilo). It is not recommended to use these medications during treatment with Verquvo.
  • are used to treat heart disease, including chest pain, known as nitrates (for example, isosorbide mononitrate).

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.

Pregnancy

Verquvo should not be used during pregnancy, as it is not known if it harms the fetus. If there is a possibility that you may become pregnant, consult your doctor about reliable contraceptive methods.

Breastfeeding

It is unknown if Verquvo passes into breast milk and if it could harm your baby. Your doctor will decide with you whether to interrupt breastfeeding or the treatment with Verquvo.

Driving and operating machinery

If you feel dizzy during treatment with this medication, do not drive vehicles, ride a bicycle, or use machines.

Verquvo contains lactose and sodium

This medication contains lactose. If your doctor has told you that you have a certain sugar intolerance, consult with him before taking this medication.

This medication contains less than 1mmol of sodium (23mg) per tablet; this is essentially “sodium-free”.

3. How to Take Verquvo

Follow exactly the administration instructions for this medication as indicated by your doctor. In case of doubt, consult your doctor or pharmacist.

Therecommended initial dose is 1tablet of 2.5mgonce a day. Your doctor will then adjust the dose according to how well you tolerate the treatment. Generally, your doctor will increase the dose after about 2weeks to 1tablet of 5mg once a day and after another 2weeks to themaximum target dose of 1tablet of 10mgonce a day.

If you havelow blood pressureduring treatment with Verquvo, this may cause you to feel dizzy and disoriented, and your doctor may temporarily reduce your Verquvo dose or interrupt your Verquvo treatment.

Take one tablet at the same time every day with food. If you cannot swallow the tablet, you can crush Verquvo and mix it with water. Take this mixture immediately.

If you take more Verquvo than you should

Consult your doctor immediately if you take more Verquvo than you should and experience any of the adverse effects listed in section4. The most likely effect would be a drop in blood pressure that may cause you to feel dizzy and disoriented.

If you forget to take Verquvo

Take the missed tablet as soon as you remember on the same day of the missed dose. Do not take a double dose to make up for the missed tablet.

If you interrupt treatment with Verquvo

Do not stop treatment with this medication without first talking to your doctor. If you stop treatment with this medication, your condition may worsen.

If you have any other questions about the use of this medication, ask your doctor or pharmacist.

4. Possible Adverse Effects

Like all medications, this medication may produce adverse effects, although not all people will experience them.

The possible adverse effects are:

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

  • Low blood pressure (hypotension)

Frequent(may affect up to 1 in 10people)

  • Low red blood cell count (anemia), which may cause pale skin, weakness, or difficulty breathing
  • Dizziness
  • Headache
  • Nausea and vomiting
  • Indigestion (dyspepsia)
  • Heartburn (gastroesophageal reflux disease)

Reporting Adverse Effects

If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect not listed in this prospectus. You can also report them directly throughthe national notification system included in theAppendixV. By reporting adverse effects, you can contribute to providing more information about the safety of this medication.

5. Verquvo Storage

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

Do not use this medication after the expiration date that appears on the box and on each blister or bottle after “CAD”. The expiration date is the last day of the month indicated.

This medication does not require special storage conditions.

Medicines should not be disposed of through drains or in the trash. Ask your pharmacist how to dispose of the containers and medications that you no longer need. This will help protect the environment.

6. Contents of the packaging and additional information

Composition of Verquvo

-The active ingredient is vericiguat. Each film-coated tablet contains 2.5mg, 5mg or 10mg of vericiguat.

-The other components are:
Core tablet:Microcrystalline cellulose, sodium croscarmellose, hypromellose 2910, lactose monohydrate, magnesium stearate, sodium lauryl sulfate (see section2 “Verquvo contains lactose and sodium”).
Film coating:Hypromellose 2910, talc, titanium dioxide (E171), iron oxide red (E172) (only Verquvo 5mg), iron oxide yellow (E172) (only Verquvo 10mg).

