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S.W.3d 507 2004 ; . Objective findings are those findings which cannot come under the voluntary control of the patient. Crawford, supra. In order to prove a compensable injury the claimant must prove, among other things, a causal relationship between his employment and the injury. Id. The determination of whether a causal relationship exists is a question of fact for the Commission to determine. Smith-Blair, Inc. v. Jones, 77 Ark. App. 273, 72 S.W.3d 560 2002 ; . It is undisputed that appellant has suffered from chronic, severe back pain since at least 1997, when he originally injured his back while working as a welder for Big John's Manufacturing. He admits never fully recovering from that injury and has continued seeking treatment and medication without significant improvement. An MRI as far back as July 1999 indicated that appellant has degenerative-disc disease and herniations at L3-4 and L4-5 in his lumbar spine, and another MRI in July 2002 showed protrusion at L3-4 and L4-5. A discogram in September 2002 showed an abnormality at L5-S1, and he was diagnosed with HNP in May 2003. The record indicates that those conditions are aggravated by numerous common factors, including damp weather, weather changes, physical activity, pressure, sitting for long periods, sitting, walking, tension, fatigue, coughing, sneezing, and driving a car. Subsequent to the alleged injury on September 2, 2003, Dr. Bivens did not indicate any sort of work-related accident or injury in his notes from an examination of appellant on September 4, 2003, and testified that he did not recall appellant mentioning the alleged work and singulair!

All options were granted at an exercise price which was greater than the market price of the Group's shares at the grant date. The following table summarizes information about share options outstanding at December 31, 2002.

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P. Ding, H. Xu, G. Wei, and J. Zheng. Biomedical Chromatography, 14: 141-143, 2000. 2255. Kingery JR, Sowinski KM, Kraus MA, et al. Vancomycin assay performance in patients with end-stage renal disease receiving hemodialysis. Pharmacotherapy. 2000; 20: 653656. Santos JV, Baudat JA, Casellas FJ, et al. Intravenous cyclosporine for steroidrefractory attacks of Crohn's Disease. J Clin Gastroenterol. 1995; 20: 207210. Santos J, Baudat S, Casellas FJ, et al. Efficacy of intravenous cyclosporine for steroid refractory attacks of ulcerative colitis. J Clin Gastroenterol. 1995; 20: 285289. Gurudu SR, Griffel LH, Gialanella RJ, et al. Cyclosporine therapy in inflammatory bowel disease. J Clin Gastroenterol. 1999; 29: 151154. Carbonnel F, Boruchowicz A, Duclos B, et al. Intravenous cyclosporine in attacks of ulcerative colitis. Dig Diseases and Sciences. 1996; 41: 24712476. Egan LJ, Sandborn WJ, Tremaine WJ. Clinical outcome following treatment of refractory inflammatory and fistulizing Crohn's Disease with intravenous cyclosporine. J Gastroenterol. 1998; 93: 442447. Cohen RD, Stein R, Hanauer SB. Intravenous cyclosporin in ulcerative colitis: a five-year experience. J Gastroenterol. 1999; 94: 15871592. Schwinghammer TL, Bloom EJ, Rosenfield CS, et al. High-dose cyclosporine and corticosteroids for prophylaxis of acute and chronic graft-versus-host disease. Bone Marrow Transplant. 1995; 16: 147154. Imashuku S, Hibi S, Ohara T, et al. Effective control of Epstein-Barr virus-related hemophagocytic lymphohistiocytosis with immunochemotherapy. Blood. 1999; 93: 18691874. Theis JG, Liau-Chu M, Chan HS, et al. Anaphylactoid reactions in children receiving high-dose intravenous cyclosporine for reversal of tumor resistance: the and terazosin. Adverse Events Occurring at an Incidence of 1% or More Among REMERON-Treated Patients The table that follows enumerates adverse events that occurred at an incidence of 1% or more, and were more frequent than in the placebo group, among REMERON mirtazapine ; Tabletstreated patients who participated in short-term US placebo-controlled trials in which patients were dosed in a range of 560 mg day. This table shows the percentage of patients in each group who had at least one episode of an event at some time during their treatment. Reported adverse events were classified using a standard COSTART-based dictionary terminology. The prescriber should be aware that these figures cannot be used to predict the incidence of side effects in the course of usual medical practice where patient characteristics and other factors differ from those which prevailed in the clinical trials. Similarly, the cited frequencies cannot be compared with figures obtained from other investigations involving different treatments, uses and investigators. The cited figures, however, do provide the prescribing physician with some basis for estimating the relative contribution of drug and non-drug factors to the side effect incidence rate in the population studied. INCIDENCE OF ADVERSE CLINICAL EXPERIENCES1 1% ; IN SHORT-TERM US CONTROLLED STUDIES Placebo Body System REMERON n 453 ; n 361 ; Adverse Clinical Experience Body as a Whole Asthenia 8% 5% Flu Syndrome 5% 3% Back Pain 2% 1% Digestive System Dry Mouth 25% 15% Increased Appetite 17% 2% Constipation 13% 7% Metabolic and Nutritional Disorders Weight Gain 12% 2% Peripheral Edema 2% 1% Edema 1% 0% Musculoskeletal System.
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