Package Leaflet: Information for the User
Januvia 25mg film-coated tablets
Januvia 50mg film-coated tablets
Januvia 100mg film-coated tablets
sitagliptin
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack and other information
Januvia 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.
This medicine helps to increase the amount 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 level, which is too high due to your type 2 diabetes. This medicine can 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, together with a diet and exercise program.
What is type 2 diabetes?
Type 2 diabetes is a condition where your body does not produce enough insulin, and the insulin that your body 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 Januvia
Warnings and precautions
There have been reports of pancreatitis (inflammation of the pancreas) in patients taking Januvia (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 Januvia.
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 your 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 10 to 17 years. It is not known if this medicine is safe and effective when used in children under 10 years of age.
Other medicines and Januvia
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 the level of digoxin in your blood if you are taking Januvia.
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 taking 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
This medicine has no or negligible influence on the ability to drive and use machines. However, dizziness and somnolence have been reported, which may affect your ability to drive or use machines.
Also, taking this medicine with the medicines called sulfonylureas or with insulin may cause low blood sugar (hypoglycemia), which may affect your ability to drive and use machines or work without a safe support.
Januvia contains sodium
This medicine contains less than 23 mg of sodium (1 mmol) per tablet; this is essentially “sodium-free”.
Take this medicine exactly as your doctor has told you. If you are not sure, ask your doctor or pharmacist.
The recommended dose is:
If you have kidney problems, your doctor may prescribe a lower dose (such as 25 mg or 50 mg).
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, which you may already be taking for your diabetes, together with a diet and exercise program.
Diet and exercise may help your body use sugar better. It is important that you follow the diet and exercise program recommended by your doctor while taking Januvia.
If you take more Januvia than you should
If you take more of this medicine than you should, contact your doctor immediately.
If you forget to take Januvia
If you forget to take a dose, take it as soon as you remember. If you do not remember until it is time for 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 Januvia
Keep taking this medicine while your doctor tells you to, so that you can continue to control your blood sugar levels. You should not stop taking this medicine without first talking to your doctor.
If you have any further questions on 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 Januvia and contact a doctor immediatelyif you experience 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/peeling of the skin, and swelling of the face, lips, tongue, and throat that may cause difficulty breathing or swallowing, stop taking this medicine and contact your doctor immediately. Your doctor will prescribe a medicine to treat the allergic reaction and change your diabetes treatment.
Some patients have reported 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 have reported different types of stomach discomfort when starting the combination of sitagliptin and metformin together (frequency classified as common).
Some patients have reported 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 have reported the following side effects while taking sitagliptin and pioglitazone:
Common: flatulence, swelling of hands or feet
Some patients have reported the following side effects while taking sitagliptin and pioglitazone and metformin:
Common: swelling of hands or feet
Some patients have reported the following side effects while taking sitagliptin in combination with insulin (with or without metformin):
Common: flu
Uncommon: dry mouth
Some patients have reported the following side effects while taking sitagliptin alone during clinical trials or during use after approval, alone and/or in combination with other diabetes medicines:
Common: low blood sugar, headache, infection of the upper respiratory tract, nasal congestion or runny nose, and sore throat, osteoarthritis, pain in the arm or leg
Uncommon: dizziness, constipation, itching
Rare: reduced number of platelets
Frequency not known: kidney problems (which may require dialysis), vomiting, joint pain, muscle pain, back pain, interstitial lung disease, bullous pemphigoid (a type of blistering skin condition)
Reporting of side effects
If you experience any side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system listed in Appendix V. 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 expiry date which is stated on the blister and carton after EXP. The expiry date refers to the last day of that month.
Store below 25°C.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
What Januvia contains
Appearance and packaging
Opaque blisters (PVC/PE/PVDC and aluminum). Packs of 14, 28, 30, 56, 84, 90, or 98 film-coated tablets and 50 x 1 film-coated tablets in single-dose blisters.
Not all pack sizes may be marketed.
