Search Results for "Immunizations"
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Searched for Immunizations. Results 271 to 280 of 414 total matches.

Zinc for the Common Cold

   
The Medical Letter on Drugs and Therapeutics • Jan 31, 1997  (Issue 993)
, Antimicrob Agents Chemother, 31:622, 1987). Whether taking zinc has any effect on the immune response ...
Results of a recent study suggested that zinc gluconate may be effective in treating the common cold (SB Mossad et al, Ann Intern Med, 125:81, July 15, 1996). Zinc gluconate lozenges, sometimes combined with vitamin C or other ingredients, are available in pharmacies and health food stores throughout the USA.
Med Lett Drugs Ther. 1997 Jan 31;39(993):9-10 |  Show IntroductionHide Introduction

Glatiramer Acetate for Relapsing Multiple Sclerosis

   
The Medical Letter on Drugs and Therapeutics • Jul 04, 1997  (Issue 1004)
is unknown, but the drug has several immune-modulating actions, including inhibition of binding of myelin ...
Glatiramer acetate (Copaxone - Teva Marion Partners), formerly known as copolymer-l, has been approved by the US Food and Drug Administration (FDA) for treatment of relapsing-remitting multiple sclerosis (MS). Interferon β-1b (Betaseron) and interferon β-1a (Avonex - Medical Letter, 38:63, 1996) were previously approved for this indication.
Med Lett Drugs Ther. 1997 Jul 4;39(1004):61-2 |  Show IntroductionHide Introduction

A New Scorpion Antivenom

   
The Medical Letter on Drugs and Therapeutics • Jun 25, 2012  (Issue 1393)
are used to immunize the horses; after extraction, digestion, fractionation and purification, the product ...
Anascorp (Rare Disease Therapeutics), an intravenously administered antivenom derived from horse serum, has been approved by the FDA for treatment of clinical signs of scorpion envenomation.
Med Lett Drugs Ther. 2012 Jun 25;54(1393):51-2 |  Show IntroductionHide Introduction

Probiotics Revisited

   
The Medical Letter on Drugs and Therapeutics • Jan 07, 2013  (Issue 1407)
an immune response. SOURCES — Probiotics can be found in various foods and dietary supplements. Yogurt ...
Probiotics are live, nonpathogenic microorganisms (usually bacteria or yeasts) marketed as dietary supplements. They have not been approved by the FDA for any indication. Since our last article on this subject, some new data have become available.
Med Lett Drugs Ther. 2013 Jan 7;55(1407):3-4 |  Show IntroductionHide Introduction

Omidubicel (Omisirge) for Neutrophil Recovery Following Myeloablative Conditioning Therapy (online only)

   
The Medical Letter on Drugs and Therapeutics • May 29, 2023  (Issue 1677)
occur with cord blood products. 1. C de Koning et al. Lymphoid and myeloid immune cell reconstitution ...
The FDA has approved omidubicel-onlv (Omisirge – Gamida Cell), a nicotinamide-modified, allogeneic hematopoietic progenitor cell therapy derived from cord blood, to reduce the time to neutrophil recovery and the risk of infection in patients ≥12 years old with hematologic malignancies who will undergo umbilical cord blood transplantation following myeloablative conditioning therapy. Hematopoietic progenitor cell (HPC) umbilical cord products (e.g., Allocord, Clevecord, Ducord) have been available in the US for years for the same indication. Cord blood banks also supply cord...
Med Lett Drugs Ther. 2023 May 29;65(1677):e93-4   doi:10.58347/tml.2023.1677h |  Show IntroductionHide Introduction

In Brief: A New OTC Naloxone Nasal Spray (RiVive)

   
The Medical Letter on Drugs and Therapeutics • Mar 18, 2024  (Issue 1698)
states, these laws grant both civil and criminal immunity to laypersons who administer the drug.3 ...
The FDA has approved RiVive (Harm Reduction Therapeutics), a 3-mg naloxone nasal spray, as an over-the-counter (OTC) product for emergency treatment of opioid overdose. Two 4-mg naloxone nasal spray formulations, Narcan and one of its generics, were approved for OTC sale in 2023.
Med Lett Drugs Ther. 2024 Mar 18;66(1698):47-8   doi:10.58347/tml.2024.1698d |  Show IntroductionHide Introduction

