Urokinase medac

Leaflet attached to the packaging: information for the user

Urokinase medac, 10,000 IU, powder for solution for injection or infusion
Urokinase medac, 50,000 IU, powder for solution for injection or infusion
Urokinase medac, 100,000 IU, powder for solution for injection or infusion
Urokinase medac, 250,000 IU, powder for solution for injection or infusion
Urokinase medac, 500,000 IU, powder for solution for injection or infusion
Urokinasum

Read the leaflet carefully before using the medicine, as it contains important information for the patient.

• Keep this leaflet, you may need to read it again.
• If you have any further questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.
• If you experience any side effects, including those not listed in this leaflet, tell your doctor or pharmacist. See section 4.

Table of contents of the leaflet:

• 1. What is Urokinase medac and what is it used for
• 2. Important information before using Urokinase medac
• 3. How to use Urokinase medac
• 4. Possible side effects
• 5. How to store Urokinase medac
• 6. Contents of the pack and other information

1. What is Urokinase medac and what is it used for

The name of the medicine is Urokinase medac. The active substance is urokinase, which helps to dissolve blood clots in:

• lungs
• deep veins
• peripheral arteries (e.g. in the legs)
• central venous catheters (catheters placed in large veins in the neck, chest, or groin) and arteriovenous fistulas for hemodialysis (surgically created connections between an artery and a vein used for blood filtration)

2. Important information before using Urokinase medac

Urokinase medac is administered by a doctor or nurse with experience in this type of therapy. You will not be asked to use the medicine on your own.

When not to use Urokinase medac

Warnings and precautions

Particular caution should be exercised when using Urokinase medac

In such circumstances, the doctor will decide whether to use Urokinase medac. During the use of Urokinase medac, the doctor will exercise particular caution if you are undergoing blood tests, intramuscular injections, or any other medical procedures that carry a high risk of bleeding, such as arterial procedures.

Children

There is very limited experience with the use of urokinase in dissolving blood clots in peripheral arteries (e.g. in the legs) in children. Therefore, urokinase should not be used in such cases.

Urokinase medac and other medicines

Tell your doctor or pharmacist about all medicines you are currently taking or have recently taken, including those that are available without a prescription, especially if you are taking any of the following medicines:

• heparin, dipyridamole, and other anticoagulant medicines or those that may affect blood coagulation
• acetylsalicylic acid (aspirin)
• non-steroidal anti-inflammatory drugs (NSAIDs)
• dextrans
• contrast agents

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 using this medicine. Urokinase medac should not be used during pregnancy or immediately after childbirth, unless it is clearly necessary. It is not known whether urokinase passes into breast milk. Therefore, breastfeeding should be avoided during treatment with Urokinase medac.

Driving and using machines

Using Urokinase medac has a negligible effect on the ability to drive and use machines.

3. How to use Urokinase medac

This medicine should always be used according to the doctor's instructions. The doctor will determine the dose and duration of treatment with Urokinase medac, depending on the indication. Urokinase medac should never be injected into muscles or under the skin.

Use in children

Urokinase medac can be used in children of any age to treat blocked central venous catheters, using the same procedures as for adult patients. If you have any further questions on the use of this medicine, ask your doctor or nurse.

4. Possible side effects

Like all medicines, Urokinase medac can cause side effects, although not everybody gets them. Urokinase medac may rarely cause serious side effects. You should immediately inform your doctor if you experience:

• any spontaneous bleeding, as urokinase increases the risk of bleeding.
• symptoms of an allergic reaction/hypersensitivity, such as
• chest tightness or breathing difficulties
• swelling of the eyelids, face, or lips
• rash or hives on the skin, itching
• fainting (drop in blood pressure) or cyanosis (blue discoloration)

Other side effects may occur: some patients may experience fever or chills, nausea and vomiting, back pain, or shortness of breath within an hour of starting the infusion.

Very common (occurred in more than 1 in 10 patients)

• bleeding
• unusual bleeding, especially from injection sites or wounds
• small amounts of blood in the urine
• nosebleeds
• gum bleeding
• bruises
• changes in blood test results

Common (occurred in less than 1 in 10 patients and more than 1 in 100)

• fever
• chills
• bleeding (in the brain, stomach, urine, muscles)
• small blood clots or cholesterol crystals may break loose and travel with the blood, causing blockages in other areas.

Uncommon (occurred in less than 1 in 100 patients and more than 1 in 1000)

• liver bleeding

Reporting side effects

If you experience any side effects, including those not listed in this leaflet, tell your doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products: Al. Jerozolimskie 181C, PL-02-222 Warsaw, Tel.: 22 49-21-301, Fax: 22 49-21-309, Website: https://smz.ezdrowie.gov.pl. Side effects can also be reported to the marketing authorization holder. By reporting side effects, you can help provide more information on the safety of this medicine.

5. How to store Urokinase medac

Keep the medicine out of the sight and reach of children. Store in a temperature below 25°C. Store in the original packaging to protect from light. Do not use this medicine after the expiry date stated on the label. The expiry date refers to the last day of the month stated. Do not use Urokinase medac if the powder in the vial is not white. The chemical and physical stability, both at room temperature and at 5°C ± 3°C, after reconstitution and further dilution with sodium chloride 9 mg/ml (0.9%) solution for injection is 72 hours. From a microbiological point of view, the product should be used immediately after reconstitution and dilution. If not used immediately, the responsibility for the storage conditions and duration before use rests with the user, and normally should not exceed 24 hours at 2°C to 8°C, unless reconstitution and dilution are performed under controlled and validated aseptic conditions. Due to the loss of urokinase activity, the solution should be used immediately after reconstitution and further dilution with 5% or 10% glucose solution.

6. Contents of the pack and other information

What Urokinase medac contains

The active substance is human urokinase. The other ingredients are disodium phosphate dodecahydrate, sodium dihydrogen phosphate dihydrate, human albumin.

What Urokinase medac looks like and contents of the pack

Each vial contains a white powder for solution for injection or infusion. Each pack contains one vial. Urokinase medac is available in different strengths: 10,000 IU, 50,000 IU, 100,000 IU, 250,000 IU, 500,000 IU. Not all strengths may be marketed.

Marketing authorization holder and manufacturer

Pharma-Zentrale GmbH
Loerfeldstraße 20
58313 Herdecke
Germany

Date of last revision of the leaflet: