Repetitive transcranial magnetic stimulation (rTMS) is approved by the US Food and Drug Administration (FDA) for treatment resistant depression (TRD), and presumably works by modulating brain circuitry. A new meta-analysis focuses specifically on using rTMS as augmentation to antidepressants in patients with TRD.
Lisdexamfetamine (Vyvanse), a stimulant approved for treating kids and adults with ADHD, is the first drug approved by the US Food and Drug Administration (FDA) for treating adults with binge-eating disorder (BED).
Dr. Carlat has disclosed that he has no relevant relationships or financial interests in any commercial company pertaining to this educational activity.
There’s a new medication on the market for the treatment of dementia—the first to come along in several years.
Dr. Carlat has disclosed that he has no relevant relationships or financial interests in any commercial company pertaining to this educational activity.
If you’re like most psychiatrists, you get your fair share of older folks who come into the office complaining of difficulties with sleep or with significant symptoms of anxiety.
Marc Agronin, MD
Geriatric Psychiatrist
Vice President, Behavioral Health and Clinical Research
Miami Jewish Health Systems, Miami, FL
Dr. Agronin has disclosed that he is principal investigator on research grants from several pharmaceutical firms and that all funds go directly to his employer, Miami Jewish Health Systems. In addition, he has been on the speakers bureaus of Forest Laboratories (Namenda XR), AssurX (GeneSightRX), and Novartis (Exelon Patch). Dr. Carlat has reviewed the content of the interview and has determined that there is no bias due to these relationships.
Get advice on how to assess and work with patients with cognitive impairment and dementia, in an interview with Marc Agronin, MD, Geriatric Psychiatrist and Vice President of Behavioral Health and Clinical Research at Miami Jewish Health Systems.
A recent study tested an intensive weight loss program in a large group of psychiatric patients. The results were…well, read on and you decide whether they were impressive.
Daniel Carlat, MD
Editor-in-Chief, Publisher, The Carlat Report.
Dr. Carlat has disclosed that he has no relevant relationships or financial interests in any commercial company pertaining to this educational activity.
With nine other atypical antipsychotics already on the market (some of which are available as generics), did we really need another one? Given the pesky side effects of antipsychotics, maybe we did. Let’s take a look at what we know so far about Latuda (lurasidone) in an effort to figure out how to incorporate it into our clinical toolbox. Latuda was first approved by the US Food and Drug Administration (FDA) for use in schizophrenia in late 2010.