Examples of using Subcutaneous administration in English and their translations into Slovenian
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Computer
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Official/political
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Programming
After subcutaneous administration of a single 40 mg dose, absorption
The terminal half-life after subcutaneous administration in patients is longer with a mean value of 160 hours(84 to 353 hours).
The apparent volume of distribution after subcutaneous administration of lixisenatide(Vz/F) is approximately 100 L.
The absolute bioavailability after the first and third subcutaneous administration ranged from 45.8 to 98.4%,
The biological efficacy of epoetin theta has been demonstrated after intravenous and subcutaneous administration in various animal models in vivo(mice, rats, dogs).
The Cmax after subcutaneous administration(20.4 ng/ml) was lower than intravenous(223 ng/ml).
The safety and efficacy of ORENCIA subcutaneous administration in children below 18 years of age have not been established.
Absorption After subcutaneous administration, omalizumab is absorbed with an average absolute bioavailability of 62%.
Subcutaneous administration could lead to a suboptimal response to the vaccine(see section 4.4).
With subcutaneous administration of 6 mg of sumatriptan for 10 minutes, the severity of
Exposures after subcutaneous administration of single dulaglutide(1.5 mg)
Simponi is registered in 50 mg and 100 mg strengths for subcutaneous administration.
The mean terminal half-lives following intravenous and subcutaneous administration are about 12 h
In the rat, subcutaneous administration at the maximum dose, 200 µg/kg/day, caused an increase in
After repeated subcutaneous administration every 48 hours for 4 doses,
VELCADE 3.5 mg powder for solution for injection is available for intravenous or subcutaneous administration.
Subcutaneous administration: The weekly dose can be given as one injection per week
The terminal half-life after subcutaneous administration is determined by the rate of absorption from the subcutaneous tissue.
Intravenous or subcutaneous administration is often used in the days immediately following a heart attack.
The absolute bioavailability of methoxy polyethylene glycol-epoetin beta after subcutaneous administration was 62%