The parity distribution of such a synthetic cohort at age 50, l50, i is treated as the final parity distribution, and from that the parity progression ratios ai from parity i to i and the total fertility index adjusted for parity and age tf ; are obtained.
Seeking to market a generic version of the drug. In 2003, Wyeth filed suit in New Jersey District Court, alleging Teva's generic extended release venlafaxine HCl formulation infringes three of Wyeth's patents. The patents were to expire in 2017. Analysts, though, had predicted a likely defeat for Wyeth, such that generics would likely have been able to launch as early as June 2008. The Court construed certain disputed claims in a September 6, 2005 opinion that slightly favored Teva. Trial was set to begin October 18, 2005; the settlement was announced that same day. Under the terms of the settlement, which are confidential and are still to be approved by the FDA and the District Court, Teva will launch its generic version of Ecfexor in June 2006, and its generic version of Efdexor XR in July 2010. In return, Wyeth will receive a percentage of gross profit from the generic sales. Global sales of Ffexor totaled about 5 million in 2004, but Efcexor XR was the best-selling antidepressant in the world in 2004, with global sales of more than .3 billion. FTC FILES ANTITRUST SUIT AGAINST BARR AND WARNER CHILCOTT In a move that appears to indicate that the FTC is taking a stronger stance against what it views as anticompetitive deals within the drug industry, the FTC has filed suit in the DC District Court against Barr and Warner Chilcott seeking to void a million "reverse payment" agreement, i.e., one under which the patent holder pays a generic manufacturer to stay off the market, to keep Barr's generic version of Warner's contraceptive Ovcon-35 off the market for five years. In addition, twenty-one states and the District of Columbia have also filed a complaint in the DC District Court. By way of explanation, this matter stems from Barr's plan to market its generic version of non-chewable Ovcon which is not patent protected at a price 30 percent lower than Warner's price, after receiving FDA approval. Barr expected approval in late 2003, but, before the FDA granted approval, Barr and Warner Chilcott entered into the agreement, under which Warner Chilcott paid Barr for the exclusive option to market Barr's generic drug; thereby effectively keeping Barr off the market. This is the second such agreement challenged by the FTC this year See G&B Update Vol. 9, No. 8 August 2005 and is additionally noteworthy because the FTC originally did not object to the agreement after reviewing Barr's letter of intent outlining the transaction before the agreement was finalized.
ESCO offers Oregon employees three health plan options, all of which include in-person or telephone tobacco-cessation counseling and medications. The programs are free or cost employees the equivalent of the standard copay. Employees in Mississippi and Kentucky smoke more, report more tobacco-related health problems, and do not have access to health plans with cessation services to the degree that their fellow employees in Oregon do ; . When ESCO implemented the Smoke-free Workplace Law, the company offered employees a financial incentive to quit--an offer seized by a handful of workers. Through Karin Drake, ESCO's Health Services Manager, ESCO has recognized employees who quit smoking with a fruit basket after they remain smokefree for six months. Every November, around the time of the Great American Smokeout, ESCO publicizes its tobacco-cessation programs. Corporate benefits manager Patrick Pine, a former smoker, wants to encourage smokers to quit and advocates that businesses consider it in their interest to assist those who attempt to quit. Businesses, he says, will see greater productivity, a safer, cleaner work environment, less interpersonal conflict and a healthier workforce. He urges managers to recognize that it can be difficult for smokers to successfully quit on the first attempt. He cautions that incentive systems should recognize hurdles that deter smokers from attempting to quit. He suggests that even one person successfully quitting likely will generate savings and benefit that far exceed an employer's investment in smoking cessation.
The British Approved Names book was currently published every two years, with four Supplements issued between new editions. Commission was invited to consider a number of options regarding future publication of the book. Proposal to abandon publication It was pointed out that WHO did not assign names to certain materials and that if these products were used in the UK a mechanism needed to be in place in order to provide a suitable name. In view of these points, it was agreed that publication of BANs should be continued but that Commission should consider how this might best be achieved. Proposal to continue publication Under the terms of the Medicines Act 1968, the BP Commission was charged with preparing or causing to be prepared a list of names that were suitable for use at the head of a monograph. It was suggested that rather than continue with publication of a separate BAN book, those names that were only used in the UK should be included in a new Appendix for the BP. It was agreed that a final edition of the BAN book should be issued during 2004 and that it should be re-named as "British Pharmacopoeia: Nonproprietary Names" in order to reflect the content of the current book. Any further new names would be included in a new BP Appendix. 960 New Monographs COM 03 ; 36.
