Примери за използване на Mg zoledronic на Английски и техните преводи на Български
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How much Zoledronic acid Mylan is given- The usual single dose given is 4 mg zoledronic acid.
Statistically significant differences are marked(*p< 0.05) for between treatment comparisons(4 mg zoledronic acid vs. placebo).
The results demonstrated that 4 mg zoledronic acid showed comparable efficacy to 90 mg pamidronate in the prevention of SREs.
Bone histology was evaluated in 7 patients with Paget' s disease 6 months after treatment with 5 mg zoledronic acid.
There was faster normalisation of corrected serum calcium at day 4 for 8 mg zoledronic acid and at day 7 for 4 mg and 8 mg zoledronic acid.
While the risk is reduced with a dose of 4 mg zoledronic acid administered over 15 minutes,
There was faster normalisation of corrected serum calcium at day 4 for 8 mg zoledronic acid and at day 7 for 4 mg and 8 mg zoledronic acid.
While the risk is reduced with a dose of 4 mg zoledronic acid administered over 15 minutes,
The multiple event analysis revealed a significant risk reduction of 16% in patients treated with 4 mg zoledronic acid in comparison with patients receiving pamidronate.
3.0 mmol/l) is a single dose of 4 mg zoledronic acid.
The efficacy of one infusion of 5 mg zoledronic acid versus daily doses of 30 mg risedronate for 2 months was demonstrated in two 6-month comparative trials.
Zometa 4 mg/100 ml solution for infusion contains 4 mg zoledronic acid in 100 ml of infusion solution for immediate use in patients with normal renal function.
One ml solution contains 0.05 mg zoledronic acid anhydrous, corresponding to 0.0533 mg zoledronic acid monohydrate.
a single dose of 4 mg zoledronic acid.
The recommended dose in the prevention of skeletal related events in patients with advanced malignancies involving bone is 4 mg zoledronic acid every 3 to 4 weeks.
The recommended dose in the prevention of skeletal related events in patients with advanced malignancies involving bone is 4 mg zoledronic acid every 3 to 4 weeks.
have been accumulated from clinical studies and post-marketing reports following predominantly chronic treatment with 4 mg zoledronic acid.
Re-treatment consists of an additional intravenous infusion of 5 mg zoledronic acid after an interval of one year
have been accumulated from clinical studies and post-marketing reports following predominantly chronic treatment with 4 mg zoledronic acid.
post-marketing reports following predominantly chronic treatment with 4 mg zoledronic acid.