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Ometop

Ometop is also used to prevent stomach ulcers and acidity that may be seen with the prolonged use of painkillers. It belongs to a class of medicines known as proton pump inhibitors (PPIs).

Other names for this medication:
Acichek, Adzole, Almac, Cucid, Domigyl, Domperon, Domril, Durazol, Emidon, Foxidom, Lexcid, Locap, Lomecid, Losec, Minisec, Odoman, Ogestrel, Omdom, Ometop, Omiup, Ompicid, Ompire, Ranispas, Tackodom, Ulcicap, Ulcirex

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Also known as: Omeprazole

Description

Ometop (omeprazole) is a proton pump inhibitor that decreases the amount of acid produced in the stomach.

Ometop is used to treat symptoms of gastroesophageal reflux disease (GERD) and other conditions caused by excess stomach acid. Omeprazole is also used to promote healing of erosive esophagitis (damage to your esophagus caused by stomach acid).

Ometop may also be given together with antibiotics to treat gastric ulcer caused by infection with Helicobacter pylori (H. pylori).

Over-the-counter Ometop OTC is used in adults to help control heartburn that occurs 2 or more days per week. Ometop OTC must be taken as a course for 14 days in a row.

Dosage

Take Ometop exactly as directed on the label, or as prescribed by your doctor. Follow all directions on your prescription label and read all medication guides or instruction sheets.

Use Ometop OTC (over-the-counter) exactly as directed on the label, or as prescribed by your doctor.

Read and carefully follow any Instructions for Use provided with your medicine. Ask your doctor or pharmacist if you do not understand these instructions.

If you cannot swallow a capsule whole, open it and sprinkle the medicine into a spoonful of applesauce. Swallow the mixture right away without chewing. Do not save it for later use.

You must dissolve Ometop powder in a small amount of water. This mixture can either be swallowed or given through a nasogastric (NG) feeding tube using a catheter-tipped syringe.

Use this medicine for the full prescribed length of time, even if your symptoms quickly improve.

OTC Ometop should be taken for only 14 days in a row. It may take 1 to 4 days before your symptoms improve. Allow at least 4 months to pass before you start a new 14-day course of treatment.

Call your doctor if your symptoms do not improve, or if they get worse.

Some conditions are treated with a combination of Ometop and antibiotics. Use all medications as directed.

This medicine can affect the results of certain medical tests. Tell any doctor who treats you that you are using Ometop.

Store at room temperature away from moisture and heat.

Detailed Ometop dosage information

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture, light and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Ometop are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Heartburn can mimic early symptoms of a heart attack. Get emergency medical help if you have chest pain that spreads to your jaw or shoulder and you feel sweaty or light-headed.

You should not use Ometop OTC if you are allergic to it, or if:

you are also allergic to medicines like Ometop OTC, such as esOmetop OTC, lansoprazole, pantoprazole, rabeprazole, Nexium, Prevacid, Protonix, and others; you had breathing problems, kidney problems, or a severe allergic reaction after taking Ometop OTC in the past; or you also take HIV medication that contains rilpivirine (such as Complera, Edurant, Odefsey, Juluca).

Ask a doctor or pharmacist if Ometop OTC is safe to use if you have:

trouble or pain with swallowing; bloody or black stools, vomit that looks like blood or coffee grounds; heartburn that has lasted for over 3 months; frequent chest pain, heartburn with wheezing; unexplained weight loss; nausea or vomiting, stomach pain; liver disease; low levels of magnesium in your blood; or osteoporosis or low bone mineral density (osteopenia).

You may be more likely to have a broken bone in your hip, wrist, or spine while taking a proton pump inhibitor long-term or more than once per day. Talk with your doctor about ways to keep your bones healthy.

Ask a doctor before using this medicine if you are pregnant or breastfeeding.

Do not give this medicine to a child without medical advice.

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Subthreshold psychiatric disorders in primary care: prevalence and associated characteristics. In this manuscript we present our experience with the use of FDP at the POI and pre-hospital setting regarding the feasibility, safety, adverse reactions and adherence to clinical practice guidelines (CPG). Acute and chronic psychosocial stress can induce pronounced changes in human singulair montelukast drug interactions immune responses. Molecular profiling holds great promise for improving our ability to diagnose, prognosticate, and select individualized treatments for lung cancer patients. A 38-year-old man underwent ligation of the superior mesenteric vein due to traumatic disruption.

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The linked Surveillance, Epidemiology, and End Results (SEER) registries and Medicare claims data on patients diagnosed with epithelial ovarian cancer in 2007-2009 were used to extract data on statin prescription fills, population characteristics, primary treatment, comorbidity and survival. Ultimately, these methods were not designed to evaluate the strength of the observed interactions. The results obtained indicate the utility of the algorithm and demonstrate the need to window the data before calculating the correlation. 727 participants from a hospital in the Southeastern United States were administered the PHQ-9 and OAHMQ during a follow-up survey. The findings suggest that ambulatory PT care is less costly than home-based services for people with RA based on The Arthritis Society model. Not only did we find the previously reported potential fetal DNA markers in our identified DMRs/DMSs but also we verified fully the identified DMRs/DMSs in the validation round by MassARRAY EpiTYPER. 1789-1701cm(-1)) of oilseed tissue during rumen in situ incubation using attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FT/IR).

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