Marketing Authorisation Holder and Manufacturer
Merck Sharp & Dohme B.V., Waarderweg 39, 2031 BN Haarlem, Netherlands
For further information, contact your local representative of the Marketing Authorisation Holder:
Belgium MSD Belgium Tel: +32(0)27766211 dpoc_belux@msd.com | Lithuania UAB Merck Sharp & Dohme Tel.: +370 5 278 02 47 msd_lietuva@merck.com |
Luxembourg MSD Belgium Tel: +32(0)27766211 dpoc_belux@msd.com | |
Czech Republic Merck Sharp & Dohme, s.r.o. Tel.: +420 233 010 111 dpoc_czechslovak@merck.com | Hungary MSD Pharma Hungary Kft. Tel.: +36 1 888 5300 hungary_msd@merck.com |
Denmark MSD Danmark ApS Tel.: +45 4482 4000 dkmail@merck.com | Malta Merck Sharp & Dohme Cyprus Limited Tel: 8007 4433 (+356 99917558) malta_info@merck.com |
Germany MSD Sharp & Dohme GmbH Tel: 0800 673 673 673 (+49 (0) 89 4561 0) e-mail@msd.de | Netherlands Merck Sharp & Dohme B.V. Tel.: 0800 9999000 (+31 23 5153153) medicalinfo.nl@merck.com |
Estonia Merck Sharp & Dohme OÜ Tel.: +372 6144 200 msdeesti@merck.com | Norway MSD (Norge) AS Tel: +47 32 20 73 00 msdnorge@msd.no |
Greece MSD Α.Φ.Ε.Ε. Tel: +30-210 98 97 300 dpoc_greece@merck.com | Austria Merck Sharp & Dohme Ges.m.b.H. Tel: +43 (0) 1 26 044 dpoc_austria@merck.com |
Spain Merck Sharp & Dohme de España, S.A. Tel: +34 91 321 06 00 msd_info@merck.com | Poland MSD Polska Sp. z o.o. Tel.: +48 22 549 51 00 msdpolska@merck.com |
France MSD France Tel: +33 (0)1 80 46 40 40 | Portugal Merck Sharp & Dohme, Lda Tel: +351 21 4465700 inform_pt@merck.com |
Croatia Merck Sharp & Dohme d.o.o. Tel: +385 1 66 11 333 croatia_info@merck.com | Romania Merck Sharp & Dohme Romania S.R.L. Tel: +4021 529 29 00 msdromania@merck.com |
Ireland Merck Sharp & Dohme Ireland (Human Health) Limited Tel: +353 (0)1 2998700 medinfo_ireland@msd.com | Slovenia Merck Sharp & Dohme, inovativna zdravila d.o.o. Tel: +386 1 5204 201 msd_slovenia@merck.com |
Iceland Vistor hf. Tel: +354 535 7000 | Slovakia Merck Sharp & Dohme, s.r.o. Tel.: +421 2 58282010 dpoc_czechslovak@merck.com |
Italy MSD Italia S.r.l. Tel: 800 23 99 89 (+39 06 361911) dpoc.italy@msd.com | Finland MSD Finland Oy Tel: +358 (0)9 804 650 info@msd.fi |
Cyprus Merck Sharp & Dohme Cyprus Limited Tel: 80000 673 (+357 22866700) cyprus_info@merck.com | Sweden Merck Sharp & Dohme (Sweden) AB Tel: +46 77 5700488 medicinskinfo@merck.com |
Latvia SIA Merck Sharp & Dohme Latvija Tel: +371 67364224 msd_lv@merck.com | United Kingdom (Northern Ireland) Merck Sharp & Dohme Ireland (Human Health) Limited Tel: +353 (0)1 2998700 medinfoNI@msd.com |
Date of last revision of this leaflet:{MM/AAAA}.
Detailed information on this medicine is available on the European Medicines Agency web site: http://www.ema.europa.eu.
The average price of JANUVIA 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.