Download PDF by Joseph F. Goldberg, Carrie L. Ernst: Managing the Side Effects of Psychotropic Medications

By Joseph F. Goldberg, Carrie L. Ernst

"Managing the unwanted effects of Psychotropic medicines offers entire, pragmatic info on expecting and countering opposed drug results once they happen. Cowritten through a study psychopharmacologist and a consultation-liaison psychiatrist, this e-book fills a void within the literature, assisting psychological overall healthiness practitioners check the dangers and advantages of particular psychotropic medicinal drugs and adopt thoughts for dealing with opposed effects."

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Extra resources for Managing the Side Effects of Psychotropic Medications

Sample text

Divalproex may cause thrombocytopenia. Serum ammonia level Not routinely measured in the absence of clinical signs of hepatic encephalopathy. Divalproex can deplete carnitine. Serum lipase and amylase Not routinely measured in the absence of clinical suspicion of acute pancreatitis. Divalproex recipients who present with an acute abdomen should be evaluated for possible acute pancreatitis, a clinical assessment that includes measurement of serum lipase and amylase. The Psychiatrist as Physician TABLE 1–2.

For example, more varied and higher rates of side effects with placebo have been reported in drug trials for patients with anxiety disorders, whereas less extensive or diverse side effects from placebo are typically observed in trials for patients with schizophrenia. , dry mouth, nausea, headache, insomnia, somnolence, and sexual dysfunction) occurred at least twice as often in a randomized comparison to sertraline among patients with dysthymic disorder (Thase et al. 1996) than reported during placebo treatment in similar comparison trials for acute major depression.

Withdrawal effects of a first drug, or the reemergence of psychiatric symptoms if a new drug is less effective than the one being discontinued), for which data from controlled trials may offer little or no guidance. The Psychiatrist as Physician 27 Research trials assess adverse effects either through subjects’ spontaneous reporting or, less often, through systematic inventories of possible side effects. com), developed by the International Conference on Harmonisation (ICH) and maintained by the International Federation of Pharmaceutical Manufacturers and Associations (IFPMA).

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