Примери за използване на Venous thromboembolic на Английски и техните преводи на Български
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The most common adverse reactions were skin reactions, venous thromboembolic events and laboratory abnormalities(hypomagnesaemia
Treatment-related venous thromboembolic events were reported in approximately 1.0% of patients with solid tumours who received sunitinib on clinical trials, including GIST and RCC.
Testosterone Cypionate may cause venous thromboembolic events which may be symptomized by extreme shortness of breath,
Venous thromboembolic events(VTE) and arterial thromboembolic events(ATE), including fatal cases,
However, you need to avoid smoking during their use because the risk for cardiovascular disease and venous thromboembolic disease increases.
Treatment-related venous thromboembolic events were reported in patients who received sunitinib including deep venous thrombosis and pulmonary embolism(see section 4.8).
Venous thromboembolic events(VTEs) were reported in approximately 8% of patients
rash, venous thromboembolic events, pruritus and urticaria.
Prophylaxis of venous thromboembolic disease in moderate and high risk surgical patients,
observed in necitumumab-treated patients are skin reactions(6.3%) and venous thromboembolic events(4.3%).
VTE= venous thromboembolic event(DVT and/or PE)*The 95% Confidence Intervals for the treatment differences for total VTE were.
Prophylaxis of venous thromboembolic disease in medical patients with an acute illness expected to induce limitation of mobility.
For the prophylaxis of venous thromboembolic disease following surgery,
The harmonised indication therefore states prophylaxis of venous thromboembolic disease in moderate
However, combined hormonal contraceptives are not recommended due to the increased risk of venous thromboembolic disease.
Intrarosa has not been studied in women with current or previous venous thromboembolic disease.
In the phase 2 trial(with a minimum of 64 months follow-up), venous thromboembolic adverse reactions have occurred in 6% of patients(treatment-emergent frequencies).
Serious venous thromboembolic adverse reactions occurred in 5% of patients(treatment-emergent frequencies)(see section 4.8).
Venous thromboembolic events were reported in 5.3% of patients treated with abemaciclib
Venous Thromboembolic Events Treatment-related venous thromboembolic events were reported in approximately 1.0% of patients with solid tumours who received SUTENT on clinical trials, including GIST and MRCC.