--> Santarus Announces Development Program For New ZEGERID Prescription Product What is Xenical? Where to buy low cost medicine.















Santarus Announces Development Program For New ZEGERID Prescription Product What is Xenical? Price comparison for Xenical Where to buy low cost medicinegeocities archive
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Santarus Announces Development Program For New ZEGERID Prescription Product

What is Xenical?

uses of Xenical

Xenical is used along with a doctor-approved reduced-calorie diet, exercise, and behavior modification program to help significantly overweight ( obese ) persons lose weight. Taking Xenical can also help prevent we from regaining weight we have lost. Losing weight and keeping it off can reduce many health risks that come with obesity, including heart disease, diabetes, high blood pressure, some forms of cancer, certain breathing problems, and a shorter lifespan.

Dietary fats need to be broken down into smaller pieces before body can absorb them. Xenical works by blocking enzyme that breaks down fats in your diet. This undigested fat then passes out of your body in your bowel movement. Xenical doesn't block absorption of calories from sugar and other non-fat foods, so we still need to restrict your total intake of calories.

how to use of Xenical

Read Patient Information Leaflet provided by your pharmacist before we start taking Xenical and each time we get a refill. If you have any questions, consult your doctor or pharmacist.

Take Xenical by mouth with liquid sometime during each main meal that contains fat or within 1 hour after meal, usually 3 times daily or as directed by your doctor. If you occasionally miss a meal or your meal contains no fat, skip that dose of medication. To decrease chance of unpleasant side effects, it is very important that no more than 30% of calories in your diet come from fat. Your daily intake of fat, protein, and carbohydrate should be evenly spread over 3 main meals.

Because Xenical can interfere with absorption of certain vitamins ( fat-soluble vitamins including A, D, E, K ) , a daily multivitamin supplement containing these nutrients is recommended. Take multivitamin at least 2 hours before or 2 hours after taking Xenical ( e. g. , at bedtime ) .

If we take cyclosporine, take it at least 2 hours before or after Xenical to make sure the full dose of cyclosporine is absorbed into your bloodstream.

You should see some weight loss within 2 weeks after we start Xenical. Tell your doctor if your condition does not improve or if it worsens.

side effects of Xenical

Changes in your bowel function frequently occur because of the unabsorbed fat. Fatty/oily stool, oily spotting, intestinal gas with discharge, a feeling of needing to have a bowel movement right away, increased number of bowel movements, or poor bowel control may occur while use Xenical. These side effects may get worse if we eat more fat than you should. If these effects persist or worsen, notify your doctor promptly.

Remember that your doctor has prescribed Xenical because he or she has judged that benefit to we is greater than the risk of side effects. Many people using Xenical don't have serious side effects.

A very serious allergic reaction to Xenical is unlikely, but seek immediate medical attention if it occurs. Symptoms of a serious allergic reaction may include:

This isn't a complete list of possible side effects. If we notice other effects not listed above, contact your doctor or pharmacist.

precautions of Xenical

Before taking Xenical, tell your doctor or pharmacist if we are allergic to it; or if we have any other allergies.

Xenical should not be used if we have certain medical conditions. Before using this medicine, consult your doctor or pharmacist if we have:

Before using Xenical, tell your doctor or pharmacist your medical history, especially of:

If you're diabetic, weight loss may improve your blood sugar control. Be sure to check your blood sugar regularly and tell your doctor results. Your diet or medications may need to be adjusted.

Xenical isn't recommended for use during pregnancy. Consult your doctor for more details.

It's not known whether Xenical passes into breast milk. Because of possible risk to infant, breast-feeding while using this drug is not recommended. Consult your doctor before breast-feeding.

interactions of Xenical

See also How to Use section.

Your healthcare professionals ( e. g. , doctor or pharmacist ) may already be aware of any possible drug interactions and may be monitoring we for them. Do not start, stop or change dosage of any medicine before checking with them first.

