Search Results for "Pneumonia"
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Searched for Pneumonia. Results 91 to 100 of 169 total matches.

Remdesivir (Veklury) for COVID-19

   
The Medical Letter on Drugs and Therapeutics • Nov 30, 2020  (Issue 1612)
(pneumonia and room-air oxygen saturation >94%) were randomized to receive remdesivir for either 5 or 10 days ...
The FDA has approved the antiviral drug remdesivir (Veklury – Gilead) for IV treatment of COVID-19 in hospitalized patients who are ≥12 years old and weigh ≥40 kg. Hospitalized children who are <12 years old or weigh <40 kg can receive remdesivir through an Emergency Use Authorization (EUA). Remdesivir is the first drug to be approved in the US for treatment of COVID-19.
Med Lett Drugs Ther. 2020 Nov 30;62(1612):186-8 |  Show IntroductionHide Introduction

Cefepime/Enmetazobactam (Exblifep) for Complicated Urinary Tract Infections

   
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024  (Issue 1707)
pneumoniae, Pseudomonas aeruginosa, Proteus mirabilis, and Enterobacter cloacae. It has limited ...
The FDA has approved Exblifep (Allecra), a fixed-dose combination of the cephalosporin cefepime and the beta-lactamase inhibitor enmetazobactam, for IV treatment of adults with complicated urinary tract infections (cUTIs), including pyelonephritis, caused by designated susceptible microorganisms (see Spectrum of Activity). Exblifep is the first product that contains enmetazobactam to be approved in the US.
Med Lett Drugs Ther. 2024 Jul 22;66(1707):117-8   doi:10.58347/tml.2024.1707d |  Show IntroductionHide Introduction

Expanded Table: Some Drugs for Inflammatory Bowel Disease (online only)

   
The Medical Letter on Drugs and Therapeutics • Jul 10, 2023  (Issue 1680)
, hepatotoxicity, renal failure, interstitial pneumonia, toxic epidermal necrolysis, Stevens-Johnson syndrome ...
View the Table: Some Drugs for Inflammatory Bowel Disease
Med Lett Drugs Ther. 2023 Jul 10;65(1680):e115-9   doi:10.58347/tml.2023.1680d |  Show IntroductionHide Introduction

Table: Treatments Considered for COVID-19 (Archived) (online only)

   
The Medical Letter on Drugs and Therapeutics • Apr 06, 2020  (Issue 1595)
(decrease exposure) B Cao et al. NEJM 20209 Population: hospitalized patients w/ pneumonia, SaO2 94 ...
View the Table: Treatments Considered for COVID-19
Med Lett Drugs Ther. 2020 Apr 6;62(1595):e1-289 |  Show IntroductionHide Introduction

CRP and Statins for Primary Prevention of Coronary Artery Disease

   
The Medical Letter on Drugs and Therapeutics • Dec 15, 2008  (Issue 1301)
pneumoniae. Because CRP is stable in serum and easily measured by commercial assays, it has become the most ...
Modestly elevated C-reactive protein (CRP) concentrations have been associated with an increased risk of coronary heart disease. The recently published and heavily publicized results of the JUPITER trial will lead many patients to ask health care professionals whether they should have a CRP test to see if they should be taking a statin.
Med Lett Drugs Ther. 2008 Dec 15;50(1301):97-8 |  Show IntroductionHide Introduction

Pneumococcal Vaccination of Adults: Polysaccharide or Conjugate?

   
The Medical Letter on Drugs and Therapeutics • Jun 15, 2009  (Issue 1314)
. It has reduced the risk of invasive pneumococcal disease (meningitis or bacteremic pneumonia), but not mortality ...
A 23-valent polysaccharide vaccine (PPSV23; Pneumovax 23 - Merck) is the only pneumococcal vaccine approved for use in adults. It has reduced the risk of invasive pneumococcal disease (meningitis or bacteremic pneumonia), but not mortality, in immunocompetent older adults.2 PPSV23 has not been shown to reduce the risk of invasive pneumococcal disease (IPD) in immunocompromised patients.

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Med Lett Drugs Ther. 2009 Jun 15;51(1314):47-8 |  Show IntroductionHide Introduction

Plazomicin (Zemdri) - A New Aminoglycoside Antibiotic

   
The Medical Letter on Drugs and Therapeutics • Nov 05, 2018  (Issue 1559)
-negative bacilli including Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, and Pseudomonas ...
The FDA has approved the new aminoglycoside antibiotic plazomicin (Zemdri – Achaogen) for IV treatment of adults with complicated urinary tract infections (cUTIs). Plazomicin is active against multi-drug- resistant Enterobacteriaceae, including strains resistant to other aminoglycosides.
Med Lett Drugs Ther. 2018 Nov 5;60(1559):180-2 |  Show IntroductionHide Introduction

Iptacopan (Fabhalta) for Paroxysmal Nocturnal Hemoglobinuria (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 30, 2024  (Issue 1712)
infections and others caused by encapsulated bacteria (e.g., Streptococcus pneumoniae, Haemophilus ...
The FDA has approved the complement factor B inhibitor iptacopan (Fabhalta – Novartis) for treatment of paroxysmal nocturnal hemoglobinuria (PNH) in adults. Iptacopan is the first oral drug to be approved in the US for this indication. Three parenterally administered drugs, the complement C5 inhibitors eculizumab (Soliris) and ravulizumab (Ultomiris) and the complement C3 inhibitor pegcetacoplan (Empaveli), are also approved for treatment of PNH.
Med Lett Drugs Ther. 2024 Sep 30;66(1712):e171-3   doi:10.58347/tml.2024.1712e |  Show IntroductionHide Introduction

Cefiderocol (Fetroja) - A New IV Cephalosporin for Complicated UTI

   
The Medical Letter on Drugs and Therapeutics • May 04, 2020  (Issue 1597)
in 298 patients with nosocomial pneumonia mainly caused by carbapenem-susceptible gram-negative ...
The FDA has approved cefiderocol (Fetroja – Shionogi), a new IV cephalosporin antibiotic, for treatment of complicated urinary tract infections (UTI) caused by susceptible gram-negative bacteria in adults who have limited or no alternative treatment options.
Med Lett Drugs Ther. 2020 May 4;62(1597):65-8 |  Show IntroductionHide Introduction

Timing of Remdesivir for COVID-19

   
The Medical Letter on Drugs and Therapeutics • Oct 19, 2020  (Issue 1609)
% CI 0.52 to 1.03).2 A clinical trial in 584 patients hospitalized with moderate COVID-19 (pneumonia ...
Remdesivir (Veklury – Gilead), an investigational antiviral drug administered by IV infusion, is now available through an FDA Emergency Use Authorization (EUA) for treatment of COVID-19 in all hospitalized patients. An earlier EUA limited use of the drug to patients hospitalized with severe disease.
Med Lett Drugs Ther. 2020 Oct 19;62(1609):161 |  Show IntroductionHide Introduction