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
The name of the medicine is Urokinase medac. The active substance is urokinase, which helps to dissolve blood clots in:
Urokinase medac is administered by a doctor or nurse with experience in this type of therapy. The patient will not be asked to administer the medicine themselves.
Particular caution should be exercised when using Urokinase medac
In such circumstances, the doctor will decide whether to use Urokinase medac in the patient. During the use of Urokinase medac, the doctor will exercise particular caution if the patient is undergoing blood tests, intramuscular injections, or any other medical procedures that carry a high risk of bleeding, such as arterial procedures.
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.
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:
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.
Using Urokinase medac has a negligible influence on the ability to drive and use machines.
This medicine should always be used as directed by your doctor. The doctor will determine the dose and duration of treatment with Urokinase medac, depending on the indication. Urokinase medac should never be injected into a muscle or under the skin.
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.
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 doctorif you experience:
Other side effects may occur: In some patients, fever or chills, nausea, and vomiting, back pain, or shortness of breath may occur within an hour of starting the infusion.
If you experience any side effects, including any not listed in this leaflet, please inform your doctor or pharmacist. Side effects can be reported directly to the Department of Medicinal Product Monitoring, 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.
Keep this medicine out of the sight and reach of children. Store in a temperature below 25°C. Store in the original package 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. 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 these should normally not exceed 24 hours at 2°C to 8°C, unless reconstitution and dilution have been carried out in 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.
The active substance is human urokinase. The other ingredients are disodium phosphate dodecahydrate, sodium dihydrogen phosphate dihydrate, human albumin.
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.
Pharma-Zentrale GmbH
Loerfeldstraße 20
58313 Herdecke
Germany
Need help understanding this medicine or your symptoms? Online doctors can answer your questions and offer guidance.