Monday, March 2, 2009

FDA Meeting on Opioid REMS Highlights the Need for Comprehensive, Integrated Risk Management

FDA Meeting on Opioid REMS Highlights the Need for Comprehensive, Integrated Risk Management

Inflexxion is uniquely positioned to assist companies with risk evaluation and mitigation strategy plans

Newton, MA (PRWEB) March 2, 2009 -- On Tuesday, March 3rd, the FDA will meet with manufacturers of extended-release (ER) opioid medications for what's expected to be the beginning of a process to develop a new Risk Evaluation and Mitigation Strategy (REMS) program. According to the Agency, strategies for minimizing the risks of opioid medications -- which have included FDA-required risk minimization and action plans, or RiskMAPs -- need to be strengthened.

"Despite [the efforts of the FDA, drug manufacturers, and other stakeholders, the rates of misuse and abuse, and of accidental overdose of opioids, have risen over the past decade," states the Agency in a media release announcing the meeting. Crafting a new REMS program, the Agency says, will entail "discussions with other federal agencies and non-government institutions, including patient and consumer advocates, representatives of the pain and addiction treatment communities, other health care professionals, and other interested parties."

Inflexxion, a company that is deeply engaged with the pain and addiction treatment communities, is uniquely prepared to assist manufacturers, federal agencies, and other stakeholders with creating a comprehensive REMS. In 2001, the company's pharmaceutical risk-management division launched development of the National Addictions Vigilance Intervention and Prevention Program (NAVIPPRO) with support from the National Institutes of Health (NIH). Now a nationally recognized public health-oriented substance risk management solution, NAVIPPRO integrates the four key components of an effective REMS: national, "real-time," product-specific surveillance; signal detection; signal verification; and empirically validated prevention and intervention programs.

"One of the key elements distinguishing REMS from RiskMAPs is the requirement for ongoing evaluation of the efficacy of a program, both by the FDA and the sponsor of the drug, so adjustments can be made to ensure that risk-mitigation goals are being met," says Kevin Zacharoff, M.D., Director of Medical Affairs at Inflexxion. "NAVIPPRO is designed to assist with this type of long-term, continuous evaluation."

In a recent study of NAVIPPRO data published in Pharmacoepidemiology and Drug Safety (December 2008, Volume 17, Issue 12), the authors evaluated the surveillance component of the program. Analyzing NAVIPPRO's proprietary, "real-time" data stream, de-identified client assessment data continuously collected from the ASI-MV® Connect network of substance abuse clinics across the U.S., they examined the representativeness, geographic coverage, and timeliness of report of the data. They found that the data allow for the characterization of product-specific and geo-spatial differences for drug abuse, and can serve as a tool for monitoring the responses of the treatment center population to particular drug formulations.

According to Zacharoff, the findings show that NAVIPPRO data can be useful for measuring, in "real time," the relative rate of abuse of a particular drug in a vulnerable population, and in a specific geographic area of the country. "These data can help detect early signals of an emerging trend of abuse, which in turn allows for targeted prevention and intervention efforts, and for gauging the impact of those initiatives," he says.

To address the need for prevention and intervention, Inflexxion has incorporated into NAVIPPRO its award-winning, empirically validated educational programs. These programs include PainEDU.org, a comprehensive pain education website for health care professionals with nearly 20,000 subscribed clinicians of varying disciplines. As part of its educational offerings, PainEDU provides clinicians with access to clinically tested practice tools, such as the Screener and Opioid Assessment for Patients with Pain (SOAPP®).

Developed by Inflexxion, SOAPP is a brief, pen-and-paper self-report tool that enables health care providers to assess a patient's risk of addiction before initiating opioid therapy. It can be used in concert with the Current Opioid Misuse Measure (COMM)®, a complementary tool for identifying whether a patient, throughout the course of long-term opioid therapy, may be exhibiting aberrant behaviors associated with abuse of opioid medications.

The utility of SOAPP and COMM were recently highlighted in new guidelines by the American Pain Society and the American Academy of Pain Medicine on the use of opioid medications to treat chronic non-cancer pain. The guidelines, published in the February 2009 issue of The Journal of Pain (Volume 10, Number 2), recommend that clinicians routinely conduct a complete benefit-to-harm evaluation before starting opioid therapy, and do periodic follow-up screenings of patients who may be at risk for abuse or addiction.

