Примери за използване на Fondaparinux should на Английски и техните преводи на Български
{-}
-
Medicine
-
Colloquial
-
Official
-
Ecclesiastic
-
Ecclesiastic
-
Computer
Fondaparinux should be used with care in these patients.
In patients with severe hepatic impairment, fondaparinux should be used with care(see section 4.4).
Fondaparinux should be used with caution in these patients(see section 4.4).
Patients with Heparin Induced Thrombocytopenia Fondaparinux should be used with caution in patients with a history of HIT.
Fondaparinux should be used with caution in elderly patients(see section 4.2).
Clinical experience is limited in patients with body weight< 50 kg. Fondaparinux should be used with caution at a daily dose of 5 mg in this population(see sections 4.2 and 5.2).
Fondaparinux should not be prescribed to pregnant women unless clearly necessary.
In these patients the use of prolonged prophylaxis with fondaparinux should be considered for up to an additional 24 days(see section 5.1).
Fondaparinux should be used with caution in patients with a history of HIT.
If follow up treatment with a Vitamin K antagonist is required,treatment with fondaparinux should be continued until the target INR value has been reached.
Renal impairment- Fondaparinux should be used with caution in patients with moderate renal impairment(see section 4.4).
Fondaparinux should be used with caution at a daily dose of 5 mg in this population(see sections 4.2 and 5.2).
In patients with severe hepatic impairment, fondaparinux should be used with care as this patient group has not been studied(see sections 4.4 and 5.2).
Fondaparinux should be used with caution in patients who have an increased risk of haemorrhage(see section 4.4).
Renal impairment• Prophylaxis of VTE- Fondaparinux should not be used in patients with creatinine clearance< 20 ml/ min(see section 4.3).
The use of fondaparinux should be considered with caution because of an increased risk of bleeding due to a deficiency of coagulation factors in patients with severe hepatic impairment see section.
Renal impairment- Fondaparinux should not be used in patients with creatinine clearance< 20 ml/ min.
Fondaparinux should be used with caution in patients who have an increased risk of haemorrhage, such as those with congenital or acquired bleeding disorders(e. g. platelet count< 50,000/ mm3), active ulcerative gastrointestinal disease and recent intracranial haemorrhage or shortly after brain, spinal or ici.
Renal impairment- Fondaparinux should not be used in patients with creatinine clearance< 20 ml/min(see section 4.3).
Fondaparinux should be used with caution in patients who have an increased risk of haemorrhage, such as those with congenital or acquired bleeding disorders(e.g. platelet count< 50,000/mm3), active ulcerative gastrointestinal disease and recent intracranial haemorrhage or shortly after brain, spinal or ophthalmic surgery and in special patient groups as outlined below.
Haemorrhage Fondaparinux should be used with caution in patients who have an increased risk of haemorrhage, ct.
In patients≥75 years, fondaparinux should be used with care, as renal function decreases with age(see section 4.4).
As for other anticoagulants, fondaparinux should be used with caution in patients who have undergone recent surgery(< 3 days) and only once surgical haemostasis has been established.
However, the use of fondaparinux should be considered with caution because of an increased risk of bleeding due to a deficiency of coagulation factors in patients with severe hepatic impairment(see section 4.2).
Severe hepatic impairment The use of fondaparinux should be considered with caution because of an increased risk of bleeding due to a deficiency of coagulation factors in patients with severe hepatic impairment(see section 4.2).
For treatment of UA/ NSTEMI and STEMI, fondaparinux should be used with caution in patients who are being treated concomitantly with other agents that increase the risk of haemorrhage(such as GPIIb/ IIIa inhibitors or thrombolytics).
The timing of restarting subcutaneous fondaparinux after sheath removal should be based on clinical judgment.
For prevention of VTE, agents that may enhance the risk of haemorrhage should not be administered concomitantly with fondaparinux.
In superficial vein thrombosis patients who are to undergo surgery or other invasive procedures, fondaparinux, where possible, should not be given during the 24 hours before surgery.
Patients eligible for fondaparinux 2.5 mg treatment should have acute, symptomatic, isolated, spontaneous superficial-vein thrombosis of the lower limbs, at least 5 cm long and documented by ultrasonographic investigation or other objective methods.