Examples of 'hours after administration' in a sentence
Meaning of "hours after administration"
hours after administration: Refers to a timeframe following the execution of a task or the application of a treatment, typically denoting a delay or gap in time
How to use "hours after administration" in a sentence
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hours after administration
Fasting for two hours after administration.
Hours after administration.
Do not redose before two hours after administration.
Six hours after administration complete blood biochemistry analysis were carried out.
The result is achieved two hours after administration.
Food intake two hours after administration did not affect the absorption of PROCYSBI.
In a matter of minutes or hours after administration.
Two hours after administration of the compounds, the mice are placed in a glass beaker.
Significant relief is obtained as early as six hours after administration.
These occurred two hours after administration of the endotoxin.
Significant relief is obtained as early as two hours after administration.
Counting is effected 3 hours after administration of the products and is repeated after 6 hours.
The clinical result becomes noticeable within a few hours after administration.
A meal was served 4 hours after administration of the drug.
Carrageenan is an irritant whose administration causes a powerful inflammation four hours after administration.
The animals are observed for two hours after administration of the pentetrazol.
The effects of the compounds on experimental parameters were followed for five hours after administration.
The rats were fed 2 hours after administration.
Results demonstrated that the optimal time of tumour localization was three hours after administration.
They were fed 2 hours after administration.
In some embodiments the polypeptide is expressed at a peak level about six hours after administration.
Reperfusion is followed for 3 hours after administration of test compound.
Methylphenidate has a rapid onset and improves symptoms within the first hours after administration.
The observation period is 2 hours after administration of the morphine.
Maximum plasma concentrations of macitentan are achieved about 8 hours after administration.
The pigs were sacrificed 2 hours after administration of contrast media.
Maximum plasma concentration is generally achieved 6 to 8 hours after administration.
All of these are done both 2 hours after administration of the test product.
Maximum serum concentrations are achieved between 1 and 4 hours after administration.
The animals are observed for 2 hours after administration of the pentamethylene tetrazole.
The mice were deprived of food again for one or two hours after administration.
The maximum effect appeared 4 hours after administration and was sustained for a further 8 hours following administration.
Blood was collected from the tail vein eight hours after administration.
Four hours after administration of arachidonic acid the rat was sacrificed with CO2.
This effect lasted for five hours after administration.
Hours after administration of a bile acid sequestrant see section 4.5.
Lymph nodes could be imaged up to several hours after administration of an effective dose.
Substantial quantities of diltiazem are not released from this bead until approximately 12 hours after administration.
Light is then administered several minutes to a few hours after administration of the photosensitive texaphyrin.
The formulation initially releases significant quantities of diltiazem within the first 8 hours after administration.
Ed should be administered approximately 24 hours after administration of cytotoxic chemotherapy.
There is little excretion or biotransformation of caspofungin during the first 30 hours after administration.
Post-dose levels were measured two hours after administration of investigational product.
Blood samples were taken before and at different times up to 72 hours after administration.
An EEG is obtained 5 hours after administration of the first and last trospium dose.
Monitoring of the serum potassium is advisable for several hours after administration of the salt.
Blood samples were removed 4 hours after administration by cardiac puncture ( 3 mice per time point ).
Lowering of potassium levels is detectable 7 hours after administration.
Two hours after administration of 5-FU, the rescue treatments with uridine or triacetyluridine were begun.
Highest concentration is reached 2 hours after administration.
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