Search Results for "anaphylaxis"
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Searched for anaphylaxis. Results 21 to 30 of 61 total matches.

Dupilumab (Dupixent) for Eosinophilic Esophagitis and Prurigo Nodularis

   
The Medical Letter on Drugs and Therapeutics • Feb 06, 2023  (Issue 1669)
reactions and infections are common. Anaphylaxis has been reported. Dosage: 300 mg SC once/week for EoE ...
The FDA has approved the subcutaneously injected interleukin (IL)-4 receptor alpha antagonist dupilumab (Dupixent – Sanofi/Regeneron) for treatment of eosinophilic esophagitis (EoE) in patients ≥12 years old who weigh ≥40 kg and treatment of prurigo nodularis in adults. Dupilumab is the first drug to be approved in the US for each of these indications. It is also FDA-approved for treatment of atopic dermatitis, asthma, and chronic rhinosinusitis with nasal polyposis.
Med Lett Drugs Ther. 2023 Feb 6;65(1669):18-20   doi:10.58347/tml.2023.1669b |  Show IntroductionHide Introduction

In Brief: Azmiro — A Single-Dose Injectable Formulation of Testosterone Cypionate

   
The Medical Letter on Drugs and Therapeutics • Mar 17, 2025  (Issue 1724)
of the risk of serious pulmonary oil microembolism reactions and anaphylaxis. The FDA has approved Azmiro ...
The FDA has approved Azmiro (Azurity), the first injectable formulation of testosterone cypionate to become available in single-dose vials and prefilled syringes for treatment of males with conditions associated with a deficiency or absence of endogenous testosterone. Injectable testosterone cypionate has been available in multidose vials (Depo-Testosterone, and generics) for many years. Testosterone enanthate (Xyosted) is available in prefilled autoinjectors for use in adult men. No testosterone products are approved for treatment of low testosterone levels due solely to aging. All...
Med Lett Drugs Ther. 2025 Mar 17;67(1724):44-5   doi:10.58347/tml.2025.1724b |  Show IntroductionHide Introduction

Baloxavir (Xofluza) for Post-Exposure Prophylaxis of Influenza

   
The Medical Letter on Drugs and Therapeutics • Jan 11, 2021  (Issue 1615)
, including anaphylaxis. Neuropsychiatric events have also been reported, but a causal relationship ...
The oral polymerase acidic endonuclease inhibitor baloxavir marboxil (Xofluza — Genentech) is now FDAapproved for post-exposure prophylaxis of influenza in patients ≥12 years old. Baloxavir was approved for treatment of acute uncomplicated influenza in patients ≥12 years old in 2018.1 Two neuraminidase inhibitors are FDA-approved for prophylaxis of influenza: oseltamivir (Tamiflu, and generics) in patients ≥1 year old, and zanamivir (Relenza) in patients ≥5 years old.2 Unlike oseltamivir and zanamivir, baloxavir is not FDA-approved for pre-exposure prophylaxis of...
Med Lett Drugs Ther. 2021 Jan 11;63(1615):2-3 |  Show IntroductionHide Introduction

Betibeglogene Autotemcel (Zynteglo) for Beta Thalassemia (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 30, 2024  (Issue 1712)
, which can cause hypersensitivity reactions, including anaphylaxis. DRUG INTERACTIONS — HIV ...
Betibeglogene autotemcel (Zynteglo — Bluebird Bio), an autologous lentiviral vector cell-based gene therapy, has been approved by the FDA for one-time treatment of transfusion-dependent beta thalassemia in children and adults. Exagamglogene autotemcel (Casgevy), a cell-based gene therapy that uses CRISPR/Cas9 gene-editing technology, was approved earlier this year for the same indication in patients ≥12 years old.
Med Lett Drugs Ther. 2024 Sep 30;66(1712):e167-8   doi:10.58347/tml.2024.1712c |  Show IntroductionHide Introduction

