Levaquin Black Box

On July 8, 2008, The FDA ordered the manufacturer of Levaquin, Ortho McNeil, to place a black box warning on the drug.  A black box warning (also referred to as a black label warning or boxed warning) is the strongest warning available for prescription drugs.  Such a warning means that the drug carries significant risk. 

 fda2 Levaquin Black Box

Levaquin has not  been recalled.  The FDA has also ordered Ortho McNeil to provide a guidebook to patients with information about the possible side effects associated with Levaquin.   If you or a loved on has experienced Levaquin complications you may have a claim against the manufacturer.  Please contact us today for a free consultation.

Call us today for a free consultation.  Toll Free 1-866-777-2557 or 612-767-2009.  24 hours a day, 7 days a week.  We are representing individuals in all 50 states.  This is a free, no obligation consultation.

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