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Searched for rapid. Results 11 to 20 of 109 total matches.
Table: Over the Counter At-Home Tests for COVID-19 (online only)
The Medical Letter on Drugs and Therapeutics • Oct 20, 2021 (Issue 5041)
test Symptomatic: 94%/98% Yes No N/A
Rapid Test (iHealth) (symptomatic) or Asymptomatic: 85-88%/N.D ...
View the Table: Over the Counter At-Home Tests for COVID-19
Med Lett Drugs Ther. 2021 Oct 20;63(5041):e1 doi:10.58347/tml.2021.5041a | Show Introduction Hide Introduction
Ophthalmic Phentolamine (Ryzumvi) for Drug-Induced Mydriasis
The Medical Letter on Drugs and Therapeutics • Jun 24, 2024 (Issue 1705)
. It
may be helpful for patients who need a more rapid
return to normal vision after dilation.
The Medical Letter ...
The FDA has approved a 0.75% ophthalmic solution
of the alpha-adrenergic antagonist phentolamine
(Ryzumvi – Viatris) for treatment of mydriasis produced
by adrenergic agonists such as phenylephrine
or parasympatholytic agents such as tropicamide in
patients ≥3 years old. Ryzumvi is the first drug to be
approved in the US for reversal of pharmacologically
induced mydriasis.
Med Lett Drugs Ther. 2024 Jun 24;66(1705):100-1 doi:10.58347/tml.2024.1705c | Show Introduction Hide Introduction
In Brief: Kirsty — An Insulin Aspart Interchangeable with NovoLog
The Medical Letter on Drugs and Therapeutics • Sep 08, 2025 (Issue 5120)
), a biosimilar
to rapid-acting insulin aspart (NovoLog), for treatment
of type 1 or type 2 diabetes. Kirsty ...
The FDA has approved Kirsty (Biocon), a biosimilar
to rapid-acting insulin aspart (NovoLog), for treatment
of type 1 or type 2 diabetes. Kirsty is the
first rapid-acting insulin to become available in
the US that has received interchangeability status
with NovoLog; Merilog, another insulin aspart
biosimilar, was approved earlier but has not received
interchangeability status with NovoLog.
Med Lett Drugs Ther. 2025 Sep 8;67(5120):1-2 doi:10.58347/tml.2025.5120a | Show Introduction Hide Introduction
Vazalore - A New Aspirin Formulation
The Medical Letter on Drugs and Therapeutics • May 02, 2022 (Issue 1649)
in immediaterelease,
buffered, and enteric-coated formulations.
Immediate-release aspirin is rapidly absorbed ...
The FDA has approved an over-the-counter (OTC)
liquid-filled capsule formulation of aspirin (Vazalore –
PLx Pharma). The manufacturer has been heavily
promoting Vazalore with claims of fast, predictable
absorption and antiplatelet activity and improved
gastrointestinal safety compared to existing OTC
aspirin formulations.
Benzgalantamine (Zunveyl) for Alzheimer's Disease
The Medical Letter on Drugs and Therapeutics • Apr 14, 2025 (Issue 1726)
,
headache, and decreased appetite are common with rapid dose
escalation of galantamine. Depression, fatigue ...
The FDA has approved Zunveyl (Alpha Cognition),
a delayed-release formulation of the prodrug
benzgalantamine, for treatment of mild to moderate
dementia of Alzheimer's disease (AD). Immediate- and
extended-release formulations of the acetylcholinesterase
inhibitor galantamine have been
available in the US for years for treatment of AD.
Med Lett Drugs Ther. 2025 Apr 14;67(1726):59-60 doi:10.58347/tml.2025.1726b | Show Introduction Hide Introduction
Comparison Chart: Some Inhaled Drugs for Treatment of Asthma (online only)
The Medical Letter on Drugs and Therapeutics • Nov 25, 2024 (Issue 1716)
to perform rapid, deep
inhalation
▶ Doses may be wasted if Ellipta inhaler is
opened/closed accidently ...
