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Happi (Rabeprazole)

Happi comes as a delayed-release (releases the medication in the intestine to prevent break-down of the medication by stomach acids) tablet and a delayed-release sprinkle capsule (capsule that contains small granules of medication that are sprinkled on food or liquid) to take by mouth. The delayed-release tablets are usually taken once a day. When used to treat ulcers, Happi tablets are taken after the morning meal. When used in combination with other medications to eliminate H. pylori, Happi tablets are taken twice a day, with the morning and evening meals, for 7 days. Happi sprinkle capsules are usually taken once a day 30 minutes before a meal. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take Happi exactly as directed. Do not take more or less of it or take it more often or for a longer period of time than prescribed by your doctor.

Swallow the tablets whole with water; do not split, chew, or crush them.

To take the sprinkle capsules, open a capsule and sprinkle the granules onto a small amount of cool soft food such as applesauce, fruit or vegetable baby food, or yogurt and swallow the mixture immediately (within 15 minutes) without chewing or crushing the granules. You can also open a capsule and pour the contents into a small amount of cool liquid such as infant formula, apple juice, or pediatric electrolyte solution and swallow the mixture immediately (within 15 minutes) without chewing or crushing the granules.

Continue to take Happi even if you feel well. Do not stop taking Happi without talking to your doctor. If your condition does not improve or gets worse, call your doctor.

Other names for this medication:
Rabeprazole, Aciphex, Barole, Eurorapi, Gastrodine, Happi, Paricel, Rabec, Rabeloc, Rabemac, Rabeprazol, Rabium, Rotec,

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We conducted a randomized study to determine whether systematic transpupillary thermotherapy (TTT) after proton beam radiotherapy could have a beneficial effect. Recurrence of full-thickness rectal prolapse was found in only 2 patients-(1.5 percent).

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Human NK cytotoxicity against pEC mediated by freshly isolated or IL-2-activated NK cells through NKG2D was completely blocked using anti-pULBP1 polyclonal Ab. Monte Carlo (MC) simulations are performed to validate the correctness of the theoretical model.

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Identification of iron-cyanide complexes in contaminated soils and wastes by Fourier transform infrared spectroscopy. This descriptive, correlational study describes academically-based nurse practice centers and the associated job satisfaction of nurse faculty members. Genomic responses in mouse models greatly mimic human inflammatory diseases. The responses of cultured phototrophic biofilms to diverse phosphorus (P) regimes were assessed using a semi-continuous flow incubator.

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Genetic analysis of aldosterone synthase in patients with idiopathic hyperaldosteronism. We used GSP to investigate SCC-25 cells with wild-type p53 gene and OEC-M1 cells with mutant p53 gene for the assessment of antiproliferative effects including cell viability, cell cycle, apoptosis, migration and invasion potential, and alterations of associated oncoproteins involved in cellular and molecular events. Much of drug discovery today is predicated on the concept of selective targeting of particular bioactive macromolecules by low-molecular-mass drugs. Prevention of local relapses and new localisations of oral leukoplakias with the synthetic retinoid fenretinide (4-HPR).

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Treatment with the demethylating drugs 5-azacytidine (AZA) and decitabine (DAC) is now recognised as an effective therapy for patients with Myelodysplastic Syndromes (MDS), a range of disorders arising in clones of hematopoietic progenitor cells. Last we evaluate its construction as a scientific concept from empirical facts. The characteristic cytological, immunological and biochemical changes in the synovial fluid in synovitis of different etiologies

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