"In the past, drug sponsors and consultants worked individually on programs designed to minimize risk in a hit-or-miss fashion, with very little modification of the initiatives based on outcomes. I believe that the FDA hopes that this new REMS development process will provide an opportunity for these groups to come together, working more closely to ensure that patients are treated appropriately, based on collected data, with the best medications available, and the highest level of safety and vigilance," says Zacharoff. "We at Inflexxion are committed to assisting all stakeholders - including the manufacturers, the FDA, and health care providers - in successfully navigating these issues and together improving the risk-benefit balance of opioid medications."

To learn more about NAVIPPRO, visit the website (www.navippro.com).

About Inflexxion, Inc.

Founded in 1989, Inflexxion creates innovative, award-winning behavioral health solutions for prevention, education, and disease management. Our grant-funded, clinically tested programs address substance abuse and addiction, chronic pain management, and other health and wellness issues. Our pharmaceutical risk management division provides Risk Evaluation and Mitigation Strategy (REMS) assistance to companies that research, manufacture, and market opioid pain medications and other therapeutic agents with potential abuse problems. Key offerings include NAVIPPROTM, ASI-MV® Connect, PainEDU.org, painACTION.com, and SOAPP®. Inflexxion is based in Newton, MA.

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Contact Information Amanda Hemm

Inflexxion, Inc.

http://www.NAVIPPRO.com

617-614-0436



CIRM Completes Briefing Visit to Stemedica Cell Technologies

CIRM Completes Briefing Visit to Stemedica Cell Technologies

Leadership of the California Institute for Regenerative Medicine ("CIRM") completed a two part visit to Stemedica Cell Technologies, Inc. ("Stemedica") to tour its manufacturing facility, R&D lab and corporate headquarters.

San Diego, Calif. (PRWEB) March 2, 2009 -- Leadership of the California Institute for Regenerative Medicine ("CIRM") completed a two part visit to Stemedica Cell Technologies, Inc. ("Stemedica") to tour its manufacturing facility, R&D lab and corporate headquarters.

"I was glad to have the opportunity to visit Stemedica and get to know more about its leadership, plans for the future and to see first hand the assets and potential they represent to the stem cell movement in California", said Dr. Alan Trounson, President of CIRM. "We want to have strong working relationships with all sectors of California's stem cell industry, including for-profit companies like Stemedica."

Prior to Dr. Trounson's visit, Dr. Marie Csete, CIRM's Chief Scientific Officer had the opportunity to visit Stemedica's manufacturing facility and R&D laboratory. "We're delighted to see Stemedica make the effort to secure a clinical grade manufacturing license from the State of California. We believe this capability will aid numerous organizations in California and around the world in their efforts to manufacture stem cell products for clinical application", said Dr. Csete.

"We were pleased to have Dr. Trounson and Dr. Marie Csete visit our facilities and receive a briefing from our leadership", said Dr. Maynard Howe, Stemedica's Vice Chairman & CEO. "We continue to play a pivotal role in the evolution of the stem cell industry in California and believe a supportive working relationship with CIRM is an essential part of this process.

Stuart Lipton, M.D., Ph.D., Scientific Director and Senior Vice President of the Del E. Webb Center for Neuroscience, Aging and Stem Cell Research at the Burnham Institute for Medical Research, San Diego, CA, joined Dr. Trounson during his visit to Stemedica's manufacturing facility. "I was impressed with the progress that Stemedica has made on the licensing process for clinical grade allogeneic stem cell manufacturing and am excited about expanding our research relationship with the Stemedica team. Having a manufacturing resource like this in California will be a great asset to our entire research community. I anticipate that many CIRM-funded stem cell research institutions will take advantage of Stemedica's manufacturing facility that will soon become FDB (Food & Drug Board) cGMP licensed."

Dr. Nikolai Tankovich, Stemedica's President and Chief Medical Officer organized the visits for Dr. Trounson, Dr. Csete and Dr. Lipton. "We're delighted that these outstanding leaders within California's stem cell movement took the time to find out more about Stemedica and our plans to lead this industry from a manufacturing standpoint. We will continue to seek the wise counsel of CIRM in an effort to align our efforts with theirs. In addition, we are expanding our collaborative research efforts with the Burnham Institute for Medical Research and several other California stem cell research institutions", said Dr. Tankovich.