Tell your doctor of all prescription and nonprescription medication we use, especially of:

This document doesn't contain all possible interactions. Therefore, before using Xenical, tell your doctor or pharmacist of all products we use. Keep a list of all your medications with you, and share list with your doctor and pharmacist.

overdose of Xenical

If overdose of Xenical is suspected, contact your local poison control center or emergency room immediately. US residents can call US national poison hotline at 1-800-222-1222. Canadian residents should call their local poison control center directly.

notes of Xenical

Do not share Xenical with others.

For best results, Xenical should be used along with a doctor-approved exercise program and diet plan. Consult your doctor or dietician for help designing an appropriate exercise and food plan for you.

missed dose of Xenical

If you miss a dose Xenical, take it as soon as you remember unless it has been more than 1-2 hours since your meal. In that case, skip missed dose since most of the fat from your meal will already be absorbed and medication will not work. Don't double the dose of Xenical to catch up.

storage of Xenical

Store Xenical at room temperature at 77 degrees F ( 25 degrees C ) away from light and moisture. Brief storage between 59-86 degrees F ( 15-30 degrees C ) is permitted. Keep all medicines away from children and pets.

Properly discard Xenical when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.

Price comparison for Xenical

Santarus Announces Development Program For New ZEGERID Prescription Product

Santarus Announces Development Program For New ZEGERID Prescription Product What is Xenical? Price comparison for Xenical Where to buy low cost medicinegeocities archive

Santarus, Inc. ( NASDAQ: SNTS ) , a specialty pharmaceutical company, announced that it's developing a new tablet formulation to add to its ZEGERID® family of branded prescription pharmaceutical products. The new formulation is a swallowable tablet that combines immediate-release omeprazole, a proton pump inhibitor ( PPI ) , with a mix of buffers. Santarus plans to undertake clinical and stability studies with the tablet in preparation for submission of a New Drug Application to U. S. Food and Drug Administration. The company's objective is to have new ZEGERID tablet product commercially available in U. S. in the second half of 2009.

" Our goal was to design an optimized tablet formulation that has potential to provide features and benefits that are important to physicians and their patients. We've evaluated new formulation in a pilot clinical study with positive results, " said Gerald T. Proehl, president and chief executive officer of Santarus. " Our progress in developing a ZEGERID tablet formulation reflects our past experience in developing other immediate-release PPI products. We've a successful track record of moving quickly through product and clinical development to regulatory approval for ZEGERID Capsules and Powder for Oral Suspension. We're focused on achieving similar results for this new ZEGERID formulation so we can expand ZEGERID family of product offerings. "

About Currently Marketed ZEGERID Prescription Products

ZEGERID ( omeprazole/sodium bicarbonate ) Capsules and Powder for Oral Suspension are indicated for treatment of heartburn and other symptoms associated with gastroesophageal reflux disease ( GERD ) , maintenance of healing and short-term treatment of erosive esophagitis, and short-term treatment of active benign gastric ulcers and active duodenal ulcers. ZEGERID Powder for Oral Suspension 40 mg is also indicated for reduction of risk of upper gastrointestinal bleeding in critically ill patients.

ZEGERID Capsules and Powder for Oral Suspension contain a combination of omeprazole, a PPI, and sodium bicarbonate, an antacid, which raises gastric pH and thus protects omeprazole from acid degradation.

ZEGERID products offer a distinct pharmacological profile - rapidly reaching maximal plasma levels ( in approximately 30 minutes ) and providing strong acid control. While correlation of pharmacodynamic data to clinical effect has not been established, median percentage of time gastric pH was greater than 4 over 24 hours in patients treated with ZEGERID in a pharmacodynamic study ranged from 12. 2 hours to 18. 6 hours, depending on the strength and dosage form, after repeated once-daily dosing. ZEGERID can be conveniently taken once-a-day on an empty stomach, at least one hour before a meal.

