Examples of using Subcutaneous administration in English and their translations into Finnish
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Subcutaneous administration at doses of 100 mg/kg/day in rats
Subcutaneous administration of Draxxin to cattle causes very commonly transient pain reactions
Subcutaneous administration of the product may induce transient local swelling at the injection site as well as inflammatory reactions which resolve within 14 days post treatment.
For patients managed with percutaneous coronary intervention(PCI): If the last enoxaparin sodium subcutaneous administration was given less than 8 hours before balloon inflation, no additional dosing is needed.
The absolute bioavailability after the first and third subcutaneous administration ranged from 45.8 to 98.4%,
The biological efficacy of erythropoietin has been demonstrated after intravenous and subcutaneous administration in various animal models in vivo rats and dogs.
Sub-populations The absolute bioavailability of somatropin seems to be similar in males and females following subcutaneous administration.
ease of use subcutaneous administration.
The rapid onset and early peak of activity of Liprolog itself is observed following the subcutaneous administration of Liprolog Mix25.
signs of hypersensitivity or tachyphylaxis following subcutaneous administration of asfotase alfa.
The pharmacokinetics of icatibant has been extensively characterized by studies using both intravenous and subcutaneous administration to healthy volunteers and patients.
cardiac depressant effects at systemic exposure slightly above the human clinical exposure, whilst subcutaneous administration elicited respiratory
Following subcutaneous administration, the protracted action profile is based on three mechanisms: self-association, which results in slow absorption;
Subcutaneous administration of 0.073 mg/ kg body weight of Valtropin resulted in a Cmax of 43.97 ng/ ml and an AUC0-24 h of 369.90 ng·h/ ml.
Absorption Following subcutaneous administration, meloxicam is completely bioavailable
subsequent relapse after chemotherapy cannot be recommended as the safety of the once weekly subcutaneous administration has not been established.
daily plerixafor subcutaneous administration in rats at doses approximately 4 fold higher than the recommended human dose.
For intramuscular and subcutaneous administration, a dosage of 0.01 mg in 0.5
For subcutaneous administration only.
Immune responses after subcutaneous administration.