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Generic Prilosec OTC is the medication of high quality, which is taken in treatment of symptoms of gastroesophageal reflux disease (GERD) and other conditions caused by excess stomach acid. It is also taken to promote healing of erosive esophagitis (damage to your esophagus caused by stomach acid). Generic Prilosec OTC is acting by decreasing the amount of acid produced in the stomach. It is proton pump inhibitor (PPI).

Other names for this medication:
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Similar Products:
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Also known as:  Omeprazole.


Generic Prilosec OTC target is the treatment of symptoms of gastroesophageal reflux disease (GERD) and other conditions caused by excess stomach acid. It is also taken to promote healing of erosive esophagitis (damage to your esophagus caused by stomach acid).

Generic Prilosec OTC is acting by decreasing the amount of acid produced in the stomach. It is proton pump inhibitor (PPI).

Prilosec is also known as Omeprazole, Omez, Protoloc.

Generic name of Generic Prilosec OTC is Omeprazole.

Brand names of Generic Prilosec OTC are Prilosec and Prilosec OTC.


Generic Prilosec OTC is available in tablets (10 mg, 20 mg, 40 mg) and capsules.

You should take Generic Prilosec OTC every day for 14 days. Do not take Generic Prilosec OTC more than one pill a day.

Take Generic Prilosec OTC before eating. Do not break, crush or open a delayed-release capsule.

Your symptoms may get better before the condition is completely treated.

Take Generic Prilosec OTC with water.

If you want to achieve most effective results do not stop taking Generic Prilosec OTC suddenly.


If you overdose Generic Prilosec OTC and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Generic Prilosec OTC overdosage: drowsiness, nausea, fast heartbeat, sweating, dry mouth, headache, blurred vision, vomiting.


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 Prilosec 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.


Do not take Generic Prilosec OTC if you are allergic to Generic Prilosec OTC components.

Do not take Generic Prilosec OTC if you're pregnant or you plan to have a baby, or you are a nursing mother.

Generic Prilosec OTC is not used for immediate relief of heartburn symptoms.

Do not take more than one tablet of Generic Prilosec OTC a day (24 hours).

Be careful with Generic Prilosec OTC if you suffer from or have a history of liver disease, bloody or black stools, heartburn which lasts for over 3 months, vomit that looks like blood or coffee grounds, frequent chest pain, heartburn with wheezing, stomach pain, nausea or vomiting, trouble or pain with swallowing, unexplained weight loss.

Take Generic Prilosec OTC with care if you are taking such medicines as disulfiram (Antabuse),a blood thinner (warfarin (Coumadin)),tacrolimus (Prograf),cyclosporine (Gengraf, Neoral, Sandimmune), phenytoin (Dilantin),ampicillin (Omnipen, Principen),itraconazole (Sporanox) or ketoconazole (Nizoral),insomnia or anxiety medicines (diazepam (Valium), alprazolam (Xanax), lorazepam (Ativan), temazepam (Restoril), clorazepate (Tranxene), chlordiazepoxide),iron (Feosol, Mol-Iron, Fergon, Femiron and the others), atazanavir (Reyataz), theophylline (TheoBid, Theo-Dur, Theochron, Theolair, Elixophyllin, Slo-Phyllin).

Avoid alcohol.

Do not stop taking Generic Prilosec OTC suddenly.

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This was a multi-center, open study conducted at 102 hospitals in Japan. Patients with reflux esophagitis received famotidine 10 mg twice daily for 2 weeks, then omeprazole 10 mg once daily for 2 weeks. Thereafter, patients were switched to famotidine 10 mg twice daily for a third 2-weekperiod, provided those with a medical condition agreed to continue the study. Patients evaluated the treatment response to each gastrointestinal symptom using a predefined patient questionnaire and gastrointestinal symptom rating scale (GSRS).

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In H. pylori-positive patients the intestinal flora is characterized by an increase in growth of acid-tolerant L. acidophilus. Eradication therapy exerts only a short-term influence on intestinal flora, whereas in the long term, the intestinal microflora is restored to a pattern similar to that of the control group.

