


Ask a doctor about a prescription for SITAGLIPTIN TEVA 100 mg FILM-COATED TABLETS
Package Leaflet:information for the user
Sitagliptin Teva 100 mg film-coated tablets EFG
sitagliptin
Read all of this leaflet carefully before you start taking this medicine,because it contains important information for you.
Contents of the pack
5 Conservation of Sitagliptin Teva
Sitagliptin Teva contains the active substance sitagliptin, which belongs to a class of medicines called DPP-4 inhibitors (dipeptidyl peptidase-4 inhibitors) that reduce blood sugar levels in adult patients with type 2 diabetes mellitus.
This medicine helps increase the levels of insulin produced after a meal and decreases the amount of sugar produced by the body.
Your doctor has prescribed this medicine to help you reduce your blood sugar levels, which are too high due to your type 2 diabetes. This medicine may be used alone or in combination with other medicines (insulin, metformin, sulfonylureas, or glitazones) that reduce blood sugar levels, which you may already be taking for your diabetes, along with your diet and exercise program.
What is type 2 diabetes?
Type 2 diabetes is a disease in which your body does not produce enough insulin, and the insulin it produces does not work as well as it should. Your body may also produce too much sugar. When this happens, sugar (glucose) builds up in the blood. This can cause serious medical problems, such as heart disease, kidney disease, blindness, and amputation.
Do not take Sitagliptin Teva
Warnings and precautions
Tell your doctor or pharmacist before taking Sitagliptin Teva.
There have been reports of pancreatitis (inflammation of the pancreas) in patients treated with sitagliptin (see section 4).
If you notice blisters on your skin, it may be a sign of a disease called bullous pemphigoid. Your doctor may ask you to stop taking Sitagliptin Teva.
Tell your doctor if you have or have had:
It is unlikely that this medicine will cause low blood sugar because it does not work when blood sugar levels are low. However, when this medicine is used in combination with a medicine that contains a sulfonylurea or with insulin, low blood sugar (hypoglycemia) may occur. Your doctor may reduce the dose of your sulfonylurea or insulin medicine.
Children and adolescents
Children and adolescents under 18 years of age should not use this medicine. It is not effective in children and adolescents aged between 10 and 17 years. It is not known if this medicine is safe and effective when used in children and adolescents under 10 years of age.
Taking Sitagliptin Teva with other medicines
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
In particular, tell your doctor if you are taking digoxin (a medicine used to treat irregular heartbeat and other heart problems). Your doctor may need to check your digoxin levels if you are taking Sitagliptin Teva.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
This medicine should not be taken during pregnancy.
It is not known if this medicine passes into breast milk. You should not take this medicine if you are breastfeeding or planning to breastfeed.
Driving and using machines
The effect of this medicine on your ability to drive or use machines is negligible. However, dizziness and somnolence have been reported, which may affect your ability to drive or use machines.
Also, taking this medicine with sulfonylureas or insulin may cause low blood sugar (hypoglycemia), which may affect your ability to drive or use machines or work without a secure support.
Sitagliptin Teva contains sodium
This medicine contains less than 23 mg of sodium (1 mmol) per tablet; it is essentially "sodium-free".
Follow exactly the instructions for administration of this medicine given by your doctor. If you are unsure, consult your doctor or pharmacist again.
The recommended dose is:
If you have kidney problems, your doctor may prescribe lower doses (such as 25 mg or 50 mg).
The tablets can be divided into equal doses.
You can take this medicine with or without food and drinks.
Your doctor may prescribe this medicine alone or with other medicines that also reduce blood sugar levels.
Diet and exercise can help your body use sugar better. It is important that you follow the diet and exercise recommended by your doctor while taking Sitagliptin Teva.
If you take more Sitagliptin Teva than you should
If you take more of this medicine than you should, contact your doctor immediately.
If you forget to take Sitagliptin Teva
If you forget a dose, take it as soon as you remember. If you do not remember until the time of your next dose, skip the missed dose and continue with your regular schedule. DO NOT take a double dose of this medicine.
If you stop taking Sitagliptin Teva
Continue taking this medicine while your doctor prescribes it for you to help control your blood sugar levels. You should not stop taking this medicine without consulting your doctor first.
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
STOP taking Sitagliptin Teva and contact your doctor immediatelyif you notice any of the following serious side effects:
If you have a severe allergic reaction (frequency not known), including skin rash, hives, blisters on the skin/exfoliative skin, and swelling of the face, lips, tongue, and throat that may cause difficulty breathing or swallowing, stop taking this medicine and consult your doctor immediately. Your doctor will prescribe a medicine to treat the allergic reaction and change your diabetes medicine.
Some patients experienced the following side effects after adding sitagliptin to their treatment with metformin:
Common(may affect up to 1 in 10 people): low blood sugar, nausea, flatulence, vomiting.
Uncommon(may affect up to 1 in 100 people): stomach pain, diarrhea, constipation, somnolence.
Some patients experienced different types of stomach discomfort when starting the combination of sitagliptin and metformin together (frequency classified as common).
