NuvaRing was first approved in The Netherlands on February 14, 2001, then by all 14 other countries then in the European Union on June 12, 2001, and in the United States by the . Food and Drug Administration (FDA) on October 3, 2001.   NuvaRing was first marketed in the United States in July 2002,  followed by a number European countries since then.  In March 2007, Organon announced the market launch of NuvaRing in Australia, bringing the total number of countries where NuvaRing is available to 32. A study by Danish researcher Dr. Øjvind Lidegaard in 2012 with million women found a times increase in the likelihood of venous thromboembolism when compared to users of non-hormonal based birth control. In Canada , Lidegaard's study led to a change in labeling warning of increased risk of blood clots, but not in the United States. 
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