About Stemedica Technologies, Inc.:

Stemedica Cell Technologies Inc. (http://www.stemedica.com (http://www.stemedica.com)) is a specialty biopharmaceutical company that is committed to the development and manufacture of best-in-class adult stem cells for use by approved research institutions and hospitals for pre-clinical and clinical studies. Within the United States, the Company is currently developing regulatory pathways for stroke, traumatic brain injury and wound repair. Outside the United States, Stemedica provides its adult stem cells to hospitals and research centers that are conducting studies under protocols approved by the appropriate regulatory agencies. These studies are focused on the treatment of neurodegenerative disease, sight restoration and wound repair. Stemedica is based in San Diego, California.

About CIRM:

The California Institute for Regenerative Medicine (CIRM) was established in 2005 with the passage of Proposition 71, the California Stem Cell Research and Cures Act. The statewide ballot measure, which provided $3 billion in funding for stem cell research at California universities and research institutions, was overwhelmingly approved by voters, and called for the establishment of an entity to make grants and provide loans for stem cell research, research facilities, and other vital research opportunities. To date, the CIRM governing board has approved 229 research and facility grants totaling more than $614 million, making CIRM the largest source of funding for human stem cell research in the world. For more information, please visit http://www.cirm.ca.gov (http://www.cirm.ca.gov/).

Media Contact for Stemedica: Dave McGuigan at dmcguigan (at) stemedica.com.

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Contact Information Dave McGuigan

Stemedica Cell Technologies Inc

http://www.stemedica.com

+1 858 658 0910



Sunday, March 1, 2009

Pennsylvania Law Firm Joins Efforts to Help Those Injured by Oral Sodium Phosphate (OSP) Products

Pennsylvania Law Firm Joins Efforts to Help Those Injured by Oral Sodium Phosphate (OSP) Products

The Pennsylvania lawfirm of Marcus & Mack have announced that they joined forces with a national law firm to help those injured by Oral Sodium Phosphate (OSP) products. The FDA issued an alert about oral sodium phosphates and the report that they were causing acute phosphate nephropathy in patients. Many patients suffered severe kidney injuries. The attorneys are reviewing and accepting cases for people who used OSP products for bowel cleansing before colonoscopy.

Indiana, Pennsylvania (PRWEB) March 1, 2009 -- The law firm of Marcus & Mack in Indiana, Pennsylvania has joined forces with the Tate Law Group to help those who may have been injured by Oral Sodium Phosphate (OSP) (http://www.marcusandmack.com). This action is a result of the December 11th announcement by the FDA alerting that Oral Sodium Phosphate products used for bowel cleansing prior to colonoscopy or other procedures may cause acute phosphate nephropathy.

The FDA stated that they have become aware of reports of acute nephropathy, a type of acute injury, associated with the use of oral sodium phosphate products.

The FDA is now requiring the manufacturer of Visicol and OsmoPrep to add Boxed Warning to the labeling for these prescriptions.

On the same day as the FDA alert, Fleet Laboratories voluntarily recalled its over-the-counter Phospho-soda products. Fleet issued a statement that "the recall decision was made to address the FDA's determination that oral sodium phosphate solutions used for bowel preparation prior to medical procedures such as colonoscopy should be available by prescription, and consumers should not be using over the counter products for bowel cleansing."

Acute phosphate nephropathy, also known as nephrocalcinosis, is a very serious kidney injury associated with the deposits of calcium-phosphate crystals in the renal tubes that can require a patient to need dialysis or a kidney transplant. In the most severe cases, acute phosphate nephropathy can lead to acute renal failure and even death.

The attorneys at Marcus & Mack are accepting clients who have suffered a kidney injury that may be the result of the use of an oral sodium phosphate. For more information about the oral sodium phosphate products or the Fleet Laboratories products please visit our website at http://www.marcusandmack.com or feel free to call our toll free number at 866-527-2161.

