Package Leaflet: Information for the Patient
Dapagliflozin Krka 5 mg film-coated tablets EFG
Dapagliflozin Krka 10 mg film-coated tablets EFG
Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.
Contents of the Package Leaflet
What is Dapagliflozin Krka
Dapagliflozin Krka contains the active substance dapagliflozin. It belongs to a group of medications called "sodium-glucose cotransporter 2 (SGLT2) inhibitors". They work by blocking the SGLT2 protein in the kidney. By blocking this protein, sugar in the blood (glucose), salt (sodium), and water are eliminated from the body through urine.
What is Dapagliflozin Krka used for
Dapagliflozin Krka is used to treat:
What is type 2 diabetes and how does Dapagliflozin Krka help?
What is heart failure and how does Dapagliflozin Krka help?
What is chronic kidney disease and how does Dapagliflozin Krka help?
Do not take Dapagliflozin Krka
Warnings and precautions
Contact a doctor or the nearest hospital immediately:
Diabetic ketoacidosis:
If you suspect you have diabetic ketoacidosis, contact a doctor or the nearest hospital immediately and do not take this medication.
Necrotizing fasciitis of the perineum:
Consult your doctor, pharmacist, or nurse before starting to take Dapagliflozin Krka:
If any of the above situations apply to you (or you are unsure), talk to your doctor, pharmacist, or nurse before taking Dapagliflozin Krka.
Diabetes and foot care
If you have diabetes, it is essential that you regularly check your feet and follow any other foot care advice provided by your healthcare professional.
Glucose in urine
Due to how Dapagliflozin Krka works, your urine will test positive for glucose while you are taking this medication.
Children and adolescents
Dapagliflozin can be used in children aged 10 years or older for the treatment of type 2 diabetes. There is no data available in children under 10 years of age.
Dapagliflozin is not recommended in children or adolescents under 18 years of age for the treatment of heart failure or for the treatment of chronic kidney disease, as it has not been studied in these patients.
Other medications and Dapagliflozin Krka
Tell your doctor, pharmacist, or nurse if you are taking, have recently taken, or might take any other medications.
Especially tell your doctor:
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, ask your doctor or pharmacist for advice before taking this medication.
You should stop taking this medication if you become pregnant, as its use is not recommended during the second and third trimesters of pregnancy. Consult your doctor about the best way to control your blood sugar levels during pregnancy.
Consult your doctor if you want to breastfeed or are breastfeeding before taking this medication. Do not use dapagliflozin during breastfeeding. It is not known if this medication passes into human breast milk.
Driving and using machines
Dapagliflozin has no or negligible influence on the ability to drive or use machines.
Taking this medication with other medications called sulfonylureas or with insulin may cause low blood sugar levels (hypoglycemia), which can cause symptoms such as shaking, sweating, and vision changes that can affect your ability to drive or use machines.
Do not drive or use tools or machines if you feel dizzy while taking Dapagliflozin Krka.
Dapagliflozin Krka contains lactose and sodium
If your doctor has told you that you have an intolerance to some sugars, consult with them before taking this medication.
This medication contains less than 1 mmol of sodium (23 mg) per tablet; this is essentially "sodium-free".
Follow the instructions for administration of this medication exactly as indicated by your doctor. If you are unsure, consult your doctor, pharmacist, or nurse again.
How much to take
How to take this medication
Your doctor may prescribe Dapagliflozin Krka along with another medication(s). Remember to take these other medication(s) following the instructions of your doctor. This will help you get the best results for your health.
Diet and exercise can help your body use blood sugar better. If you have diabetes, it is essential that you follow any diet and exercise program recommended by your doctor while taking dapagliflozin.
If you take more Dapagliflozin Krka than you should
If you take more dapagliflozin tablets than you should, consult your doctor or go to the hospital immediately. Bring the medication package with you.
In case of overdose or accidental ingestion, consult your doctor or pharmacist or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medication and the amount taken.
If you forget to take Dapagliflozin Krka
What you should do if you forget to take a tablet depends on how much time is left until your next dose.
If you stop taking Dapagliflozin Krka
Do not stop taking dapagliflozin without first consulting your doctor. If you have diabetes, your blood sugar levels may increase without this medication.
