Relevant bibliographies by topics / Rabeprazole

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Rabeprazole'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Rabeprazole"

1

Cusimano, Joseph. "Rabeprazole." WikiJournal of Medicine 9, no. 1 (2022): 6. http://dx.doi.org/10.15347/wjm/2022.006.

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Rabeprazole is a proton pump inhibitor that suppresses gastric acid production in the stomach. Available under different brand name products as well as in a variety of combination products, rabeprazole has several medical uses concerning the management of problems of pathological gastric acid. Rabeprazole's adverse effects tend to be mild but can be serious, including deficiencies in essential nutrients, rare incidences of liver damage, and immune-mediated reactions. As a class effect, rabeprazole can increase the risk for osteoporosis, serious infections (including Clostridium difficile infec
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Duan, Zhenya, Yan Wang, Ling Zhang, et al. "An application of continuous flow microreactor in the synthesis and extraction of rabeprazole." International Journal of Chemical Reactor Engineering 19, no. 3 (2021): 287–94. http://dx.doi.org/10.1515/ijcre-2020-0173.

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Abstract The oxidation of rabeprazole sulfide is a key step in the synthesis of rabeprazole, a drug for the treatment of stomach acid-related disorders. The current rabeprazole production process adopts one pot batch process, which has low reaction efficiency and poor stability. A continuous process can greatly improve the production efficiency and solve the above problems. Therefore, the reaction parameters of rabeprazole in microreactor were explored through laboratory experiments to explore the possibility of continuous production of rabeprazole. Rabeprazole sodium was synthesized by using
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&NA;. "Rabeprazole." Reactions Weekly &NA;, no. 1394 (2012): 35. http://dx.doi.org/10.2165/00128415-201213940-00129.

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&NA;. "Rabeprazole." Reactions Weekly &NA;, no. 1159 (2007): 25. http://dx.doi.org/10.2165/00128415-200711590-00075.

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&NA;. "Rabeprazole." Reactions Weekly &NA;, no. 1373 (2011): 27. http://dx.doi.org/10.2165/00128415-201113730-00091.

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Prakash, Amitabh, and Diana Faulds. "Rabeprazole." Drugs 55, no. 2 (1998): 261–67. http://dx.doi.org/10.2165/00003495-199855020-00009.

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Bank, Simmy. "Rabeprazole." Drugs 55, no. 2 (1998): 268. http://dx.doi.org/10.2165/00003495-199855020-00010.

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Takeguchi, Noriaki. "Rabeprazole." Drugs 55, no. 2 (1998): 268. http://dx.doi.org/10.2165/00003495-199855020-00011.

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Langtry, Heather D., and Anthony Markham. "Rabeprazole." Drugs 58, no. 4 (1999): 725–42. http://dx.doi.org/10.2165/00003495-199958040-00014.

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Carswell, Christopher I., and Karen L. Goa. "Rabeprazole." Drugs 61, no. 15 (2001): 2327–56. http://dx.doi.org/10.2165/00003495-200161150-00016.

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Dissertations / Theses on the topic "Rabeprazole"

1

Garcia, Cassia Virginia. "Validação de métodos analíticos e estudo da estabilidade de rabeprazol sódico." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2007. http://hdl.handle.net/10183/10382.

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Neste trabalho, foram desenvolvidos e validados métodos qualitativos e quantitativos para o controle de qualidade de rabeprazol sódico, um inibidor da bomba de prótons. O fármaco apresenta eficácia comprovada na cicatrização, alívio de sintomas e prevenção de recidivas de úlceras pépticas e doença do refluxo gastroesofágico. A substância química de referência utilizada nas análises foi caracterizada por espectrofotometria no infravermelho e por espectroscopia de ressonância magnética nuclear. A análise qualitativa foi realizada por cromatografia em camada delgada, espectrofotometria no ultravi
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2

Naghmeh, Jabarizadekivi. "A Comparison of the Effect of Omeprazole and Rabeprazole on Clozapine Serum Concentrations." University of Sydney, 2008. http://hdl.handle.net/2123/2471.

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Master of Philosophy<br>Clozapine is a drug of choice for treatment of refractory schizophrenia, which is primarily metabolized by Cytochrome P450 1A2 (CYP1A2). Norclozapine is its main metabolite. There are reports of wide ranging gastrointestinal side effects associated with clozapine therapy, that result in concomitant administration of proton pump inhibitors to treat acid-related disorders. Omeprazole is an established CYP1A2 inducer, while an in vitro study has shown that rabeprazole is much less potent in this regard. There is no available information about the impact of rabeprazole on C
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Naghmeh, Jabarizadekivi. "A Comparison of the Effect of Omeprazole and Rabeprazole on Clozapine Serum Concentrations." Thesis, The University of Sydney, 2007. http://hdl.handle.net/2123/2471.

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Clozapine is a drug of choice for treatment of refractory schizophrenia, which is primarily metabolized by Cytochrome P450 1A2 (CYP1A2). Norclozapine is its main metabolite. There are reports of wide ranging gastrointestinal side effects associated with clozapine therapy, that result in concomitant administration of proton pump inhibitors to treat acid-related disorders. Omeprazole is an established CYP1A2 inducer, while an in vitro study has shown that rabeprazole is much less potent in this regard. There is no available information about the impact of rabeprazole on CYP1A2 activity in patien
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Tu, Cheng-Wen, and 杜正文. "Modified Release of Rabeprazole and Oxybutynin Using Enteric Coating System." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/99887508463695080407.

