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Drugs for Chronic Insomnia
The Medical Letter on Drugs and Therapeutics • Jan 09, 2023 (Issue 1667)
.
Pregnancy and Lactation – No adequate data on
use of orexin receptor antagonists in pregnant ...
Cognitive behavioral therapy for insomnia (CBT-I) is
recommended for initial treatment of chronic insomnia.
CBT-I includes stimulus control, sleep education
and hygiene, sleep restriction, relaxation training, and
cognitive therapy. When CBT-I alone is not effective,
pharmacologic treatment should be added.
Med Lett Drugs Ther. 2023 Jan 9;65(1667):1-6 doi:10.58347/tml.2023.1667a | Show Introduction Hide Introduction
Antiviral Drugs for Seasonal Influenza for 2024-2025
The Medical Letter on Drugs and Therapeutics • Dec 09, 2024 (Issue 1717)
,
and death.20-22
No data are available on the efficacy of baloxavir
started >48 hours after illness onset ...
Influenza is generally a self-limited illness, but
pneumonia, respiratory failure, and death can occur,
especially in persons at increased risk for influenza
complications (see Table 1). Updated information on
influenza activity and antiviral resistance is available
from the CDC at cdc.gov/flu.
Med Lett Drugs Ther. 2024 Dec 9;66(1717):193-8 doi:10.58347/tml.2024.1717a | Show Introduction Hide Introduction
In Brief: Fentanyl Sublingual Tablets (Abstral) for Breakthrough Cancer Pain
The Medical Letter on Drugs and Therapeutics • May 16, 2011 (Issue 1364)
(March 31, 2011) data from retail
pharmacies nationwide available from Wolters Kluwer Health ...
The FDA has approved the marketing of fentanyl sublingual tablets (Abstral – ProStrakan) for treatment of breakthrough pain in adult cancer patients who are already receiving and are tolerant to opioid therapy. It is the fourth transmucosal formulation of fentanyl to become available in the US for this indication.1-3The manufacturer recommends an initial dose of 100 mcg, a maximum of 2 doses per breakthrough pain episode, and use for no more than 4 breakthrough pain episodes per day. As with all formulations of fentanyl, strong inhibitors of CYP3A4 such as clarithromycin (Biaxin, and others)...
COVID-19 Update: mRNA COVID-19 Vaccines and Myocarditis
The Medical Letter on Drugs and Therapeutics • Jun 04, 2025 (Issue 5110)
vaccination.
Based on health insurance claims data, the estimated
incidence of myocarditis ...
The FDA has required the manufacturers of the mRNA
COVID-19 vaccines Comirnaty (Pfizer-BioNTech)
and Spikevax (Moderna) to revise their labels to
include updated information about the risks of
myocarditis/pericarditis. The FDA requested that
the manufacturers submit the proposed labeling
changes or contest the agency's requirement for the
safety update by May 17, 2025. As of June 4th, to our
knowledge, the labels of Comirnaty and Spikevax
have not been updated and neither manufacturer has
submitted a rebuttal.
Med Lett Drugs Ther. 2025 Jun 4;67(5110):1 doi:10.58347/tml.2025.5110a | Show Introduction Hide Introduction
Lamotrigine For Epilepsy
The Medical Letter on Drugs and Therapeutics • Mar 17, 1995 (Issue 944)
of lamotrigine would probably be even lower, but no data are available.
The Medical Letter, Vol. 37 (Issue 944 ...
Lamotrigine (la mo tri jeen; Lamictal - Burroughs Wellcome), a phenyltriazine derivative, has been approved by the US Food and Drug Administration for use in addition to other antiepileptic drugs in adults with partial seizures. Since this diagnostic category includes the largest number of patients with intractable epilepsy, new drugs with antiepileptic activity are usually tried first for this indication. Lamotrigine was first marketed abroad in 1990 and is now available in more than 50 other countries.
Mirtazapine - A New Antidepressant
The Medical Letter on Drugs and Therapeutics • Dec 20, 1996 (Issue 990)
effects on sedation and on cognitive and motor impairment. No data are available to evaluate ...
Mirtazapine (mir taz a peen; Remeron - Organon) has been approved by the US Food and Drug Administration for treatment of depression. A tetracyclic piperazinoazepine, it is an analog of mianserin, an antidepressant available in Europe, but is structurally unrelated to antidepressants previously available in the USA.
Repaglinide for Type 2 Diabetes Mellitus
The Medical Letter on Drugs and Therapeutics • May 22, 1998 (Issue 1027)
with metformin than either drug alone (R Moses et
al, Diabetologia, 40 suppl 1:A322, 1997). Unpublished data ...
Repaglinide (Prandin - Novo Nordisk) is a new oral glucose-lowering agent for treating type 2 diabetes (formerly called non-insulin-dependent diabetes mellitus or NIDDM). It has been approved by the FDA for monotherapy or for use in combination with metformin.
Vardenafil (Levitra) for Erectile Dysfunction
The Medical Letter on Drugs and Therapeutics • Sep 29, 2003 (Issue 1166)
of erections (50-67% vs. 32%). No data were presented on the time to onset of
action (WJ Hellstrom et al ...
Vardenafil (Levitra -Bayer) is the second oral drug approved by the FDA for treatment of erectile dysfunction. Sildenafil (Viagra - Medical Letter 1998; 40:51), the first oral drug, has been available for 5 years. Pharmacokinetics, effectiveness, adverse effects, dosage and cost of the new drug are reviewed. Whether it offers any benefits over sildenafil is discussed.
Efalizumab (Raptiva) for Treatment of Psoriasis
The Medical Letter on Drugs and Therapeutics • Dec 08, 2003 (Issue 1171)
208).
No data are available comparing efalizumab directly with either alefacept or the TNF-α ...
Efalizumab (Raptiva - Genentech/XOMA), a humanized monoclonal antibody that inhibits T-cell activation, has been approved by the FDA for treatment of adults with moderate to severe chronic plaque psoriasis.
Alfuzosin (Uroxatral) -- Another Alpha1-blocker for Benign Prostatic Hyperplasia
The Medical Letter on Drugs and Therapeutics • Jan 05, 2004 (Issue 1173)
. Cost for 30 days’ treatment with the maintenance dosage, according to data from retail pharmacies ...
Alfuzosin hydrochloride (Uroxatral - Sanofi-Synthelabo) is now available in the US in a new formulation for once-daily treatment of benign prostatic hyperplasia (BPH). The drug has been used in Europe since 1987. Alpha1-blockers cause relaxation of smooth muscle tone in the bladder neck, prostatic capsule and prostatic urethra, relieving symptoms of urinary obstruction.