2011
DOI: 10.1007/s12325-011-0038-9
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Preservative-free tafluprost 0.0015% in the treatment of patients with glaucoma and ocular hypertension

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Cited by 26 publications
(11 citation statements)
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“…The tolerability had improved after the change to preservative-free tafluprost with a total of 85.7% of patients rating the tolerability as "very good" and "good." 40 …”
Section: Tafluprost Efficacy and Safety -Clinical Studiesmentioning
confidence: 99%
“…The tolerability had improved after the change to preservative-free tafluprost with a total of 85.7% of patients rating the tolerability as "very good" and "good." 40 …”
Section: Tafluprost Efficacy and Safety -Clinical Studiesmentioning
confidence: 99%
“…Even within existing drug classes, there are clear options for optimizing the balance between efficacy, safety, tolerability, potential quality concerns, impact on patient quality of life, and cost. Among prostaglandin analogues, for example, tafluprost provides efficacy in IOP lowering in various settings, with improvements in OSD symptoms and patient satisfaction when compared with latanoprost 8898. Travoprost and tafluprost monotherapies were suggested to be cost-effective relative to latanoprost alone 99,100.…”
Section: Objectives and Methodsmentioning
confidence: 99%
“…Erb et al evaluated “real-life” data on the efficacy and safety of preservative-free tafluprost from participating ophthalmologists. 37 Data were collected from 2123 patients with glaucoma or ocular hypertension receiving preservative- free tafluprost with or without a previous history of using other intraocular pressure-lowering agents 37. The preservative- free tafluprost lowered intraocular pressure from 19.5 ± 4.4 mmHg at baseline to 16.4 ± 2.9 mmHg after 6–12 weeks.…”
Section: Intraocular Pressure-lowing Effects In Human Subjectsmentioning
confidence: 99%