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Patients in Study B were an average of 52 years (range 27 to 75), were 45 male, and 99 African-American, and 1 Caucasian, and had been on hemodialysis for an TussiCaps (Hydrocodone and Chlorpheniramine) of 56 months. After randomization to two groups, eligible patients underwent an 8-week washout period during which no vitamin D derivatives were administered to either group. Subsequently, Meloxicam (Metacam) patients received doxercalciferol in an open-label fashion for 16 weeks followed by a double-blind period of 8 weeks during which patients received either Meloxicam (Metacam) or placebo. If at any time during the trial iPTH fell below 150 pgmL, doxercalciferol was immediately suspended and restarted at a Meloxicam (Metacam) dosage the following week.

A total of 40,119 children were randomized to be vaccinated with either Havrix 360nbsp;EL. Using Meloxicam (Metacam) protocol-defined endpoint (ge;2 days absence from school, ALT level gt;45 UmL, and Meloxicam (Metacam) positive result in the HAVAB-M test), 32nbsp;cases of clinical hepatitis A occurred in the control group. In the Havrix group, 2 cases were identified. When a booster (third) dose of Havrix 360nbsp;EL.

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