Table 3

Percentage of women who reported specific adverse events during clinical trials of hormonal contraceptive methods

AEContraceptiveAE frequency (%)Sample size (n)Publication
Sore breastsCOC8.32837Yasmin12
COC3.82501NuvaRing17
IUS8.5*5091Mirena15
Injection2.8>3900Depo-Provera16
Nausea/vomitingCOC4.52837Yasmin12
COC16.31723Ortho Tri-Cyclen Lo11
Injection3.3>3900Depo-Provera16
Transdermal system16.63322Ortho Evra18
Vaginal ring5.92501NuvaRing17
Changes in premenstrual syndromeCOC13.22837Yasmin12
Vaginal dischargeIUS14.9*5091Mirena15
Vaginal ring5.72501NuvaRing17
Alteration of menstrual bleeding patternsIUS31.9*5091Mirena15
VulvovaginitisIUS10.5*5091Mirena15
Back painIUS7.9*5091Mirena15
DysmenorrheaVaginal ring3.52501NuvaRing17
COC6.4*5091Mirena15
Injection1.7>3900Depo-Provera16
Transdermal system7.83322Ortho Evra18
  • *Crude incidence per person-years.

  • AE, adverse event; COC, combined oral contraceptive; IUS, intrauterine system.