Matching articles for "lumateperone"
Addendum: Urinary Incontinence with Second-Generation Antipsychotic Drugs
The Medical Letter on Drugs and Therapeutics • March 2, 2026; (Issue 1749)
Our recent article entitled Lumateperone (Caplyta) for Adjunctive
Treatment of Depression should have included
urinary incontinence among the adverse effects associated
with use of second-generation...
Our recent article entitled Lumateperone (Caplyta) for Adjunctive
Treatment of Depression should have included
urinary incontinence among the adverse effects associated
with use of second-generation antipsychotic drugs. Urinary
incontinence has been reported with both first- and second-generation antipsychotics. Possible causes include the
anti-alpha-adrenergic, antidopaminergic, and anticholinergic
effects of these drugs, as well as sedation. In an observational
study in 200 women 20-40 years old, urinary incontinence
was reported by 29% of those taking antipsychotic drugs and
by 13% of age-matched controls.
Lumateperone (Caplyta) for Adjunctive Treatment of Depression
The Medical Letter on Drugs and Therapeutics • February 2, 2026; (Issue 1747)
The FDA has approved the second-generation
antipsychotic drug lumateperone (Caplyta — Intra-Cellular Therapies) for adjunctive treatment of major
depressive disorder (MDD) in adults. Lumateperone
was...
The FDA has approved the second-generation
antipsychotic drug lumateperone (Caplyta — Intra-Cellular Therapies) for adjunctive treatment of major
depressive disorder (MDD) in adults. Lumateperone
was approved earlier for treatment of schizophrenia
and bipolar depression.
Iloperidone (Fanapt) — A New Indication for Bipolar Disorder
The Medical Letter on Drugs and Therapeutics • July 22, 2024; (Issue 1707)
The oral second-generation antipsychotic drug
iloperidone (Fanapt – Vanda) has been approved
by the FDA for acute treatment of manic or mixed
episodes associated with bipolar I disorder in adults.
First...
The oral second-generation antipsychotic drug
iloperidone (Fanapt – Vanda) has been approved
by the FDA for acute treatment of manic or mixed
episodes associated with bipolar I disorder in adults.
First approved in 2009 for treatment of schizophrenia,
iloperidone is the eighth second-generation antipsychotic
to be approved for acute treatment of manic
or mixed episodes of bipolar I disorder (see Table 1).
Drugs for Bipolar Disorder
The Medical Letter on Drugs and Therapeutics • April 1, 2024; (Issue 1699)
Bipolar disorder is characterized by episodes of
mania, hypomania, and depression. Recurrences of
manic or (more frequently) depressive symptoms
are common. About 15-20% of patients with bipolar
disorder...
Bipolar disorder is characterized by episodes of
mania, hypomania, and depression. Recurrences of
manic or (more frequently) depressive symptoms
are common. About 15-20% of patients with bipolar
disorder die by suicide.
Lumateperone (Caplyta) for Bipolar Depression
The Medical Letter on Drugs and Therapeutics • August 8, 2022; (Issue 1656)
The oral second-generation antipsychotic drug
lumateperone (Caplyta – Intra-Cellular Therapies),
which was approved by the FDA in 2020 for treatment
of schizophrenia, is now approved for use...
The oral second-generation antipsychotic drug
lumateperone (Caplyta – Intra-Cellular Therapies),
which was approved by the FDA in 2020 for treatment
of schizophrenia, is now approved for use as
monotherapy or as an adjunct to lithium or valproate
for treatment of depressive episodes associated with
bipolar I or II disorder in adults.
Lumateperone (Caplyta) for Schizophrenia
The Medical Letter on Drugs and Therapeutics • July 27, 2020; (Issue 1603)
The FDA has approved lumateperone (Caplyta —
Intracellular Therapies), an oral second-generation
antipsychotic, for once-daily treatment of schizophrenia
in adults. It is the 13th second-generation...
The FDA has approved lumateperone (Caplyta —
Intracellular Therapies), an oral second-generation
antipsychotic, for once-daily treatment of schizophrenia
in adults. It is the 13th second-generation antipsychotic
drug to be approved by the FDA for this indication.