Appearance of the product and contents of the pack

Verquvo 2.5mg film-coated tablets (tablets) are round, biconvex, white tablets with a diameter of 7mm, marked with “2.5” on one face and “VC” on the other.

Verquvo 5mg film-coated tablets (tablets) are round, biconvex, brown-red tablets with a diameter of 7mm, marked with “5” on one face and “VC” on the other.

Verquvo 10mg film-coated tablets (tablets) are round, biconvex, yellow-orange tablets with a diameter of 9mm, marked with “10” on one face and “VC” on the other.

Verquvo is available

  • in blisters in boxes of 14, 28 or 98film-coated tablets
  • in perforated unit dose blisters in boxes of 10x1 or 100x1 film-coated tablets
  • in bottles of 100film-coated tablets

Only some pack sizes may be marketed.

Marketing authorisation holder

Bayer AG

51368 Leverkusen

Germany

Responsible for manufacturing

Bayer AG

Kaiser-Wilhelm-Allee

51368 Leverkusen

Germany

For further information about this medicinal product, please contact the local representative of the marketing authorisation holder:

België/Belgique/Belgien

Bayer SA-NV

Tél/Tel: +32-(0)2-535 63 11

Lietuva

UAB Bayer

Tel. +37 05 23 36 868

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T??.: +359 02 4247280

Luxembourg/Luxemburg

Bayer SA-NV

Tél/Tel: +32-(0)2-535 63 11

Ceská republika

Bayer s.r.o.

Tel: +420 266 101 111

Magyarország

Bayer Hungária KFT

Tel: +36 14 87-41 00

Danmark

Bayer A/S

Tlf: +45 45 23 50 00

Malta

Alfred Gera and Sons Ltd.

Tel: +35 621 44 62 05

Deutschland

Bayer Vital GmbH

Tel: +49 (0)214-30 513 48

Nederland

Bayer B.V.

Tel: +31-(0)297-28 06 66

Eesti

Bayer OÜ

Tel: +372 655 8565

Norge

Bayer AS

Tlf:+47 23 13 05 00

Ελλ?δα

Bayer Ελλ?ς ΑΒΕΕ

Τηλ: +30-210-61 87 500

Österreich

Bayer Austria Ges.m.b.H.

Tel: +43-(0)1-711 46-0

España

Bayer Hispania S.L.

Tel: +34-93-495 65 00

Polska

Bayer Sp. z o.o.

Tel: +48 22 572 35 00

France

Bayer HealthCare

Tél (N° vert): +33-(0)800 87 54 54

Portugal

Bayer Portugal, Lda.

Tel: +351 21 416 42 00

Hrvatska

Bayer d.o.o.

Tel: +385-(0)1-6599 900

România

SC Bayer SRL

Tel: +40 21 529 59 00

Ireland

Bayer Limited

Tel: +353 1 216 3300

Slovenija

Bayer d. o. o.

Tel: +386 (0)1 58 14 400

Ísland

Icepharma hf.

Sími:+354 540 8000

Slovenská republika

Bayer spol. s r.o.

Tel. +421 2 59 21 31 11

Italia

Bayer S.p.A.

Tel: +39 02 397 8 1

Suomi/Finland

Bayer Oy

Puh/Tel: +358- 20 785 21

Κ?προς

NOVAGEM Limited

Tηλ: +357 22 48 38 58

Sverige

Bayer AB

Tel: +46 (0) 8 580 223 00

Latvija

SIA Bayer

Tel: +371 67 84 55 63

United Kingdom (Northern Ireland)

Bayer AG

Tel: +44-(0)118 206 3000

Date of the last revision of this leaflet:

Other sources of information

The detailed information on this medicinal product is available on the website of the European Medicines Agency:http://www.ema.europa.eu.

Страна регистрации
Активное вещество
Требуется рецепт
Да
Производитель
Состав
Croscarmelosa sodica (8,48 mg mg), Lactosa monohidrato (58,52 mg mg), Laurilsulfato de sodio (0,56 mg mg)
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