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Generated Narrative: Bundle TEST PURPOSES ONLY - ryzodeg
Language: en
Profile: Bundle - ePI
Final Document at 2022-02-16 13:28:17+0000 by Organization ACME industry for Bundle: identifier = http://ema.europa.eu/identifier#None; type = document; timestamp = 2023-06-27 10:09:22+0000
Document Subject
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identifier: http://ema.europa.eu/identifier
/EU/1/12/806/001
type: Medicinal Product
domain: Human use
status: active
legalStatusOfSupply: Medicinal product subject to medical prescription
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Country Jurisdiction Language EU EU en
Document Content
Generated Narrative: Composition composition-en-47f74762e12054bd07cc18f7f2dc9dfb
Language: en
Profile: Composition (ePI)
identifier: http://ema.europa.eu/identifier
/EU/1/12/806/001
status: Final
type: Package Leaflet
category: Raw
date: 2022-02-16 13:28:17+0000
author: Organization ACME industry
title: TEST PURPOSES ONLY - ryzodeg
Mode | Time |
Official | 2022-02-16 13:28:17+0000 |
What is in this leaflet:
Ryzodeg is used to treat diabetes mellitus in adults, adolescents and children from the age of 2 years. It helps your body reduce your blood sugar level.
This medicine contains two types of insulin:
Do not use Ryzodeg
Warnings and precautions Talk to your doctor, pharmacist or nurse before using Ryzodeg. Be especially aware of the following:
If you have poor eyesight, please see section 3. Skin changes at the injection site The injection site should be rotated to help prevent changes to the fatty tissue under the skin, such as skin thickening, skin shrinking or lumps under the skin. The insulin may not work very well if you inject into a lumpy, shrunken or thickened area (see section 3 How to use Ryzodeg ). Tell your doctor if you notice any skin changes at the injection site. Tell your doctor if you are currently injecting into these affected areas before you start injecting in a different area. Your doctor may tell you to check your blood sugar more closely, and to adjust your insulin or your other antidiabetic medications dose.
Children and adolescents Ryzodeg can be used in adolescents and children from the age of 2 years with diabetes mellitus. Ryzodeg should be used with special caution in children 2 to 5 years old. The risk for very low blood sugar may be higher in this age group. There is no experience with the use of this medicine in children below the age of 2 years.
Other medicines and Ryzodeg Tell your doctor, pharmacist or nurse if you are taking, have recently taken or might take any other medicines. Some medicines affect your blood sugar level, this may mean your insulin dose has to be changed.
Listed below are the most common medicines which may affect your insulin treatment.
Your blood sugar level may fall (hypoglycaemia) if you take:
Your blood sugar level may rise (hyperglycaemia) if you take:
Octreotide and lanreotide: used to treat a rare condition involving too much growth hormone (acromegaly). They may increase or decrease your blood sugar level.
Pioglitazone: oral antidiabetic medicine used to treat type 2 diabetes mellitus. Some patients with long-standing type 2 diabetes mellitus and heart disease or previous stroke who were treated with pioglitazone and insulin experienced the development of heart failure. Inform your doctor immediately if you experience signs of heart failure such as unusual shortness of breath, rapid increase in weight or localised swelling (oedema).
If any of the above applies to you (or you are not sure), talk to your doctor, pharmacist or nurse.
Ryzodeg with alcohol If you drink alcohol, your need for insulin may change. Your blood sugar level may either rise or fall. You should therefore monitor your blood sugar level more often than usual.
Pregnancy and breast-feeding It is not known if Ryzodeg affects the baby in pregnancy or during breast-feeding. 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. Your insulin dose may need to be changed during pregnancy and after delivery. Careful control of your diabetes is needed in pregnancy. Avoiding too low blood sugar (hypoglycaemia) is particularly important for the health of your baby.
Driving and using machines Having too low or too high blood sugar can affect your ability to drive or use any tools or machines. If your blood sugar is too low or too high, your ability to concentrate or react might be affected. This could be dangerous to yourself or others. Ask your doctor whether you can drive if:
Important information about some of the ingredients in Ryzodeg This medicine contains less than 1 mmol sodium (23 mg) per dose. This means that the medicine is essentially sodium-free .
Always use this medicine exactly as your doctor has told you. Check with your doctor, pharmacist or nurse if you are not sure.
If you are blind or have poor eyesight and cannot read the dose counter on the pen, do not use the pen without help. Get help from a person with good eyesight who is trained to use the FlexTouch pre-filled pen.
The pre-filled pen can provide a dose of 1 80 units in one injection in steps of 1 unit.
Your doctor will decide with you:
Flexibility in dosing time
Based on your blood sugar level, your doctor may change your dose.
When using other medicines, ask your doctor if your treatment needs to be adjusted.
Use in elderly ( 65 years old) Ryzodeg can be used in elderly, but you may need to check your blood sugar level more often. Talk to your doctor about changes in your dose.
If you have kidney or liver problems If you have kidney or liver problems, you may need to check your blood sugar level more often. Talk to your doctor about changes in your dose.
Injecting your medicine Before you use Ryzodeg for the first time, your doctor or nurse will show you how to use the pre-filled pen.
Do not use Ryzodeg
How to inject
Detailed instructions for use are provided on the other side of this leaflet.
If you use more Ryzodeg than you should If you use too much insulin, your blood sugar may get too low (hypoglycaemia), see advice in section 4 Too low blood sugar .
