Primeri uporabe Coagulation tests v Angleški in njihovi prevodi v Slovenski
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Hematology, including coagulation tests.
Blood coagulation tests are not 100% accurate.
Menstrual cycle, fibrinolysis, blood coagulation tests.
Blood coagulation tests and bleeding time.
Citrate is in liquid form in the tube and is used for coagulation tests, as well as in blood transfusion bags.
Use of coagulation tests and their interpretation.
In the case of concomitant administration of these products, prothrombin time(PT)or other suitable coagulation tests should be monitored.
The use of coagulation tests and their interpretation.
In the case of concomitant administration of these products, prothrombin time(PT)or other suitable coagulation tests should be monitored.
Coagulation tests, therefore, should be monitored in patients treated with vitamin K antagonists(see section 4.4).
Oritavancin binds to and prevents theaction of the phospholipid reagents which activate coagulation in commonly used laboratory coagulation tests.
Coagulation tests such as INR, prothrombin time(PT), or activated partial thromboplastin time(aPTT) are not a useful measure of the effect of Lixiana.
Due to limited data in patients, heparins should be used with care in patients receiving palifermin andappropriate blood coagulation tests should be carried out to monitor their treatment.
Increased coagulation tests(PT/INR) and/or bleeding, which may be severe, have been reported in patients treated with levofloxacin in combination with a vitamin K antagonist(e.g. warfarin).
These effects result from oritavancin binding to and preventing theaction of the phospholipid reagents which activate coagulation in commonly used laboratory coagulation tests.
Blood samples for coagulation tests should be collected as closely as possible prior to a patient's next dose of telavancin or consideration given to using a test unaffected by telavancin.
Therefore neonates whose mothers are treated with drugs valproic acid during pregnancy,it is essential to carry out coagulation tests(to determine the number of platelets in peripheral blood, the plasma concentration of fibrinogen, coagulation factors and coagulation). .
Due to possible increases in coagulation tests(PT/INR) and/or bleeding in patients treated with levofloxacin incombination with a vitamin K antagonist(e.g. warfarin), coagulation tests should be monitored when these active substances are given concomitantly(see section 4.5).
At the doses used for treatment, fondaparinux does not, to a clinically relevant extent,affect routine coagulation tests such as activated partial thromboplastin time(aPTT), activated clotting time(ACT) or prothrombin time(PT)/International Normalised Ratio(INR) tests in plasma nor bleeding time or fibrinolytic activity.
At the 2.5 mg dose, fondaparinux does not affect routine coagulation tests such as activated partial thromboplastin time(aPTT), activated clotting time(ACT) or prothrombin time(PT)/International Normalised Ratio(INR) tests in plasma nor bleeding time or fibrinolytic activity.
A coagulation test helps to identify.
Table 2: Coagulation test thresholds at trough that may be associated with an increased risk of bleeding.
Table 2 shows coagulation test thresholds at trough that may be associated with an increased risk of bleeding(see section 5.1).
In such cases a coagulation test(see sections 4.4 and 5.1) may help to determine whether haemostasis is still impaired.
A coagulation test helps to identify patients with an increased bleeding risk due to increased dabigatran exposure.
A coagulation test helps to identify patients with an increased bleeding risk due to increased dabigatran exposure.
A coagulation test(see section 4.4) may help to identify patients with an increased bleeding risk caused by excessive dabigatran exposure.
A coagulation test helps to identify patients with an increased bleeding risk due to increased dabigatran exposure(see sections 4.2, 4.4 and 5.1).
In healthy volunteer studies, no changes in platelet P-selectin and soluble CD40 ligand(sCD40L)expression or coagulation test parameters(TT, PT, aPTT, ACT, ECT) occurred after single or multiple dose(28 days) administration of vorapaxar.