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1 esomeprazole but not with dexlansoprazole or lansoprazole.
2 All patients received lansoprazole.
3 pH (confirmed by 24-hour pH monitoring) with lansoprazole.
4 negative breath test result while receiving lansoprazole.
5 nsoprazole and 67% of recipients of 30 mg of lansoprazole.
6 azole and 90% of patients receiving 30 mg of lansoprazole.
7 g bolus followed by 9-mg/h infusion) or oral lansoprazole (120-mg bolus followed by 30 mg every 3 hou
8 ontrol 68.3+/-37.8; ranitidine 38.4 +/-94.2; lansoprazole 14.6+/-84.4; and omeprazole 15.1+/-48.9.
10 ren were randomly assigned to receive either lansoprazole, 15 mg/d if weighing less than 30 kg or 30
11 groups of media: a) control; b) control plus lansoprazole (25 microg/mL); c) control plus omeprazole
12 ith or without a PPI (dexlansoprazole 60 mg, lansoprazole 30 mg, esomeprazole 40 mg, or, as a positiv
14 -pyridyl)methylsulfinyl]-1H-ben zimida zole (lansoprazole), 5-difluoromethoxy-2-[3, 4-methoxy-2-pyrid
15 >/=18 years, 50 mg for those <18 years) and lansoprazole (60 mg for participants >/=18 years, 30 mg
16 relatively acid stable analogue, N(1)-methyl lansoprazole, (6b), allowed direct determination of both
17 They were randomly assigned to intravenous lansoprazole (90-mg bolus followed by 9-mg/h infusion) o
18 ceftriaxone (a cephalosporin antibiotic) and lansoprazole (a proton-pump inhibitor) will prolong the
19 whom acid secretion status was monitored on lansoprazole, all were free of significant gastrointesti
20 a dynamic balancing procedure to: 14 days of lansoprazole, amoxicillin, and clarithromycin (standard
21 omization to 1 of 3 treatment groups: 14-day lansoprazole, amoxicillin, and clarithromycin (triple th
22 in, and metronidazole (sequential); or 5-day lansoprazole, amoxicillin, clarithromycin, and metronida
23 clarithromycin (standard therapy); 5 days of lansoprazole, amoxicillin, clarithromycin, and metronida
24 e 50.0% (10.0%-72.0%) for participants given lansoprazole and 5.0% (0.0%-40.0%) for participants give
25 compared with 72% of recipients of 15 mg of lansoprazole and 67% of recipients of 30 mg of lansopraz
26 ared with 79% of patients receiving 15 mg of lansoprazole and 90% of patients receiving 30 mg of lans
27 nidazole (concomitant therapy); or 5 days of lansoprazole and amoxicillin followed by 5 days of lanso
28 , and clarithromycin (triple therapy); 5-day lansoprazole and amoxicillin followed by 5-day lansopraz
29 ive control, we evaluated the combination of lansoprazole and cefuroxime (another cephalosporin), whi
32 s of many TB drugs, further investigation of lansoprazole as a potential antituberculosis agent is wa
34 e is no evidence that, in clinical practice, lansoprazole can treat or prevent incident tuberculosis
35 nsoprazole and amoxicillin followed by 5-day lansoprazole, clarithromycin, and metronidazole (sequent
36 razole and amoxicillin followed by 5 days of lansoprazole, clarithromycin, and metronidazole (sequent
37 s suggested this interaction was specific to lansoprazole combined with ceftriaxone but not with othe
39 ing inhaled corticosteroids, the addition of lansoprazole, compared with placebo, improved neither sy
45 Patients enrolled in a long-term trial of lansoprazole for Zollinger-Ellison syndrome and other ac
46 on of hospital stay was 1.8 days in the oral lansoprazole group and 3.9 days in the intravenous esome
48 tive metabolite (omeprazole > esomeprazole > lansoprazole > dexlansoprazole) and showed a correspondi
49 patients with a hypersensitivity reaction to lansoprazole had a positive OPT or skin test result with
50 nd that patients taking both ceftriaxone and lansoprazole had significantly longer QTc intervals (up
53 clinical trial to investigate the effects of lansoprazole (LANZO) administration, a proton pump inhib
56 ffects of Multiple Doses of Dexiansoprazole, Lansoprazole, Omeprazole or Esomeprazole on the Pharmaco
57 HODS AND We studied a cohort of new users of lansoprazole, omeprazole, or pantoprazole from the Unite
59 8 weeks, along with a proton-pump inhibitor (lansoprazole or omeprazole) and bismuth subsalicylate.
61 e minimized by the use of dexlansoprazole or lansoprazole rather than esomeprazole or omeprazole.
62 months, 35% of placebo recipients and 2% of lansoprazole recipients had three or more recurrences.
65 rly, esomeprazole but not dexlansoprazole or lansoprazole significantly reduced the effect of clopido
66 st results were positive after completion of lansoprazole therapy were 91% (95% CI, 83% to 96%) at 3
67 s have found the proton pump inhibitor (PPI) lansoprazole to be highly active against Mycobacterium t
71 ctice Research Datalink to determine whether lansoprazole users have a lower incidence of TB disease
72 a positive pH study, no treatment effect for lansoprazole vs placebo was observed for any asthma outc
73 There was a significant difference between lansoprazole vs. ranitidine (p< .01), and omeprazole vs.
74 ommonly prescribed and cheaply available PPI lansoprazole was associated with reduced incidence of TB
76 After 8 and 16 weeks, participants given lansoprazole were 3.12-fold (1.28-7.59) and 3.50-fold (1
77 y the coadministration of dexlansoprazole or lansoprazole with clopidogrel than by the coadministrati
78 olled, parallel clinical trial that compared lansoprazole with placebo in children with poor asthma c
79 transmission, nor could we determine whether lansoprazole would have a beneficial effect if given to
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