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| 15 Sep 2009 by insciences After 90 days, 56.4 per cent of patients who received Aggrenox ® treatment from Day 1 had little or no disability (mRS 0-1) compared with 52.4 per cent of patients in the ASA initial therapy group (odds ratio 0.96; 95% CI: 0.65. ... Articles - http://insciences.org/articles.php |
| 14 Sep 2009 by Prne 283 patients received Aggrenox(R) (extended-release dipyridamole [200 mg] plus ASA [25mg]) twice daily from day 1 to day 90 after an ischaemic stroke or TIA - 260 patients received ASA 100 mg once daily between days one and seven, ... PR Hub - http://blog.taragana.com/pr/ [ More results from PR Hub ] |
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| 15 Jan 2009 Absorption: Peak plasma levels of dipyridamole are achieved 2 hours (range 1-6 hours) after administration of a daily dose of 400 mg AGGRENOX (given as 200 mg b.i.d.). The peak plasma concentration at steady-state is 1.98 g/mL ... Recent Discussions at PrescriptionDrug-Info.com - http://www.prescriptiondrug-info.com/forums/pre... [ More results from Recent Discussions at PrescriptionDrug-Info.com ] |
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