On March 22, 2004, FDA issued a public health advisory that cautions physicians, their patients, and families and caregivers to closely monitor adults and children with depression. Results of antidepressant studies in children since June 2003 appeared to suggest an increased risk of suicidal thoughts and actions in those children taking certain antidepressants. FDA has initiated a review of these reports, but it is not clear whether or not antidepressants contribute to suicidal thinking and behavior. As a result of the studies, FDA is asking manufacturers to change the labels of 10 drugs to include stronger cautions and warnings to monitor patients for worsening depression and the emergence of suicidal ideation. The drugs affected include bupropion Wellbutrin ; , citalopram CelexaTM ; , escitalopram LexaproTM ; , fluvoxamine Luvox not FDA approved for treatment of depression in the US ; , fluoxetine Prozac ; , mirtazapine Remeron ; , nefazodone Serzone ; , paroxetine Paxil ; , venlaxafine Effrxor ; , and sertraline Zoloft ; . It should be noted that Page 2.
If you miss a dose of effexor xr, take it as soon as you remember it and emsam.
National Association of Chain Drug Stores, "2003 Community Pharmacy Results, " downloaded September 17, 2004, at : nacds user-assets PDF files 2003results . 2 Dee Mahan, "Sticker Shock: Rising Prescription Drug Prices for Seniors, " Families USA, June 2004. 3 David Gross, "Trends in Manufacturer Prices of Brand Name Prescription Drugs Used by Older Americans, 2000 through 2003, " AARP Public Policy Institute, May 2004. 4 David Gross, "Trends in Manufacturer Prices of Brand Name Prescription Drugs Used by Older Americans, 2000 through 2003--First Quarter Update, " AARP Public Policy Institute, July 2004. 5 For an excellent summary of the Medicare Prescription Drug Benefit, see the Kaiser Family Foundation Fact Sheet titled: "The Medicare Prescription Drug Law, " Fact Sheet #7044, published in March 2004, available at kff . 6 U.S. Census Bureau. Income, Poverty, and Health Insurance Coverage in the United States: 2003. 7 Kaiser Commission on Medicaid and the Uninsured, "Health Insurance Coverage in America: 2003 Data Update Highlights, " issued on September 27, 2004: Figure 6. 8 Kaiser Commission on Medicaid and the Uninsured, Fact Sheet #1420-06, September 2004. 9 ibid 10 Bill Brubaker, "Drug Spending Falls As Co-Payments Rise, " Washington Post, October 9, 2002: E03. 11 "Pharmaceuticals Rank as Most Profitable Industry, Again." Public Citizen, April 2002. 12 "Profiting from Pain: Where Prescription Drug Dollars Go, " Families USA, July 2002. 13 Public Citizen Congress Watch, "2002 Drug Industry Profits: Hefty Pharmaceutical Margins Dwarf Other Industries, " June 2003. Available at citizen documents Pharma Report . 14 Pharmaceutical Research and Manufacturers of America, "Intellectual Property Overview, " : phrma issues intprop . 15 Pharmaceutical Research and Manufacturers of America, "Why Do Prescription Drugs Cost So Much?. and Other Questions About Your Medicine, " available at phrma publications publications brochure questions questions . 16 Public Citizen, "Would Lower Prescription Drug Prices Curb Drug Company Research and Development?", : citizen congress reform drug industry r d articles ?ID 7909, accessed October 11, 2004. 17 Scott Hensley, "Drug Prices Rise at Faster Clip, Placing Burden on Consumers, " Wall Street Journal, April 15, 2002. 18 "Profiting from Pain: Where Drug Dollars Go, " Families USA, July 2002, 3. 19 Julie Appleby, "Drugmakers spend more on dividends than research, " USA Today, October 11, 2004. 20 Marcia Angell, M.D. The Truth About Drug Companies: How the Deceive Us and What to Do About It, Random House, New York, 2004: 179. 21 Gardiner Harris and Joanna Slater, "Generic Drug Makers Use Altered Copies to Outmaneuver Patients in Legal Battles, " Wall Street Journal, April 17, 2003. 22 Wyeth obtained the 6-month extension referenced here legally. Under The Best Pharmaceuticals for Children Act enacted in 1997 and recently reauthorized until 2007 ; , drug companies that test their drug for use in children are given an additional six months of market exclusivity for that drug. Pub L. No. 107-109 ; . Wyeth tested Effexor for use in children. Although Wyeth did not find the drug to be more effective for treating pediatric depression than a placebo, the company still received the 6-month exclusivity extension. 23 From testimony submitted by Congressman Henry Waxman at "Hearing on Publication and Disclosure Issue in Anti-Depressant Pediatric Clinical Trials" in Subcommittee on Oversight and Investigations of the House Energy and Commerce Committee, September 9, 2004 24 "Generic Drug Entry Prior to Patent Expiration: An FTC Study", Federal Trade Commission, July 2002. 25 ibid.
