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Brux (Omeprazole)
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Omeprazole

Brux and esBrux are proton pump inhibitors (PPIs) and potent inhibitor of gastric acidity which are widely used in the therapy of gastroesophageal reflux and peptic ulcer disease. Brux and esBrux therapy are both associated with a low rate of transient and asymptomatic serum aminotransferase elevations and are rare causes of clinically apparent liver injury.

Other names for this medication:
Omeprazole, Prilosec, Acimax, Acimed, Agastin, Agrixal, Alboz, Alsidol, Altosec, Anadir, Antra, Antramups, Aprazole, Asec, Aspra, Audazol, Biocid, Bioprazol, Brux, Buscogast, Candazol, Ceprandal, Cizole, Cosec, Criogel, Danlox, Desec, Domer, Dudencer, Elcontrol, Elgam, Elkostop, Emage, Emeproton, Emez, Emilok, Erbolin, Eselan, Exter, Ezol, Flusal, Fordex, Gasec, Gastec, Gastracid, Gastral, Gastrimut, Gastrium, Gastronorm, Gastroplex, Gastrotem, Gastrozol, Gastrozole, Getzome, Glaveral, Grizol, Helicid, Hycid, Inhibitron, Inhipump, Inpro, Ipproton, Klomeprax, Lanex, Lenar, Limnos, Locid, Locimez, Logastric, Lokev, Lokit, Lomac, Lomex, Lopraz, Lordin, Losamel, Losec, Losectil, Losepine, Loseprazol, Medoprazole, Mepral, Meprazol, Merofex, Metsec, Minisec, Miol, Miracid, Mopral, Nansen, Nocid, Nogacid, Norpramin, Norsec, Novek, Nozer, Nuclosina, Ocid, Ogal, Olark, Olexin, Olit, Omag, Omalcer, Omapren, Omapro, Omax, Omebeta, Omec, Omecap, Omecip, Omedar, Omel, Omep, Omepra, Omepradex, Omepral, Omeprazol, Omeprazolum, Omepren, Omeprol, Omepron, Omeral, Omeran, Omesec, Omestad, Ometab, Ometac, Omez, Omezol, Omezolan, Omezole, Omezyn, Omezzol, Omicap, Omig, Omisec, Omiz, Omizac, Omolin, Onic, Opaz, Opep, Oprazole, Oraz, Ortanol, Ozid, Parizac, Penrazol, Pepticum, Peptidin, Polprazol, Pratiprazol, Pravil, Prazidec, Prazol, Prazole, Prazolen, Prazolit, Presec, Prevas, Probitor, Procap, Procelac, Proceptin, Proclor, Prohibit, Prolok, Promisec, Protoloc, Protop, Prysma, Pumpitor, Regulacid, Risek, Sanamidol, Seclo, Sopral, Stomex, Tulzol, Ulceral, Ulcesep, Ulcid, Ulcosan, Ulcozol, Ulsen, Ultop, Ulzol, Xoprin, Zanprol, Zefxon, Zegerid, Zenpro, Zepral, Zolcer, Zollocid, Zoltum, Zomepral,

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Brux is used to treat certain conditions where there is too much acid in the stomach. It is used to treat gastric and duodenal ulcers, erosive esophagitis, and gastroesophageal reflux disease (GERD). GERD is a condition where the acid in the stomach washes back up into the esophagus. Sometimes Brux is used in combination with antibiotics (eg, amoxicillin, clarithromycin) to treat ulcers associated with the infection caused by the H. pylori bacteria.

Brux is also used to treat Zollinger-Ellison syndrome, a condition where the stomach produces too much acid.

Brux is also used to treat dyspepsia, a condition that causes sour stomach, belching, heart burn, or indigestion.

In addition, Brux is used to prevent upper gastrointestinal tract bleeding in seriously ill patients.

Brux is a proton pump inhibitor (PPI). It works by decreasing the amount of acid produced by the stomach.

This medicine is available both over-the-counter (OTC) and with your doctor's prescription.

This product is available in the following dosage forms:

  • Powder for Suspension
  • Tablet Disintegrating, Delayed Release
  • Capsule, Delayed Release
  • Tablet, Delayed Release
  • Packet

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Incontinence-Associated Dermatitis (IAD) is one of the clinical manifestations of Moisture- Associated Skin Damage (MASD). Among these post-translational modifications, protein phosphorylation represents the one that has been most thoroughly investigated. The effects of epidermal growth factor and chondroitin sulfate on the animal corneal endothelial cell culture. We present an atypical clinical case of a foreign body in the maxillary sinus. In contrast to the effect favorable body weight on bone mineral density, high percentage body fat and waist circumference are related to low BMD and a vertebral fracture.

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Toxic-metabolic Risk Factors in Pediatric Chronic Pancreatitis-Single Center Experience. An earlier study with spider phobic participants documented that perceptual stimuli are particularly potent to trigger fear responses. But the released amount of alkane fractions using these hydrogels is higher than that in the reference (without using hydrogel). The results suggest that different axial transmission approaches reflect different bone properties.

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