Package Leaflet: Information for the Patient
Komboglyze 2.5mg/850mg film-coated tablets
saxagliptin/metformin hydrochloride
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
This medicine contains two different active substances called:
saxagliptin, which is part of a class of medicines called DPP-4 inhibitors (dipeptidyl peptidase-4 inhibitors), and
metformin, which is part of a class of medicines called biguanides.
Both belong to a group of medicines called oral antidiabetics.
What Komboglyze is used for
This medicine is used to treat a type of diabetes called ‘type 2 diabetes’.
How Komboglyze works
Saxagliptin and metformin work together to control the sugar in your blood. They increase the levels of insulin after meals. They also reduce the amount of sugar your body makes. Along with diet and exercise, they help reduce your blood sugar. This medicine can be used alone or with other antidiabetic medicines, including insulin.
To control your diabetes, you should continue with diet and exercise, even when taking this medicine. So, it is important that you follow the diet and exercise recommendations given by your doctor or healthcare professional.
Do not take Komboglyze
The symptoms of a severe allergic reaction can include:
If you get any of these symptoms, stop taking this medicine and contact your doctor or healthcare professional immediately.
Do not take this medicine if you are in any of the above situations. If you are unsure, consult your doctor or pharmacist before taking this medicine.
Warnings and precautions
Risk of lactic acidosis
Komboglyze may cause a very rare but very serious side effect called lactic acidosis, especially if your kidneys are not working properly. The risk of developing lactic acidosis is also increased with uncontrolled diabetes, severe infections, prolonged fasting, or alcohol intake, dehydration, liver problems, and any medical condition in which a part of the body has a reduced supply of oxygen (such as acute and severe heart diseases).
If any of the above applies to you, consult your doctor for further instructions.
Stop taking Komboglyze for a short period if you have a condition that may be associated with dehydration(significant loss of body fluids), such as severe vomiting, diarrhea, fever, heat exposure, or if you drink less fluid than usual. Consult your doctor for further instructions.
Stop taking Komboglyze and contact a doctor or the nearest hospital immediately if you experience any of the symptoms of lactic acidosis, as this condition can lead to coma.
The symptoms of lactic acidosis include:
Lactic acidosis is a medical emergency and should be treated in a hospital.
Consult your doctor quickly to find out how to proceed if
Consult your doctor or pharmacist before taking Komboglyze
If you need to undergo major surgery, you should stop taking Komboglyze during the procedure and for some time after. Your doctor will decide when you should stop taking Komboglyze and when you can restart it.
Diabetic skin lesions are a common complication of diabetes. Skin rash has been observed with saxagliptin and with certain antidiabetic medicines in the same class as saxagliptin. Follow the skin and foot care recommendations given by your doctor or healthcare professional. Contact your doctor if you find blisters on your skin, as it may be a sign of a disease called bullous pemphigoid. Your doctor may ask you to stop taking Komboglyze.
If you are in any of the above situations, or if you are unsure, consult your doctor or pharmacist before taking this medicine.
Kidney tests
During treatment with this medicine, your doctor will check your kidney function at least once a year or more frequently if you are an elderly person and/or if your kidney function is worsening.
Children and adolescents
Komboglyze is not recommended for use in children and adolescents below 18 years. It is not known if this medicine is safe and effective when used in children and adolescents below 18 years.
Other medicines and Komboglyze
If you need to be given an injection of a contrast medium that contains iodine into your bloodstream, for example, in the context of an X-ray or scan, you should stop taking Komboglyze before or at the time of the injection. Your doctor will decide when you should stop taking Komboglyze and when you can restart it.
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines. You may need more frequent blood glucose and kidney function tests, or your doctor may need to adjust the dose of Komboglyze. It is especially important to mention the following:
If you are in any of the above situations, or if you are unsure, consult your doctor or pharmacist before taking this medicine.
Taking Komboglyze with alcohol
Avoid excessive alcohol intake while taking Komboglyze, as this may increase the risk of lactic acidosis (see section “Warnings and precautions”).
Pregnancy and breast-feeding
Do not take this medicine if you are pregnant or might become pregnant, as it may affect your baby.
Do not take this medicine if you are breast-feeding or plan to breast-feed. This is because metformin passes into human breast milk in small amounts.
Consult your doctor or pharmacist before taking any medicine.
Driving and using machines
Saxagliptin and metformin have a negligible effect on the ability to drive and use machines. Hypoglycemia may affect your ability to drive and use machines or work with a firm support, and there is a risk of hypoglycemia when taking this medicine in combination with medicines with a known hypoglycemic effect, such as insulin or sulfonylureas.
Follow exactly the administration instructions of this medicine given by your doctor. If you are unsure, consult your doctor or pharmacist again.
If your doctor prescribes this medicine for you together with a sulfonylurea or insulin, remember to take this other medicine as directed by your doctor to achieve the best results for your health.
How much to take
If you have reduced kidney function, your doctor may prescribe a lower dose.
How to take this medicine
Diet and exercise
To control your diabetes, you should continue with diet and exercise, even when taking this medicine. So, it is important that you follow the diet and exercise recommendations given by your doctor or healthcare professional. In particular, if you are following a weight-control diet for diabetics, continue it while taking this medicine.
