January 1, 2009
Posted by healthandsurvival in Diseases, Drugs, Herbal Medicine, Wellness.Tags: depression, Drugs, health, healthcare, herbs, Life, medicines, news, prevention, st. john's wort, supplements, vitamins, Wellness, zoloft
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(NaturalNews) The herbal supplement St. John’s Wort has long been promoted as an effective alternative for treating depression. Unfortunately, St. John’s Wort has proven ineffective for people suffering severe clinical depression. In fact, the results of a recent study revealed that St. John’s Wort is completely ineffective at treating severe depression. There is another effective natural alternative, however, and it is called SAM-E (S-adenosylmethionine).
Symptoms of Depression:
•Feelings of sadness and emptiness
•Feelings of helplessness, hopelessness, guilt, or worthlessness
•Loss of interest in previously enjoyed activities
•Excessive sleeping or insomnia
•Fatigue
•Lack of energy
•Difficulty concentrating and in decision-making
•Headaches or digestive disorders
•Crying and tearfulness
•Overeating or under eating
In the aforementioned study, St. John’s Wort was tested for eight weeks on 200 patients who were suffering a degree of depression that made daily functioning difficult. St. John’s Wort was no more effective than a placebo.
In a significant number of previous studies, however, St. John’s Wort was found effective for mild to moderate cases of depression. There is some evidence that points to the fact that St. John’s Wort can help with some symptoms of depression. In Germany, in fact, St. John’s Wort is available by prescription.
There have been questions about the quality of some of this research, though. One such criticism cites a lack of studies using a placebo and another drug such as Zoloft. Zoloft is classified as an SSRI (selective serotonin reuptake inhibitor) and these are commonly used drugs for treating depression. These newer drugs also have numerous side-effects, however, and while many claim to be “non-habit forming,” this does not seem to be the case.
To satisfy these criticisms about the St. John’s Wort studies, researchers gave participating patients either St. John’s Wort, Zoloft, or a placebo for up to 26 weeks. When the study concluded, researchers found that neither the prescription drug nor the St. John’s Wort was more effective than the placebo. Almost 33% of the placebo patients showed a large response to their treatment and this was compared to approximately 24% of both the Zoloft group and the St. John’s Wort group.….read more here…
Risky Asthma Drugs December 7, 2008
Posted by healthandsurvival in Asthma, Children's Health, Drugs.Tags: advair, Asthma, children, health, kids, news, pediatrics, symbicort
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Warning Given on Use of 4 Popular Asthma Drugs, but Debate Remains
WASHINGTON — Two federal drug officials have concluded that asthma sufferers risk death if they continue to use four hugely popular asthma drugs — Advair, Symbicort, Serevent and Foradil. But the officials’ views are not universally shared within the government.
The two officials, who work in the safety division of the Food and Drug Administration, wrote in an assessment on the agency’s Web site on Friday that asthma sufferers of all ages should no longer take the medicines. A third drug-safety official concluded that Advair and Symbicort could be used by adults but that all four drugs should no longer be used by people age 17 and under.
Dr. Badrul A. Chowdhury, director of the division of pulmonary and allergy products at the agency, cautioned in his own assessment that the risk of death associated with the drugs was small and that banning their use “would be an extreme approach” that could lead asthmatics to rely on other risky medications.
Once unheard of, public disagreements among agency experts have occurred on occasion in recent years. The agency is convening a committee of experts on Wednesday and Thursday to sort out the disagreement, which has divided not only the F.D.A. but also clinicians and experts for more than a decade.
Sudden deaths among asthmatics still clutching their inhalers have fed the debate. But trying to determine whether the deaths were caused by patients’ breathing problems or the inhalers has proved difficult.
The stakes for drug makers are high. Advair sales last year were $6.9 billion and may approach $8 billion this year, making the medication GlaxoSmithKline’s biggest seller and one of the biggest-selling drugs in the world. Glaxo also sells Serevent, which had $538 million in sales last year. Symbicort is made by AstraZeneca and Foradil by Novartis.
Whatever the committee’s decision, the drugs will almost certainly remain on the market because even the agency’s drug-safety officials concluded that they were useful in patients suffering from chronic obstructive pulmonary disease, nearly all of whom are elderly.
Dr. Katharine Knobil, global clinical vice president for Glaxo, dismissed the conclusions of the agency’s drug-safety division as “not supported by their own data.” Dr. Knobil said that Advair was safe and that Serevent was safe when used with a steroid.
Michele Meeker, a spokeswoman for AstraZeneca, said that the F.D.A.’s safety division improperly excluded most studies of Symbicort in its analysis, and that a review of all of the information shows that the drug does not increase the risks of death or hospitalization.
Dr. Daniel Frattarelli, a Detroit pediatrician and member of the American Academy of Pediatrics’s committee on drugs, said that he was treating children with Advair and that his committee had recently discussed the safety of the medicines.
“Most of us felt these were pretty good drugs,” Dr. Frattarelli said. “I’m really looking forward to hearing what the F.D.A. committee decides.”
About 9 percent of Advair’s prescriptions go to those age 17 and under, according to Glaxo. Ms. Meeker could not provide similar figures for Symbicort.
In 1994, Serevent was approved for sale, and the F.D.A. began receiving reports of deaths. A letter to the New England Journal of Medicine described two elderly patients who died holding Serevent inhalers. Glaxo warned patients that the medicine, unlike albuterol, does not work instantly and should not be used during an attack.
