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1 ion rate was low (5% EBd) and mitigated with premedication.
2 oses of ipilimumab safely, the majority with premedication.
3 receive additional doses of ipilimumab with premedication.
4 reactions were reported despite the lack of premedication.
5 was attributable, in part, to corticosteroid premedication.
6 significantly higher (p = .03) with atropine premedication.
7 urs and use of antiemetics and antigastritis premedication.
8 All patients received standard premedication.
9 Frequent HSR may warrant prophylactic premedication.
10 tributed solely to the use of corticosteroid premedications.
11 2 [95% CI, 70-73]; n = 330) compared with no premedication (73 [95% CI, 71-74]; n = 319) or placebo (
12 he frequency of reactions despite the use of premedication (a "breakthrough reaction"), and the frequ
14 s who underwent contrast-enhanced CT without premedication and who had similar rates of 13 comorbid d
15 sciplinary preoperative assessment, adequate premedications, and close intra- and postoperative monit
17 armacological interventions such as sedative premedication are used to treat this clinical phenomenon
18 avior Checklist [CBCL]) were administered at premedication baseline and at the end of the MPH trial w
20 n with lorazepam compared with placebo or no premedication did not improve the self-reported patient
21 avenously over 1 hour without corticosteroid premedications every 3 weeks with weekly hematologic mon
22 roup (68 [95% CI, 65-72]; n = 87) and the no premedication group (73 [95% CI, 69-77]; n = 57) or the
23 2 minutes (95% CI, 11-13 minutes) for the no premedication group, and 13 minutes (95% CI, 12-14 minut
24 ticoids, although intravenous glucocorticoid premedication improved tolerability during the first rit
26 it with routine use of lorazepam as sedative premedication in patients undergoing general anesthesia.
30 er ABI-007 260 mg/m(2) intravenously without premedication (n = 229) or standard paclitaxel 175 mg/m(
33 utes without corticosteroid or antihistamine premedications on days 1, 8, and 15 of a 28-day cycle.
34 ents (8%) who were subsequently treated with premedications; one patient had grade 3 hypersensitivity
35 cocorticoids, intravenous methylprednisolone premedication, or intravenous methylprednisolone premedi
39 who received an oral 13-hour corticosteroid premedication regimen before contrast material-enhanced
40 ccelerated 5-hour intravenous corticosteroid premedication regimen before low-osmolality contrast-enh
45 utic index and elimination of corticosteroid premedication required for solvent-based taxanes make th
46 inistration of high paclitaxel doses without premedication, resulting in significant antitumor activi
48 oses and with antihistamine and beta-agonist premedication, stem cell factor therapy has been well to
49 on to outline the differences among sedative premedications such as midazolam, clonidine, and dexmede
53 bation, the use of atropine and lidocaine as premedications, the choice of sedative agents depending
54 s a 1-hour IV infusion every 3 weeks without premedication to prevent hypersensitivity reactions (HSR
57 ydramine hydrochloride and/or corticosteroid premedication was added after hypersensitivity-like reac
59 material, the patient's age and sex, whether premedication was given, the contrast agent used, the vo
64 mammography were randomly divided to receive premedication with acetaminophen, ibuprofen, and/or 4% l
69 m-tolerated dose of IT mafosfamide following premedication with dexamethasone and morphine was 14 mg.
73 d 62 women; mean age, 37 years); 43 received premedication with intravenous morphine sulfate (0.04 mg
74 e surgery under general anesthesia, sedative premedication with lorazepam compared with placebo or no
76 re imaged with a 64-section CT scanner after premedication with oral atenolol and/or intravenous meto
78 ty are effective lambdaU similar to sedative premedications, with the exception of parent present ind
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