Edistride 5 mg film-coated tablets and 10 mg film-coated tablets
dapagliflozin
1. What Edistride is and what it is used for
What Edistride is
Edistride contains the active substance dapagliflozin. It belongs to a group of medicines called sodium-glucose transporter (SGLT2) ‘inhibitors’. They work by blocking the SGLT2‑ protein in your kidneys. By blocking this protein, blood sugar ( glucose ), salt ( sodium ), and water are removed from your body via the urine.
What Edistride is used for
Edistride is used in adult patients (18 years and older) to treat:
- Type 2 diabetes
- if your type 2 diabetes cannot be controlled with diet and exercise.
- Edistride can be used alone or in combination with other medicines to treat diabetes.
- It is important to continue to follow the advice on diet and exercise that you have received from your doctor, pharmacist, or nurse.
- Heart failure
- in patients with symptoms due to weak pumping function of the heart.
What is Type 2 Diabetes Diabetes and how can Edistride help?
- In type 2 diabetes, your body does not produce enough insulin or cannot use the insulin that is formed properly. This leads to a high blood sugar level. This can lead to serious problems such as heart or kidney disease, blindness, and poor circulation in your arms and legs.
- Edistride works by removing excess sugar from your body. If you have type 2 diabetes, it can also help prevent heart disease.
What is heart failure and how can Edistride help?
- This type of heart failure occurs when the heart is weak and cannot pump enough blood to the lungs and the rest of the body. This can lead to serious medical problems and the need for hospital care.
- The most common symptoms of heart failure are shortness of breath, feeling tired or very tired all the time, and swollen ankles.
- Edistride helps protect your heart from getting weaker and improves your symptoms. It can reduce the need to go to the hospital and can help some patients live longer.
2. What you need to know before you take 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 cautions
Contact a doctor or nearest hospital immediately
Diabetic ketoacidosis:
- If you have diabetes and experience nausea or vomiting, abdominal pain, thirst, rapid and deep breathing, confusion, unusual sleepiness or fatigue, a sweet breath, a sweet taste or metallic taste in the mouth, a different smell of urine or sweat, or rapid weight loss.
- The above symptoms may be signs of “diabetic ketoacidosis” – a serious, sometimes life-threatening problem that you can get in diabetes due to increased levels of “ketone bodies” in the urine or blood. This is shown in tests.
- The risk of developing diabetic ketoacidosis may increase with prolonged fasting, high alcohol consumption, dehydration, a sudden decrease in insulin dose, or a greater need for insulin due to major surgery or a serious illness.
- When you are being treated with Edistride, diabetic ketoacidosis can occur even if your blood sugar level is normal.
If you suspect you have diabetic ketoacidosis, contact your doctor or nearest hospital immediately and do not take this medicine.
Necrotizing fasciitis in the perineum:
- Talk to your doctor immediately if you experience a combination of symptoms such as pain, tenderness, redness, or swelling of the genitals or the area between the genitals and the rectum along with fever or general malaise. These symptoms can be a sign of a rare but serious and in the worst-case life-threatening infection called necrotizing fasciitis of the perineum or Fournier’s gangrene which destroys the tissue under the skin. Fournier’s gangrene must be treated immediately.
Talk to your doctor, pharmacist, or nurse before taking Edistride
- if you have “type 1 diabetes” – the type that usually begins when you are young, and your body does not produce any insulin.
- if you have liver problems – your doctor may start giving you a lower dose.
- if you are taking medicines that lower blood pressure (blood pressure-lowering drugs) and have had low blood pressure ( hypotension ). More information is given below under “Other medicines and Edistride”.
- if you have very high levels of sugar in your blood that can cause you to become dehydrated (lose too much body fluid). Possible symptoms of dehydration are listed in section 4. Tell your doctor before taking Edistride if you have any of these signs.
- if you get nausea, vomiting, or fever or if you can not eat or drink. These conditions can cause dehydration. Your doctor may ask you to stop taking Edistride until you have recovered 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 get a serious infection.
If any of the above apply 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 to check your feet regularly and follow the advice on foot care provided by healthcare professionals.
Renal function
If you have diabetes, your kidneys should be checked before you start taking Edistride. During treatment with this medicine, your doctor will check your kidney function once a year or more often if your kidney function deteriorates. If you have kidney problems, your doctor may ask you to take another medicine or other medicine to control your blood sugar.
Sugar in the urine
Because of the way Edistride works, your urine will show positive test results for sugar when you take this medicine.
Elderly (65 years and older)
If you are older, there may be a higher risk that your kidneys are not working well and that you are being treated with other medicines (see also “Kidney function” above and “Other medicines and Edistride” below).
Children and young people
Edistride is not recommended for use in children and adolescents below 18 years of age, as it has not been studied in these patients.
Other medicines and Edistride
Tell your doctor, pharmacist, or nurse if you are taking, have recently taken, or might take any other medicines.
In particular, tell your doctor:
- if you are taking a medicine that is used to remove fluid from the body ( diuretics).
- if you are taking other medicines that lower your blood sugar, such as insulin or medicine containing ‘sulphonylureas’. Your doctor may want to lower the dose of one of the other medicines to prevent you from getting low blood sugar (hypoglycemia).
Pregnancy and breastfeeding
If you are pregnant or breast-feeding, 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 (last six months of pregnancy). Talk to your doctor about the best way to control your blood sugar when you are pregnant.
Talk to your doctor if you want to breast-feed or breast-feeding before taking this medicine. Do not use Edistride if you are breast-feeding. It is not known if this medicine passes into breast milk.
Driving and using machines
Edistride has no or negligible effect on the ability to drive and use machines.
