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1 following cardiac parasympathetic blockade (glycopyrrolate).
2 in salivary response to an anti-sialogogue (glycopyrrolate).
3 ts with and without cholinergic blockade via glycopyrrolate.
4 lder--60-77 yrs) received 4.0 microg/kg i.v. glycopyrrolate.
8 daily), indacaterol (27.5 mug twice daily), glycopyrrolate (15.6 mug twice daily), or placebo, all d
9 nts were randomized (1:1:1:1) to indacaterol/glycopyrrolate (27.5/15.6 mug twice daily), indacaterol
10 ith subjects who received the active placebo glycopyrrolate (4 microg/kg) and subjects who were not i
11 P < 0.05, n = 3) following administration of glycopyrrolate (-8.1 +/- 4.5 ms) compared to PS alone (-
12 e efficacy and safety of QVA149 (indacaterol/glycopyrrolate), a fixed-dose combination of a long-acti
14 control (no drug), parasympathetic blockade (glycopyrrolate) and beta-adrenergic blockade (metoprolol
16 ol) and a long-acting muscarinic antagonist (glycopyrrolate), compared with its monocomponents and pl
19 inistration of either propranolol (PROP), or glycopyrrolate (GLYC), or PROP and GLYC in combination (
20 blockade (NMB) reversal with neostigmine and glycopyrrolate has been reported to cause cardiac arrest
30 o demonstrate the superiority of indacaterol/glycopyrrolate versus its monocomponents for standardize
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