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The basics on 1st diet pill approved in 13 years

The Food and Drug Administration has approved the first new prescription diet drug in 13 years: Belviq, developed by Arena Pharmaceuticals of San Diego.

Doctors say Belviq is a welcome addition to treating obesity, which is almost at 35% in the U.S., even though some call the weight-loss results modest.

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The FDA will continue to monitor studies on the drug’s safety, including whether it could lead to heart attacks or strokes, after it is on the market.

The cost of the drug is not available yet..Dr. Peter Vash executive medical director of Costa Mesa-based Lindora Medical Clinics, gives us a quick look at Belviq:

Q. How does this drug work?

A. Belviq sends a message to the brain to increase serotonin levels,  which in turn reduces appetite and triggers a sense of fullness.

Q. Who are prime candidates?

A. People who are obese with Body Mass Index (BMI) of more than 30 and overweight people who have Type II diabetes or hypertension.

Q. Who should not take this drug? 

A. Women who are pregnant, anyone on SSRI anti-depressants (i.e. Prozac, Zoloff, etc.) or people taking migraine headache medication.

Q. can it be used as a standalone as opposed to part of an overall weight-loss regimen?

A. Belviq has the potential to be an extremely effective and useful tool in the fight against obesity. it should only be used under the proper guidance of a physician and in conjunction with a low-calorie diet, moderate exercise and behavioral modification program. it will not have the same effect if used as a standalone.

Q. When and where will it be available?

 A. it will be available after the 1st of the year and only in licensed physician offices.

Q. What’s the difference between Belviq and Fen-Phen, and how do we know there won’t be similar health problems?  

A. Fenfluramine is one half of the Fen-Phen drug, which caused the combination to be taken off the market because of its damaging effect on the heart valve.  Belviq has all of the positive aspects. it decreases appetites but does not affect the heart valve.  The FDA has investigated the drug in a clinical manner and in their studies have found Belviq does not have the same damaging effect.  

Q. Are there any warning signs doctors are on the lookout for?

A. Each patient will respond differently to the drug so it is difficult to say exactly what the warning signs might be.  it should always be used under the guidance of a qualified physician. 

Some highlights from Time:

How well it works: “According to clinical trial data submitted by Arena to the FDA, nearly half of dieters without Type 2 diabetes who used the medication lost at least 5% of their starting weight — or an average of 12 lbs. — over a year, compared with 23% of those taking a placebo.”

Side effects: “The most common side effects of Belviq in non-diabetic patients are headache, dizziness, fatigue, nausea, dry mouth and constipation; in patients with diabetes, side effects include low blood sugar, headache, back pain, cough and fatigue.”

Health concerns: “In 2010, the FDA rejected Arena’s first request for approval, asking for more evidence of its safety. New data provided by the company showed that heart problems would not occur at the low doses at which Belviq would be prescribed.”

The FDA news release is here

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The basics on 1st diet pill approved in 13 years

Renaissance Surgical Arts at Newport Harbor Announces Single-Dose Radiation Treatment Alternative for Women with Early Breast Cancer

Posted on: Thursday, 10 February 2011, 18:03 CST

COSTA MESA, Calif., Feb. 10, 2011 /PRNewswire/ — Renaissance Surgical Arts at Newport Harbor announced today that it is the first outpatient surgery center in the Western United States to offer intraoperative radiotherapy (IORT) using the INTRABEAM® System – the only device used in the TARGIT-A multicenter human clinical trial that demonstrated IORT to be as effective as traditional radiation for certain women with early breast cancer.

IORT has the potential to replace as many as six and a half weeks of routine radiation therapy with 20-30 minutes of targeted radiation administered during surgery directly to the tumor site after lumpectomy.

“IORT is a game-changer for women facing breast cancer – I like to call it one and done,” said Dr. Alice Police, breast surgeon at Renaissance and co-founder of Pacific Breast Care in Newport Beach, Calif. “For some women in the earlier stages of breast cancer, IORT makes it possible for them to have one surgery consisting of lumpectomy and single-dose radiation therapy and then go on with their life having completed their breast cancer treatment.”

Unlike whole breast radiation treatment, which is administered five times per week for as many as six and a half weeks, IORT provides patients with a targeted single-dose radiation treatment delivered intraoperatively after removal of the tumor. Radiation is applied for 20-30 minutes, exposing the affected tissue in the tumor bed from the inside.

“Dr. Police’s passion for IORT as a revolutionary development in treating early breast cancers aligned with our mission to deliver the best surgical technologies available to patients in a comfortable and private outpatient environment,” said Bruce Wallace, CEO and Administrator for Renaissance Surgical Arts at Newport Harbor. “We looked at IORT device manufacturers and it was clear that the INTRABEAM System was the only responsible choice given its exclusive use in the TARGIT-A Clinical trial which provides 10 years of study and follow-up data to back its safety and efficacy.”

The INTRABEAM System was the only radiotherapy device used in the TARGIT-A clinical trial, the largest randomized clinical trial conducted in the field of IORT for the treatment of breast cancer. the TARGIT-A trial was launched in 2000 and it enrolled 2,232 human patients throughout 28 centers in nine countries. with up to 10-years of follow-up data, the study results demonstrate the equivalency of single-dose targeted IORT in comparison to external beam radiation therapy (EBRT) based on local recurrence.

Renaissance is one of only two outpatient surgery centers in the entire country to offer IORT using the INTRABEAM System, and is the only outpatient facility in the Western United States. It is also the only location at all offering treatment in Orange, Riverside and San Diego counties using the clinically proven INTRABEAM System technology.

“After learning about IORT from Dr. Police, I did my own research on the options, risks and benefits of whole breast and partial breast radiation in comparison to IORT,” said Gila Jones, 58, of San Juan Capistrano, Calif. “After feeling confident about effectiveness based on the TARGIT-A outcomes and considering my own lifestyle and other health concerns, IORT became the obvious choice for me. Dr. Police did my surgery at Renaissance where I was treated as an honored guest.”

Patients need to be evaluated by a specialist to determine if they are a good candidate for IORT. to find out if you or someone you know is an IORT candidate, contact Renaissance Surgical Arts at Newport Harbor at 949-629-1400. for more information about the TARGIT-A clinical trial, please visit www.targit-research.org or www.targit.org.uk. for more information about the INTRABEAM® system, please visit www.meditec.zeiss.com/intrabeam.

Renaissance Surgical Arts at Newport Harbor

Renaissance Surgical Arts at Newport Harbor is a professionally managed, but majority physician-owned facility in Orange County, Calif. with eight ORs and two procedure rooms, the 20,000-plus square foot outpatient facility demonstrates how to mere cutting edge technology into a patient-centric environment that is as beautiful as it is functional. the multispecialty outpatient center supports the area’s best physicians representing a wide variety of specialties, including Cardiology, Ear Nose and Throat, Gastroenterology, Neurosurgery, Orthopedics, Spinal, Ophthalmology, Plastic and Reconstructive Surgery, Podiatry, Oncology, Interventional Radiology, GYN and General Surgery. Learn more at www.mysurgerycenter.net.

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This release was issued on behalf of the above organization by Send2Press(R), a unit of Neotrope(R). http://www.Send2Press.com

SOURCE Renaissance Surgical Arts at Newport Harbor

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Renaissance Surgical Arts at Newport Harbor Announces Single-Dose Radiation Treatment Alternative for Women with Early Breast Cancer