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.
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.
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.
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.
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 Introduction Hide 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 Introduction Hide 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.
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...
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.
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.