4 patient profiles for whom I choose famotidine Review article
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Published:
Mar 31, 2023
Keywords:
famotidine, acid-dependent disease, NAB
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Abstract
The presented patient profiles indicate the possibility of including famotidine in the treatment in order to optimize the treatment of acid-dependent diseases based on available literature data and practical recommendations.
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How to Cite
Waśko-Czopnik , D. (2023). 4 patient profiles for whom I choose famotidine. Medycyna Faktow (J EBM), 16(1(58), 43-45. https://doi.org/10.24292/01.MF.0123.07
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References
1. McCullough AJ, Graham DY, Knuff TE et al. Suppression of nocturnal acid secretion with famotidine accelerates gastric ulcer healing. Gastroenterology. 1989; 97(4): 860-6. http:// doi.org/10.1016/0016-5085(89)91489-3.
2. Ryan JR, Vargas R, McMahon FG et al. Comparison of effects of oral and intravenous famotidine on inhibition of nocturnal gastric acid secretion. Am J Med. 1986; 81(4B): 60-4. http://doi.org/10.1016/0002-9343(86)90601-7.
3. Yamashita Y, Kinoshita Y, Chihara K et al. [Comparison of the effects between standard doses of H2-blocker (famotidine 20 mg b.d.) and proton pump inhibitor (omeprazole 20 mg o.d.) in the treatment of refractory reflux esophagitis by ambulatory 24-hr intra-gastroesophageal pH monitoring]. Nihon Shokakibyo Gakkai Zasshi. 1994; 91(12): 2166-73.
4. McRorie JW, Kirby JA, Miner PB. Histamine2-receptor antagonists: Rapid development of tachyphylaxis with repeat dosing. World J Gastrointest Pharmacol Ther. 2014; 5(2): 57-62. http://doi.org/10.4292/wjgpt.v5.i2.57.
5. Fandriks L, Lonroth H, Petterson A et al. Can famotidine and omeprazole be combined on a once-daily basis? Scand J Gastroenterol. 2007; 42(6): 689-94. http://doi. org/10.1080/00365520601026665.
6. Humphries TJ. Famotidine: a notable lack of drug interactions. Scand J Gastroenterol Suppl. 1987; 134: 55-60. http://doi.org/10.3109/00365528709090142.
7. Echizen H, Ishizaki I. Clinical pharmacokinetics of famotidine. Clin Pharmacokinet. 1991; 21(3): 178-94. http://doi.org/10.2165/00003088-199121030-00003.
8. Lin JH. Pharmacokinetic and pharmacodynamic properties of histamine H2-receptor antagonists. Relationship between intrinsic potency and effective plasma concentrations. Clin Pharmacokinet. 1991; 20(3): 218-36. http://doi.org/10.2165/00003088-19912003000004.
9. Mills JG, Wood JR. The pharmacology of histamine H2-receptor antagonists. Methods Find Exp Clin Pharmacol. 1989; 11(suppl 1): 87-95.
2. Ryan JR, Vargas R, McMahon FG et al. Comparison of effects of oral and intravenous famotidine on inhibition of nocturnal gastric acid secretion. Am J Med. 1986; 81(4B): 60-4. http://doi.org/10.1016/0002-9343(86)90601-7.
3. Yamashita Y, Kinoshita Y, Chihara K et al. [Comparison of the effects between standard doses of H2-blocker (famotidine 20 mg b.d.) and proton pump inhibitor (omeprazole 20 mg o.d.) in the treatment of refractory reflux esophagitis by ambulatory 24-hr intra-gastroesophageal pH monitoring]. Nihon Shokakibyo Gakkai Zasshi. 1994; 91(12): 2166-73.
4. McRorie JW, Kirby JA, Miner PB. Histamine2-receptor antagonists: Rapid development of tachyphylaxis with repeat dosing. World J Gastrointest Pharmacol Ther. 2014; 5(2): 57-62. http://doi.org/10.4292/wjgpt.v5.i2.57.
5. Fandriks L, Lonroth H, Petterson A et al. Can famotidine and omeprazole be combined on a once-daily basis? Scand J Gastroenterol. 2007; 42(6): 689-94. http://doi. org/10.1080/00365520601026665.
6. Humphries TJ. Famotidine: a notable lack of drug interactions. Scand J Gastroenterol Suppl. 1987; 134: 55-60. http://doi.org/10.3109/00365528709090142.
7. Echizen H, Ishizaki I. Clinical pharmacokinetics of famotidine. Clin Pharmacokinet. 1991; 21(3): 178-94. http://doi.org/10.2165/00003088-199121030-00003.
8. Lin JH. Pharmacokinetic and pharmacodynamic properties of histamine H2-receptor antagonists. Relationship between intrinsic potency and effective plasma concentrations. Clin Pharmacokinet. 1991; 20(3): 218-36. http://doi.org/10.2165/00003088-19912003000004.
9. Mills JG, Wood JR. The pharmacology of histamine H2-receptor antagonists. Methods Find Exp Clin Pharmacol. 1989; 11(suppl 1): 87-95.