Examples of using Normalised ratio in English and their translations into German
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Discontinue the VKA and start Lixiana when the international normalised ratio(INR) is≤ 2.5.
It is recommended that the international normalised ratio(INR) be monitored upon co-administration of Genvoya.
Selexipag did not influence the pharmacodynamic effect of warfarin on the international normalised ratio.
It is recommended that the international normalised ratio(INR) be monitored when warfarin is combined with INTELENCE.
Hyperglycaemia, decreased haemoglobin, hypokalaemia, hyponatraemia, decreased white blood cell count,increased international normalised ratio INR.
Or prothrombin time(PT)/ International Normalised Ratio(INR) tests in plasma nor bleeding time or fibrinolytic activity.
Co-administration with REYATAZ/ritonavir has the potential to produce a decrease or, less often,an increase in INR International Normalised Ratio.
It is recommended that the international normalised ratio(INR) be monitored upon co-administration and following ceasing treatment with idelalisib.
Co-administration with REYATAZ/ ritonavir has the potential to produce a decrease or, less often,an increase in INR International Normalised Ratio.
It is recommended that the International Normalised Ratio(INR) be monitored carefully during treatment with REYATAZ, especially when commencing therapy.
Therefore, when warfarin or anothercoumarin anticoagulant is co-administered,close international normalised ratio(INR) follow-up and monitoring is recommended.
International Normalised Ratio(INR) should be closely monitored after initiating dronedarone in patients taking vitamin K antagonists as per their label.
Dronedarone(600 mg twice daily) increased by 1.2-fold S-warfarin with no change in R-warfarin andonly a 1.07 increase in International Normalised Ratio INR.
Infrequent bleeding events or elevations in the International Normalised Ratio(INR) have been reported in some patients taking warfarin while on Nexavar therapy.
And general status of the patient so thatthe contribution of the fluoroquinolone to the increase in INR(international normalised ratio) is difficult to assess.
Coagulation parameters, specifically international normalised ratio(INR), should be monitored in the days immediately following the initiation of Pixuvri concurrent therapy.
ZEPATIER should be discontinued if ALT elevation is accompanied by signs or symptoms of liver inflammation or increasingconjugated bilirubin, alkaline phosphatase, or international normalised ratio INR.
The readout for PT is to be donein seconds, because the INR(International Normalised Ratio) is only calibrated and validated for coumarins and cannot be used for any other anticoagulant.
The risk may vary with the underlying infection, age and general status of the patient so thatthe contribution of the fluoroquinolone to the increase in INR(international normalised ratio) is difficult to assess.
Consequently, APTIVUS co-administered with low dose ritonavir,may be associated with changes in INR(International Normalised Ratio) values, and may affect anticoagulation(thrombogenic effect) or increase the risk of bleeding.
Tell your doctor if you are taking warfarin or other blood thinners asyou might need to have blood tests more often to measure how thick your blood is called‘International Normalised Ratio' or INR test.
Pancytopenia, prothrombin time prolonged, international normalised ratio increased, hypoprothrombinaemia, prothrombin time shortened, granulocytosis, leukocytosis, eosinophilia, lymphocytosis, monocyte count decreased, monocyte count increased, thrombocythaemia.
After concomitant administration of warfarin 25 mg with repeated dosing of lixisenatide 20 mcg,there were no effects on AUC or INR(International Normalised Ratio) while Cmax was reduced by 19% and tmax was delayed by 7 hours.
Oritavancin has been shown to artificially prolong prothrombin time(PT) and international normalised ratio(INR) for up to 12 hours, making the monitoring of the anticoagulation effect of warfarin unreliable up to 12 hours after an oritavancin dose.
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.
Prolonged prothrombin time, prolonged activated partial thromboplastin time,increased International Normalised Ratio, increased blood alkaline phosphatase, increased blood lactate dehydrogenase, increased C-Reactive Protein, Cytomegalovirus antibody positive.
For some medicinal products that can cause serious or life-threatening undesirable effects, such as carbamazepine, phenobarbital, phenytoin,tricyclic antidepressants and warfarin(monitor International Normalised Ratio), concentration monitoring is available; this should minimise the risk of potential safety problems with concomitant use.
Common Blood bilirubin increased, Weight decreased, White blood cell count decreased, Haemoglobin decreased, Neutrophil count decreased,International normalised ratio increased, Activated partial thromboplastin time prolonged, Blood glucose increased, Blood albumin decreased, Electrocardiogram QT prolonged.
Seventy-three percent(73%) of patients enrolled into the ACTIVE-A study were unable to take VKA due to physician assessment,inability to comply with INR(international normalised ratio) monitoring, predisposition to falling or head trauma, or specific risk of bleeding; for 26% of the patients, the physician's decision was based on the patient's unwillingness to take VKA.
