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Do not take Vipidia
Warnings and precautions
Consult your doctor or pharmacist before starting to take Vipidia:
Contact your doctor if blisters appear on your skin, as this could be one of the signs of a condition called bullous pemphigoid. Your doctor will ask you to stop treatment with alogliptin.
Children and adolescents
Vipidia is not recommended for use in children and adolescents under 18 years of age, due to a lack of efficacy in these patients.
Other medications and Vipidia
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
There is no experience with the use of Vipidia in pregnant women or during breastfeeding.Vipidia should not be used during pregnancy or breastfeeding. Your doctor will help you decide whether to continue breastfeeding or using Vipidia.
Driving and operating machinery
It is not known whether Vipidia affects the ability to drive and operate machinery.The combination of Vipidia with other diabetes medications called sulfonylureas, insulin, or combined therapy with thiazolidinedione plus metformin may cause excessively low blood sugar (hypoglycemia), which could affect your ability to drive and operate machinery.
Vipidia contains sodium
This medication contains less than 1 mmol of sodium (23 mg) per tablet; it is essentially "sodium-free".
Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.
Your doctor will prescribe Vipidia along with one or more additional medications to control your blood sugar levels.Your doctor will inform you if you need to adjust the amount of the other medications you take.
The recommended dose of Vipidia is 25mg once a day.
Patients with kidney disease
If you have kidney disease, your doctor may recommend a reduced dose. This may be 12.5mg or 6.25mg once a day, depending on the severity of your kidney disease.
Patients with liver disease
If your liver function is mildly or moderately reduced, the recommended dose of Vipidia is 25mg once a day. This medication is not recommended for patients with severely reduced liver function, due to the lack of data in these patients.
Swallow the whole tablets with water.You can take this medication with or without food.
If you take more Vipidia than you should
If you take more tablets than you should, or if someone else or a child takes your medication, contact or go immediately to the nearest emergency center.Bring this leaflet or some tablets with you, so your doctor knows exactly what you have taken.
If you forget to take Vipidia
If you forget to take a dose, take it as soon as you remember.Do not take a double dose to make up for a missed dose.
If you interrupt treatment with Vipidia
Do not stop taking Vipidia without first consulting your doctor. Your blood sugar levels may increase if you stop taking Vipidia.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine may cause side effects, although not everyone will experience them.
STOP taking Vipidia and contact your doctor immediatelyif you notice any of the followingserious side effects:
Of unknown frequency(cannot be estimated from available data):
You should alsoconsult your doctorif you experience any of the following side effects:
Frequent(may affect up to 1 in 10people):
Of unknown frequency:
Reporting side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through thenational notification system included in theAppendix V.By reporting side effects, you can contribute to providing more information about the safety of this medicine.
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 the blister pack after CAD/EXP. 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 the drains or in the trash. Ask your pharmacist how to dispose of the containers and medications that you no longer need. In this way, you will help protect the environment.
Composition of Vipidia
Each 25mg tablet contains alogliptina benzoate equivalent to 25mg of alogliptina.
Each 12.5mg tablet contains alogliptina benzoate equivalent to 12.5mg of alogliptina.
Each 6.25mg tablet contains alogliptina benzoate equivalent to 6.25mg of alogliptina.
Appearance of the product and contents of the pack
Vipidia is available in blister packs containing 10, 14, 28, 30, 56, 60, 84, 90, 98, or 100tablets.
Only some pack sizes may be marketed.
of the pack.
Marketing Authorization Holder
Takeda Pharma A/S
Delta Park 45
2665 Vallensbaek Strand
Denmark
Responsible for Manufacturing
Takeda Ireland Limited
Bray Business Park
Kilruddery
Co. Wicklow
Ireland
For further information about this medicinal product, please contact the local representative of the marketing authorization holder:
Takeda Belgium NV Tel:+32 2 464 06 11 | Lietuva Takeda, UAB Tel:+370 521 09 070 | |
???????? ?????? ???????????? ???.: +359 2 958 27 36 medinfoEMEA@takeda.com | Luxembourg/Luxemburg Takeda Belgium NV Tél/Tel: +32 2 464 06 11 | |
Ceská republika Takeda Pharmaceuticals Czech Republic s.r.o. Tel:+420 234722722 | Magyarország Takeda Pharma Kft. Tel.: +36 1 270 7030 | |
Danmark Takeda Pharma A/S Tlf: +45 46 77 10 10 | Malta Takeda HELLAS S.A. Tel: +30 210 6387800[email protected] | |
Deutschland Takeda GmbH Tel: +49 (0)800 825 3325 | Nederland Takeda Nederland B.V. Tel: +31 20 203 5492 | |
Eesti Takeda Pharma AS Tel: +372 6177 669 | Norge Takeda AS Tlf:+47 800 800 30 | |
Ελλ?δα TakedaΕΛΛΑΣ Α.Ε. Τηλ: +30 210 6387800 | Österreich Takeda Pharma Ges.m.b.H. Tel: +43(0) 800‑20 80 50 | |
España Laboratorios Menarini, S.A. Tel: +34934 628 800 | Polska Takeda Pharma Sp.z o.o. Tel.: +48223062447 | |
France Takeda France SAS Tél:+ 33 1 40 67 33 00 | Portugal Tecnimede‑Sociedade Técnico‑Medicinal, S.A Tel: +351 21 041 41 00 | |
Hrvatska Takeda Pharmaceuticals Croatia d.o.o Tel: +385 1 377 88 96 | România Takeda Pharmaceuticals SRL Tel:+40 21 335 03 91 | |
Ireland Takeda Products Ireland Ltd Tel:1800 937 970 | Slovenija Takeda Pharmaceuticals farmacevtska družba d.o.o. Tel: +386 (0) 59 082 480 | |
Ísland Vistor hf. Sími:+354 535 7000 | Slovenská republika Takeda Pharmaceuticals Slovakia s.r.o. Tel:+421 (2) 20 602 600 | |
Italia Takeda Italia S.p.A. Tel: +39 06 502601 | Suomi/Finland Takeda Oy Puh/Tel: 0800 774 051 | |
Κ?προς TakedaΕΛΛΑΣ Α.Ε. Τηλ: +30 210 6387800 | Sverige Takeda Pharma AB Tel:020 795 079 medinfoE[email protected] | |
Latvija Takeda Latvia SIA Tel:+371 67840082 | United Kingdom(Northern Ireland) Takeda UK Ltd Tel:+44 (0) 2830 640 902 |
Last update of the summary of product characteristics:
Other sources of information
Further information on this medicinal product is available on the website of the European Medicines Agency:http://www.ema.europa.eu.
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