Примери за използване на Platelet counts should на Английски и техните преводи на Български
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Platelet counts should be≥ 70 x 10.
Since either repeat exposure with any GP IIb/IIIa ligand-mimetic agent(like abciximab or eptifibatide) or first-time exposure to a GP IIb/IIIa inhibitor may be associated with immune-mediated thrombocytopenic responses,monitoring is required, i.e. platelet counts should be monitored prior to treatment, within 6 hours of administration, and at least once daily thereafter while on therapy and immediately at clinical signs of unexpected bleeding tendency.
Platelet counts should be closely monitored.
Prior to initiating a new cycle of therapy:• Platelet counts should be≥ 70 x 109/ l and the absolute neutrophils count should be≥ 1.0 x 109/ l• Non-haematological toxicities should have resolved to Grade 1 or baseline.
Platelet counts should therefore be monitored closely.
Therefore, platelet counts should be monitored prior to each dose of bortezomib.
Platelet counts should be assessed monthly thereafter.
Platelet counts should be monitored frequently during treatment with Kyprolis.
Platelet counts should be monitored at least twice a week until≥50 x 109/l.
Platelet counts should be monitored at least monthly during ixazomib treatment.
Platelet counts should be monitored every week prior to starting antiviral therapy.
Platelet counts should be monitored on an ongoing basis, in accordance with oncology guidelines.
Platelet counts should be≥ 70 x 109/l and the absolute neutrophils count should be≥ 1.0 x 109/l.
Platelet counts should be checked prior to olaratumab dosing on Day 1 and Day 8 of each cycle.
Platelet counts should be measured frequently and the condition of patients should be observed closely.
Platelet counts should be≥ 100,000 cells/μL and the absolute neutrophils count(ANC) should be≥ 1,500 cells/μL.
Platelet counts should be≥ 75,000 cells/μL in patients with bone marrow infiltration or splenic sequestration.
Platelet counts should be monitored according to medical judgment until platelet engraftment and platelet recovery are achieved.
Platelet counts should be assessed weekly until a stable platelet count(≥ 50 x 109/ l for at least 4 weeks without dose adjustment) has been achieved.
Platelet counts should be monitored prior to each dose of bortezomib(i.e. on days 1, 4, 8 and 11 of cycles 1-8, see Table 1, and on days 1 and 8 of cycles 9-16, see Table 2).
Platelet counts should be monitored weekly during antiviral therapy until a stable platelet count is achieved, normally around 50,000-75,000/µl.
Platelet counts should be monitored when reducing or discontinuing other ITP treatments in order to avoid platelet counts below the recommended range(see section 4.2).
Platelet counts should be monitored when combining romiplostim with other medicinal products for the treatment of ITP in order to avoid platelet counts outside of the recommended range(see section 4.2).
Platelet counts should be closely monitored and consideration given to reducing the dose or discontinuing eltrombopag treatment if the platelet count exceeds the target levels(see section 4.2).
Platelet counts should be monitored prior to treatment, within 6 hours of administration, and at least once daily thereafter while on therapy and immediately at clinical signs of unexpected bleeding tendency.
Platelet counts should be assessed monthly thereafter and appropriate dose adjustments made as per the dose adjustment table(table 2) in order to maintain platelet counts within the recommended range.
Platelet count should be measured prior to the procedure.
If the use of romiplostim is deemed necessary, platelet count should be closely monitored to minimise the risk of thromboembolic complications.
If use of romiplostim is deemed necessary, platelet count should be closely monitored to minimise the risk of thromboembolic complications.
Platelet count should be closely monitored in order to ensure appropriate medical management of the dose of eltrombopag when lopinavir/ritonavir therapy is initiated or discontinued.