View the Comparison Chart: Some Inhaled Drugs for Treatment of Asthma
Med Lett Drugs Ther. 2024 Nov 25;66(1716):e192-5 doi:10.58347/tml.2024.1716b | Show Introduction Hide Introduction
A Fixed-Dose Combination of Meloxicam and Rizatriptan (Symbravo) for Migraine
The Medical Letter on Drugs and Therapeutics • Apr 28, 2025 (Issue 1727)
.
PHARMACOKINETICS — The meloxicam component in
Symbravo is absorbed more rapidly than conventional
oral meloxicam ...
The FDA has approved Symbravo (Axsome), an oral
fixed-dose combination of the nonsteroidal anti-inflammatory
drug (NSAID) meloxicam and the
5-HT1B/1D receptor agonist (triptan) rizatriptan (Maxalt,
and generics), for acute treatment of migraine with or
without aura in adults. It is the second combination
of an NSAID and a triptan to be approved for migraine
treatment. An oral fixed-dose combination of
sumatriptan and naproxen (Treximet, and generics) is
approved for use in patients ≥12 years old.
Med Lett Drugs Ther. 2025 Apr 28;67(1727):68-70 doi:10.58347/tml.2025.1727b | Show Introduction Hide Introduction
Treatment of Common Respiratory Tract Infections
The Medical Letter on Drugs and Therapeutics • Apr 17, 2023 (Issue 1674)
Diagnosis – GAS pharyngitis should be diagnosed
by nucleic acid amplification test or rapid antigen ...
Most respiratory tract infections are caused by
viruses. Bacterial respiratory tract infections are
usually treated empirically with antibiotic therapy
that targets the most probable causative pathogens.
Recommended antibiotic regimens for outpatient
treatment of some common respiratory tract
infections are listed in Table 1 for adults and Table 2
for children.
Med Lett Drugs Ther. 2023 Apr 17;65(1674):57-62 doi:10.58347/tml.2023.1674a | Show Introduction Hide Introduction
In Brief: Furoscix - A Subcutaneous Furosemide Infusor for Heart Failure
The Medical Letter on Drugs and Therapeutics • Jan 23, 2023 (Issue 1668)
of loop diuretics is often used to
achieve rapid diuresis in acute decompensation or
to overcome ...
The FDA has approved Furoscix (scPharmaceuticals),
a subcutaneous formulation of the loop diuretic
furosemide administered via a single-use, on-body
infusor, for treatment of congestion due to fluid
overload in adults with New York Heart Association
(NYHA) Class II-III chronic heart failure (HF).
Furosemide (Lasix, and generics) has been available
for years in oral and IV formulations.
Med Lett Drugs Ther. 2023 Jan 23;65(1668):14-5 doi:10.58347/tml.2023.1668d | Show Introduction Hide Introduction
COVID-19 Update: Tocilizumab (Actemra) FDA-Approved for Treatment of COVID-19 (online only)
The Medical Letter on Drugs and Therapeutics • Jan 09, 2023 (Issue 1667)
dexamethasone and
have rapidly increasing conventional oxygen needs
and systemic inflammation. Dexamethasone ...
The interleukin-6 (IL-6) receptor antagonist
tocilizumab (Actemra – Genentech) has been
approved by the FDA for IV treatment of COVID-19
in hospitalized adults who are receiving a systemic
corticosteroid and require supplemental oxygen,
mechanical ventilation, or extracorporeal membrane
oxygenation (ECMO). Tocilizumab was previously
available for this indication under an Emergency
Use Authorization (EUA); it remains available under
an EUA for treatment of children 2-17 years old
who are hospitalized with COVID-19 and require
oxygen support.
Med Lett Drugs Ther. 2023 Jan 9;65(1667):e9 doi:10.58347/tml.2023.1667d | Show Introduction Hide Introduction