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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 IntroductionHide 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 IntroductionHide 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)...
Med Lett Drugs Ther. 2011 May 16;53(1364):40 |  Show IntroductionHide Introduction

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 IntroductionHide 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.
Med Lett Drugs Ther. 1995 Mar 17;37(944):21-3 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 1996 Dec 20;38(990):113-4 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 1998 May 22;40(1027):55-6 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 2003 Sep 29;45(1166):77-8 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 2003 Dec 8;45(1171):97-8 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 2004 Jan 5;46(1173):1-2 |  Show IntroductionHide Introduction