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1 dities and drug-drug interactions in case of polypharmacy.
2 specially in elderly patients and those with polypharmacy.
3 an antiretroviral regimen, increase risk for polypharmacy.
4 scontinuation than those assigned to stay on polypharmacy.
5 inuations entailed returning to the original polypharmacy.
6 tors, including age, sex, comorbidities, and polypharmacy.
7 tic demonstration of rational anticonvulsant polypharmacy.
8 h, syncope in the elderly often results from polypharmacy and abnormal physiologic responses to daily
9 hout statins, although statin users had more polypharmacy and circulatory illnesses than non-users.
10 spite the presence of greater comorbidities, polypharmacy, and altered pharmacokinetics in this age g
11 omplicated by the presence of comorbidities, polypharmacy, and concomitant functional impairment, but
12 omorbid medical illnesses, social isolation, polypharmacy, and factors associated with end-of-life ca
13 eviewing evidence-based approaches to reduce polypharmacy, and outlining the potential benefits of de
14 MCI, clinicians should consider depression, polypharmacy, and uncontrolled cardiovascular risk facto
15 extremely common, but evidence regarding all polypharmacy approaches for schizophrenia from randomize
20 were also more likely to report weight loss, polypharmacy, consumption of a special diet, and functio
22 cancer, we expect that greater attention to polypharmacy could lead to improvements in adverse drug
23 and less than 10 medications, and excessive polypharmacy (EPP) was defined as 10 or more medications
24 licensing trials, the increasing problems of polypharmacy (especially in the elderly), the lack of tr
25 iovascular perspectives with multimorbidity, polypharmacy, frailty, cognitive decline, and other clin
26 , during which drug-drug interactions due to polypharmacy further enhance the risk of adverse effects
29 at that patients should be free to return to polypharmacy if an adequate trial on antipsychotic monot
30 s Review examines the existing literature on polypharmacy in advanced cancer and end-of-life settings
34 re has been a recent significant increase in polypharmacy involving antidepressant and antipsychotic
38 Epidemiology studies have demonstrated that polypharmacy is extremely common, but evidence regarding
39 es, specifically poor compliance to lifelong polypharmacy, lifestyle modifications, and physician ine
41 19 sites) were randomly assigned to stay on polypharmacy or switch to monotherapy by discontinuing o
43 ith hospitalization were eating problems and polypharmacy (positive predictive value: 17.9%; sensitiv
44 nal dependence, organ function, comorbidity, polypharmacy, social support, cognitive and/or psychosoc
45 gents identified to date display significant polypharmacy that severely compromises interpretation of
50 h 6, 86% (N=48) of those assigned to stay on polypharmacy were still taking both medications, whereas
51 rapy for individuals receiving antipsychotic polypharmacy, with the caveat that patients should be fr
52 examine patterns and trends in psychotropic polypharmacy within nationally representative samples of
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