PMID- 19624787 OWN - NLM STAT- MEDLINE DCOM- 20101029 LR - 20211020 IS - 1742-1241 (Electronic) IS - 1368-5031 (Print) IS - 1368-5031 (Linking) VI - 63 IP - 8 DP - 2009 Aug TI - Tolterodine extended release is well tolerated in older subjects. PG - 1198-204 LID - 10.1111/j.1742-1241.2009.02108.x [doi] AB - OBJECTIVES: To investigate the tolerability of tolterodine extended release (ER) in older subjects with overactive bladder (OAB). METHODS: This was a retrospective analysis of pooled data from five large, randomised, double-blind, placebo-controlled trials. Subjects with OAB symptoms, including urinary frequency and urgency (and nocturia in two studies) with or without urgency urinary incontinence, received qd treatment with tolterodine ER (4 mg) or placebo for 8-12 weeks. Data were stratified post hoc by age group: < 65 (n = 2531), 65-74 (n = 1059) and > or = 75 years (n = 573). Tolerability was assessed by evaluating the occurrence of adverse events (AEs). AE occurrences from each study were mapped to the MedDRA coding dictionary of preferred terms. RESULTS: Discontinuation rates were slightly higher among subjects > or = 75 years of age vs. those < 65 years of age; however, this was observed in subjects treated with placebo as well as tolterodine ER. Overall, there were no significant differences in the occurrence of dry mouth, headache, constipation, nausea, urinary tract infection, blurred vision, dry eye, dizziness and micturition disorder in older (65-74 or > or = 75 years) vs. younger (< 65 years) subjects treated with tolterodine ER relative to placebo (treatment x age; all p > 0.1). Dry mouth was the only AE consistently associated with tolterodine ER treatment (< 65 years, 17%; 65-74 years, 16%; > or = 75 years, 15%). The occurrence of all other AEs was < or = 5% in most age and treatment cohorts. Most AEs were mild or moderate in all age and treatment cohorts. CONCLUSION: The nature and frequency of AEs associated with tolterodine ER treatment were similar across age groups in subjects with OAB, suggesting that tolterodine ER was not associated with an increased risk of AEs in older vs. younger subjects and, thus, is a suitable first-line pharmacotherapy treatment for OAB in this population. FAU - Griebling, T L AU - Griebling TL AD - Department of Urology and The Landon Center on Aging, University of Kansas, 3901 Rainbow Boulevard, Kansas City, KS 66160, USA. tgriebling@kumc.edu FAU - Kraus, S R AU - Kraus SR FAU - Richter, H E AU - Richter HE FAU - Glasser, D B AU - Glasser DB FAU - Carlsson, M AU - Carlsson M LA - eng GR - U01 DK058234/DK/NIDDK NIH HHS/United States GR - U01 DK058234-09/DK/NIDDK NIH HHS/United States PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PL - India TA - Int J Clin Pract JT - International journal of clinical practice JID - 9712381 RN - 0 (Benzhydryl Compounds) RN - 0 (Cresols) RN - 0 (Delayed-Action Preparations) RN - 0 (Muscarinic Antagonists) RN - 33RU150WUN (Phenylpropanolamine) RN - 5T619TQR3R (Tolterodine Tartrate) SB - IM MH - Adult MH - Aged MH - Benzhydryl Compounds/*administration & dosage/adverse effects MH - Cresols/*administration & dosage/adverse effects MH - Delayed-Action Preparations MH - Female MH - Humans MH - Male MH - Middle Aged MH - Muscarinic Antagonists/*administration & dosage/adverse effects MH - Phenylpropanolamine/*administration & dosage/adverse effects MH - Randomized Controlled Trials as Topic MH - Retrospective Studies MH - Tolterodine Tartrate MH - Treatment Outcome MH - Urinary Bladder, Overactive/*drug therapy PMC - PMC2737749 EDAT- 2009/07/25 09:00 MHDA- 2010/10/30 06:00 CRDT- 2009/07/24 09:00 PHST- 2009/07/24 09:00 [entrez] PHST- 2009/07/25 09:00 [pubmed] PHST- 2010/10/30 06:00 [medline] AID - IJCP2108 [pii] AID - 10.1111/j.1742-1241.2009.02108.x [doi] PST - ppublish SO - Int J Clin Pract. 2009 Aug;63(8):1198-204. doi: 10.1111/j.1742-1241.2009.02108.x.