Search Results for "days"
Search again or select article below to purchase. Single article price: $45. Order 3 or more at one time and receive a 10% discount.
Sort by relevance | Sort by date
Searched for days. Results 481 to 486 of 486 total matches.
Risks of Tramadol and Gabapentin Use for Pain
The Medical Letter on Drugs and Therapeutics • Feb 02, 2026 (Issue 1747)
was associated with an increased risk of
dementia; the risk was highest with >90 days of use.5
In a recently ...
Tramadol (Ultram, and others) and gabapentin
(Neurontin, and others) are increasingly being
prescribed for treatment of chronic pain despite reports
of serious adverse events associated with their use.
Both drugs are touted as safer and less addictive than
strong opioids, but supporting evidence is lacking.
Med Lett Drugs Ther. 2026 Feb 2;68(1747):22-4 doi:10.58347/tml.2026.1747d | Show Introduction Hide Introduction
Booster Dose of the Pfizer/BioNTech COVID-19 Vaccine (Comirnaty)
The Medical Letter on Drugs and Therapeutics • Oct 18, 2021 (Issue 1635)
-CoV-2
infection (by 11.3-fold) and severe COVID-19 (by 19.5-
fold) beginning 12 days after ...
On September 22, on the advice of its Vaccines and
Related Biologic Products Advisory Committee, the
FDA expanded the Emergency Use Authorization
(EUA) for the Pfizer/BioNTech mRNA-based COVID-19
vaccine (Comirnaty) to include administration of a
booster dose ≥6 months after a 2-dose primary series
in adults who are ≥65 years old or at high risk for severe
COVID-19 because of an underlying medical condition
or frequent institutional or occupational exposure
to SARS-CoV-2 (see Table 1). The FDA Advisory
Committee recommended against authorization of a
booster dose of Comirnaty...
Ublituximab (Briumvi) for Relapsing Multiple Sclerosis
The Medical Letter on Drugs and Therapeutics • Mar 06, 2023 (Issue 1671)
Metabolism Proteolysis
Half-life 22 days
STANDARD TREATMENT ― Patients with highly-active
relapsing MS ...
The FDA has approved the recombinant chimeric
anti-CD20 antibody ublituximab-xiiy (Briumvi – TG Therapeutics) for IV treatment of adults with
relapsing forms of multiple sclerosis (MS), including
clinically isolated syndrome (initial neurological
episode), relapsing-remitting disease, and active
secondary progressive MS (SPMS). Two other anti-CD20 antibodies, IV ocrelizumab (Ocrevus) and SC
ofatumumab (Kesimpta), are also FDA-approved for
these indications.
Med Lett Drugs Ther. 2023 Mar 6;65(1671):36-8 doi:10.58347/tml.2023.1671c | Show Introduction Hide Introduction
Depemokimab (Exdensur) for Severe Eosinophilic Asthma
The Medical Letter on Drugs and Therapeutics • Mar 16, 2026 (Issue 1750)
pens and syringes
Route Subcutaneous
Metabolism Degradation by proteolytic enzymes
Half-life 48 days ...
The FDA has approved depemokimab (Exdensur –
GSK), a long-acting interleukin-5 (IL-5) antagonist,
for add-on maintenance treatment of severe asthma
characterized by an eosinophilic phenotype in
patients ≥12 years old. Depemokimab is the fourth
IL-5-directed treatment to be approved in the US for
this indication; the IL-5 antagonists mepolizumab
(Nucala) and reslizumab (Cinqair) and the IL-5
receptor alpha antagonist benralizumab (Fasenra)
were approved earlier.
Med Lett Drugs Ther. 2026 Mar 16;68(1750):44-6 doi:10.58347/tml.2026.1750b | Show Introduction Hide Introduction
Risankizumab (Skyrizi) - An IL-23 Antagonist for Crohn's Disease
The Medical Letter on Drugs and Therapeutics • Dec 26, 2022 (Issue 1666)
days (in patients with Crohn’s disease)
Table 2. Risankizumab Clinical Trial Results
Clinical ...
The injectable interleukin (IL)-23 antagonist
risankizumab-rzaa (Skyrizi – Abbvie) has been
approved by the FDA for treatment of moderately
to severely active Crohn's disease (CD) in adults.
Risankizumab was approved earlier for treatment of
plaque psoriasis and psoriatic arthritis.
Drugs for Open-Angle Glaucoma
The Medical Letter on Drugs and Therapeutics • Apr 28, 2025 (Issue 1727)
/day 183.50
Istalol (Bausch + Lomb) 0.5% soln* 2.5, 5 mL 1 drop qAM 208.40
Carbonic Anhydrase ...
Glaucoma is a progressive optic neuropathy
associated with increased intraocular pressure
(IOP; normal range 8-22 mm Hg), which is the only
disease-related factor that can be modified. Topical
drugs that lower IOP are the first line of treatment for
open-angle glaucoma.
Med Lett Drugs Ther. 2025 Apr 28;67(1727):65-8 doi:10.58347/tml.2025.1727a | Show Introduction Hide Introduction