Have you heard of any connection between effexor and the above mentioned sleep problems and geodon.
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My wellbutrin xl was changed to effexor xr and my abilify was changed to geodon and i still have my topomax and paxil.
What Is Effexor? Effexor is in a class of medicines called serotonin and norepinephrine reuptake inhibitors SNRIs ; . Effexor is used to treat depression. Effexor XR is used to treat: Depression Generalized anxiety disorder GAD ; Social anxiety disorder SAD ; Who Should Not Take Effexor? Never take Effexor if you are taking another drug used to treat depression, called a Monoamine Oxidase Inhibitor MAOI ; , or if you have stopped taking an MAOI in the last 14 days. Taking Effexor close in time to an MAOI can result in serious, sometimes fatal, reactions, including: - High body temperature - Coma - Seizures convulsions ; MAOI drugs include Nardil phenelzine sulfate ; , Parnate tranylcypromine sulfate ; , Marplan isocarboxazid ; , and other brands. What Are The Risks? Possible life-threatening serotonin syndrome when used with triptan medicines: See FDA Alert [07 2006] above. Suicidal thoughts or actions: Persons taking Effexor may be more likely to think about killing themselves or actually try to do so, especially when Effexor is first started or the dose is changed. People close to persons taking Effexor can help by paying attention to changes in user's moods or actions. Contact your healthcare professional right away if someone using Effexor talks about or shows signs of killing him or herself. If you are taking Effexor yourself and you start thinking about killing.
Dr. D. stated that as a complicating factor the Applicant might have experienced a full blown hypomanic episode approximately 4 - 6 weeks after he was prescribed Effexor. This was described to the Tribunal by the Applicant as the interval when he was on the significant winning streak at the casino. It was also noted in this report by Dr. D. that the Applicant admitted to cannabis abuse. Dr. P.D. recommended that the Applicant undergo a psychiatric assessment and stated that he had an appointment with Dr. S. on May 8, 2007. Other recommendations would be provided after his psychiatric assessment. Mr. Biel then described in item number 4C of his summary a report by Dr. V.S. Dr. V.S. a psychiatrist ; referred to the detailed assessment by Dr. P.D., which was attached, and whcih the Tribunal has summarized above. Dr. V.S. reported that the Applicant has been psychiatrically well, up to the fall of 2006 when a breakup with his girlfriend resulted in the Applicant slipping into a major depressive episode with insomnia, lethargy, poor concentration and vague suicidal ideation. At that time the Applicant was placed on Effexor XR. Several weeks later the period of the winning streak at the casino was described. He gambled all night and worked during the day. The Applicant, on questioning from the Tribunal, indicated that this truly was a winning streak. Confusing the diagnostic and therapeutic picture was the fact that the Applicant continued to use marijuana on a regular basis. Exposure to this drug was being combated by the Applicant and he was down from three and a half grams a day to half a gram a day. Prior to the depression, the Applicant was more and more concerned about his girlfriend's faithfulness. At this time he became increasingly suicidal and homicidal as well as delusional through the winter of 2007. The doctor stated that the Applicant showed relatively little insight into this problem. He began to feel that his ex-girlfriend and her new boyfriend were harassing and taunting him. This led to him making a number of threats against her for which he was arrested and jailed. Apparently there were charges still outstanding despite the fact that he was in a Court Diversion Program. In late March of 2007, the Applicant was brought to the emergency department again voicing threats against his ex-girlfriend. He stated that she had harassed him in the past but this had stopped. He denied any other persecutory ideas, ideas of reference, or other psychotic symptoms. It was unclear whether the change in mental state from when he was seen by Dr. P.D. reflected his discontinuing the use of Effexor or his reduction in smoking marijuana. His mental state at that examination was within normal limits. The doctor did report that he and cymbalta.