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Double-blind, placebo-controlled randomized clinical trials.

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Recently approved single-enantiomer drugs showed no evidence of superior efficacy over the older racemic precursors in the pivotal trials leading to their approval, and in a majority of cases, they were not directly compared.

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Twenty of the 45 patients were symptomatic (mean score 1.9) on pre-study treatment (mainly omeprazole < 20 mg once daily); on omeprazole 20 mg twice daily, only six patients remained symptomatic (mean score 1.6). Ten patients (22%) had persisting GOR on omeprazole 20 mg twice daily (median % total time with pH < 4 was 8%). Abnormal nocturnal reflux was found in nine and abnormal daytime reflux in only four patients. Heartburn persisted in three of these 10 patients (30%). Those remaining symptomatic had more daytime acid reflux than the asymptomatic patients with persistent reflux (median percentage daytime at pH < 4 was 13.6% vs 0.6%, respectively; P < 0.01). By increasing the omeprazole dose to 20 mg three times daily, only three of the 10 had persistent acid reflux.

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Despite 30 years of its discovery, the ideal therapeutic regimen against Helicobacter pylori is still evasive. Clarithromycin-based standard triple therapy which has been considered the first line empirical therapy has been failing in many parts of the world, due to rising resistance against Clarithromycin, forcing the use of alternate regimens. In this context, we studied the local antibiotic resistance patterns against H. pylori and its impact on standard triple therapy in our region. All patients undergoing diagnostic upper endoscopy during the study period and detected to be positive for rapid urease test (RUT) underwent cultures of gastric mucosal specimens and had their antibiotic resistance patterns mapped out. Standard triple therapy was administered to those tested positive for H. pylori by RUT and eradication rates checked by urea breath test 4 weeks after the completion of treatment. Eradication rates with Clarithromycin-based standard triple therapy were suboptimal with a success of only (71.28%). H. pylori culture and antibiotic susceptibility studies showed high resistance to Clarithromycin (21.2%), Metronidazole (78.1%), and Levofloxacin (15%). However, the resistance to Amoxicillin (2.9%), Tetracycline (0%), and Rifabutin (4.5%) were low. Standard triple therapy is failing in our region due to high Clarithromycin resistance. We need to abandon empirical and blind triple therapy without post-treatment testing and devise alternate effective treatment strategies against H. pylori based on the local resistance patterns observed.

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There is much controversy as to whether or not treatment of Helicobacter pylori reduces the occurrence of peptic ulcers during therapy with a non-steroidal anti-inflammatory drug (NSAID).

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The economic evaluation of new medicines is increasingly important for pricing, registration and selection for use. A decision-analytic strategy was performed to assess the economic impact of antacids alone (phase I therapy), and in combination with either omeprazole, 20 mg once daily, or ranitidine, 150 mg twice daily, for patients with persistent, symptomatic gastro-oesophageal reflux disease of grade II or more (Savary-Miller classification). Data were obtained from published literature, an expert panel of gastroenterologists and actual payments by a private insurer in the USA. Over the 7-month period of the analysis, omeprazole reduced both symptoms and overall costs when compared with ranitidine or antacids. Consequently, the cost per symptom-free month was 43% lower with omeprazole than with ranitidine. Thus, omeprazole should be considered as the initial therapeutic approach for patients in whom phase I therapy fails.

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buy prilosec 2015-08-26

These results suggest that not only the eradication but also the suppression of H. pylori may improve ulcer Buy Zithromax Suspension Online healing and reduce the rate of relapse.

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Three hundred consecutive patients were included. Mean age was 48 yr, 47% were male, 38% had peptic ulcer, and 62% functional dyspepsia. Almost all (97%) patients took all the medications correctly. Per-protocol and intention-to-treat eradication rates were 81% (95% CI 77-86%) and 77% (73-82%). Adverse effects were reported in 22% of the patients, mainly including nausea (8%), metallic taste (5 Paracetamol To Buy %), abdominal pain (3%), and myalgias (3%); none of them were severe.

