AccessMyLibrary provides FREE access to over 30 million articles from top publications available through your library.

Are you dying to be thin? If you'd do anything to slim down, read this. Cosmo examines the weight-loss herb ephedra and its serious--sometimes fatal--side effects. (Warning to Women).(Brief Article)

Cosmopolitan

| May 01, 2002 | Grumman, Rachel | COPYRIGHT 2002 Hearst Communications, reprinted with permission of Hearst. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

* Three years ago, Dawn Shuster was a healthy 33-year-old who wanted to lose about 25 pounds. So she took an over-the-counter diet pill to speed up the process. Little did she know that this supposedly safe weight-loss aid would bring her to the brink of death.

Dawn followed the bottle's instructions, popping four pills a day for two-and-a-half weeks. On the 19th day, at the West Palm Beach, Florida, doctor's office where she worked screening patients for clinical trials, she complained to a coworker that she had a stomachache and felt like she was going to pass out. A few minutes later, her coworker heard a loud thump. When she turned around to see what had happened, she was horrified: Dawn had fallen on the floor and vomited and was in cardiac arrest. By the time she arrived at Columbia Hospital, Dawn had lost so much oxygen that she was blue from her navel to her head. She was deprived of air long enough that she could have sustained long-term brain damage ... but luckily didn't.

fighting for her life

On the way to the hospital, Dawn had to be intubated, a technique where a tube is inserted into the windpipe to help the patient breathe. However, during intubation, she threw up, and the vomit went into her lungs, which led to a severe bacterial infection. Doctors were forced to put her into a morphine-induced coma-like state for about two weeks so that she could fight it off. "I flat-lined three times and was declared dead. My family was asked to come in and say good-bye to me, and a priest even performed last rites!" says Dawn, who suffered a total of three heart attacks despite having no history of heart problems.

She spent a month in the cardiac intensive-care unit, then was transferred to another hospital, where she had a pacemaker and defibrillator surgically implanted. These devices help to regulate her heart rate and keep her alive, at least for now. Because the pacemaker is doing 97 percent of the work, Dawn's doctor told her that there's a strong chance she will eventually need a heart transplant.

"To think that I only wanted to lose some weight," laments Dawn. "Now I have to take up to 22 pills a day just to function --from blood thinners to beta blockers, which slow my heart rate and decrease the stress. I'm often so wiped out that I have trouble walking and breathing. Some days are so bad, I can't make it out of bed. I'm very grateful to be here, but I'm mad as hell that the manufacturers allowed me to play. Russian roulette with my life."

danger in the aisles

Related articles from newspapers, magazines, journals, and more
'Dawn of a New Era' Geron Soars as First ESC Trial Clears FDA Hurdle.
Magazine article from: BIOWORLD Today Boggs, Jennifer January 26, 2009 700+ words
...largest IND ever received by the FDA -- was put on hold by the agency...he added, calling it the "dawn of a new era in medical therapeutics...help wonder at the timing of the FDA's decision. But Okarma maintained...the first company to get the FDA's blessing wasn't easy...
Macular degeneration treatment on fast track for FDA approval.
Newspaper article from: South Florida Sun-Sentinel (Fort Lauderdale, FL) June 14, 2006 700+ words
...300 million. The strong results also prompted the FDA to allow doctors who participated in earlier trials...another drug after, Michels said. Genentech spokeswoman Dawn Kalmar said the FDA has promised to rule on the application for Lucentis...
Canadian International Pharmacy Association (CIPA) Responds to FDA Release.
Press release article from: PR Newswire August 31, 2006 700+ words
...it issued yesterday," said Dawn Polley, President of CIPA. Characterizing the FDA latest press release as nothing...pointed out that "In the past the FDA has intimated that a drug is...the version approved by the FDA even if it is the equivalent...
FDA investigators respond to mad cow emergency.(Food and Drug Administration)
Magazine article from: FDA Consumer Bren, Linda May 1, 2004 700+ words
...director of investigations in the FDA's Seattle district. Investigators...rendering plant by 9:30 a.m. FDA investigator Dawn Barkans got the word three days later...investigation was completed, 30 FDA employees in the Seattle area and...
A quarter-century of rewriting the rules.(THE DAWN OF DTC)
Magazine article from: Medical Marketing & Media Arnold, Matthew October 1, 2006 700+ words
...TO think of 1997 as being the dawn of DTC advertising. In that year, the FDA released its draft guidance effectively...Digest in 1981. In 1982, the FDA prompted Lilly to retract a press...Under pressure from doctors, FDA was adamant. "We thought that...
NOVANTRONE(R) One Step Closer to FDA Approval to Treat Multiple Forms Of...
Press release article from: PR Newswire April 7, 2000 700+ words
...approval made last month by the FDA's Peripheral and Central Nervous...Drugs Advisory Panel. "The FDA's 'approvable letter' brings...forms of this disease," said Dawn Viveash, vice president, regulatory...productive interaction with the FDA will continue, as we work with...
Radiologicals/mammography.
Newspaper article from: Warning Letter Bulletin June 2, 2003 700+ words
...the actual SID was measured to be greater than 2%. FDA notified Diagnostic Imaging that if it determined the...11, inspection by investigators Joseph Teixeira and Dawn Braswell, FDA disapproved of the firm's microwave oven quality control...
Drug coming into focus.
Newspaper article from: South Florida Sun-Sentinel (Fort Lauderdale, FL) June 13, 2006 700+ words
...300 million. The strong results also prompted the FDA to allow doctors who participated in earlier trials...another drug after, Michels said. Genentech spokeswoman Dawn Kalmar said the FDA has promised to rule on the application for Lucentis...
For more facts and information, see all results
©2009 Gale, a part of Cengage Learning. All rights reserved.
About us | FAQs | Contact us | Privacy policy | Terms and conditions
Other Gale sites: Encyclopedia.com | HighBeam Research | Acquire Content | Books & Authors | Goliath | MovieRetriever | Smart QandA