Примери за използване на Maximal dose на Английски и техните преводи на Български
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Maximal dose of Vascace.
This dose should be considered as a maximal dose for all patients.
The maximal dose is 8 mg/ 24 h.
All studies have been performed with the maximal dose proposed in the product information.
The maximal dose is 10 mg daily.
(1.8) mg 1995.5(682.6) mg*Similar relative effective doses(i.e approximately half maximal dose) for other sulphonylureas.
It is the maximal dose which may be used within a day.
The full blood pressure lowering effect was achieved 2 weeks after being on their maximal dose of Imprida HCT.
The recommended and maximal dose is 8 mg every 12 hours(i.e. 16 mg per day).
If an inadequate response has been observed, the dose should be increased to 5 mg, with a maximal dose of 10 mg.
At a maximal dose of 96.2 ml/kg/d Numeta G16%E delivers 0.3 mmol/kg/d of magnesium which is above the recommended levels.
IDELVION contains upto 25.8 mg(1.13 mmol) sodium per dose(bodyweight 70 kg) if the maximal dose(15 ml= 6000 IU) is applied.
INOmax is given in dose of 10 to 20 ppm,(maximal dose 20 ppm in children and 40 ppm in adults) part per million of the gas that you or your child inhale.
Depending on the individual patient response, the dose may be increased in weekly increments of 1 mg/ 24 h to a maximal dose of 3 mg/ 24 h.
(682.6) mg*Similar relative effective doses(i.e approximately half maximal dose) for other sulphonylureas(glibenclamide and glicazide).
Follitropin delta had a negative effect on fertility andearly embryonic development in rats when administered in doses≥0.8 micrograms/kg/day which is above the recommended maximal dose in humans.
Of importance the efficacy was confirmed in patients at maximal dose of metoprolol as well as in patients with recurrent angina.
Burosumab has been administered in paediatric clinical trials without dose limiting toxicity using doses up to 2.0 mg/kg body weight with a maximal dose of 90 mg every two weeks.
INOmax is given in dose of 10 to 20 ppm,(maximal dose 20 ppm in children and 40 ppm in adults) part per million of the gas that you or your child inhale.
Studies in animals have shown reproductive toxicity with REKOVELLE doses above the recommended maximal dose in humans(section 5.3).
With respect to the maximal dose, the applicant reviewed 6 clinical studies addressing the safety and efficacy of the proposed high dose ciprofloxacin treatment regimens in critically ill patients.
In contrast, a single nutrient(ascorbic acid or vitamin C)produced only 20% inhibition at its maximal dose, suggesting cooperative inhibitory effects of the nutrients in the mixture.
This medicine when diluted with sodium chloride 9 mg/mL(0.9%) solution for injection for IV administration contains 2.65 g sodium(maincomponent of cooking/table salt) in 720 mL at the maximal dose.
This medicinal product when diluted withsodium chloride 9 mg/mL(0.9%) solution for injection contains 2.65 g sodium per 720 mL at the maximal dose, equivalent to 133% of the WHO recommended maximum daily intake of 2 g sodium for an adult.
The recommended starting dose in patients> 20 to< 50 kg is 0.7 mg/kg once daily(up to 25 mg total,in exceptional cases where target doses above 25 mg are required, the maximal dose is 50 mg).
In patients with moderate hepatic impairment(Child-Pugh B) two weeks after initiation of treatment, the daily dose can be increased without exceeding a maximal dose of 18 mg(see section 5.2). Pitolisant is contra-indicated in patients with severe hepatic impairment(Child-Pugh C)(see section 4.3).
In male rats after 13 weeks of inhaled mannitol dosing, elevated circulating lymphocyte numbers andmandibular lymph node plasmacytosis was observed at doses greater than 9.3 fold the maximal dose.
After completing induction therapy, patients were randomized to receive either Zevalin(250 mg/m rituximab on day -7 andon day 0 followed on day 0 by Zevalin 15 MBq/kg body weight; maximal dose 1200 MBq;[n=208]) or no further treatment(control; n=206).
A few cases of Ehlers-Danlos like syndrome on elbows have been reported in children treated with high doses of different cysteamine preparations(cysteamine chlorhydrate or cystamine or cysteamine bitartrate)mostly above the maximal dose 1.95 g/ m2/ day.
In patients with moderate hepatic impairment(Child-Pugh B) two weeks after initiation of treatment,the daily dose can be increased without exceeding a maximal dose of 18 mg(see section 5.2).