EDISTRIDE 10 mg FILM-COATED TABLETS

2. What you need to know before you start taking Edistride

Do not take Edistride

• if you are allergic to dapagliflozin or any of the other ingredients of this medicine (listed in section 6).

Warnings and precautions

Consult a doctor or the nearest hospital immediately

Diabetic ketoacidosis:

• If you have diabetes and experience nausea or vomiting, have stomach pain, excessive thirst, rapid and deep breathing, confusion, drowsiness or unusual tiredness, sweet smell on your breath, a sweet or metallic taste in your mouth, or a different smell in your urine or sweat, or rapid weight loss.
• The above symptoms may be a sign of "diabetic ketoacidosis" - a rare but serious, potentially life-threatening problem that occurs with diabetes due to an increase in "ketone bodies" in your urine or blood, which is detected in tests.
• The risk of developing diabetic ketoacidosis may be increased with prolonged fasting, excessive alcohol consumption, dehydration, sudden reductions in insulin dose, or a greater need for insulin due to major surgery or serious illness.
• When you are being treated with Edistride, diabetic ketoacidosis may occur even if your blood sugar levels are normal.

If you suspect you have diabetic ketoacidosis, contact a doctor or the nearest hospital immediately and do not take this medicine.

Necrotizing fasciitis of the perineum:

• Consult your doctor immediately if you have a combination of symptoms of pain, tenderness, redness, or swelling of the genitals or the area between the genitals and the anus, with fever or general feeling of being unwell. These symptoms could be a sign of a rare but serious, potentially life-threatening infection called necrotizing fasciitis of the perineum or Fournier's gangrene, which destroys tissue under the skin. Fournier's gangrene needs to be treated immediately.

Consult a doctor, pharmacist, or nurse before you start taking Edistride

• if you have "type 1 diabetes" - the type that usually appears when you are young and your body does not produce any insulin. Edistride should not be used to treat this condition
• if you have diabetes and have any kidney problems - your doctor may ask you to take an additional medicine or a different one to control your blood sugar.
• if you have any liver problems - your doctor may start with a lower dose.
• if you are taking medicines to lower your blood pressure (antihypertensives) or have a history of low blood pressure (hypotension). More information is included later in "Taking Edistride with other medicines".
• if you have very high blood sugar levels that can cause dehydration (loss of too much fluid from the body). Possible signs of dehydration are listed in section 4. Tell your doctor before you start taking Edistride if you have any of these signs.
• if you have nausea (feeling sick), vomiting, or fever, or are unable to eat or drink. These conditions can cause dehydration. Your doctor may ask you to stop taking Edistride until you recover to prevent dehydration.
• if you often get urinary tract infections. This medicine may cause urinary tract infections, and your doctor may want to monitor you more closely. Your doctor may consider changing your treatment temporarily if you develop a severe infection.

If any of the above applies to you (or you are not sure), talk to your doctor, pharmacist, or nurse before taking Edistride.

Diabetes and foot care

If you have diabetes, it is important that you regularly check your feet and follow any other foot care advice given to you by your healthcare professional.

Glucose in urine

Due to how Edistride works, your urine will test positive for glucose while you are taking this medicine.

Elderly (65 years or older)

If you are elderly, there may be a greater risk that your kidneys are not working as well as they should, and you may be treated with other medicines (see also "kidney function" above and "Taking Edistride with other medicines" below)

Children and adolescents

Edistride can be used in children aged 10 years and older to treat type 2 diabetes. There is no data available in children under 10 years of age.

Edistride is not recommended in children and adolescents under 18 years of age to treat heart failure or to treat chronic kidney disease, as it has not been studied in these patients.

Taking Edistride with other medicines

Tell your doctor, pharmacist, or nurse if you are taking, have recently taken, or might take any other medicines.

Especially tell your doctor:

• if you are taking a medicine used to remove fluid from the body (diuretic).
• if you are taking other medicines that lower blood sugar, such as insulin or a "sulfonylurea" medicine. Your doctor may decide to reduce the dose of these medicines to avoid you getting low blood sugar (hypoglycemia).
• if you are taking lithium, as Edistride may lower the amount of lithium in your blood.

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. You should stop taking this medicine if you become pregnant, as it is not recommended during the second and third trimesters of pregnancy. Ask your doctor about the best way to control your blood sugar during pregnancy.

Ask your doctor if you want to breastfeed before taking this medicine. Do not use Edistride during breastfeeding. It is not known if this medicine passes into human breast milk.

Driving and using machines

Edistride has no or negligible influence on the ability to drive and use machines.

Taking this medicine with other medicines called sulfonylureas or with insulin may cause low blood sugar levels (hypoglycemia), which can cause symptoms such as shaking, sweating, and changes in vision that can affect your ability to drive or use machines.

Do not drive or use tools or machines if you feel dizzy while taking Edistride.

Edistride contains lactose

Edistride contains lactose. If your doctor has told you that you have an intolerance to some sugars, contact them before taking this medicine.

3. How to take Edistride

Always take this medicine exactly as your doctor has told you. Check with your doctor, pharmacist, or nurse if you are not sure.

What dose should you take

• The recommended dose is one 10 mg tablet a day.
• Your doctor may start with a dose of 5 mg if you have a liver problem.
• Your doctor will prescribe the dose that is right for you.

How to take this medicine

• Swallow the tablet whole with half a glass of water.
• You can take the tablet with or without food.
• You can take the tablet at any time of the day. However, try to take it at the same time each day. This will help you remember to take it.

Your doctor may prescribe Edistride with another medicine(s). Remember to take these other medicine(s) as instructed by your doctor. This will help you get the best results for your health.

