By allowing the transfer of the leases to prospective buyers on Wednesday, the county board basically gave the green light for hope in Magnetations future. The official approved action was to withdraw the objection authorized on Dec. 12, as pertaining to expedited relief, approving the sale and transfer of certain assets and liabilities free and clear of encumbrances; and authorized the assumption and assignment of contracts and unexpired leases in connection with related relief of Magnetation LLC. In other business during this weeks county board meeting, commissioners: Recognized county employees: Tony Fremont, promoted to deputy auditor – real estate; Kristin Isaacs, hired as human services support specialist; Kyle Buckingham, hired as part-time sheriffs dispatcher; and Peter Johnson, hired as part-time sheriffs dispatcher. Held a moment of silence for late county employees Darrell Lauber and MariJean Davis. Approved six letters of understanding regarding vacation payout for ICEA and Local 639 employees. Approved Commissioner Warrants of $589,002.40 with a check date of Dec. 16, 2016. Approved Procurement Standards Policy for Federal Awards.
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Eliquis lacks an antidote, or reversal agent, that counters the drugs blood thinning effects if the patient suffers excessive bleeding. Warfarin can be reversed with vitamin K, but no such antidote exists for Eliquis. The FDA approved a Pradaxa reversal agent last October. Plaintiffs allege that Eliquis makers knew about the lack of an antidote but failed to warn patients or the medical community. Another lawsuit was recently filed on behalf of a Louisiana man who suffered internal eye bleeding and eventual partial blindness, allegedly due to Eliquis. He took the drug from June 2013 to April 2016 to reduce the risk of blood clots associated with his atrial fibrillation. He alleges that neither he nor his doctor knew about the risk of irreversible bleeding with Eliquis. Eliquis Bleeding Lawsuits Consolidated into MDL Eliquis uncontrollable bleeding lawsuits have been consolidated into a federal multidistrict litigation (MDL) in the U.S. District Court for the Southern District of New York. Plaintiffs similarly allege that BMS and Pfizer failed to disclose the lack of an antidote, which ultimately caused plaintiffs to suffer bleeding injuries such as gastrointestinal bleeding and brain bleeding.
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