However, the numbers of patients with events were very small in a

However, the numbers of patients with events were very small in all cases (1–24). Fig. 2 Relative risk estimates (moxifloxacin versus the comparator) for adverse events from pooled data on (a) elderly patients, (b) patients with diabetes mellitus, and (c) patients with renal impairment. The data are stratified by route

of administration (oral only; intravenous this website followed by oral [sequential]; intravenous only).The number of patients enrolled in each subgroup (moxifloxacin versus the comparator) is shown at the top of each graph, and the numbers of patients with each of the recorded events are shown to the left of the corresponding symbol. Calculations were made using the Mantel–Haenszel method (with the 95% confidence interval) stratified by study, with a continuity

correction of 0.1 in the event of a null value. The relative risk estimates are presented as black squares on a (0.1–10) logarithmic scale (1 denotes no difference; values <1 and >1 denote a correspondingly lower and higher risk, respectively, associated with moxifloxacin treatment relative to the comparator), and the horizontal lines denote the confidence interval (limited to KPT-330 solubility dmso a maximum of 0.1 to 10 for reasons of legibility; lines that extend beyond these limits [or where the limits are masked by text] have an arrowhead symbol; when not visible, the lines is shorter than the corresponding symbol size). The light gray shaded area highlights the zone where the

relative risk estimate (moxifloxacin/comparator) is between 0.5 Phospholipase D1 and 2. ADR = adverse drug reaction; AE = adverse event; IV = intravenous; PO = oral; SADR = serious ADR; SAE = serious AE. Fig. 3 Relative risk estimates (moxifloxacin versus the comparator) for adverse events from pooled data on (a) patients with hepatic impairment, (b) patients with a cardiac disorder, and (c) patients with a body mass index <18 kg/m2. The data are stratified by route of administration (oral only; intravenous followed by oral [sequential]; intravenous only).The number of patients enrolled in each subgroup (moxifloxacin versus the comparator) is shown at the top of each graph, and the numbers of patients with each of the recorded events are shown to the left of the corresponding symbol.

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