If you forget to use Ryzodeg If you forget a dose, inject the missed dose with your next large meal on that day and thereafter resume your usual dosing schedule. Do not inject a double dose to make up for a forgotten dose.
If you stop using Ryzodeg Do not stop using your insulin without talking to your doctor. If you stop using your insulin, this could lead to a very high blood sugar level and ketoacidosis (a condition with too much acid in the blood), see advice in section 4 Too high blood sugar .
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Hypoglycaemia (too low blood sugar) may occur very commonly with insulin treatment (may affect more than 1 in 10 people). It can be very serious. If your blood sugar level falls too much, you may become unconscious. Serious hypoglycaemia may cause brain damage and may be life-threatening. If you have symptoms of low blood sugar, take actions to increase your blood sugar level immediately. See advice in Too low blood sugar below.
If you have a serious allergic reaction (seen rarely) to the insulin or any of the ingredients in Ryzodeg, stop using this medicine and see a doctor straight away. The signs of a serious allergic reaction are:
Other side effects include:
Common (may affect up to 1 in 10 people) Local reactions: Local reactions at the place you inject yourself may occur. The signs may include: pain, redness, hives, swelling and itching. The reactions usually disappear after a few days. See your doctor if they do not disappear after a few weeks. Stop using Ryzodeg and see a doctor straight away if the reactions become serious. For more information, see serious allergic reaction above.
Uncommon (may affect up to 1 in 100 people) Swelling around your joints: When you first start using your medicine, your body may keep more water than it should. This causes swelling around your ankles and other joints. This is usually only short-lasting.
Rare (may affect up to 1 in 1,000 people) This medicine can cause allergic reactions such as hives, swelling of the tongue and lips, diarrhoea, nausea, tiredness and itching.
Frequency not known (cannot be estimated from the available data) Skin changes at the injection site: If you inject insulin at the same place, the fatty tissue may either shrink (lipoatrophy) or thicken (lipohypertrophy). Lumps under the skin may also be caused by build- up of a protein called amyloid (cutaneous amyloidosis). The insulin may not work very well if you inject into a lumpy, shrunken or thickened area. Change the injection site with each injection to help prevent these skin changes.
General effects from diabetes treatment
Too low blood sugar may happen if you: drink alcohol; use too much insulin; exercise more than usual; eat too little or miss a meal.
Warning signs of too low blood sugar these may come on suddenly:
Headache; slurred speech; fast heartbeat; cold sweat, cool pale skin; feeling sick, feeling very hungry; tremor or feeling nervous or worried; feeling unusually tired, weak and sleepy; feeling confused, difficulty in concentrating; short-lasting changes in your sight.
What to do if you get too low blood sugar
What others need to do if you pass out
Tell everyone you spend time with that you have diabetes. Tell them what could happen if your blood sugar gets too low, including the risk of passing out.
Let them know that if you pass out, they must:
You may recover more quickly from passing out with an injection of glucagon. This can only be given by someone who knows how to use it.
Talk to your doctor if:
your blood sugar got so low that you passed out
you have used an injection of glucagon
you have had too low blood sugar a few times recently. This is because the dosing or timing of your insulin injections, food or exercise may need to be changed.
Too high blood sugar (hyperglycaemia)
Too high blood sugar may happen if you: eat more or exercise less than usual; drink alcohol; get an infection or a fever; have not used enough insulin; keep using less insulin than you need; forget to use your insulin or stop using insulin without talking to your doctor.
Warning signs of too high blood sugar these normally appear gradually:
Flushed, dry skin; feeling sleepy or tired; dry mouth, fruity (acetone) breath; urinating more often, feeling thirsty; losing your appetite, feeling or being sick (nausea or vomiting).
These may be signs of a very serious condition called ketoacidosis. This is a build-up of acid in the blood because the body is breaking down fat instead of sugar. If not treated, this could lead to diabetic coma and eventually death.
What to do if you get too high blood sugar
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.
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 pen label and carton, after EXP . The expiry date refers to the last day of that month.
Before first use Store in a refrigerator (2 C to 8 C). Do not freeze. Keep away from the freezing element. Keep the cap on the pen in order to protect from light.
After first opening or if carried as a spare You can carry your Ryzodeg pre-filled pen (FlexTouch) with you and keep it at room temperature (not above 30 C) or in a refrigerator (2 C to 8 C) for up to 4 weeks.
Always keep the cap on the pen when you are not using it in order to protect from light.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.
What Ryzodeg contains
What Ryzodeg looks like and contents of the pack Ryzodeg is presented as a clear and colourless solution for injection in pre-filled pen (300 units per 3 mL).
Pack sizes of 1 (with or without needles), 5 (without needles) and multipack of 10 (2 x 5) (without needles) pre-filled pens of 3 mL. Not all pack sizes may be marketed.
Marketing Authorisation Holder
Novo Nordisk A/S Novo All
DK-2880 Bagsv rd, Denmark
Manufacturer
The manufacturer can be identified by the batch number printed on the slip of the carton and on the label:
If the second and third characters are P5, ZF or FG, the manufacturer is Novo Nordisk A/S, Novo All , DK-2880 Bagsv rd, Denmark.
If the second and third characters are T6, the manufacturer is Novo Nordisk Production SAS, Avenue d Orl ans, 28000 Chartres, France.
This leaflet was last revised in
Detailed information on this medicine is available on the European Medicines Agency web site:
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