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Some medications have a range of mg kg day recommended there is usually a maximum allowable total amount per day also specified ; . Dosages that are over the recommended amounts can be dangerous. Dosages that are under the recommended amount can also be dangerous because they are considered to be subtherapeutic. Consider this example. A drug reference book indicated that the safe medication range for this medication is 2535mg kg day. You are working with a 35 pound 4 ounce child. If a medication order asked you to give 425mg once, would you give it? Is 425mg a safe dose to give? Solution: You will need to calculate two numbers the minimum and maximum safe doses ; . Then, you can determine if the dose for this patient falls within the range safe ; or outside the range unsafe ; . 1. Convert pounds and ounces to kg 4 ounces 16 0.25 pounds 0.25 pounds + 35 pounds 35.25 pounds 35.25 2.2 16.023 kg 2. Calculate the maximum and minimum doses: 3. Minimum of range: 16.023 kg ; x 25mg ; 400.575 mg Maximum of range: 16.023 kg ; x 35mg ; 560.875 mg 4. The order asked you to give 425mg to this 16.02kg child. Since 425mg falls between 400.575mg and 560.875 425mg is a safe dose to administer.
Figure 30 is an identical plot to Figure 29, except that the sales for 2010 are forecast rather than actual sales used to calculate the CNS CV focus parameter and revenue Figure 26: Percentage of 2005 sales derived from CV products for Mid size. The above graph shows a similar segregation when the Mid Pharma peer set is Pharma examined by therapy area focus and 2010 revenues. As in 2005, there are four distinct groups that show a correlation between size of company and range of 100% therapeutic focus. In general terms, the companies form identical clusters to the 200580% with the plot, exception that Schwarz Pharma appears to lose its strong CV focus due to its schedule of launching three new products within the field of CNS between 2006 and 60% 2010, including oral lacosamide indicated for the potential treatment of epilepsy and neuropathic pain ; . The three new launches are forecast to generate 2m by 2010, a considerable 41.4% of the company's total revenues for that year. Thus, by 2010, 40% Schwarz may become the one example of a Mid Pharma company that does have a combined focus in both CNS and CV and
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We do not have information about use of infliximab in chronic active outpatient UC. Infliximab is licensed for use in moderate to severe UC. 5. Relevant guidelines include those produced by the European Colitis and Crohn's Organisation ECCO ; in preparation ; and by the American Gastroenterological Association Gastroenterology 2006; 130: 940-987 ; . These guidelines were drawn up following exhaustive reviews of the literature followed by an iterative process of consultation between acknowledged experts in IBD in Europe and the USA respectively; the quality of evidence on which recommendations were based was meticulously graded. The principal evidence supporting use of infliximab in steroidrefractory acute severe inpatient UC comes from the trial by Jarnerot Gastroenterology 2005; 128: 1805-1811 ; , which showed that a single infusion of infliximab 5 mg kg was associated with a colectomy rate of 30% after three months, in comparison with nearly 70% in patients treated with placebo; in this study infliximab was less effective in fulminant UC than in less severe acute attacks. A discordant note was provided by Probert et al Gut 2003; 52: 998-1002 ; , who reported that infliximab 5 mg kg at weeks 0 and 2 in in-patients with steroid-refractory acute severe UC was no better than placebo in inducing clinical remission 39% versus 30% respectively ; or sigmoidoscopic remission 26% versus 30% ; . The key data supporting use of infliximab in chronic active refractory UC in outpatients is provided by the ACT I and ACT II trials Rutgeerts P, New Eng J Med 2005; 353: 2462-76.