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Contact Information Cynthia Miklos

Marcus & Mack

http://www.marcusandmack.com

(866)527-2161



Saturday, February 28, 2009

SinoFresh Healthcare Inc. Files SEC Form 15

SinoFresh Healthcare Inc. Files SEC Form 15

SinoFresh Healthcare Inc. ("the Company") (OTCBB: SFSH.OB) announced that the Company voluntarily filed a Form 15 with the Securities and Exchange Commission ("SEC") on February 18, 2009, thereby, voluntarily suspending its reporting obligations under the Securities Exchange Act of 1934.

Venice, FL (PRWEB) February 26, 2009 --SinoFresh Healthcare Inc. ("the Company") (OTCBB: SFSH.OB) announced that the Company voluntarily filed a Form 15 with the Securities and Exchange Commission ("SEC") on February 18, 2009, thereby, voluntarily suspending its reporting obligations under the Securities Exchange Act of 1934.

As a result of filing the Form 15, the Company will no longer be required to file annual and quarterly reports with the SEC. The Company took this action in order to focus its resources on further developing and marketing its unique antiseptic nasal and sinus care product.

The Company's common stock will continue to be eligible for public trading, only now it will occur through the Pink Sheets ( www.pinksheets.com ) quotations system instead of the OTC Bulletin Board. The change in trading venue is to become effective within 90 days of filing with the SEC; however, SinoFresh Healthcare Inc. will suspend all periodic report filing with the SEC, effective immediately.

"An overwhelming amount of resources have been expended over the past several years for auditing, filing and legal expenses in the desire to maintain an OTC Bulletin Board listing," stated Charles Fust, CEO of Sinofresh Healthcare Inc. "Focusing our limited resources on reducing our debt load and establishing strategic relationships to market our Sinofresh Nasal Spray product best serves the interests of our shareholders. The Company takes this step after carefully considering the advantages and disadvantages of continuing registration reporting. The costs and administrative burdens associated with being a public company have significantly increased, particularly in light of the Sarbanes-Oxley requirements make current on-going reporting financially infeasible.

The Company plans to provide timely quarterly and annual reports pertaining to its financial performance and other announcements on its website and through the Pink Sheets Disclosure and News Service.

About SinoFresh HealthCare, Inc.

SinoFresh HealthCare, Inc. is dedicated to research efforts and products designed to eliminate causal agents in the area of upper respiratory health and the potential positive impact upon the reduction of mold, fungus, viral and bacterial pathogens using patented, innovative preventative measures. The company's lead product, SinoFresh(TM) Nasal and Sinus Care is a hygienic cleansing spray that kills germs and removes other nasal-sinus irritants is available nationwide.

This press release contains forward-looking statements. Words such as "anticipates," "expects," "intends," "plans," "targets," "projects," "believes," "seeks," "estimates" and similar expressions are intended to identify such forward-looking statements. These statements are based on the current expectations or beliefs of Sinofresh Healthcare Inc. management. They are not guarantees of future performance and are subject to a number of factors and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. You should not place undue reliance on these forward-looking statements, which speak only as of the date of this press release. Unless legally required, we undertakes no obligation to update publicly any forward-looking statements, whether as a result of new information, future events or otherwise.

Contacts: Sinofresh Healthcare Inc. 941-484-2929

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Contact Information Charles Fust

SinoFresh HealthCare, Inc.

http://www.sinofresh.com

941-488-6464



Friday, February 27, 2009

Hissey Kientz, LLP Announces Its Support For A New Bill That Would Protect The Rights Of Victim Of Asbestos Exposure Who Have Developed Malignant Mesothelioma

Hissey Kientz, LLP Announces Its Support For A New Bill That Would Protect The Rights Of Victim Of Asbestos Exposure Who Have Developed Malignant Mesothelioma

Hissey Kientz, LLP announces its support for a new bill that would protect the rights of victim of asbestos exposure who have developed malignant mesothelioma. “This is an important bill that would ensure that the legal rights of individuals in Texas who have developed mesothelioma after being exposed to asbestos are protected,” said attorney Robert Kientz.

February, 26, 2009, Austin, Texas (Vocus) February 27, 2009 -- The law firm of Hissey Kientz, LLP wishes to announce its support for a new bill that would make it easier for sufferers of malignant mesothelioma to prove that their injuries were caused by exposure to asbestos. The bill (Senate Bill No. 1123 and House Bill 1811) was filed jointly this week by congressmen from the Texas State Senate and House of Representatives.

