Примери за използване на Subsequent infusions на Английски и техните преводи на Български
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Subsequent infusions.
The incidence of IRRs declined with subsequent infusions.
Subsequent infusions*.
The risk of such reactions decreases in subsequent infusions.
All subsequent infusions for CLL and FL.
The proportion of affected patients decreases with subsequent infusions.
For subsequent infusions, please see premedication section.
It is recommended to maintain this lower infusion rate in all subsequent infusions.
Subsequent infusions may need to occur in a clinical setting.
The median interval time between the first and the subsequent infusions of Zalmoxis cells was 30 days.
Subsequent infusions may need to occur in a clinical setting.
Patients who tolerate the first 90-minute infusion can receive subsequent infusions over 30 minutes.
Subsequent infusions can be given by a caregiver or by the patient.
If the first infusion is tolerated, then subsequent infusions may be administered over 30 to 60 minutes.
Subsequent infusions can be administered by a caregiver or by the patient(see section 4.4).
If the 60-minute infusion is well tolerated, all subsequent infusions may be administered over 30-minutes.
Subsequent infusions may be administered no sooner than 16 weeks following the previous infusion. .
If the 60 minute infusion is well tolerated, all subsequent infusions may be administered over 30 minutes.
Less than 1% of patients had a Grade 3/4 infusion-related reaction with the Week 2 or subsequent infusions.
The incidence of IRRs with subsequent infusions was 3% with the second 1,000 mg dose and 1% thereafter.
The overall incidence of IRRs in clinical trials was 23% with the first infusion and decreased with subsequent infusions.
Premedication for subsequent infusions and other premedication should be administered as described below.
The first two infusions are given two weeks apart and subsequent infusions are given every six months.
If a patient experiences a Grade 1 or2 infusion-related reaction premedication must be given for all subsequent infusions.
If the infusion is well tolerated within 60 minutes, all subsequent infusions can be carried out within 30 minutes.
The incidence of IRR symptoms was highest during or after the first infusion(9%)and decreased with subsequent infusions(< 4%).
For subsequent infusions, the dose should be reduced to 12 mg/kg for serious Grade 3 toxicities and to 10 mg/kg for Grade 4 toxicities.
If well-tolerated, you may increase the infusion rate up to 2.0 ml/min/site(120 ml/hour/site) for subsequent infusions.
Beyond Cycle 1 the incidence of IRRs in subsequent infusions was comparable between the Gazyvaro and the relevant comparator arms.
In patients receiving Gazyvaro plus chemotherapy, the incidence of IRRs was highest on Day 1 andgradually decreased with subsequent infusions.