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Nexx (Esomeprazole)
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Esomeprazole

Nexx is a drug used to treat certain stomach and esophagus problems. Nexx is approved for the treatment of gastroesophageal reflux disease (GERD), and in combination with antibiotics for the treatment of patients with H. pylori infection. It's also used to reduce the risk of gastric ulcers and in the treatment of Zollinger-Ellison syndrome. Nexx relieves heartburn, difficulty swallowing, and persistent cough caused by acid reflux. It also helps heal acid damage to the stomach and esophagus, prevents ulcers, and may help prevent cancer in the esophagus. Nexx belongs to a class of drugs called proton pump inhibitors, which block the production of acid in the stomach. Other proton pump inhibitors include omeprazole (Prilosec), lansoprazole (Prevacid), rabeprazole (Aciphex), and pantoprazole (Protonix). The Food and Drug Administration (FDA) approved Nexx in 2001. Pfizer bought the rights to the over-the-counter (OTC) version of Nexx from AstraZeneca in 2012. In 2014, the patent expired, and a new OTC Nexx was introduced. AstraZeneca reportedly slashed thousands of jobs in the face of diminished revenues due to the expiration of the Nexx patent.

Other names for this medication:
Esomeprazole, Axagon, Ceso, Emep, Esofag, Esomac, Esomep, Esomeprazol, Esomezol, Esonix, Esopral, Esoprax, Esoprazol, Esoral, Esoz, Espram, Inexium, Izra, Lucen, Maxpro, Nedox, Neksium, Neptor, Nexe, Nexiam, Nexium, Nexpro, Nexum, Nexx, Opton, Progut, Pronex, Raciper, Sergel, Sompraz, Ulcratex, Zosec,

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Mucous from bottom-dwelling juvenile plaice (Pleuronectes platessa) and pelagic adult herring (Clupea harengus) elicit similar responses, suggesting that the behavioural reactions are species independent. Changes in the pepsin activity of the gastric mucosa of rats in the early stages of carcinogenesis Longitudinal evidence on the association between interleukin-6 and C-reactive protein with the loss of total appendicular skeletal muscle in free-living older men and women. Most of the reviewed information was present in the prescriptions. Identification of differentially expressed proteins by treatment with PUGNAc in 3T3-L1 adipocytes through analysis of ATP-binding proteome.

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We use objective boundary conditions and self-consistent charge density-functional-based tight-binding to simulate at the atomistic scale the formation of helices in narrow graphene nanoribbons with armchair edges terminated with fluorine and hydrogen. Differentiating the effects of three benzodiazepines on non-REM sleep EEG spectra. Ultimately, identification and use of susceptibility factors in workplace settings has both scientific and ethical issues that need addressing. While plasmacytoid dendritic cells (pDCs), a natural type I interferon (IFN)-producing cell type, are regarded as critical for innate immunity to viruses, their role in defense against fungal infections remains unknown.

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