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REMERON has an elimination half-life of approximately 20 to 40 hours; therefore, dose changes should not be made at intervals of less than 1 to 2 weeks in order to allow sufficient time for evaluation of the therapeutic response to a given dose. The clearance of mirtazapine is reduced in elderly patients and in patients with moderate to severe renal or hepatic impairment. Based on these limited data, it is unknown whether or not the dose of REMERON needed for maintenance treatment is identical to the dose needed to achieve an initial response. Do not start REMERON in a patient who is being treated with linezolid or intravenous methylene blue because there is an increased risk of serotonin syndrome. If acceptable alternatives to linezolid or intravenous methylene blue treatment are not available and the potential benefits of linezolid or intravenous methylene blue treatment are judged to outweigh the risks of serotonin syndrome in a particular patient, REMERON should be stopped promptly, and linezolid or intravenous methylene blue can be administered. The patient should be monitored for symptoms of serotonin syndrome for 2 weeks or until 24 hours after the last dose of linezolid or intravenous methylene blue, whichever comes first.

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Mirtazapine is a tetracyclic piperazino-azepine antidepressant agent that was initially approved for the treatment of major depressive disorder MDD in the Netherlands in In addition to its beneficial effects in depression, mirtazapine has been reported to be efficacious in the off-label management of various other conditions.

   
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Since the coronavirus first hit the United States, doctors at a number of hospitals have noticed a pattern. Fewer patients are being treated for heart attacks at a time when Nighttime high blood pressure could harm the brain, a new study says.

   
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