Search Results for "Pregnancy"
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Searched for Pregnancy. Results 111 to 120 of 355 total matches.

Ciltacabtagene Autoleucel (Carvykti) for Multiple Myeloma (online only)

   
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022  (Issue 1663)
, such as neutropenia, anemia, and leukopenia, were common. PREGNANCY AND LACTATION — Ciltacabtagene autoleucel ...
The FDA has approved ciltacabtagene autoleucel (Carvykti – Janssen), a B-cell maturation antigen (BCMA)-directed genetically-modified cellular product, for treatment of relapsed or refractory multiple myeloma in adults who received ≥4 prior lines of therapy, including a proteasome inhibitor, an immunomodulatory drug, and an anti-CD38 monoclonal antibody. Carvykti is an individualized cellular product prepared from the patient's own T cells, which are genetically modified to express chimeric antigen receptors (CAR) and then infused back into the patient. Idecabtagene...
Med Lett Drugs Ther. 2022 Nov 14;64(1663):e188-9 |  Show IntroductionHide Introduction

In Brief: A New Indication for Dabrafenib (Tafinlar) and Trametinib (Mekinist) Combination Therapy (online only)

   
The Medical Letter on Drugs and Therapeutics • Feb 06, 2023  (Issue 1669)
does not affect CYP isoenzymes and has no clinically significant drug interactions. PREGNANCY ...
The oral kinase inhibitors dabrafenib (Tafinlar – GSK) and trametinib (Mekinist – Novartis) have received accelerated approval by the FDA for use together for a fifth indication: treatment of unresectable or metastatic solid tumors with a BRAF V600E mutation in patients ≥6 years old who have progressed following prior treatment and have no satisfactory alternative treatment options. The combination is not approved for treatment of colorectal cancer because of known intrinsic resistance to BRAF inhibition and dabrafenib is not approved for use in patients with wild-type BRAF...
Med Lett Drugs Ther. 2023 Feb 6;65(1669):e26-7   doi:10.58347/tml.2023.1669f |  Show IntroductionHide Introduction

Emrosi — Low-Dose, Biphasic Oral Minocycline for Rosacea

   
The Medical Letter on Drugs and Therapeutics • Jan 20, 2025  (Issue 1720)
. PREGNANCY AND LACTATION — Because of their adverse effects on tooth and bone development, tetracyclines ...
Emrosi (Journey), an oral, low-dose, biphasic-release formulation of the tetracycline antibiotic minocycline, has been approved by the FDA for once-daily treatment of inflammatory lesions of rosacea (papules and pustules) in adults. Low-dose, biphasic-release doxycycline (Oracea, and generics) has been available for years for treatment of papulopustular rosacea.
Med Lett Drugs Ther. 2025 Jan 20;67(1720):10-1   doi:10.58347/tml.2025.1720b |  Show IntroductionHide Introduction

Dupilumab (Dupixent) for COPD

   
The Medical Letter on Drugs and Therapeutics • Jan 20, 2025  (Issue 1720)
should be avoided in patients being treated with dupilumab. PREGNANCY AND LACTATION — Dupilumab ...
The FDA has approved the subcutaneously injected interleukin (IL)-4 receptor alpha antagonist dupilumab (Dupixent – Sanofi/Regeneron) for add-on maintenance treatment of adults with inadequately controlled chronic obstructive pulmonary disease (COPD) and an eosinophilic phenotype. Dupilumab is the first biologic drug to be approved in the US for this indication. It has been available for years for treatment of asthma, atopic dermatitis, chronic rhinosinusitis with nasal polyps, eosinophilic esophagitis, and prurigo nodularis.
Med Lett Drugs Ther. 2025 Jan 20;67(1720):11-3   doi:10.58347/tml.2025.1720c |  Show IntroductionHide Introduction