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Standard-dose lansoprazole is better than high-dose ranitidine in moderately severe reflux Buy Fenofibrate 160 Mg oesophagitis.

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A prospective, physician-blinded, randomized, controlled clinical study was conducted. The patients were randomly assigned to receive TRE every day before taking medicine (TRE group) or no TRE (control group). The patients in the TRE group received regular instructions before taking medicine for the eradication of H. Buy Valtrex Uk pylori during the entire course of treatment through telephone calls. The patients in the control group received detailed instructions at the time of seeing a doctor for the guidance. The primary outcome was the H. pylori eradication rate after treatment. The secondary outcomes included the clinical remissions after treatment, adverse events, compliance, and patients' satisfaction.

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Before endoscopy the health-related quality of life was Buy Atarax compromised in comparison with a normal population, but 1 week after a negative endoscopy it is increased to a level which was close to the normal range despite no major change in symptoms. Physical activity and sleep scores improved significantly after endoscopy.

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After 7 days, the percentage of time Buy Viagra Using Paypal with intragastric pH >4 over 24 hours was 59.7% (14.3 hours) with immediate-release omeprazole, 48.8% (11.7 hours) with lansoprazole (P=0.005), and 41.8% (10.0 hours) with pantoprazole (P<0.001). Median intragastric pH was significantly higher with immediate-release omeprazole than with lansoprazole (P=0.003) or pantoprazole (P<0.001). All drugs were well tolerated.

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Of 37 children, 21 were diagnosed with acid Buy Generic Tamoxifen GERD where pre- and post-treatment reflux indexes were 14.09±1.47 vs. 7.73±1.36; (p<0.001). The number of obstructive apneas and hypopneas decreased after PPI treatment, resulting in an AHI reduction from 13.08±3.11/h to 8.22±2.52/h; (p<0.01). Respiratory response to PPI ranged from complete resolution of OSA (three children with mild OSA; AHI<5/h; 10.31years; 14.29%) to lack of significant AHI change (six children with severe OSA; AHI>10/h; 3.62 years; 28.57%). Post-treatment AHI was predicted by pre-treatment reflux index (adjusted R(2)=0.487; p<0.001).

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From September, 2004 to April, 2007, we retrospectively reviewed 2,297 patients with NUD (1,050 patients) or PUD (1,247 patients) infected with H. pylori. All patients received a standard 1 week triple therapy comprising of one of the five PPIs (pantoprazole, esomeprazole, omeprazole, lansoprazole, rabeprazole), clarithromycin and amoxicillin. The follow-up H. pylori test was performed 4 weeks after the completion of therapy.

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Plasma, gastric mucosa and gastric juice antibiotic concentrations were measured following either low- or high-dose amoxicillin (750 or 1000 mg b.i.d.) and clarithromycin (400 or 500 mg b.i.d.) given in combination with omeprazole 20 mg bid to 12 male volunteers in an open crossover design. Gastric juice and mucosal biopsy collection was performed either 2 (n=6) or 6 hours (n=6) after dosing.

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Proton pump inhibitor and histamine-2 receptor antagonist can prevent aspirin-related ulcers/erosions but few studies compare the efficacy of these two agents. Aims. We evaluated the efficacy of omeprazole and famotidine in preventing recurrent ulcers/erosions in low-dose aspirin users.

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Patients in this study (n = 15; 6 to 13 years old, 9 boys) had reflux esophagitis grade Ic or II (Vandenplas classification). The efficacy of pantoprazole to reduce esophageal acid exposure time (pH < 4), reduce the number and duration of reflux episodes, and to increase the percentage of time with gastric pH > 3 was assessed by continuous 24-hour pH monitoring. The intensity of 5 common symptoms of esophagitis was scored before and after treatment on a 4-point scale. Esophagitis was assessed at baseline and after treatment by visual inspection and by the histology of biopsies from the distal third of the esophagus.