Примери за използване на When administered intravenously на Английски и техните преводи на Български
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When administered intravenously causes heart attacks.
The terminal half-life of darbepoetin alfa is 21 hours(SD 7.5) when administered intravenously.
When administered intravenously, it will simulate a heart attack.
Fosaprepitant, a prodrug of aprepitant, when administered intravenously is rapidly converted to aprepitant.
When administered intravenously, tacrolimus has been shown to have a low clearance rate.
Pegaspargase was well tolerated both in rats and dogs when administered intravenously in single dose up to 500 U/kg body weight.
When administered intravenously, adult patients are allowed a maximum of 3 to 4 grams.
Fosaprepitant is the prodrug of aprepitant and when administered intravenously is converted rapidly to aprepitant(see section 5.2).
When administered intravenously in low doses, this agent may convert methemoglobin to hemoglobin.
Atropine administered in most cases and usually at a dose of 2 mg when administered intravenously and subcutaneously with 0.5-1 mg.
When administered intravenously, b-endorphin can cause an increase in plasma HGH level by a factor of 20-30(!).
Plasma concentrations of midazolam were not affected when administered intravenously as simeprevir does not inhibit hepatic CYP3A4.
When administered intravenously at doses up to 30 mg/kg, oritavancin did not affect the fertility or reproductive performance of male and female rats.
This dosage can be hundreds(some time thousands) of times bigger than the one used when administered intravenously, since, due to the peritoneal barrier, it is not absorbed into the systematic circulation.
In addition, when administered intravenously, diuretics may enhance neomycin toxicity by altering the antibiotic concentration in serum and tissue.
Immediately after the institution of these ventilatory measures, the adequacy of the circulation should be evaluated,keeping in mind that drugs used to treat convulsions sometimes depress the circulation when administered intravenously.
When administered intravenously, mannitol is eliminated largely unchanged by glomerular filtration and 87% of the dose is excreted in the urine within 24 hours.
The influence of hepatic and renal impairment on the pharmacokinetics of the medicinal 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.
When administered intravenously, an excess amount of calcium and vitamin D toxic doses of nerves and muscles can relax to the extent that it can lead to coma or lethargic sleep.
The distribution and elimination of povidone when administered intravenously has been well investigated and studies using radioactive labelled povidone of different molecular weight have demonstrated that clearance of polymers after intravenous administration is dependent on molecular weight.
However, when administered intravenously to opioid-dependent patients the presence of naloxone in Zubsolv produces marked opioid antagonist effects, thereby deterring intravenous abuse.
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.
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.
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.
For example, if, when administered intravenously, the effect of the drug develops within the first minutes, while with the intramuscular or enteral route of administration, the effect may develop within the first two hours.
No systemic accumulation was observed when ibandronic acid was administered intravenously once every 4 weeks for 48 weeks to patients with metastatic bone disease.
When tacrolimus is administered intravenously as rapid infusion/bolus injection at a dose of 0.1 to 1.0 mg/kg, QTc prolongation has been observed in some animal species.
Zoledronic acid was well tolerated when administered subcutaneously to rats and intravenously to dogs at doses up to 0.02 mg/kg daily for 4 weeks.
Also, bacteria located in the central nervous system may not respondto penicillin during the tertiary stage, even when high doses are administered intravenously.