Diet and exercise may help your body use blood sugar better. If you have diabetes, it is important that you follow any diet and exercise program recommended by your doctor while taking Edistride.

If you take more Edistride than you should

If you take more Edistride tablets than you should, contact your doctor or go to the hospital immediately. Take the medicine pack with you.

If you forget to take Edistride

What you should do if you forget to take a tablet depends on how much time is left until your next dose.

• If there are 12 hours or more until your next dose, take a dose of Edistride as soon as you remember. Then take the next dose at the usual time.
• If there are less than 12 hours until the next dose, skip the missed dose. Take the next dose at the usual time.
• Do not take a double dose of Edistride to make up for a forgotten dose.

If you stop taking Edistride

Do not stop taking Edistride without first talking to your doctor. If you have diabetes, your blood sugar levels may increase without this medicine.

If you have any further questions on the use of this product, ask your doctor, pharmacist, or nurse.

4. Possible side effects

Like all medicines, Edistride can cause side effects, although not everybody gets them.

Contact a doctor or the nearest hospital immediately if you get any of the following side effects:

• angioedema,seen very rarely (may affect up to 1 in 10,000 people).

These are the signs of angioedema:

• swelling of the face, tongue, or throat
• difficulty swallowing
• hives and breathing problems

• diabetic ketoacidosis, this is rare in patients with type 2 diabetes (may affect up to 1 in 1,000 people)

These are the signs of diabetic ketoacidosis (see also section 2 Warnings and precautions):

• increase in "ketone bodies" in your urine or blood
• nausea or vomiting
• stomach pain
• excessive thirst
• rapid and deep breathing
• confusion
• drowsiness and unusual tiredness
• sweet smell on your breath, a sweet or metallic taste in your mouth, or a different smell in your urine or sweat.
• rapid weight loss

This can happen regardless of your blood sugar levels. Your doctor will decide whether to temporarily or permanently stop your treatment with Edistride.

necrotizing fasciitis of the perineumor Fournier's gangrene, a serious infection of the soft tissues of the genitals or the area between the genitals and the anus, seen very rarely.

Stop taking Edistride and contact a doctor immediately if you notice any of these serious side effects:

• urinary tract infection, occurs frequently (may affect up to 1 in 10 people).

These are the signs of a severe urinary tract infection:

• fever and/or chills
• burning sensation when urinating
• back or side pain.

Although it is not common, if you see blood in your urine, tell your doctor immediately.

Contact your doctor as soon as possible if you get any of the following side effects:

• low blood sugar (hypoglycemia), very common (may affect more than 1 in 10 people) in patients with diabetes who take this medicine with a sulfonylurea or insulin

These are the signs of low blood sugar:

• chills, sweating, feeling of great anxiety, rapid heartbeat
• feeling hungry, headache, changes in vision
• change in mood or feeling confused.

Your doctor will explain how to treat low blood sugar and what to do if you get any of the above signs.

Other side effects of Edistride treatment:

Common

• genital infections (candidiasis) of the penis or vagina (signs may include irritation, itching, and discharge or unusual smell)
• back pain
• difficulty urinating, increased amount of urine, or need to urinate more frequently
• changes in cholesterol or lipid levels in the blood (seen in tests)
• increases in the number of red blood cells in the blood (seen in tests)
• decreases in renal clearance of creatinine (seen in tests) at the start of treatment
• dizziness
• rash

Uncommon (may affect up to 1 in 100 people)

• fungal infection
• excessive loss of fluids from the body (dehydration, signs may include a very dry or sticky mouth, reduced or no urination; or rapid heartbeat)
• thirst
• constipation
• waking up at night to urinate
• dry mouth
• weight loss
• increase in creatinine (seen in blood tests) at the start of treatment
• increase in urea (seen in blood tests)

Rare

• kidney inflammation (tubulointerstitial nephritis)

Reporting of side effects

If you get 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.

5. Storage of Edistride

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 or carton after EXP/CAD. The expiry date is the last day of the month shown.

No special storage conditions are required.

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.

6. Contents of the pack and additional information

Composition of Edistride

• The active substance is dapagliflozin.

Each film-coated tablet (tablet) of Edistride 5 mg contains dapagliflozina propanediol monohydrate equivalent to 5 mg of dapagliflozin.

Each film-coated tablet (tablet) of Edistride 10 mg contains dapagliflozina propanediol monohydrate equivalent to 10 mg of dapagliflozin.

• The other ingredients are:
• • tablet core: microcrystalline cellulose (E460i), lactose (see section 2 "Edistride contains lactose"), crospovidone (E1202), silicon dioxide (E551), magnesium stearate (E470b).
  • film coating: polyvinyl alcohol (E1203), titanium dioxide (E171), macrogol (3350) (E1521), talc (E553b), yellow iron oxide (E172).

Appearance of the product and pack contents

The film-coated tablets of Edistride 5 mg are yellow and round with a diameter of 0.7 cm. They are engraved with "5" on one side and "1427" on the other.

The film-coated tablets of Edistride 10 mg are yellow and diamond-shaped, approximately 1.1 x 0.8 cm in diagonal. They are engraved with "10" on one side and "1428" on the other.

Edistride 5 mg tablets and Edistride 10 mg tablets are available in aluminum blisters in pack sizes of 14, 28 or 98 film-coated tablets in non-perforated calendar blisters and in packs of 30x1 or 90x1 film-coated tablets in perforated unit-dose blisters.

Not all pack sizes may be marketed in your country.

Marketing authorisation 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

SK10 2NA

United Kingdom

For further information about this medicinal product, contact the local representative of the marketing authorisation holder:

Date of last revision of this prospectus:

Other sources of information

Detailed information on this medicinal product is available on the European Medicines Agency website: http://www.ema.europa.eu.