Ortho Evra Recall
Though there has not been an official Ortho Evra recall by the federal government, doctors and health professionals are turning away from the risky birth control patch. The Ortho Evra patch adheres to the skin for weeklong periods at a time. It was initially designed to create a simple and effective approach to birth control requiring less maintenance than the standard oral contraceptive. The transdermal patch time releases the hormones estrogen and progestin into the bloodstream to prevent ovulation and pregnancy. However, an Ortho Evra recall seems to be looming in the near future due to mounting evidence that the easy method can cause fatal side effects.
Ortho Evra Recall
Ortho Evra attorneys from Nadrich Law are dedicated Ortho Evra lawyers that will aggressively represent your Ortho Evra Lawsuit. The FDA issued an Ortho Evra Patch recall due to serious symptoms and side effects, including heart failure. If you or women you know have developed a symptom of any type or health problems from using a birth control patch, specifically the Ortho Evra birth control patch, our personal injury attorneys will file your claim.
In November 2005, Ortho McNeil, the manufacturer of the Ortho Evra birth control patch, released a consumer warning about serious health risks and side effects from using the product, which prompted an FDA Ortho Evra patch recall. The patch releases 60% more estrogen directly into the bloodstream than birth control pills, and the elevated levels of hormones lead to blood clots, heart failure, and other medical problems.
Ortho Evra Recall
Patch side effects are related to the transdermal application of the weekly birth control patch. The FDA Ortho Evra recall/Ortho Evra patch alerts have stemmed from serious side effects from higher levels of estrogen in the bloodstream because the patch is attached directly to the skin. Many blood clot warning signs have been linked to the birth control patch, and Ortho-McNeil, the manufacturer, has been ordered by the FDA to label the drug by detailing the dangers of a transdermal patch. Other contraceptives are not placed directly on the skin, and release 60% less estrogen than the birth control patch.
Ortho Evra Recall - Label Change
Ortho Evra has garnered a great deal of negative publicity as of late because of the adverse health effects associated with use of the contraceptive. An official Ortho Evra recall has not yet been issued; however, there as some in the medical community who believe one to be on the horizon. Ortho McNeil, a subsidiary of Johnson & Johnson and the manufacturer/marketer of Ortho Evra, has thus far refused to accept liability for a failure to adequately warn consumers of the risks involved with use of the birth control patch.
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