Table 4.
Outcome | Total Comparisons | Total Studies | All Studies | Oxybutynin IR | Oxybutynin ER | Tolterodine IR | Tolterodine ER | Trospium | Darifenacin | Solifenacin | Fesoterodine |
---|---|---|---|---|---|---|---|---|---|---|---|
RR (95% CI) | RR (95% CI)(Szonyi et al., 1995) | RR (95% CI)(Lackner et al., 2008) | RR (95% CI)(Malone-Lee et al., 2001) | RR (95% CI)(DuBeau et al., 2012; Wagg et al., 2014; Zinner et al., 2002) | RR (95% CI)(Sand et al., 2011) | RR (95% CI)(Chapple et al., 2007a; Foote et al., 2005) | RR (95% CI)(Wagg et al., 2006) | RR (95% CI)(DuBeau et al., 2012; Kraus et al., 2010b; Wagg et al., 2013) | |||
AEs | 13 | 12 | 1.41 (1.12–1.78) NNH = 47.4 |
-- | 2.78 (0.12–4.57) | 3.53 (0.47–26.56) | 1.02 (0.67–1.56) | 1.14 (0.28–4.57) | 0.78 (0.42–1.48)[45,42] | 1.44 (0.89–2.33) | 1.96
(1.45–2.64)[50,47,51] NNH =22.5 |
Dry Mouth | 6 | 5 | 3.01 (1.18–7.68) NNH =86.3 |
-- | -- | 0.64 (0.06–6.91) | 2.61 (0.31–22.25) | -- | 2.51 (0.12–51.90)[45] | -- | 4.79
(1.16–19.74)[50,47,51] NNH =60.8 |
I2 >25%;
Adverse Event noted in Study but 0 count
AEs = Adverse Events; CI = confidence intervals; ER = extended release; IR = immediate release; NNH = Number Needed to Harm; RR = rate ratio