Teva's overall sales growth for 2006 was driven principally by the effects of the Ivax acquisition, which impacted mainly the pharmaceutical segment, as well as organic growth in the U.S. resulting from new product launches with exclusivity. Pharmaceutical Sales North America In 2006, pharmaceutical sales in North America amounted to , 759 million, representing an increase of 68% over 2005. The increase in sales was attributable to: four major new generic product launches in the U.S., with 180 days exclusivity: the generic versions of Zocor simvastatin ; , Zoloft sertraline ; , Wellbutrin XL bupropion ; and Pravachol pravastatin ; . In addition, during 2006, Teva sold generic versions of the following products in the U.S. listed in the order of their launch during the year ; : DDAVP, Clozaril, Desferal, Zonegran, Novantrone, MiraLaxTM, Proscar, Mobic, Effexor, Cipro, Depo-Medrol, Ditropan XL and Zofran. the consolidation of the results of Ivax commencing February 1, 2006, including significant sales of Ivax's respiratory products; the continued growth in sales of Copaxone; and the continued substantial growth of sales in Canada due to 15 new product launches, the most significant of which was the generic version of Effexor venlafaxine ; , the largest generic launch in Canadian pharmaceutical market history, as well as the revaluation of the Canadian dollar against the U.S. dollar and
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Several treatments for fibromyalgia were reviewed, including: LILLY'S Cymbalta duloxetine ; , an SNRI. A speaker said, "This has a significant direct effect on fibromyalgia pain, but insomnia, dry mouth, and constipation are more common than placebo.Duloxetine shows a lot of promise for the treatment of fibromyalgia. In trials ; female subjects demonstrated significantly greater improvement on most efficacy measures vs. placebo, but male subjects failed to show a significantly greater improvement on any efficacy measure compared with placebo-treated males." CYPRESS BIOSCIENCE'S Ixel milnacipran ; , an SNRI. Phase II data has already been completed and presented on this BID agent, and that showed a significant improvement in weekly pain assessment, physical function, and the number of days patients reported feeling good. However, QD dosing did not show a statistically significant improvement over placebo. A speaker said, "We're not sure why, but this indicates the drug needs to be dosed BID." The improvement in females was described as "similar to duloxetine." PFIZER'S pregabalin Speakers expressed frustration with the long time it is taking to get this drug approved by the FDA. One expert commented, "Pregabalin, which is son of gabapentin, is supposed to be available soon but it's had that status for about five years." Another expert said, "We may some day see pregabalin. That's another drug I've been waiting and waiting for." A third noted that the higher doses 300 mg day and 450 mg day ; appear to be more effective than a lower dose 150 mg day ; , saying, "There was a pretty significant reduction in mean pain score after one week at the 450 mg day dose, which is about equivalent to 2400 mg of gabapentin Pfizer's Neurontin ; .Pregabalin behaves like gabapentin in many ways reduces pain at the study endpoints and improves fatigue and sleep quality." WYETH'S Effexor venlanfaxine ; Effexor has been shown to work in rats, and it is my drug of choice for fibromyalgia by virtue of being the only one SNRI ; out there that works. The problem with it is that when the headaches stop, you get anorgasmia.
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The Following Drugs Will Move To A Higher Higher Copay ; Tier: Necon 10 11-28 Regonol Inj. Prior Authorization Status Has Been Changed On The Drugs Below: Prior Authorization no longer applies to: Ambien Elidel Leflunomide Lunesta Nexium Omeprazole Prevacid Prilosec Protopic Raptiva Sonata Soriatane Testosterone Cyprionate Inj. Zegerid Zolpidem Step Therapy Has Been Added To: Elidel Protopic Drugs With Quantity Limits Added In 2008: Accuneb Duoneb Xopenex Nebulization Drugs Added To 2008 Formulary: Chorionic Gonadotropin Cyklokapron Inj Depo-Provera 400 mg. Inj. Elaprase Emsam Gamastan S D Gamunex Gardasil Glycopyrrolate Increlex M-R-Vax II Naglazyme Nitrostat Oxandrolone Pentoxyphylline Primaxin Rituxan Rotateq Tyzine Vaqta Zostavax Drugs No Longer Covered in 2008: Accuzyme Spray Antipyrine Benzocaine Eardrop Benzoyl Peroxide Gel Wash Cipro Inj * Climara * Colestid Granules * Diprolene Lotion * Dritho-Scalp Cream Effexor * Hyoscyamine Sulfate Ketek Klaron 10% Lotion * Lamisil * Levsin Inj. Nitroglycerin 6.5mg caps Omnicef 300mg * Papain Urea Oint, Spray Parnate * Pilocarpine Eye Drops Plan B Potassium Chloride Liquid Pravachol 80 mg * Prostigmin Tab Salsalate Scopolamine Inj. Vantin Susp * Vospire ER * Zithromax Susp * Zoloft * * Even though the brand name drug will no longer be covered, generic equivalents for these drugs are still available on the formulary and
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Preservation techniques and flexible menu patterns for long duration missions. 28 ; However, some major differences exist between the two space nutrition pro rams regarding the respective dietary habits. These differences are shown in ables 2 and 3.
