Exemplos de uso de When administered intravenously em Inglês e suas traduções para o Português
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When administered intravenously fosaprepitant is rapidly converted to aprepitant.
The terminal half-life of darbepoetin alfa is 21 hours(SD 7.5) when administered intravenously.
When administered intravenously, adult patients are allowed a maximum of 3 to 4 grams.
The drug is not only ineffective when administered intravenously, but it has been known to be fatal.
The terminal half-life of darbepoetin alfa is 21 hours(SD 7.5) when administered intravenously.
When administered intravenously in rabbits, psilocybin's LD50 is approximately 12.5 mg/kg.
Fosaprepitant, a prodrug of aprepitant, when administered intravenously is rapidly converted to aprepitant.
When administered intravenously at doses up to 30 mg/kg, oritavancin did not affect the fertility or reproductive performance of male and female rats.
Pegaspargase was well tolerated both in rats and dogs when administered intravenously in single dose up to 500 U/kg.
Elimination When administered intravenously, tacrolimus has been shown to have a low clearance rate.
These symptoms are consistent with the accumulation of phenylacetate,which showed dose-limiting neurotoxicity when administered intravenously at doses up to 400 mg/ kg/ day.
When administered intravenously, mannitol is eliminated largely unchanged by glomerular filtration and 87% of the dose is excreted in the urine within 24 hours.
Fosaprepitant is the prodrug of aprepitant and when administered intravenously is converted rapidly to aprepitant see section 5.2.
When administered intravenously, ocriplasmin enters the endogenous protein catabolism pathway through which it is rapidly inactivated via its interactions with protease inhibitor α2-antiplasmin or α2-macroglobulin.
Trastuzumab emtansine when administered intravenously every 3 weeks exhibited linear PK across doses ranging from 2.4 to 4.8 mg/kg; patients who received doses less than or equal to 1.2 mg/kg had faster clearance.
Methylthioninium chloride was mutagenic in gene mutation assays in bacteria and mouse lymphoma cells butnot in vivo mouse micronucleus assay when administered intravenously at 62 mg/kg.
However, when administered intravenously to opioid dependent persons, the presence of naloxone in Suboxone produces marked opioid antagonist effects and opioid withdrawal, thereby deterring intravenous abuse.
The influence of hepatic and renal impairment on the pharmacokinetics of Instanylhave not been evaluated; however, when administered intravenously the clearance of fentanyl has shown to be altered due to hepatic and renal impairment caused by alterations in metabolic clearance and plasma proteins.
When administered intravenously with beta-adrenergic blocking medication, the patient may experience a serious decrease in blood pressure, an increase in particular adverse inotropic effects, as well as a general acute decompensation of the heart.
The influence of hepatic and renal impairment on the pharmacokinetics of themedicinal product has not been evaluated, however, when administered intravenously the clearance of fentanyl has been shown to be altered in hepatic and renal impairment due to alterations in metabolic clearance and plasma proteins.
Aflibercept has been shown to be embryotoxic and teratogenic when administered intravenously to pregnant rabbits every 3 days during the organogenesis period(gestation days 6 to 18) at doses approximately 1 to 15 times the human dose of 4 mg/kg every 2 weeks.