LAST NAME EMERGENCY MEDICAL TREATMENT & CONSENT FORM Parent’s or guardian’s medical authorization for student’s participating in and traveling with the Niceville High School Band. This authorization is good for entire school year, from July 2010 through July 2011 (or graduation). · Part I—Student’s Personal and Family Information Person to call if parents not available:
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Zostavax™ reduced the Incidence, Severity and Duration of Shingles Pain in a
New Study Published in The New England Journal of Medicine
In the Study, Zostavax™ Also Reduced the Incidence of Both Postherpetic Neuralgia
Lyon, June 2, 2005 – ZOSTAVAX™ (zoster vaccine live [Oka/Merck]) a shingles vaccine currently developed by Sanofi Pasteur MSD / Merck & Co., Inc., reduced the total burden of pain and discomfort caused by shingles by 61 percent, according to a new study that compared the investigational vaccine to placebo in more than 38,500 men and women age 60 and older. In the study, ZOSTAVAX also reduced by 67 percent the incidence of persistent nerve pain -- the most frequent complication of shingles known as postherpetic neuralgia (“PHN”) -- and reduced the incidence of shingles by 51 percent. “We are delighted that the results from this study published in The New England Journal of Medicine met or exceeded the predefined criteria for success,” said Michael N. Oxman, M.D, an infectious disease specialist at the San Diego VA Healthcare System and the University of California, San Diego, who was study leader and lead author on the article. “Shingles is a common, frequently painful disease that can occur without warning in anyone who has had chickenpox. For those people who develop the most common complication of shingles, PHN, pain can last for weeks, months or even years. Even the touch of one’s own shirt against the affected area can be very painful for someone suffering from PHN.” The Phase III Shingles Prevention Study, published in the June 2 issue of The New England Journal of Medicine, was a Department of Veterans Affairs (VA) study conducted in
collaboration with the National Institute of Allergy and Infectious Diseases (NIAID), part of the
National Institutes of Health (NIH) and Merck at 22 research sites across the United States
over a period of more than five years.
Zostavax™ is the Sanofi Pasteur MSD / Merck trademark for zoster vaccine live
[Oka/Merck]). Study design
The randomized, double-blind, placebo-controlled study was conducted to determine whether vaccination with a single dose of a live attenuated investigational vaccine, ZOSTAVAX™, would decrease the incidence and/or severity of shingles and persistent nerve pain (PHN) in men and women age 60 and older who had no previous history of shingles. In the study, participants were randomized to groups given either ZOSTAVAX™ (n=19,270) or a placebo (n=19,276) and followed for the development of shingles for a median duration of 3.1 years. Suspected cases of shingles were assessed by polymerase-chain-reaction (PCR) assay, virus culture and clinically by an evaluation committee consisting of five physicians with expertise in shingles. All subjects with clinically diagnosed shingles were offered antiviral treatment (famciclovir) when indicated or as appropriate and were offered standard-of-care treatment for pain. The primary endpoint of the study was the burden of illness (BOI) caused by shingles over the first six months after shingles rash onset, a measure affected by the incidence, severity and duration of shingles-associated pain and discomfort. Severity of pain was evaluated according to a “worst pain” score on a 0-to-10 scale using a validated questionnaire (Zoster Brief Pain Inventory) with a zero being no pain and a 10 being worst pain imaginable. Those in the study who did not develop shingles were assigned a score of zero. The BOI score represented the average severity of illness among all subjects in the vaccine or placebo group. The study also evaluated the incidence of persistent long-term nerve pain after shingles (PHN) in the group that received ZOSTAVAX™ compared to placebo. PHN was
defined as shingles-associated pain (rated as > 3 on a 0-to-10 scale, using the Zoster Brief
Pain Inventory) that persisted or appeared more than 90 days after the onset of the shingles
rash. The incidence of shingles in the group vaccinated with ZOSTAVAX compared to
placebo recipients was also evaluated in the study.
Reductions seen in burden of illness and incidence of both PHN and shingles
The study showed efficacy with ZOSTAVAX™ on all measured endpoints compared to placebo: • ZOSTAVAX™ significantly reduced the incidence, severity and duration (burden of illness) of pain and discomfort associated with shingles -- by 61.1 percent (p<0.001); the overall BOI score was 2.21 for the vaccine group (N=19,254) compared to a score of 5.68 in the placebo group (N=19,247); ZOSTAVAX™ significantly reduced the incidence of persistent nerve pain after shingles (PHN) -- by two-thirds (66.5 percent) (p<0.001); 27 cases of PHN occurred in the vaccine group (N=19,254) compared to 80 cases in the placebo group (N=19,247); ZOSTAVAX™ significantly reduced the overall incidence of shingles by 51.3 percent (p<0.001); 315 cases of shingles occurred in the vaccine group (N=19,254) compared to 642 cases in the placebo group (N=19,247). “In this study, the investigational vaccine, ZOSTAVAX™, significantly reduced the shingles
pain burden of illness and led to a significant reduction in the incidence of PHN. The
investigational vaccine also reduced the incidence of shingles itself,” said Jeffrey L. Silber,
M.D., senior director for Biologics and Vaccines Clinical Research, Merck Research
Laboratories, leader of the Merck research team for the study and one of the article’s
authors. “The investigational vaccine showed efficacy on these endpoints, regardless of
participants’ gender, age and other demographic factors.”
