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1 labeling was protected by a molar excess of famotidine.
2 -generated randomisation sequence to receive famotidine 20 mg twice daily (n=204) or placebo twice da
3 y used agents for SUP were ranitidine (31%), famotidine (24%), sucralfate (24%), and cimetidine (12%)
4 We therefore investigated the efficacy of famotidine, a well-tolerated histamine H(2)-receptor ant
6 ected ranitidine for ease of administration, famotidine because of formulary availability, sucralfate
15 reflective of acid secretion inhibited by a famotidine or acid neutralized by calcium carbonate tabl
18 received the histamine2-receptor antagonist famotidine (Pepcid AC, 10 mg), calcium carbonate antacid
19 ak effect, 210 minutes after administration, famotidine reduced acid secretion by 7.3 mmol per 30 min
20 stamine receptor antagonists (pyrilamine and famotidine, respectively) greatly diminishes recruitment
21 and cytokine production in H2 R-deficient or famotidine-treated animals, while dimaprit dampened the
23 At 12 weeks, comparing patients assigned to famotidine with patients assigned to placebo, gastric ul
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