“This is an important bill that would ensure that the legal rights of individuals in Texas who have developed mesothelioma after being exposed to asbestos are protected,” said attorney Robert Kientz of Hissey Kientz, LLP.

Mesothelioma (http://www.mesotheliomalawyershelp.com/about-mesothelioma/what-is-mesothelioma/) is a deadly form of cancer caused by exposure to asbestos that can attack the lining of the heart, chest or abdomen. Thousands of individuals in the United States are diagnosed with mesothelioma every year as a result of asbestos exposure that occurred in the workplace or from products containing asbestos.

Under current standards of causation enacted by the Texas State Supreme Court (Georgia-Pacific Corporation v. Fred and Betty Stephens), plaintiffs who bring mesothelioma claims must meet the same strict legal requirements that were established for cases involving asbestosis. If enacted by the Texas Senate and House of Representatives, the new bill would provide for a lower causation standard for mesothelioma lawsuits (http://www.mesotheliomalawyershelp.com/about-mesothelioma/mesothelioma-lawsuits/), making it easier for the victims of asbestos exposure to prove their case in court and recover fair compensation for their injuries.

“In an asbestosis case, the individual’s likelihood of developing the disease increases the more they were exposed to asbestos. But with mesothelioma, any level of exposure—no matter how small—is sufficient to cause the disease to develop,” said Kientz. “By forcing defendants in mesothelioma cases to meet the standard of causation for asbestosis, the Texas Supreme Court has set a benchmark for justice that is almost impossible these victims to meet.”

The new bill would remove the requirement for mesothelioma claimants “to prove, for any purpose, a quantitative dose, approximate quantitative dose or estimated quantitative dose of asbestos fibers to which the exposed person was exposed” in order to meet the standard of causation. Additionally, the law would protect defendants who were not involved in the manufacturing or sale of asbestos (http://www.mesotheliomalawyershelp.com/asbestos-info/what-is-asbestos/) but who may, under current law, be unfairly held responsible for injuries caused by asbestos products.

“By enacting this bill, the Texas legislature will help to bring the state’s laws relating to asbestos in accord with mainstream legal standards for mesothelioma cases and restore the intended function of these laws: to protect the legal rights of individuals who have suffered at the hands of the asbestos industry,” said Kientz.

About Hissey Kientz, LLP

Hissey Kientz, LLP (http://www.hkllp.com) is currently accepting cases involving individuals who may have contracted mesothelioma, asbestosis or lung cancer as a result of asbestos exposure, as well as those injured by the Ortho Evra patch, digoxin toxicity from Digitek, PPH caused by Fen-Phen, the Composix Kugel mesh hernia patch, renal failure caused by Trasylol, the Duragesic patch (fentanyl), gadolinium MRI contrast dyes or other defective drugs and devices. To learn more about the firm and other drug cases, visit Hissey Kientz, LLP (www.hkllp.com) or call toll-free at (866) 275-4454.

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Contact Information Craig Whitney

Hissey Kientz, LLP

http://www.hkllp.com

512-320-9100



Thursday, February 26, 2009

Healthy Living Network Announces Launch of New Detox Web Site

Healthy Living Network Announces Launch of New Detox Web Site

The Healthy Living Network, a division of Healthy Directions, LLC, is proud to announce the launch of searchbodydetox.com, a new informational Web site devoted to all aspects of whole body cleansing and detoxification.

Potomac, MD (PRWEB) February 25, 2009 -- The Healthy Living Network, a division of Healthy Directions, LLC, is proud to announce the launch of searchbodydetox.com (http://www.searchbodydetox.com), a new informational Web site devoted to all aspects of whole body cleansing and detoxification.

Visitors to searchbodydetox.com can expect to find original articles, blogs, studies, forums, encyclopedias, and more on a variety of topics and concerns, including environmental toxins, colon cleansing, liver detox, lymph and blood detox, skin detox, detox and weight loss, and nutrition and detox, as well as information on daily and quarterly detox programs. Searchbodydetox.com will also offer weekly eLetters so consumers can have continuous access to breaking news and up-to-date information.

According to Ed Hauck, President of Healthy Directions, "Each day, Americans are exposed to a staggering number of chemicals. Every time you eat, drink, clean your home, fertilize your lawn, or drive your car, this toxic load increases. In fact, more than 80,000 chemicals are registered with the Environmental Protection Agency, and more are added each year.

