Page 20 - RxExam's Naplex Theory Book Part 2
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                Miscellaneous:
                                Dose               Special Notes

                Colchicine      1. Gout, prophylaxis:   1). Colchicine (Colcrys) disrupts cytoskeletal functions through
                (Tablet)                           inhibition of β-tubulin polymerization into microtubules, and
                                0.5 to 0.6 mg PO   consequently prevents the activation, degranulation, and migration of
                                once a day.        neutrophils thought to mediate some gout symptoms. It is indicated
                                                   for the following:
                                2. Gout, treatment:
                                                   a). Treatment and prophylaxis of gout flares
                                1.2 mg PO at the   b). Familial Mediterranean Fever (FMF) in adults and children 4 years
                                first sign of flare   or older
                                followed by 0.6
                                mg I hour later.   2). Co-administration of Colchicine (Colcrys) with drugs known to
                                Do not exceed 1.8   inhibit CYP3A4 and/or P-glycoprotein (P-gp) increases the risk of
                                mg within 1 hour.   colchicine-induced toxic effects. If patients are taking or have recently
                                                   completed treatment with such drugs within the prior 14 days, the
                                3. FMF:            dose adjustments of Colchicine (Colcrys) are required.

                                1.2 to 2.4 mg per   3). The most commonly reported adverse reaction in clinical trials of
                                day given in 1 or 2  colchicine for the prophylaxis of gout was diarrhea. Nausea, vomiting,
                                divided doses.     abdominal discomfort, headache and fatigue are also reported with
                                                   the therapy.

                Terminology

                Familial                           Familial Mediterranean Fever (FMF) is also called recurrent
                Mediterranean                      polyserositis. The salient features of FMF include brief recurrent
                Fever (FMF)                        episodes of peritonitis, pleuritis, and arthritis, usually with
                                                   accompanying fever. FMF occurs within families and is much more
                                                   common in individuals of Mediterranean descent than in persons of
                                                   any other ethnicity.























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