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The use of\n                      <jats:styled-content style=\"fixed-case\">COC<\/jats:styled-content>\n                      s containing cyproterone acetate, desogestrel, drospirenone, or gestodene was associated with a significantly increased risk of\n                      <jats:styled-content style=\"fixed-case\">VTE<\/jats:styled-content>\n                      compared with the use of levonorgestrel\u2010containing\n                      <jats:styled-content style=\"fixed-case\">COC<\/jats:styled-content>\n                      s (pooled risk ratios 1.5\u20132.0). The analysis restricted to monophasic\n                      <jats:styled-content style=\"fixed-case\">COC<\/jats:styled-content>\n                      formulations with 30\u00a0\u03bcg of ethinyl estradiol yielded similar findings. After adjustment for study characteristics, the risk estimates were slightly attenuated.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Compared with the use of levonorgestrel\u2010containing\n                      <jats:styled-content style=\"fixed-case\">COC<\/jats:styled-content>\n                      s, the use of\n                      <jats:styled-content style=\"fixed-case\">COC<\/jats:styled-content>\n                      s containing other progestogens could be associated with a small increase in risk for\n                      <jats:styled-content style=\"fixed-case\">VTE<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  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