"At searchbodydetox.com, you'll have access to experts and authorities who can deliver effective answers to all of your detoxification (http://www.searchbodydetox.com) and body cleansing questions and concerns. Additionally, you'll find a plan of action to help reduce your risk of chemical exposure and toxic build up."

All information and advice found on searchbodydetox.com has been carefully screened and selected to provide the most current, ground-breaking, well-researched, and highly effective recommendations. While the majority of the experts and authorities on the site are doctors, the material on the Web site is intended to provide timely and accurate medical news and education, not personal medical advice, diagnosis, or treatment.

For more information about this exciting new resource for detox- and cleanse-related information, visit www.searchbodydetox.com (http://www.searchbodydetox.com).

About Healthy Directions, LLC

Healthy Directions, LLC, is the recognized leader in providing authoritative health and wellness solutions to consumers. Healthy Directions' subsidiary, Doctors' Preferred, LLC, is a leading vitamin and nutritional supplement business that develops and sells proprietary, branded nutritional supplements based upon the research of the Healthy Directions health experts, marketed primarily through direct mail. For more information on Healthy Directions, please visit www.healthydirections.com.

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Contact Information Annette Payne

Healthy Directions, LLC

http://www.searchbodydetox.com

301-340-7788



Wednesday, February 25, 2009

Pharmacists Encourage Patients To Seek Their Guidance When Choosing OTC Medications

Pharmacists Encourage Patients To Seek Their Guidance When Choosing OTC Medications

Eighty-three percent of Patients Select OTC Products Recommended by Their Pharmacist

Washington, D.C. (Vocus) February 25, 2009 -- According to the most recent Pharmacy Today Over-the-Counter Product Survey conducted by the American Pharmacists Association (http://www.pharmacist.com/) (APhA), pharmacists believe that 83 percent of consumers purchase over-the-counter products that were recommended by their pharmacist. With more than 100,000 nonprescription medications on the market and more than 1,000 active ingredients, it's critical that patients consult their pharmacist to maximize the benefits from medications and minimize the potential for harmful drug interaction and/or side effects.

The survey, completed by nearly 1,000 APhA member and non-member pharmacists, also reveals that on average pharmacists counsel 31 patients per week about over the counter medications. Patients who seek their pharmacist's advice include patients suffering from an acute or chronic condition (92 percent), patients that are worried about using an OTC product with other prescription medications (84 percent), and patients worried about taking OTC products with a specific disease/condition (74 percent).

"Pharmacists are the only health professionals specifically trained in nonprescription medications," said John A. Gans, APhA's Chief Executive Officer. "Patients can take an active role in self care by reading medication labels, knowing the active ingredients in their medications, and asking their pharmacist questions."

One of APhA's goal in conducting the annual Pharmacy Today Over-the-Counter Product Survey is to educate consumers that pharmacists have the knowledge and training to help them select right OTC medications. As part of the survey, pharmacists are asked to tabulate the OTC products they recommend per week in 77 different product categories. The results of the survey are published as a supplement to the February issue of Pharmacy Today (http://www.pharmacytoday.org/index.htm). Click here to view the entire Pharmacy Today Over-the-Counter (http://www.pharmacytoday.org/index.htm) Supplement.

As the medication experts, pharmacists are trained in both prescription and over-the-counter medications and can provide patients with important information about how medications may interact with certain foods, other medicines or dietary supplements. Pharmacists are the most accessible health care providers and APhA encourages patients to actively seek their advice about the proper use of medications.

About the American Pharmacists Association (APhA)

The American Pharmacists Association (http://www.pharmacist.com/), founded in 1852 as the American Pharmaceutical Association, represents more than 62,000 practicing pharmacists, pharmaceutical scientists, student pharmacists, pharmacy technicians, and others interested in advancing the profession. APhA, dedicated to helping all pharmacists improve medication use and advance patient care, is the first-established and largest association of pharmacists in the United States. APhA members provide care in all practice settings, including community pharmacies, health systems, long-term care facilities, managed care organizations, hospice settings, and the uniformed services.

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Contact Information Erin Wendel

American Pharmacists Association

http://www.pharmacist.com/

202.429.7558