Taking this medicine with other medicines called sulphonylureas or with insulin may cause low blood sugar (hypoglycemia), which may cause symptoms such as shaking, sweating, and altered vision and affect your ability to drive and use machines.
Do not drive or use any tools or machines if you feel dizzy while taking Edistride.
Edistride contains lactose
Edistride contains lactose (milk sugar). If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.
3. How to take Edistride
Always take this medicine exactly as your doctor has told you. If you are not sure, talk to your doctor, pharmacist, or nurse.
How much to take
- The recommended dose is one 10 mg tablet every day.
- Your doctor may start you with a dose of 5 mg if you have liver problems.
- Your doctor will prescribe the strength that is right for you.
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. It will help you remember to take it.
Your doctor may prescribe Edistride with other medicines. Remember to take these other medicines according to your doctor’s instructions. It gives the best result for your health.
Diet and exercise can help your body make better use of blood sugar. If you have diabetes, you must continue to follow the diet and exercise programs recommended by your doctor while taking Edistride.
If you take more Edistride than you should
If you have taken too many Edistride tablets, talk to a doctor or go to a hospital immediately. Take the medicine pack with you.
If you forget to take Edistride
What to do if you forget to take a tablet depends on how much time is left until the next dose.
- If it is 12 hours or more until you take the next dose, take one dose of Edistride as soon as you remember. Then take the next dose at the usual time.
- If it is less than 12 hours until you take the next dose, skip the missed dose. Then 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 talking to your doctor first. If you have diabetes, your blood sugar may rise if you do not take 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, this medicine can cause side effects, although not everybody gets them.
Contact your doctor or nearest hospital immediately if you get any of the following side effects:
- angioedema is very rare (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 difficulty breathing
- 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):
- elevated levels of “ketone bodies” in the urine or blood
- nausea or vomiting
- abdominal pain
- strong thirst
- rapid and deep breathing
- confusion
- unusual drowsiness or fatigue
- a sweet smell on the breath, a sweet taste or metallic taste in the mouth, or a different smell on urine or sweat
- rapid weight loss.
This can occur regardless of the blood sugar level. Your doctor may decide to temporarily or permanently discontinue treatment with Edistride.
- necrotizing fasciitis of the perineum or Fournier’s gangrene, a severe soft tissue infection of the genitals or the area between the genitals and the rectum, is very rare.
Stop taking Edistride and see a doctor as soon as possible if you notice any of the following serious side effects:
- urinary tract infection is common (may affect up to 1 in 10 people).
The following are symptoms of severe urinary tract infection:
- fever and/or chills
- burning sensation when urinating (urination)
- back or side pain.
Although unusual, tell your doctor immediately if you notice any blood in your urine.
Contact your doctor as soon as possible if you have any of the following side effects:
- low blood sugar (hypoglycemia) – this is very common (may affect more than 1 in 10 people) in patients with diabetes who are taking this medicine with sulphonylureas or insulin following are symptoms of low blood sugar:
- tremors, sweating, strong anxiety, rapid heartbeat
- feeling hungry, headache, vision changes
- mood swings or feelings of confusion.
Your doctor can tell you how to treat low blood sugar levels and what to do if you get any of the above symptoms.
Other side effects when using Edistride:
Usual
- genital infection (cod) on the penis or vagina (may cause irritation, itching, abnormal discharge, or odor)
- back pain
- discomfort when urinating, the greater amount of urine than usual, or need to urinate more often
- changes in blood cholesterol or blood fat levels (shown in tests)
- increases in the number of red blood cells in the blood (shown in tests)
- reduction of creatinine clearance, a measure of renal function (shown in tests) at the beginning of treatment
- dizziness
- rash
Uncommon (may affect up to 1 in 100 people)
- fungal infection
- loss of too much fluid from your body ( dehydration, signs may include the very dry or sticky mouth, urinating little or nothing at all, or rapid heartbeat)
- thirst
- constipation
- waking up at night to pee
- dry mouth
- weight loss
- increase in creatinine (shown by laboratory blood tests) at the beginning of treatment
- increase in urea (shown by laboratory blood tests)
5. How to store 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”. The expiration date is the last day of the specified month.
No special storage instructions.
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 to protect the environment.
6. Contents of the packaging and other information
Content declaration
- The active substance is dapagliflozin.
Each Edistride 5 mg film-coated tablet (tablet) contains dapagliflozin-propanediol monohydrate equivalent to 5 mg dapagliflozin.Each Edistride 10 mg film-coated tablet (tablet) contains dapagliflozin-propanediol monohydrate equivalent to 10 mg dapagliflozin. - Other ingredients are:
- tablet core: microcrystalline cellulose (E460i), lactose (see section 2 “Edistride contains lactose”), crospovidone (E1202), silica (E551), magnesium stearate (E470b).
- film coating: poly (vinyl alcohol) (E1203), titanium dioxide (E171), macrogol (3350), talc (E553b), yellow iron oxide (E172).
What the medicine looks like and the contents of the pack
Edistride 5 mg film-coated tablets are yellow and round with a diameter of 0.7 cm. They have “5” on one side and “1427” on the other side.
Edistride 10 mg film-coated tablets are yellow and rhombic, approximately 1.1 x 0.8 cm diagonally. They have “10” on one side and “1428” on the other side.
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 30×1 or 90×1 film-coated tablets in perforated unit dose blisters.
Not all pack sizes may be marketed.
Manufacturer
AstraZeneca GmbH
Tinsdaler Weg 183
22880 Wedel
Germany
AstraZeneca UK Limited
Silk Road Business Park
Macclesfield
SK10 2NA
UK
Contact the representative of the marketing authorization holder to find out more about this medicine:
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