Examples of 'following intravenous administration' in a sentence
Meaning of "following intravenous administration"
following intravenous administration: This medical phrase is used to describe the process of providing medication or fluids directly into a vein through a needle or catheter. It commonly refers to the route of drug delivery in a clinical or hospital setting
How to use "following intravenous administration" in a sentence
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following intravenous administration
Serious adverse events following intravenous administration.
Following intravenous administration concentrations of micafungin show a biexponential decline.
Some degree of enterohepatic recirculation is anticipated following intravenous administration of CellCept.
Phlebitis following intravenous administration.
Reversible cardiotoxic effects were observed in rabbits following intravenous administration of tacrolimus.
Anaphylactic reactions following intravenous administration of free cytarabine have been rarely reported.
There is no evidence of tissue retention of alprostadil or its metabolites following intravenous administration.
Pharmacokinetics following intravenous administration in beagle dogs.
Bioavailability was calculated by comparison with plasma concentrations of rofleponide following intravenous administration.
Aniline is the major product following intravenous administration of the substituted diphenyl heterocycle.
Pharmacokinetics of amoxycillin and clavulanic acid in haemodialysis patients following intravenous administration of Augmentin.
Observed aldesleukin serum levels following intravenous administration are proportional to the dose of Proleukin.
Following intravenous administration of a 3 mg dose of bazedoxifene, the volume of distribution is.
This does not occur to the same extent following intravenous administration.
Following intravenous administration of pantoprazole, serum / plasma concentrations decline biexponentially.
See also
Peak plasma levels and total systemic exposure following intravenous administration of.
Following intravenous administration in rats, sapropterin dihydrochloride is mainly excreted in the urine.
Thus, all treatments were well tolerated following intravenous administration.
Following intravenous administration of umeclidinium to healthy volunteers, the mean volume of distribution was 86 litres.
The elimination half-life of prilocaine following intravenous administration is approximately.
Following intravenous administration of rocuronium bromide, plasma levels of rocuronium follow a three-compartment open model.
The secondary response was measured following intravenous administration of VSV-hDCT.
The elimination half-life of intramuscularly administered midazolam is comparable to that observed following intravenous administration.
The concentration-time profile following intravenous administration is well described by a twocompartment model.
In vivo transduction efficiency of AAV2i8 of various muscle groups following intravenous administration.
The pharmacokinetic properties of lepirudin following intravenous administration are well described by a two-compartment model.
However, polymers were detected and quantitated in plasma of animals following intravenous administration.
The concentration-time profile following intravenous administration is well described by a two - compartment model.
L-dC represented the majority of drug present in the plasma following intravenous administration.
Following intravenous administration to CKD patients on dialysis, the total systemic clearance was.
The estimated pharmacokinetic parameters following intravenous administration of ketorolac are listed in Table 12.
Following intravenous administration of TAXOL, paclitaxel plasma concentrations declined in a biphasic manner.
Hypotension, tachycardia and ECG changes have been observed following intravenous administration of concentrated solutions.
Following intravenous administration the volume of distribution of emtricitabine was approximately 1.4 l / kg.
Tissue distribution of different forms of recombinant human secreted a-Gal A following intravenous administration to mice.
Following intravenous administration the volume of distribution of emtricitabine was approximately 1.4 i / kg.
Toxicological and pharmacokinetic properties of chemically modified siRNAs targeting p53 RNA following intravenous administration.
Following intravenous administration, the mean plasma clearance is approximately 9 i/ h.
Figure 7 shows the percent reporting disability following intravenous administration of Compound I.
Following intravenous administration the volume of distribution of tenofovir was approximately 800 ml / kg.
Intravenously administered dival-L-dC was converted rapidly to L-dC following intravenous administration.
Following intravenous administration to healthy subjects, the mean volume of distribution was 86 litres.
Plasma clearance of vilanterol following intravenous administration was 108 litres / hour.
Following intravenous administration to healthy volunteers, the mean volume of distribution was 86 litres.
The volume of distribution at steady-state following intravenous administration is approximately 5.4 l.
Following intravenous administration to healthy adults, the volume of distribution ( Vdss ) of nevirapine was.
The terminal half-time of elimination following intravenous administration is about 20 minutes.
The apparent terminal half-life was 0.39 hours, indicating rapid elimination, as observed following intravenous administration.
The volume of distribution following intravenous administration in healthy male middle-aged volunteers was 3.2 L / kg.
Plasma concentrations fell by more than 95 % within 6 hours following intravenous administration.
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