If you have any other questions about the use of this product, ask your doctor, pharmacist, or nurse.
Like all medications, Dapagliflozin Krka can cause side effects, although not everyone gets them.
Contact a doctor or the nearest hospital immediately if you experience any of the following side effects:
These are the signs of angioedema:
These are the signs of diabetic ketoacidosis (see also section 2 Warnings and precautions):
This can occur regardless of blood sugar levels. Your doctor should decide whether to temporarily or permanently stop your treatment with dapagliflozin.
Stop taking Dapagliflozin Krka and consult a doctor immediately if you notice any of these serious side effects:
These are the signs of a serious urinary tract infection:
Although it is not very common, if you see blood in your urine, inform your doctor immediately.
Contact your doctor as soon as possible if you experience any of the following side effects:
Your doctor will explain how to treat low blood sugar levels and what to do if you experience any of the above signs.
Other side effects of treatment with Dapagliflozin Krka:
Frequent (may affect up to 1 in 10 people)
Uncommon (may affect up to 1 in 100 people)
Rare (may affect up to 1 in 10,000 people)
Reporting side effects
If you experience any side effects, consult your doctor or pharmacist, even if they are side effects not listed in this package leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medications: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date stated on the blister or packaging after EXP. The expiration date is the last day of the month indicated.
This medication does not require special storage conditions.
Medications should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of the packaging and any unused medication. In case of doubt, ask your pharmacist how to dispose of the packaging and any unused medication in the SIGRE collection point of the pharmacy. This will help protect the environment.
Composition of Dapagliflozina Krka
Dapagliflozina Krka 5 mg film-coated tablets EFG
Each film-coated tablet contains 5 mg of dapagliflozina (as dapagliflozina propanediol monohydrate).
Dapagliflozina Krka 10 mg film-coated tablets EFG
Each film-coated tablet contains 10 mg of dapagliflozina (as dapagliflozina propanediol monohydrate).
Appearance and Package Contents of the Product
5 mg: light yellow-brown, round, biconvex film-coated tablets, engraved with "5" on one side. Tablet size: approximate diameter 7 mm.
10 mg: light yellow-brown, oval, biconvex film-coated tablets, scored on one side, one side of the score is engraved with "1" and the other with "0". The tablet can be divided into equal doses. Tablet size: approximately 13 x 6.5 mm.
Dapagliflozina Krka is available in packages containing:
Only some package sizes may be marketed.
Marketing Authorization Holder and Manufacturer
KRKA, d.d., Novo mesto
Šmarješka cesta 6,
8501 Novo mesto
Slovenia
You can request more information about this medicine by contacting the local representative of the marketing authorization holder:
KRKA Farmacéutica, S.L., Calle de Anabel Segura, 10, 28108 Alcobendas, Madrid, Spain
This pharmaceutical product is authorized in the Member States of the European Economic Area under the following names:
Member State Name | Medicine Name |
Slovenia | Dapagliflozin Krka 5 mg film-coated tablets Dapagliflozin Krka 10 mg film-coated tablets |
Denmark | Dapagliflozin Krka |
Finland | Dapagliflozin Krka 5 mg film-coated tablets Dapagliflozin Krka 10 mg film-coated tablets |
France | Dapagliflozine Krka 5 mg, film-coated tablet Dapagliflozine Krka 10 mg, scored film-coated tablet |
Iceland | Dapagliflozin Krka 5 mg film-coated tablets Dapagliflozin Krka 10 mg film-coated tablets |
Ireland | Dapagliflozin Krka 5 mg film-coated tablets Dapagliflozin Krka 10 mg film-coated tablets |
Italy | Dapagliflozin Krka |
Norway | Dapagliflozin Krka |
Portugal | Dapagliflozina Krka |
Spain | Dapagliflozina Krka 5 mg film-coated tablets EFG Dapagliflozina Krka 10 mg film-coated tablets EFG |
Sweden | Dapagliflozin Krka 5 mg film-coated tablets Dapagliflozin Krka 10 mg film-coated tablets |
Date of the last revision of this prospectus:March 2024
Detailed information about this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/)