Its molecular weight is The Pulvules also contain starch, gelatin, silicone, titanium dioxide, iron oxide, and other inactive ingredients. PROZAC monotherapy is not indicated for the treatment of depressive episodes associated with Bipolar I Disorder or the treatment of treatment resistant depression. Consider a dose increase after several weeks if insufficient clinical improvement is observed. As with other drugs effective in the treatment of Major Depressive Disorder, the full effect may be delayed until 4 weeks of treatment or longer. The full therapeutic effect may be delayed until 5 weeks of treatment or longer. In one of these studies, no dose-response relationship for effectiveness was demonstrated.
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Suicidality in Children and Adolescents --Antidepressants increased the risk of suicidal thinking and behavior suicidality in short-term studies in children and adolescents with major depressive disorder MDD and other psychiatric disorders. Anyone considering the use of Prozac or any other antidepressant in a child or adolescent must balance this risk with the clinical need. Patients who are started on therapy should be observed closely for clinical worsening, suicidality, or unusual changes in behavior. Families and caregivers should be advised of the need for close observation and communication with the prescriber. Pooled analyses of short-term 4 to 16 weeks placebo-controlled trials of 9 antidepressant drugs SSRIs and others in children and adolescents with major depressive disorder MDD, obsessive compulsive disorder OCD, or other psychiatric https://www.wegmans.com disorders a total of 24 trials involving over patients have revealed a greater risk of adverse events representing suicidal thinking or behavior suicidality during the first few months of treatment in those receiving antidepressants.
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In the treatment of depression, primary care providers are often faulted for failing to give an antidepressant medication at a high enough dose. What is high enough?
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