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碩士<br>嘉南藥理科技大學<br>藥學系<br>101<br>In recent years, scientific and technological advancements have been made in the development of controlled drug delivery system. Controlled drug delivery technology has many advantages, such as improve effectiveness, convenience and reduce side effects. It also helps to improve quality of life. In order to obtain optimum formulation to ensure efficacy and safety profiles, the effect of formulation variables on drug release and stability are crucial. Rabeprazole and oxybutynin are used in the present study as the model drugs. Formulations with different polymer
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Swayze, Emma. "The effects of CTDSP1 on topoI degradation and cellular resistance to topoI inhibitors chemotherapy treatment." Thesis, 2017. https://hdl.handle.net/2144/23723.

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The anticancer drug Camptothecin (CPT) specifically targets topoisomerase I (topoI). While this class of drug is used to treat various solid tumors, CPT is only effective in 13-30 percent of the patient population. Although the mechanism of the CPT resistance pathway is not fully understood, we found cancer cells degrade topoisomerase I (topoI) in response to CPT. The observed relationship between higher basal DNA-PKcs mediated phosphorylation of topoI, rapid degradation of topoI, and resistance to CPT suggested that DNA-PKcs is a critical regulator of the phosphorylation status of topoI and t
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Yang, Yu-Fan, and 楊喻帆. "Role of CYP2C19 polymorphisms in short-term rabeprazole-based triple therapy- Implication of PK/PD correlation." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/12890224878228433172.

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邢惠婷. "The effect of regimen on the pharmacokinetics and pharmacodynamics of Rabeprazole in healthy volunteers:a relation to CTP2C19 genetic polymorphism in Taiwanese." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/13952164826798061242.

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碩士<br>國立臺灣大學<br>臨床藥學研究所<br>90<br>Abstract Sodium Rabeprazole is a relative new agent in the class of proton pump inhibitors. Rabeprazole is metabolized partially by CYP2C19, and one of its metabolites, thioether-rabeprazole is considered to be metabolized by CYP2C19, too. In addition, CYP2C19 exhibits a genetic polymorphism and there are more PMs in Asians than in Caucasians. Although CYP2C19 is not the major enzyme involved in its metabolism, it has been shown that people with different CYP2C19 genotypes have different abilities to metabolize rabeprazole either after single dose or
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Books on the topic "Rabeprazole"

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Blokdijk, G. J. Rabeprazole Sodium; Complete Self-Assessment Guide. CreateSpace Independent Publishing Platform, 2018.

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2

Ankita, Thacker, and Pujara Naisarg. Formulation and Evaluation of Sublingual Tablet of Rabeprazole Sodium. LAP Lambert Academic Publishing, 2014.

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3

Simonis, Kaylin. RabeprazoIe: A Strong Drug Used to Treat Any Gastroesophageal Reflux Disease in Adults and Children. Independently Published, 2019.

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Book chapters on the topic "Rabeprazole"

1

de Groot, Anton C. "Rabeprazole." In Monographs In Contact Allergy. CRC Press, 2022. http://dx.doi.org/10.1201/9781003158004-431.

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"Rabeprazole." In Meyler's Side Effects of Drugs: The International Encyclopedia of Adverse Drug Reactions and Interactions. Elsevier, 2006. http://dx.doi.org/10.1016/b0-44-451005-2/00604-5.

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"Rabeprazole." In Meyler's Side Effects of Drugs. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-444-53717-1.01383-4.

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"RABEPRAZOLE." In Litt's Drug Eruptions and Reactions Manual. CRC Press, 2014. http://dx.doi.org/10.1201/b15347-170.

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"Rabeprazole." In Drugs Handbook 2012–2013. Bloomsbury Academic, 2011. http://dx.doi.org/10.5040/9781350363595.art-1483.

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Jewell, Richard. "Rabeprazole." In xPharm: The Comprehensive Pharmacology Reference. Elsevier, 2007. http://dx.doi.org/10.1016/b978-008055232-3.62509-7.

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"RABEPRAZOLE." In Litt's Drug Eruption Reference Manual Including Drug Interactions. CRC Press, 2004. http://dx.doi.org/10.3109/9780203492079-158.

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8

"Rabeprazole." In PharmacotherapyFirst Drug Information. The American Pharmacists Association, 2017. http://dx.doi.org/10.21019/druginformation.rabeprazole.

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"Rabeprazole." In PharmacotherapyFirst Drug Information. The American Pharmacists Association, 2017. http://dx.doi.org/10.21019/pfdi.rabeprazole.

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"Rabeprazole." In Hale’s Medications & Mothers’ Milk™ 2019. Springer Publishing Company, 2018. http://dx.doi.org/10.1891/9780826150356.0879.

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Conference papers on the topic "Rabeprazole"

1

Mohammed, Mustafa J., Ashraf Saad Rasheed, and Bashar Qasim. "Retention behavior of pantoprazole and rabeprazole on zwitterionic stationary phases in hydrophilic interaction chromatography." In 4TH INTERNATIONAL CONFERENCE ON INNOVATION IN IOT, ROBOTICS AND AUTOMATION (IIRA 4.0). AIP Publishing, 2025. https://doi.org/10.1063/5.0254790.

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Akahoshi, K., S. Nagatomo, S. Osada, et al. "ESOMEPRAZOLE VS RABEPRAZOLE IN THE HEALING OF ARTIFICIAL ULCERS AFTER THE ENDOSCOPIC SUBMUCOSAL DISSECTION USING THE CLUTCH CUTTER: A PROSPECTIVE RANDOMIZED CONTROLLED STUDY." In ESGE Days 2018 accepted abstracts. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1637389.

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You might also be interested in the extended bibliographies on the topic 'Rabeprazole' for particular source types:
Journal articles
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