Odefsey - Another NNRTI Combination for HIV

   
The Medical Letter on Drugs and Therapeutics • May 09, 2016  (Issue 1494)
of emtricitabine/TAF (taken with elvitegravir and cobicistat) was nausea (10%). Immune reconstitution syndrome ...
The FDA has approved Odefsey (Gilead), a once-daily, fixed-dose combination of the non-nucleoside reverse transcriptase inhibitor (NNRTI) rilpivirine and the nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) emtricitabine and tenofovir alafenamide, for initial treatment of HIV-1 infection in patients with HIV-1 RNA (viral load) ≤100,000 copies/mL or to replace a stable antiretroviral regimen in patients who have been virologically suppressed (viral load <50 copies/mL) for at least six months with no history of treatment failure.
Med Lett Drugs Ther. 2016 May 9;58(1494):60-1 |  Show IntroductionHide Introduction

Tenofovir Alafenamide (Vemlidy) for Hepatitis B

   
The Medical Letter on Drugs and Therapeutics • Jan 02, 2017  (Issue 1511)
with immune-active chronic HBV infection. 4. Dosage for nucleoside/nucleotide analog-naive patients ...
The FDA has approved tenofovir alafenamide (Vemlidy – Gilead) for treatment of chronic hepatitis B virus (HBV) infection in adults with compensated liver disease. It is the first single-drug product containing tenofovir alafenamide (TAF), a prodrug of the nucleotide reverse transcriptase inhibitor tenofovir, to become available; several combination products containing TAF are approved for treatment of HIV-1 infection. Tenofovir disoproxil fumarate (TDF; Viread – Gilead), another tenofovir prodrug, has been used for many years for treatment of chronic HBV infection; a generic...
Med Lett Drugs Ther. 2017 Jan 2;59(1511):6-8 |  Show IntroductionHide Introduction

Cladribine (Mavenclad) for Multiple Sclerosis

   
The Medical Letter on Drugs and Therapeutics • Jul 29, 2019  (Issue 1577)
(patients who are antibodynegative should receive a varicella-zoster virus vaccine), standard age ...
The FDA has approved cladribine (Mavenclad – EMD Serono), a purine antimetabolite, for oral treatment of adults with relapsing forms of multiple sclerosis (MS), including relapsing-remitting disease and active secondary progressive MS (SPMS), who cannot tolerate or have had an inadequate response to other drugs indicated for treatment of MS. It is not recommended for use in patients with clinically isolated syndrome (CIS). IV cladribine, which is FDA-approved for treatment of hairy cell leukemia, has been used off-label for treatment of MS.
Med Lett Drugs Ther. 2019 Jul 29;61(1577):118-20 |  Show IntroductionHide Introduction

Upadacitinib (Rinvoq): A Second JAK Inhibitor for Ulcerative Colitis

   
The Medical Letter on Drugs and Therapeutics • Sep 05, 2022  (Issue 1658)
in immune responses and inflammation. Upadacitinib is a more potent inhibitor of JAK1 and JAK2 than ...
The FDA has approved the oral Janus kinase (JAK) inhibitor upadacitinib (Rinvoq – Abbvie) for treatment of moderately to severely active ulcerative colitis in adults who have had an inadequate response to or cannot tolerate one or more tumor necrosis factor (TNF) inhibitors. Upadacitinib is the second JAK inhibitor to be approved for this indication; tofacitinib (Xeljanz) was the first. Upadacitinib is also approved for treatment of rheumatoid arthritis, psoriatic arthritis, atopic dermatitis, and ankylosing spondylitis.
Med Lett Drugs Ther. 2022 Sep 5;64(1658):142-4 |  Show IntroductionHide Introduction