


Ask a doctor about a prescription for Humulin N
(Human insulin)
Humulin N contains human insulin as the active substance, which is used to treat diabetes.
The cause of diabetes is the pancreas's inability to produce insulin in quantities that allow
control of blood glucose levels (blood sugar). Humulin N is used to control blood glucose levels
in the long term. The duration of action of this insulin has been prolonged by the use of protamine sulfate in the suspension.
Your doctor may recommend using Humulin N and fast-acting insulin. Each type of insulin has a different patient leaflet. You should not change your insulin unless your doctor has told you to. When changing insulin, you should be very careful. Each type of insulin has a different symbol and color on the packaging and cartridge to make it easier to distinguish.
Before starting treatment with Humulin N, you should talk to your doctor, pharmacist, or nurse.
Skin changes at the injection site
You should change the injection site to prevent skin changes, such as lumps under the skin. Insulin injected into an area with lumps may not work properly (see "How to use Humulin N"). If you are currently injecting insulin into an area with lumps, you should contact your doctor before changing it. Your doctor may recommend more frequent blood glucose monitoring and adjusting the dose of insulin or other antidiabetic medicines.
You should tell your doctor or pharmacist about all the medicines you are taking or have recently taken, as well as any medicines you plan to take.
Your body's need for insulin may change if you are taking:
Your body's need for insulin usually decreases during the first three months of pregnancy and increases during the next six months. Breastfeeding women may need to adjust their insulin dose or diet.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
If you have hypoglycemia (low blood glucose), your ability to concentrate and react may be impaired. You should be aware of this in all situations where it could put you or others at risk (e.g., when driving a car or operating machinery).
You should ask your diabetes nurse or doctor for advice on driving if:
This medicine contains less than 1 mmol sodium (23 mg) per dose, i.e., it is essentially "sodium-free".
This medicine should always be used as instructed by your doctor or pharmacist. If you are not sure, ask your doctor or pharmacist.
To avoid the risk of transmitting diseases, each cartridge can only be used by one person, even if the needle is changed.
Humulin N should be injected as instructed by your doctor or diabetes nurse.
If you inject more Humulin N than prescribed, you may experience low blood glucose. You should check your blood glucose level (see subsection A in section 4)
If you inject less Humulin N than prescribed, you may experience high blood glucose. You should check your blood glucose level. Do not inject a double dose to make up for a missed dose.
If you inject less Humulin N than prescribed, you may experience high blood glucose. Do not change your insulin unless your doctor has told you to.
If you have any further questions about using this medicine, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Generalized allergyis very rare (less than 1 in 10,000 patients). The symptoms are:
If you experience any of these symptoms while using Humulin N, you should contact your doctor immediately.
Local allergyis common (less than 1 in 10 patients). The symptom may be redness, swelling, or itching at the injection site. These symptoms usually disappear after a few days or weeks. If you experience any of these symptoms, you should tell your doctor.
If insulin is injected into the same area too frequently, the fatty tissue may shrink (lipoatrophy) or thicken (lipohypertrophy) (less than 1 in 100 patients).
Lumps under the skin can also be caused by the accumulation of a protein called amyloid (amyloidosis, frequency not known). Insulin injected into an area with lumps may not work properly. You should change the injection site each time to prevent these skin changes.
Swelling (e.g., swelling of the arms, ankles; fluid retention) has been reported, especially at the start of insulin treatment or when changing treatment to improve blood glucose control.
Hypoglycemia (low blood glucose) is a condition in which there is too little glucose in the blood. It can occur if:
Alcohol and some medicines can affect your blood glucose level.
The first symptoms of low blood glucose usually come on quickly and include:
If you are not sure about recognizing the warning signs of hypoglycemia, you should avoid situations where you might put yourself or others at risk (e.g., driving a car).
If your blood glucose level is low, you should eat glucose tablets, sugar, or a sweet drink. Then, you should eat fruit, biscuits, or a sandwich, as your doctor has advised, and rest. This usually works for mild hypoglycemia or a small overdose of insulin. If your condition worsens, or you experience shallow breathing, and your skin becomes pale, you should contact your doctor immediately. An injection of glucagon may help in severe hypoglycemia. After injecting glucagon, you should eat glucose tablets or sugar. If you do not improve after glucagon injection, you should go to the hospital. For more information about glucagon, ask your doctor.
Hyperglycemia (high blood glucose) means that your body is not getting enough insulin. Hyperglycemia can be caused by:
Hyperglycemia can lead to diabetic ketoacidosis. The first symptoms develop slowly over a few hours or days. They include:
Severe symptoms include difficulty breathing and rapid pulse. You should seek medical help immediately.
Untreated hypoglycemia (low blood glucose) or hyperglycemia (high blood glucose) can lead to serious complications and cause headaches, nausea, vomiting, dehydration, loss of consciousness, coma, or even death.
Three simple waysto avoid hypoglycemia or hyperglycemia:
When you are ill, especially if you have vomiting or diarrhea, your body's need for insulin may change. People with diabetes need insulin even when they are not eating their normal meals.You should do a urine or blood test, follow the general rules for treating illness, and contact your diabetes nurse or doctor.
If you experience any side effects, including any not listed in this leaflet, you should tell your doctor, pharmacist, or nurse. You can also report side effects directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products: Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl .
You can also report side effects to the marketing authorization holder or its representative. By reporting side effects, you can help provide more information on the safety of this medicine.
Medicines should be kept out of the sight and reach of children.
Before first use, you should store Humulin N in the refrigerator (2°C - 8°C). Do not freeze.
The used pen and cartridge should be kept at room temperature (below 30°C) and used within 28 days. Do not store the used pen or cartridge in the refrigerator.
Do not store them near heat sources or in direct sunlight.
Do not use this medicine after the expiry date stated on the label and carton. The expiry date refers to the last day of that month.
Do not use this medicine if you notice clumps or white particles sticking to the bottom or sides of the cartridge, and the glass is cloudy. You should check the appearance of the insulin before each injection.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Humulin N is a white, sterile suspension of human insulin isophane. One milliliter of the suspension contains 100 international units of insulin (100 IU/ml). Each cartridge contains 300 units (3 ml suspension).
The cartridges are sold in packs of 5.
Marketing authorization holder:
Eli Lilly Nederland B.V., Papendorpseweg 83, 3528 BJ Utrecht, Netherlands
Manufacturer:
Lilly France S.A.S., Rue du Colonel Lilly, 67640 Fegersheim, France
Eli Lilly Italia S.p.A., Via A. Gramsci 731-733, 50019 Sesto Fiorentino, Italy
To obtain more detailed information, you should contact the representative of the marketing authorization holder:
Eli Lilly Polska Sp.z o.o.
ul. Żwirki i Wigury 18A
02-092 Warsaw
Tel: +48 22 440 33 00
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