If you take more Komboglyze than you should
If you take more tablets of Komboglyze than you should, talk to your doctor or go to the hospital immediately. Take the medicine pack with you.
If you forget to take Komboglyze
If you stop taking Komboglyze
Keep taking this medicine until your doctor tells you to stop. This will help keep your blood sugar under control.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.
Stop taking this medicine and contact your doctor immediately if you notice any of the following serious adverse effects:
You should contact your doctor if you experience the following adverse effect:
Other Adverse Effects of Komboglyze are:
Frequent (may affect up to 1 in 10 people)
Uncommon (may affect up to 1 in 100 people)
Adverse Effects Observed During Treatment with Saxagliptin Alone:
Frequent
Adverse Effects Observed During Treatment with Saxagliptin Alone or in Combination:
Unknown (frequency cannot be estimated from available data):
Some patients have presented a small reduction in the number of a type of white blood cell (lymphocytes) detected by blood tests while taking saxagliptin alone or in combination. Some patients have also presented eruptions and skin reactions (hypersensitivity) during treatment with saxagliptin.
During the post-authorization use of saxagliptin, additional adverse effects have been reported, including severe allergic reactions (anaphylaxis), and swelling of the face, lips, tongue, and throat that can cause difficulty breathing or swallowing. If you experience an allergic reaction, stop taking this medicine and contact your doctor immediately. Your doctor may prescribe a medicine to treat your allergic reaction and a different medicine for your diabetes.
Adverse Effects Observed During Treatment with Metformin Alone:
Very Frequent (may affect more than 1 in 10 people)
Frequent
Very Rare
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is a possible adverse effect that is not listed in this leaflet. You can also report them directly through the national reporting system included in Appendix V. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of sight and reach of children.
Do not use this medicine after the expiration date shown on the blister pack and carton after "EXP/CAD". The expiration date is the last day of the month indicated.
Store below 25°C.
Do not use this medicine if the packaging shows visible signs of deterioration or tampering.
Medicines should not be disposed of through wastewater or household waste. Ask your pharmacist how to dispose of the packaging and medicines you no longer need. This will help protect the environment.
Komboglyze Composition
The active ingredients are saxagliptin and metformin hydrochloride. Each film-coated tablet contains 2.5 mg of saxagliptin (as hydrochloride) and 850 mg of metformin hydrochloride.
The other ingredients (excipients) are:
Product Appearance and Package Contents
It is possible that not all pack sizes are marketed in your country.
Marketing Authorization Holder
AstraZeneca AB
SE-151 85 Södertälje
Sweden
Manufacturer
AstraZeneca AB
Gärtunavägen
SE-152 57 Södertälje
Sweden
AstraZeneca UK Limited
Silk Road Business Park
Macclesfield
Cheshire
SK10 2NA
United Kingdom
You can request more information about this medicine by contacting the local representative of the marketing authorization holder:
Belgium AstraZeneca S.A./N.V. Tel: +32 2 370 48 11 | Lithuania UAB AstraZeneca Lietuva Tel: +370 5 2660550 |
Luxembourg AstraZeneca S.A./N.V. Tel: +32 2 370 48 11 | |
Czech Republic AstraZeneca Czech Republic s.r.o. Tel: +420 222 807 111 | Hungary AstraZeneca Kft. Tel: +36 1 883 6500 |
Denmark AstraZeneca A/S Tel: +45 43 66 64 62 | Malta Associated Drug Co. Ltd Tel: +356 2277 8000 |
Germany AstraZeneca GmbH Tel: +49 40 809034100 | Netherlands AstraZeneca BV Tel: +31 85 808 9900 |
Estonia AstraZeneca Tel: +372 6549 600 | Norway AstraZeneca AS Tel: +47 21 00 64 00 |
Greece AstraZeneca A.E. Tel: +30 2 106871500 | Austria AstraZeneca Österreich GmbH Tel: +43 1 711 31 0 |
Spain AstraZeneca Farmacéutica Spain, S.A. Tel: +34 91 301 91 00 | Poland AstraZeneca Pharma Poland Sp. z o.o. Tel: +48 22 245 73 00 |
France AstraZeneca Tel: +33 1 41 29 40 00 | Portugal AstraZeneca Produtos Farmacêuticos, Lda. Tel: +351 21 434 61 00 |
Croatia AstraZeneca d.o.o. Tel: +385 1 4628 000 | Romania AstraZeneca Pharma SRL Tel: +40 21 317 60 41 |
Ireland AstraZeneca Pharmaceuticals (Ireland) DAC Tel: +353 1609 7100 | Slovenia AstraZeneca UK Limited Tel: +386 1 51 35 600 |
Iceland Vistor Tel: +354 535 7000 | Slovakia AstraZeneca AB, o.z. Tel: +421 2 5737 7777 |
Italy AstraZeneca S.p.A. Tel: +39 02 00704500 | Finland AstraZeneca Oy Tel: +358 10 23 010 |
Cyprus ΑλÉκτωρ Φαρµακευτικn Λτδ Tel: +357 22490305 | Sweden AstraZeneca AB Tel: +46 8 553 26 000 |
Latvia SIA AstraZeneca Latvija Tel: +371 67377100 |
Date of Last Revision of this Leaflet:
Detailed information on this medicine is available on the European Medicines Agency website: http://www.ema.europa.eu