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Teal Wand — An At-Home Cervical Cancer Screening Device

   
The Medical Letter on Drugs and Therapeutics • Jul 21, 2025  (Issue 1733)
by high-risk human papillomavirus (HPV).1 The conventional Papanicolaou (Pap) test for cervical cytology ...
The FDA has authorized use of Teal Wand (Teal Health), an at-home vaginal sample self-collection device, for cervical cancer screening.
Med Lett Drugs Ther. 2025 Jul 21;67(1733):116   doi:10.58347/tml.2025.1733c |  Show IntroductionHide Introduction

Plozasiran (Redemplo) for Familial Chylomicronemia Syndrome

   
The Medical Letter on Drugs and Therapeutics • Apr 13, 2026  (Issue 1752)
-directed antisense oligonucleotide olezarsen (Tryngolza) was approved in 2024.1 FCS ― FCS is a rare ...
Plozasiran (Redemplo – Arrowhead), an apolipoprotein C-III (apoC-III)-directed small interfering ribonucleic acid (siRNA), has been approved by the FDA to reduce triglyceride levels in adults with familial chylomicronemia syndrome (FCS). It is the second drug to be approved in the US for this indication; the apoC-III-directed antisense oligonucleotide olezarsen (Tryngolza) was approved in 2024.
Med Lett Drugs Ther. 2026 Apr 13;68(1752):61-2   doi:10.58347/tml.2026.1752c |  Show IntroductionHide Introduction

The Stretta Procedure for GERD

   
The Medical Letter on Drugs and Therapeutics • Dec 04, 2006  (Issue 1249)
and prescription drugs, and sometimes surgery. 1 Emerging endoscopic anti-reflux procedures that are less ...
Standard approaches to therapy for gastroesophageal reflux disease (GERD) include lifestyle changes, over-the-counter and prescription drugs, and sometimes surgery. Emerging endoscopic anti-reflux procedures that are less invasive than surgery are potential additions to current treatment options. An endoscopicallyguided radiofrequency (RF) energy delivery system, Stretta (Curon Medical), was approved by the FDA for treatment of GERD in 2000.
Med Lett Drugs Ther. 2006 Dec 4;48(1249):99-100 |  Show IntroductionHide Introduction

Pramipexole (Mirapex) for Restless Leg Syndrome

   
The Medical Letter on Drugs and Therapeutics • Mar 26, 2007  (Issue 1257)
for RLS in 2005. 1 Both of these drugs were first approved for treatment of Parkinson’s disease ...
The dopamine agonist pramipexole (Mirapex - Boehringer Ingelheim) is the second drug approved by the FDA for treatment of moderate to severe restless legs syndrome (RLS). Ropinirole (Requip), another dopamine agonist, was approved for RLS in 2005. Both of these drugs were first approved for treatment of Parkinson's disease.
Med Lett Drugs Ther. 2007 Mar 26;49(1257):26-8 |  Show IntroductionHide Introduction

In Brief: Erenumab (Aimovig) Hypersensitivity

   
The Medical Letter on Drugs and Therapeutics • Mar 25, 2019  (Issue 1568)
of erenumabaooe (Aimovig)1, a once-monthly, subcutaneously injected calcitonin gene-related peptide (CGRP ...
The FDA has approved changes to the labeling of erenumab-aooe (Aimovig)1, a once-monthly, subcutaneously injected calcitonin gene-related peptide (CGRP) blocker approved in 2018 for prevention of migraine. The new label contains a warning about hypersensitivity reactions, including rash, angioedema, and anaphylaxis, that have been reported with post-marketing use of the drug.According to the label, most of these reactions were not serious and occurred within hours after receiving the drug, but some occurred more than one week after administration. Because these reactions are voluntarily...
Med Lett Drugs Ther. 2019 Mar 25;61(1568):48 |  Show IntroductionHide Introduction

Acesulfame - A New Artificial Sweeteners

   
The Medical Letter on Drugs and Therapeutics • Dec 16, 1988  (Issue 781)
) and aspartame (NutraSweet; Equal) (Medical Letter, 24:1, 1982). PROPERTIES — Acesulfame has some structural ...
Acesulfame potassium (Sunette - Hoechst), an oxathiazinondioxide, was recently approved by the US Food and Drug Administration (FDA) for use as a non-caloric table-top sweetener and as an ingredient in chewing gum, powdered beverages, gelatins and puddings. The other non-caloric artificial sweeteners available in the USA are saccharin (Sweet 'N Low; and others) and aspartame (NutraSweet; Equal) (Medical Letter, 24:1, 1982).
Med Lett Drugs Ther. 1988 Dec 16;30(781):116 |  Show IntroductionHide Introduction

Tiopronin for Cystinuria

   
The Medical Letter on Drugs and Therapeutics • Jan 27, 1989  (Issue 784)
is 1 gram daily; for children more than nine years old, the initial dosage is 15 mg/kg/day. The drug ...
Tiopronin (Thiola - Mission), a thiol compound (mercaptopropionyl glycine) that solubilizes cystine by reacting with it to form a mixed disulfide, is now available in the USA for treatment of refractory cystinuria.
Med Lett Drugs Ther. 1989 Jan 27;31(784):7-8 |  Show IntroductionHide Introduction

Sudden Death in children A Tricyclic Antidepressant

   
The Medical Letter on Drugs and Therapeutics • Jun 01, 1990  (Issue 819)
resulting from any error, inaccuracy or omission. Copyright  1988-2002. The Medical Letter, Inc. Phone: 1 ...
The 1990 labeling for Norpramin, the Merrell Dow brand of the tricyclic antidepressant desipramine, reports the occurrence of sudden death in an eight-year-old child treated with the drug. Desipramine is also available as Pertofrane (Rorer) and generically.
Med Lett Drugs Ther. 1990 Jun 1;32(819):53 |  Show IntroductionHide Introduction

Breathe Right Nasal Strips to Decrease Snoring

   
The Medical Letter on Drugs and Therapeutics • Oct 28, 1994  (Issue 934)
nasal dilators (CNS, Chanhassen, MN) are adhesive strips 2 or 2 ⁄ 1 2 inches long with a plastic ...
Breathe Right, an adhesive bandage device that pulls open the nostrils, has been approved by the US Food and Drug Administration and is being heavily promoted to the general public as a treatment for snoring and night-time nasal congestion. The manufacturer's suggested retail price is $4.99 for a box of 10 strips.
Med Lett Drugs Ther. 1994 Oct 28;36(934):100 |  Show IntroductionHide Introduction

Peginterferon Alfa-2b (Sylatron) for Melanoma

   
The Medical Letter on Drugs and Therapeutics • Sep 19, 2011  (Issue 1373)
different between the two groups.1 ADVERSE EFFECTS — During the clinical trial, the most common adverse ...
The FDA has approved peginterferon alfa-2b (Sylatron – Merck) for adjuvant treatment of node-positive melanoma after surgical resection. Pegylated interferon has a longer duration of action than interferon alfa-2b (Intron A), which is also FDA-approved for adjuvant treatment of malignant melanoma after surgery, and can be given once a week, compared to 3-5 times a week for standard interferon.
Med Lett Drugs Ther. 2011 Sep 19;53(1373):76 |  Show IntroductionHide Introduction