Drugs for Asthma

   
The Medical Letter on Drugs and Therapeutics • Nov 25, 2024  (Issue 1716)
and for as long as 24 hours after administration. PREGNANCY — Poorly controlled asthma symptoms and acute ...
The goal of asthma treatment is to control symptoms, prevent exacerbations, and maintain normal lung function. Management of acute exacerbations in the emergency department is not discussed here.
Med Lett Drugs Ther. 2024 Nov 25;66(1716):185-92   doi:10.58347/tml.2024.1716a |  Show IntroductionHide Introduction

Nonopioid Drugs for Pain

   
The Medical Letter on Drugs and Therapeutics • Mar 07, 2022  (Issue 1645)
) in some patients.7 Pregnancy – Occasional use of oral acetaminophen during pregnancy is generally ...
Nonopioid drugs can be used in the treatment of many nociceptive and neuropathic pain conditions. For severe pain, especially severe chronic cancer pain, use of opioids may be necessary. Noninvasive nonpharmacologic treatments, including physical and psychological therapies, have been shown to improve pain and function in patients with some common chronic pain conditions and are unlikely to cause serious harms. A multimodal approach to analgesic therapy can increase pain control while reducing opioid use and adverse effects.
Med Lett Drugs Ther. 2022 Mar 7;64(1645):33-40 |  Show IntroductionHide Introduction

FDA Authorizes Johnson & Johnson COVID-19 Vaccine

   
The Medical Letter on Drugs and Therapeutics • Mar 22, 2021  (Issue 1620)
guidance on management of anaphylaxis risk related to COVID-19 vaccination.7 PREGNANCY AND LACTATION ...
On February 27, 2021, the FDA issued an Emergency Use Authorization (EUA) for the Johnson & Johnson adenovirus-based vaccine for prevention of COVID-19 in persons ≥18 years old. It is the third COVID-19 vaccine to become available in the US and the first to require only a single dose. Two-dose mRNA-based vaccines manufactured by Pfizer-BioNTech and Moderna received EUAs in December 2020.
Med Lett Drugs Ther. 2021 Mar 22;63(1620):41-2 |  Show IntroductionHide Introduction

Vericiguat (Verquvo) for Heart Failure

   
The Medical Letter on Drugs and Therapeutics • Mar 08, 2021  (Issue 1619)
-5 (PDE5) inhibitors such as sildenafil (Viagra, and others) is not recommended. PREGNANCY ...
The FDA has approved vericiguat (Verquvo – Merck), an oral soluble guanylate cyclase (sGC) stimulator, to reduce the risk of hospitalization for heart failure and cardiovascular (CV) death following a worsening heart failure event (hospitalization for heart failure or treatment with IV diuretics as an outpatient) in patients with symptomatic chronic heart failure and left ventricular ejection fraction (LVEF) <45%. Vericiguat is the second sGC stimulator to be marketed in the US. Riociguat (Adempas), which is FDA-approved for treatment of pulmonary arterial hypertension...
Med Lett Drugs Ther. 2021 Mar 8;63(1619):36-7 |  Show IntroductionHide Introduction

Evinacumab (Evkeeza) for Homozygous Familial Hypercholesterolemia

   
The Medical Letter on Drugs and Therapeutics • May 03, 2021  (Issue 1623)
, and nausea. Anaphylaxis occurred in one patient who received the drug. PREGNANCY AND LACTATION — Evinacumab ...
The FDA has approved evinacumab-dgnb (Evkeeza – Regeneron), an angiopoietin-like 3 (ANGPTL3) inhibitor, for adjunctive IV treatment of homozygous familial hypercholesterolemia (HoFH) in patients ≥12 years old. Evinacumab is the first ANGPTL3 inhibitor to be approved in the US.
Med Lett Drugs Ther. 2021 May 3;63(1623):66-7 |  Show IntroductionHide Introduction

Comparison Table: H2-Receptor Antagonists and PPIs (online only)

   
The Medical Letter on Drugs and Therapeutics • Apr 04, 2022  (Issue 1647)
use Pregnancy: Generally safe, but no adequate human studies in pregnant women May decrease serum ...
View the Comparison Table: H2-Receptor Antagonists and PPIs
Med Lett Drugs Ther. 2022 Apr 4;64(1647):e56-7 |  Show IntroductionHide Introduction