Imetelstat (Rytelo) for Myelodysplastic Syndromes (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 30, 2024  (Issue 1712)
. Zynteglo contains dimethyl sulfoxide, which can cause hypersensitivity reactions, including anaphylaxis ...
The FDA has approved imetelstat (Rytelo – Geron), a first-in-class telomerase inhibitor, for treatment of low- to intermediate-1 risk myelodysplastic syndromes (MDS) in adults with transfusion-dependent anemia requiring 4 or more red blood cell (RBC) units over 8 weeks who have not responded to, are no longer responding to, or are ineligible for erythropoiesis-stimulating agents (ESAs).
Med Lett Drugs Ther. 2024 Sep 30;66(1712):e169-70   doi:10.58347/tml.2024.1712d |  Show IntroductionHide Introduction

Drugs for Asthma

   
The Medical Letter on Drugs and Therapeutics • Nov 25, 2024  (Issue 1716)
of anaphylaxis. Omalizumab should generally be administered by healthcare providers who are prepared to manage ...
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

Casirivimab and Imdevimab (REGEN-COV) for Post-Exposure Prophylaxis of COVID-19

   
The Medical Letter on Drugs and Therapeutics • Aug 23, 2021  (Issue 1631)
) variant.2 ADVERSE EFFECTS — Infusion- and injection-related reactions and anaphylaxis have been reported ...
The investigational monoclonal antibodies casirivimab and imdevimab (REGEN-COV – Regeneron) have been available in the US under an Emergency Use Authorization (EUA) since late 2020 for use together to treat mild to moderate COVID-19 in persons ≥12 years old who weigh ≥40 kg and are at high risk of progression to severe disease or hospitalization. The FDA has now expanded this EUA to allow use of the antibodies together for post-exposure prophylaxis of COVID-19 in such persons, if they are not fully vaccinated against COVID-19 or are unlikely to have an adequate immune response...
Med Lett Drugs Ther. 2021 Aug 23;63(1631):130-1 |  Show IntroductionHide Introduction

Expanded Table: Some Conventional DMARDs for Rheumatoid Arthritis (online only)

   
The Medical Letter on Drugs and Therapeutics • Nov 15, 2021  (Issue 1637)
loss, rash, myelosuppression, and aminotransferase elevations Anaphylaxis, Stevens-Johnson syndrome ...
View Expanded Table: Some Conventional DMARDs for Rheumatoid Arthritis
Med Lett Drugs Ther. 2021 Nov 15;63(1637):e185-6 |  Show IntroductionHide Introduction

Epsolay - A Benzoyl Peroxide Cream for Rosacea

   
The Medical Letter on Drugs and Therapeutics • Feb 06, 2023  (Issue 1669)
. The Medical Letter ® Vol. 65 (1669) February 6, 2023 22 Hypersensitivity reactions, including anaphylaxis ...
Epsolay (Galderma), a 5% benzoyl peroxide cream, has been approved by the FDA for treatment of inflammatory lesions of rosacea in adults. It is the first product containing benzoyl peroxide to be approved in the US for treatment of rosacea. Benzoyl peroxide formulations approved for acne have been used off-label to treat rosacea for years, but itching and burning have limited their use.
Med Lett Drugs Ther. 2023 Feb 6;65(1669):21-2   doi:10.58347/tml.2023.1669c |  Show IntroductionHide Introduction

Anifrolumab (Saphnelo) for Systemic Lupus Erythematosus

   
The Medical Letter on Drugs and Therapeutics • Sep 20, 2021  (Issue 1633)
%), and cough (5%) were reported with use of anifrolumab in the pivotal trials. Anaphylaxis and serious ...
The FDA has approved anifrolumab-fnia (Saphnelo – AstraZeneca), a type I interferon receptor antagonist, for IV treatment of adults with moderate to severe systemic lupus erythematosus (SLE) who are receiving standard treatment. Anifrolumab has not been studied in patients with severe active lupus nephritis or severe active CNS lupus. It is the first type I interferon receptor antagonist to become available in the US.
Med Lett Drugs Ther. 2021 Sep 20;63(1633):146-7 |  Show IntroductionHide Introduction