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Merofex (Omeprazole)
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Omeprazole

Merofex is a medication used in the treatment of gastroesophageal reflux disease, peptic ulcer disease, and Zollinger–Ellison syndrome. It is also used to prevent upper gastrointestinal bleeding in people who are at high risk. Merofex is acting by decreasing the amount of acid produced in the stomach. It is proton pump inhibitor (PPI). Merofex is available in tablets (10 mg, 20 mg, 40 mg) and capsules.

Other names for this medication:
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Merofex 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 Merofex is used in combination with antibiotics (eg, amoxicillin, clarithromycin) to treat ulcers associated with the infection caused by the H. pylori bacteria.

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

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

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

Merofex 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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ATPase activity of transcription-termination factor rho: functional dimer model. pentaphyllum total plant extracts on immune cells was evaluated in this study. Overall morbidity and mortality rate of mediastinal surgery might appear remarkable but has to be related to the favorous long-term results after different individual treatment modalities in patients with mediastinal masses. In 9 of the 10 DM families an amplification was identified as the mechanism of mutation.

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This immunosuppression appears to be part of the inflammatory response that accompanies trauma, and in part, to represent the need for conditional nutrients in this setting. In several cases, the specific substrates transported by the new karyopherins have been identified, allowing the characterization of new pathways into and out of the nucleus. A case of lithium poisoning with lithium salts in a man of 66 years is reported. The CD (circular dichroism) and CPL (circular polarization of luminescence) spectra of NADPH in aqueous solution were studied and found to be markedly different.

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To retrospectively compare outcome after surgery by laparoscopy or laparotomy for borderline tumors. An overview on adsorptive separation of cephalosporin antibiotics has been presented.

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A new antiplatelet drug and a number of trials involving HMG Co-A reductase inhibitors are important advances in the secondary prevention of stroke. A case of cutaneous sterile pyogranuloma/granuloma syndrome in a golden retriever. Capillary electrophoresis is a sensitive monitor of the hairpin-random coil transition in DNA oligomers. Recent studies from our group have demonstrated the existence of a disynaptic excitatory cortico-motoneuronal (CM) pathway in macaque monkeys via propriospinal neurons in the midcervical segments. Correlation of bacterial mutagenicity and hamster cell transformation with tumorigenicity induced by 2,4-toluenediamine.

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Recent studies have shown that the neural regulation of pair bonding in the monogamous prairie vole (Microtus ochrogaster) is similar to that of drug seeking in more traditional laboratory rodents. We have used 51Cr labelled herpes virus infected target cells to examine the K-cell activity of peripheral blood lymphocytes in patients who have either malignant reticuloendothelial diseases or who are receiving cytotoxic and steroid therapy for other reasons. Bradykinin-induced hyperalgesia was abolished by co-administration with the B(2) receptor antagonist Hoe 140 (5 pmol/site), the NMDA antagonist MK-801 (5 nmol/site), the cyclooxygenase inhibitor indomethacin (10 nmol/site) and the glial metabolic inhibitor fluorocitrate (1 nmol/site). These data indicate that RDSs in Manoa basin are generally contaminated with certain potentially toxic elements and the legacy of past use of leaded gasoline is still a concern in this urban drainage system. This is one of the first cases of opsoclonus-myoclonus syndrome developing, following a streptococcal infection in adults.

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The purpose of this study was to assess the tracking (degree of stability) of several categories of self-reported dental health behavior in adolescence over a 3-year period. Indirect immunofluorescence indicates that XORC2 binds to chromatin well before the commencement of DNA synthesis, and even under conditions that prevent the association of replication licensing factor(s) with the DNA. Wound length, width, and linear healing rate based on wound area were measured for 2 weeks postwounding.

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