PPIs are widely prescribed for a variety of diseases and disorders of upper digestive tract. All currently marketed oral PPIs in the U. S. , other than ZEGERID, are delayed-release formulations that utilize an enteric coating to protect PPI from acid degradation, thereby delaying absorption and initial acid suppression. Unlike delayed-release PPIs, ZEGERID Capsules and Powder for Oral Suspension utilize an antacid in lieu of an enteric coating. The antacid neutralizes stomach acid and protects the PPI, omeprazole, from gastric acid degradation and allows for its rapid absorption and suppression of gastric acid.

Important Safety Information

The most frequently reported adverse events with ZEGERID are headache, diarrhea, and abdominal pain. In 178 critically ill patients treated with ZEGERID Powder for Oral Suspension, adverse events generally reflected serious, underlying medical condition of patients, but some adverse events occurred with more frequency in patients treated with ZEGERID Powder for Oral Suspension than in those treated with comparator ( acid-controlling ) drug. For more information about these and other events, please see Table 13 of full Prescribing Information. Symptomatic response to therapy does not preclude the presence of gastric malignancy. Atrophic gastritis has been noted occasionally in gastric corpus biopsies from patients treated long term with omeprazole.

ZEGERID Capsules contain 304 mg of sodium per dose. ZEGERID Powder for Oral Suspension contains 460 mg of sodium per dose. This should be taken into consideration for patients on a sodium-restricted diet.

Sodium bicarbonate is contraindicated in patients with metabolic alkalosis and hypocalcemia. ZEGERID is contraindicated in patients with known hypersensitivity to any component of the formulation.

Since both 20 mg and 40 mg ZEGERID contain the same amount of sodium bicarbonate ( 1100 mg in capsules, 1680 mg in packets of powder for oral suspension ) , two 20 mg capsules are not equivalent to, and shouldn't be substituted for, one 40 mg capsule, and two 20 mg packets aren't equivalent to, and shouldn't be substituted for, one 40 mg packet.

About Santarus

Santarus, Inc. is a specialty pharmaceutical company focused on acquiring, developing and commercializing proprietary products that address needs of patients treated by gastroenterologists or primary care physicians. The company's current marketing efforts are primarily focused on ZEGERID Capsules and Powder for Oral Suspension. These products are immediate-release formulations of omeprazole, a widely prescribed PPI. More information about Santarus is available on the company's Web site at http: //www. santarus. com.

Santarus cautions we that statements included in this press release that are not a description of historical facts are forward-looking statements. The inclusion of forward-looking statements should not be regarded as a representation by Santarus that any of its plans will be achieved. Actual results may differ materially from those set forth in this release due to the risks and uncertainties inherent in Santarus' business, including, without limitation: difficulties or delays associated with Santarus' product development activities, including product stability, and clinical testing for the new tablet formulation; whether the new tablet formulation achieves the intended safety and efficacy profile and demonstrates features and benefits that are important to physicians and their patients; timing for commercial availability of the new tablet product and potential for delays associated with clinical testing and regulatory approval processes; adverse side effects or inadequate therapeutic efficacy of Santarus' products that could result in product recalls, market withdrawals or product liability claims; competition from other pharmaceutical or biotechnology companies and evolving market dynamics, including impact of currently available generic PPI products and introduction of additional generic PPI products; scope and validity of patent protection for new tablet formulation and Santarus' other ZEGERID products, including the outcome and duration of the pending patent infringement lawsuits against Par Pharmaceutical, Inc. , and Santarus' ability to commercialize new tablet formulation and its other ZEGERID products without infringing the patent rights of others; other difficulties or delays in development, testing, manufacturing and marketing of, and maintaining regulatory approvals for, Santarus' products; and other risks detailed in Santarus' prior press releases as well as in public periodic filings with the Securities and Exchange Commission.

You're cautioned not to place undue reliance on these forward-looking statements, which speak only as of date hereof. All forward-looking statements are qualified in their entirety by this cautionary statement and Santarus undertakes no obligation to revise or update this news release to reflect events or circumstances after date hereof. This caution is made under safe harbor provisions of Section 21E of the Private Securities Litigation Reform Act of 1995.

Santarus® and ZEGERID® are registered trademarks of Santarus, Inc.

http: //www. santarus. com


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