In the study, the rates of serious adverse events, systemic adverse events and hospitalization were low. During safety evaluations conducted during the first 42 days following vaccination, the number and types of serious adverse events were similar in the vaccine (N=255/19,270) and the placebo groups (N=254/19,276) and the distribution of serious adverse events by organ system were also similar between the groups. Only five subjects had serious adverse events that were assessed by site investigators as possibly vaccine related, two in the vaccine group (exacerbation of asthma and polymyalgia rheumatica) and three in the placebo group (anaphalactoid reaction, polymyalgia rheumatica and Good Pasture’s syndrome). During this period, varicella-like (chickenpox) rashes at the injection site appeared more frequently in the vaccine group (N=20/19,270) compared to the placebo group (N=7/19,276). However, these rashes occurred at other sites at similar rates in the vaccine (N=18/19,270) and placebo groups (N=14/19,276). In an adverse events sub-study that included more than 6,600 subjects from all 22 research sites, significantly more people in the vaccine group (N=1,929/3,345) had one or more adverse events compared to the placebo group (N=1,117/3,271) reflecting a greater frequency of injection-site adverse events in vaccine recipients. The most frequently observed injection-site adverse events among those in the vaccine group were erythema (redness) (N=1,188/3,345, or 35.8 percent, compared to =227/3,271, or 7.0 percent, with placebo); pain or tenderness (N=1,147/3,345, or 34.5 percent, compared to N=278/3,271, or 8.5 percent, with placebo); swelling (N=871/3,345, or 26.2 percent compared to N=147/3,271, or 4.5 percent, with placebo); and pruritus (itching) (N=237/3,345, or 7.1 percent, compared to N=33/3,271, or 1.0 percent, with placebo). Reactions at the injection site were generally mild. No other adverse event at the injection site was observed in more than 2 percent of those in the vaccine group. In the sub-study, significantly more people in the vaccine group experienced serious adverse events (N=64/3345, or 1.9 percent) than in the placebo group (N=41/3271, or 1.3
percent; p=0.03); there were no significant differences in the distribution of serious adverse
events by body system or event. A subject-by-subject chart review of these serious adverse
events revealed no clinically meaningful differences between the vaccine and placebo
groups in the pathophysiology, nature, timing, intensity or outcome of these events.
About The Shingles Prevention Study (SPS)
Participants in the Shingles Prevention Study were enrolled between November 1998 and September 2001. Follow-up was completed in April 2004. Participants had a history of
varicella (chickenpox) or had resided in the continental United States for at least 30 years.
Immunocompromised persons and those unable to adhere to assessments specified in the
protocol were excluded from the study. More than 95 percent of the subjects were actively
followed to the end of the study. An independent data and safety monitoring board reviewed
the safety data and interim results from the study.
Shingles is caused by the reactivation of latent varicella zoster virus – the same virus that causes chickenpox. Shingles may first appear as tingling, itching or pain on one side of the body or face. It then progresses to a blistering rash accompanied by pain in almost every case that varies in intensity and duration. Shingles also can lead to complications, including persistent nerve pain (PHN) that can follow an episode of shingles. PHN can last for months or even years and can range from a tender, burning pain to a throbbing, stabbing pain. Shingles can affect anyone who has had chickenpox -- more than 90 percent of adults in the United States -- and occurs most frequently in older adults. Estimates of the number of cases of shingles occurring each year vary from up to 800,000 to 1 million cases in the United States. The incidence of shingles is expected to increase as the population ages. In fact, it is estimated that up to half of all people who reach age 85 will have developed shingles during their lifetime. Approximately 25 to 50 percent of shingles patients older than 50 years of age develop persistent long-lasting pain after shingles (PHN). About ZOSTAVAX™
Merck submitted a Biologics License Application for ZOSTAVAX™ on April 25, 2005. The FDA will determine within 60 days of that date whether it will accept for review Merck’s application as submitted. Sanofi Pasteur MSD has submitted a Marketing Authorisation Application for ZOSTAVAX™ to the European Medicines Agency (EMEA) on May 27, 2005.
About Sanofi Pasteur MSD
Sanofi Pasteur MSD is a joint venture between sanofi pasteur, the vaccine division of sanofi-aventis, and Merck & Co., Inc. Combining innovation and expertise, Sanofi Pasteur
MSD is the only company in Europe dedicated exclusively to vaccines. Sanofi Pasteur MSD
is able to draw on the research expertise of sanofi pasteur and Merck & Co., Inc., together
with their teams throughout the world, to focus on the development of new vaccines for
Europe, which aim to extend protection to other diseases and perfect existing vaccines in
order to improve the acceptability, efficacy and tolerability of vaccination.
Telephone: +33 4 37 28 40 41
2A - E L M A Ñ A N A - Domingo 29 de diciembre de 2013 Hace rabieta niña; le regalan camisa equivocada Una pequeña fanática del Benfica recibió la camiseta de su rival, el Porto, para Navidad y perdió toda la emoción que tenía por las celebraciones. La niña al ver la camiseta listada azul y blanco se enfureció y se puso a llorar. Al final, en otra bolsa le obs