In 1996, Glaxo began a study of Serevent’s safety, but the company refused for years to report the results publicly. In 2001, the company introduced Advair, whose sales quickly cannibalized those of Serevent and then far surpassed them.
Finally in 2003, Glaxo reported the results of its Serevent study, which showed that those given the medicine were more likely to die than those given placebo inhalers. Glaxo said problems with the trial made its results impossible to interpret.
Asthma is caused when airways within the lungs spasm and swell, restricting the supply of oxygen. The two primary treatments are steroids, which reduce swelling, and beta agonists, which treat spasms. Rescue inhalers usually contain albuterol, which is a beta agonist with limited duration. Serevent and Foradil are both beta agonists but have a longer duration than albuterol and were intended to be taken daily to prevent attacks.
Advair contains Serevent and a steroid. Symbicort, introduced last year, contains Foradil and a steroid. In the first nine months of this year, Symbicort had $209 million in sales.
The problem with albuterol is that it seems to make patients’ lungs more vulnerable to severe attacks, which is why asthmatics are advised to use their rescue inhalers only when needed. The long-acting beta agonists may have the same risks.
But drug makers say this risk disappears when long-acting beta agonists are paired with steroids. The labels that accompany Serevent and Foradil instruct doctors to pair the medicines with an inhaled steroid.
RFK on the “Vaccine Autism Coverup” October 17, 2008
Posted by healthandsurvival in Children's Health, Drugs, Society, Survival, Wellness, medicine, vaccines.Tags: autism, children, family, health, Life, medicine, news, thimerosol, vaccine, Wellness
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Become informed- talk to your doctor about vaccinations and your children… I do not recommend anyone avoid vaccinations- simply make informed choices. Evidence shows that vaccinations have great public health benefits but some children may be sensitive to added preservatives put in the vaccines. Fortunately, these preservatives are not required for the vaccine to work.
FDA Cites Bayer on Yaz Birth Control Pill October 7, 2008
Posted by healthandsurvival in Drugs, Society, Survival, health, medicine.Tags: contraception, Drugs, family, Life, medicines, meds, news, yaz
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Tue Oct 7, 8:10 PM ET
Source: http://news.yahoo.com/s/nm/20081008/us_nm/us_bayer_yaz&printer=1;_ylt=AtUep_djRS93bt_0Ee1bqFoXIr0F
Two television commercials for Bayer AG’s birth control pill Yaz give a misleading impression of its benefits, U.S. health regulators warned the company in a letter released on Tuesday.
The ads wrongly suggest the pills are approved for relieving premenstrual syndrome, the U.S. Food and Drug Administration said in a letter dated October 3. The ads also minimize the drug’s risks, the agency said.
Bayer will stop running the only one of the two ads currently in use, company spokeswoman Rose Talarico said. The other campaign ended in 2007.
The commercial no longer being broadcast featured women singing “We’re not gonna take it” and kicking, punching and pushing balloons with words such as “irritability,” “moodiness” and “bloating.”
Those symptoms are common with PMS. Yaz, however, is cleared for a more serious condition called premenstrual dysphoric disorder (PMDD), which causes anxiety, tension, persistent anger and other symptoms.
“The TV ads misleadingly suggest that Yaz is approved to treat women with any severity of the symptoms presented, regardless of whether their symptoms are actually severe enough to constitute PMDD,” the FDA letter said.
A second ad featured the song “Good-Bye to You” with women releasing balloons labeled with symptoms. The commercial suggests “women are saying ‘goodbye’ to their symptoms and are now symptom-free, when such an elimination of symptoms has not been demonstrated by substantial evidence or substantial clinical experience,” the FDA said.
Bayer will pull that ad and work with the FDA regarding other promotions for Yaz, Talarico said.
The FDA said both commercials “suggest that Yaz is approved for acne of all severities when this is not the case,” the agency said.
In addition, the FDA said the ads distracted viewers with fast-moving images and background music, while information about potential side effects was described.
“These complex presentations distract from and make it difficult for viewers to process and comprehend the important risks being conveyed. This is particularly troubling as some of the risks being conveyed are serious, even life-threatening,” the agency said.
Blood clots are among the potential side effects.
The letter was posted on the FDA Website at http://www.fda.gov/cder/warn/2008/YAZ_wl.pdf.
(Reporting by Susan Heavey and Lisa Richwine, editing by Bernard Orr and Andre Grenon)
Role for Mailmen in Case of Anthrax Attack October 1, 2008
Posted by healthandsurvival in Diseases, Drugs, Politics and Medicine, Society, Survival, Wellness, health.Tags: antrhrax, bioterrorism, family, health, Life, medicine, news, terror, Wellness
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WASHINGTON (AP) — If there ever is another anthrax attack, a letter carrier may deliver antibiotics to those who might be infected.
Federal health officials are beginning a project in Minneapolis-St. Paul to let letter carriers stockpile personal supplies of emergency antibiotics so they are protected and ready to deliver aid to the rest of the city.
The project seeks to overcome a big hurdle of emergency planning. The government has many drugs stockpiled in case of bioterrorism but few ways to get them quickly to people who need them.
Carriers could provide “a front-end quick strike,” said William Raub, senior science counselor to Michael O. Leavitt, health and human services secretary.
Test projects in Seattle, Philadelphia and Boston over the past two years paired carriers with police officers on holidays. Carriers volunteered to do double routes, delivering empty pill bottles along with fliers explaining what was happening. In Philadelphia, 50 carriers reached about 53,000 households in eight hours, Mr. Raub said…...read rest of story……