Prescription medications. Price takes Felodipine high blood pressure ; , Effexor depression ; , oral morphine for pain, Vicodin, Naprosin, and Gabapentin aka Neurontin ; arthritis bursitis in the hips ; . She testified that the medications affect her ability to concentrate, to retain information, and to operate machinery. Activities of daily living. Price attempts to do as many activities of daily living as she can. She stays home all day, depending on how much pain she is in. She moves from the bed to the sofa. Her granddaughter and niece help her do her hair, and she gets cooking help from her granddaughter, son, niece, and nephew. She brought a chair into the kitchen in order to do kitchen work. She cannot get into the bathtub by herself, and whoever is home helps her. She has a shower chair. She does home exercises. Driving ability. Price has a drivers license. She does not own a car and has not driven one in weeks. She chooses when to drive based on her level of medication. Also, driving was prohibited for several weeks before getting the neural stimulators. The neural stimulators could not be inserted if there was a recent spasm. Climbing stairs, sitting and standing. Price has high blood pressure and has to be careful going up and down stairs, and in and out of chairs. She testified that with changes of level she can become disoriented and lightheaded. The activities of daily living and the home exercises help to keep her blood flowing as well as being beneficial to her musculoskeletal system and
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Washingtonpost antidepressant makers withhold data on children by shankar vedantam washington post staff writer thursday, january 29, 2004; page a01 makers of popular antidepressants such as paxil, zoloft and effexor have refused to disclose the details of most clinical trials involving depressed children, denying doctors and parents crucial evidence as they weigh fresh fears that such medicines may cause some children to become suicidal.
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Veryone wants to be healthy. That's a "given" in our society. No reasonable person would prefer sickness, fatigue, and pain over a vigorous, vital and healthy body. But while the goal may be the same, people take different paths in an effort to reach it. First, they can turn to the medical and pharmaceutical industries in hopes of finding health. They can visit medical doctors and surgeons, take prescriptions and over-the-counter drugs -- all in an effort to treat their symptoms and diseases. This path has created a multi-billion-dollar disease business in this country. But, according to almost every study done in the past few decades, it hasn't helped make us healthier. We're just as sick and out of shape as we've ever been. Major life-threatening diseases like cancer, heart disease, and diabetes are striking more people than ever. New epidemics like AIDS and Ebola are sweeping the globe. And so-called "medical science" isn't able to stem the tide. In fact, the overuse, misuse and abuse of drugs and surgical procedures are adding to the death toll. Practices like chemotherapy and radiation therapy -- labeled "barbaric" by many health practitioners -- are, in many cases, killing the very people they're supposed to help.
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FINAL SWAMP CONSERVATION PLAN COMPLETED The Conservation Plan for the Southern Watershed Area was completed and submitted to Hampton Roads Planning District Commission HRPDC ; on March 21, 2001. Submission of this document fulfills the DCR-Natural Heritage contractual role of developing this Plan as a key part for the Southern Watershed Area Management Program SWAMP ; . The product is intended to assist the Cities of Chesapeake and Virginia Beach, as well as the HRPDC, with long-term planning to protect natural resources, open space, and water quality. DNH TO ASSIST DEQ WITH DATA FOR REVIEW OF WETLANDS DEVELOPMENT APPLICATIONS DNH staff met with DEQ staff to discuss their needs for natural heritage data, which will be required for proper review of wetlands development notifications and applications under new wetland regulations published by DEQ for implementation October 1, 2001. DNH proposed to develop a password-secured Internet application, with funding assistance from DEQ, that would allow DEQ staff to screen projects for their proximity to natural heritage resources. This would reduce the tremendous increased workload on DNH Project Review that might otherwise be required by the new regulations. DEQ is considering our proposal. NORTHEASTERN BEACH TIGER BEETLE POPULATION MONITORING During July, the Chesapeake Bay Region Steward and Summer Intern monitored population status for Northeastern beach tiger beetles at Natural Area Preserves flanking the Chesapeake Bay. Mid-summer is a peak activity period for adults of this federally threatened species, and populations are monitored annually at this time to establish trends, detect change in population health and habitat status, and abate threats. Populations were monitored at Bethel Beach, Hughlett Point and Dameron Marsh during the.
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