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Chicago defective medical device lawyersOver the last decade, an estimated 750,000 women have received the Essure birth control implant. Thousands have reported health complications, some of which were life-altering. In response, the U.S. Food and Drug Administration has moved to issue a “black box” warning – their most serious type – for Essure. Yet the devices remain on the market. If you or someone you love has the Essure implant, the following information covers what you should know about the possible risks, and what you can do, should you experience any of them.

Current Warning Label and Potential Complications

Pitched as the only non-surgical permanent birth control option, Essure consists of two nickel-titanium coils. They are implanted into the fallopian tubes, through the cervix, during a 15-minute procedure. Within three months, scar tissue is supposed to develop around the coils, preventing the fallopian tubes from releasing eggs into the uterus. Until a follow-up check at that three-month mark, women are told to use alternative forms of contraception to prevent pregnancy. The device’s current warning says women may experience pelvic pain and bleeding immediately after the procedure.

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Xarelto side effects, drug makers, Chicago product liability attorneyDrug manufacturers have to put drugs through testing before they are approved for use by consumers. But what happens when adverse side effects start appearing in patients using the drug because information given to the Food and Drug Administration (FDA) was incomplete? Eventually the drug may be pulled off the shelf, but patients who used the drug become a statistic to be used for further tests. Patients should not be another defective drug product liability statistic for pharmaceutical companies.

study by the Institute for Safe Medication Practices revealed that drug manufacturers often do not file complete, basic reports about adverse side effects with the FDA. Just over 50 percent of the reports filed did not meet the basic reporting standard, which should contain age, gender, and an event date.

Throughout the years, “blockbuster drugs” have been approved by the FDA, and then later pulled off the shelves, but not before the cost of lives or life-altering side effects were paid. A blockbuster drug is one that:

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