Some patients experienced the following side effects while taking sitagliptin in combination with a sulfonylurea and metformin:
Very common(may affect more than 1 in 10 people): low blood sugar
Common:constipation
Some patients experienced the following side effects while taking sitagliptin and pioglitazone:
Common:flatulence, swelling of hands or feet
Some patients experienced the following side effects while taking sitagliptin in combination with pioglitazone and metformin:
Common:swelling of hands or feet
Some patients experienced the following side effects while taking sitagliptin in combination with insulin (with or without metformin):
Common:flu
Uncommon:dry mouth
Some patients experienced the following side effects while taking sitagliptin alone during clinical trials or after approval, alone and/or with other diabetes medicines:
Common:low blood sugar, headache, upper respiratory tract infection, nasal congestion or runny nose, and sore throat, arthrosis, pain in the arm or leg
Uncommon:dizziness, constipation, itching
Rare:reduced platelet count
Frequency not known:kidney problems (which may require dialysis), vomiting, joint pain, muscle pain, back pain, interstitial lung disease, bullous pemphigoid (a type of skin blister).
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist, even if you think they are not serious. You can also report side effects directly to the Spanish Medicines Agency's Pharmacovigilance System for Human Use: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiration date stated on the packaging and blister or label of the bottle after EXP. The expiration date is the last day of the month indicated.
This medicine does not require special storage conditions.
Medicines should not be disposed of via wastewater or household waste. Return the packaging and any unused medicine to the pharmacy's SIGRE collection point. Ask your pharmacist how to dispose of the packaging and any unused medicine. This will help protect the environment.
Composition of Sitagliptin Teva 100 mg film-coated tablets EFG
Coating contains: hydrolyzed polyvinyl alcohol, macrogol 3350, titanium dioxide (E171), talc, red iron oxide (E172), yellow iron oxide (E172).
Appearance of the product and contents of the pack
Sitagliptin Teva 100 mg tablets are orange, round, marked with "S|100" and have a score line on one side, and are scored on the other side.
Each pack contains 14, 28, 30, 56, 60, 84, 90, 98, 100, and 120 tablets, calendar packs containing 14, 28, 56, and 98 tablets, single-dose packs containing 28x1, 100x1, 56x1, 98x1, 100x1, and 10x1 tablets, or a bottle (which includes a desiccant bag) containing 100 or 250 tablets.
Not all pack sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
Teva Pharma, S.L.U.
c/Anabel Segura, 11 Edificio Albatros B 1ª Planta
Alcobendas 28108 Madrid
Spain
Manufacturer
TEVA Gyógyszergyár Zrt.
Debrecen, Pallagi út 13, H-4042
Hungary
or
Teva Operations Poland Sp. z.o.o
ul. Mogilska 80., 31-546 Krakow
Poland
or
Merckle GmbH
Ludwig-Merckle-Straße 3, 89143
Blaubeuren, Baden-Wuerttemberg
Germany
or
Teva Pharma B.V.
Swensweg 5, 2031 GA Haarlem
Netherlands
Or
Actavis International Ltd
4, Sqaq tal-Gidi off, Valletta Road,
Luqa LQA 6000
Malta
Or
Balkanpharma-Dupnitsa AD
3 Samokovska Shosse,
Str.Dupnitsa 2600
Bulgaria
This medicine is authorized in the Member States of the European Economic Area under the following names:
Austria: Sitagliptin-ratiopharm 100 mg Filmtabletten
Bulgaria: Sitagliptin Teva 100 mg film-coated tablets
Czech Republic: Sitagliptin Teva 100 mg, film-coated tablets
Germany: Sitagliptin-ratiopharm 100 mg Filmtabletten
Denmark: Sitagliptin Teva
Estonia: Sitagliptin Teva
Spain: Sitagliptina Teva 100 mg film-coated tablets EFG
Finland: Sitagliptin ratiopharm 100 mg tablets, film-coated
France: Sitagliptine Teva 100 mg film-coated tablets
Croatia: Sitagliptin Teva 100 mg film-coated tablets
Hungary: Sitagliptin Teva 100 mg film-coated tablets
Ireland: Sitagliptin Teva 100 mg film-coated tablets
Iceland: Sitagliptin ratiopharm 100 mg film-coated tablets
Italy: Sitagliptin Teva 100 mg film-coated tablets
Lithuania: Sitagliptin Teva 100 mg film-coated tablets
Luxembourg: Sitagliptin-ratiopharm 100 mg Filmtabletten
Latvia: Sitagliptin Teva 100 mg film-coated tablets
Malta: Sitagliptin Teva 100 mg film-coated tablets
Netherlands: Sitagliptine Teva 100 mg, film-coated tablets
Poland: Sitagliptin Teva
Portugal: Sitagliptina Teva 100 mg film-coated tablets
Romania: Sitagliptina Teva 100 mg film-coated tablets
Sweden: Sitagliptin Teva, 100 mg film-coated tablets
Slovenia: Sitagliptin Teva 100 mg film-coated tablets
Slovakia: Sitagliptin Teva 100 mg
United Kingdom: Sitagliptin Teva 100 mg film-coated tablets
Date of last revision of this leaflet: September 2020
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es
The average price of SITAGLIPTIN TEVA 100 mg FILM-COATED TABLETS in October, 2025 is around 26.52 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for SITAGLIPTIN TEVA 100 mg FILM-COATED TABLETS – subject to medical assessment and local rules.