Examples of using The intravenous administration in English and their translations into Swedish
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Preparation for the intravenous administration.
The intravenous administration of CEPROTIN provides for an immediate
Preparation of the intravenous administration.
The intravenous administration line should be flushed with normal sodium chloride solution or 5% glucose solution
Preparation for the intravenous administration.
safety of the subcutaneous administration of bortezomib versus the intravenous administration.
Preparation for the intravenous administration.
The intravenous administration of doses up to 4000 mg diluted in 100 ml of 0.9% sodium chloride infused over 15 minutes
If a rapid antibiotic effect is needed, the intravenous administration should be considered.
If possible, the intravenous administration of isavuconazole should be completed within 6 hours after reconstitution and dilution at room temperature.
Pharmacokinetic studies were performed after the intravenous administration of the product.
Once there is the intravenous administration of this drug, its volume of distribution is around 1 L/kg.
Anaphylactic and other hypersensitivity reactions have been reported following the intravenous administration of proteins to patients.
Following the intravenous administration of a 2 micrograms/kg/min infusion of[3H] cangrelor to healthy male volunteers, 93% of total radioactivity was recovered.
other hypersensitivity reactions have been reported in fewer than 1% of patients following the intravenous administration of proteins to patients.
Furthermore, the intravenous administration of Apta-1 resulted in a significantly higher positive impact on clinical biomarkers pertaining to organ health and inflammation.
Treatment of Tumour Induced Hypercalcaemia The safety profile for Bondronat in tumour-induced hypercalcaemia is derived from controlled clinical trials in this indication and after the intravenous administration of Bondronat at the recommended doses.
Adverse reactions following the intravenous administration of 64Cu-labelled medicinal products prepared by radiolabelling with Cuprymina, will be dependent on the specific medicinal product being used.
Prevention of Skeletal Events in Patients with Breast Cancer and Bone Metastases The safety profile of intravenous Bondronat in patients with breast cancer and bone metastases is derived from a controlled clinical trial in this indication and after the intravenous administration of Bondronat at the recommended dose.
Possible side effects following the intravenous administration of Yttrium(90Y)-labelled medicinal products prepared by radiolabelling with YTRACIS,
Following the intravenous administration of 500 and 1000 mg doses of rituximab on two occasions,
In clinical studies, the intravenous administration of Cinryze resulted in a significant increase in systemic levels of antigenic
Following intravenous administration, the elimination phase half-life averaged 15.1 hours.
Following intravenous administration, the volume of distribution approximates to total blood volume.
Following intravenous administration the volume of distribution of emtricitabine was approximately 1.4 i/ kg.
Vedolizumab does not pass the blood brain barrier after intravenous administration.
After intravenous administration the plasma clearance of dronedarone ranges from 130 to 150 L/h.
Intravenous administration of the usual subcutaneous dose could result in severe hypoglycaemia.
Or ozonize the physiological solution for intravenous administration;