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Searched for blue light. Results 1 to 6 of 6 total matches.
See also: Clearlight
A Dexamethasone Ophthalmic Insert (Dextenza) for Allergic Conjunctivitis
The Medical Letter on Drugs and Therapeutics • Mar 20, 2023 (Issue 1672)
of a polyethylene glycol (PEG)-based hydrogel
conjugated with fluorescein, which makes it visible
under blue light ...
The FDA has approved Dextenza (Ocular Therapeutix),
a dexamethasone ophthalmic insert, for
treatment of ocular itching associated with allergic
conjunctivitis. Dextenza was approved earlier for
treatment of ocular inflammation and pain following
ophthalmic surgery.
Med Lett Drugs Ther. 2023 Mar 20;65(1672):45-6 doi:10.58347/tml.2023.1672b | Show Introduction Hide Introduction
Tirbanibulin 1% Ointment (Klisyri) for Actinic Keratosis
The Medical Letter on Drugs and Therapeutics • May 03, 2021 (Issue 1623)
of
the photosensitizer aminolevulinic acid (Levulan
Kerastick) and blue light phototherapy (BLU-U) is
highly effective ...
Tirbanibulin, a microtubule inhibitor, has been
approved by the FDA as a 1% ointment (Klisyri –
Almirall) for topical treatment of actinic keratosis of
the face or scalp.
Vaccination Recommendations for Updated 2024-2025 COVID-19 Vaccines (online only)
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025 (Issue 1723)
≥8 weeks after last dose5
5-11 years4 10 mcg/0.3 mL; light blue cap and label Not previously ...
View the Vaccination Recommendations for Updated 2024-2025 COVID-19 Vaccines
Med Lett Drugs Ther. 2025 Mar 3;67(1723):e1 doi:10.58347/tml.2025.1723g | Show Introduction Hide Introduction
COVID-19 Update: New Novavax Vaccine Formulation for 2023-2024
The Medical Letter on Drugs and Therapeutics • Nov 13, 2023 (Issue 1689)
doses: 1 dose ≥2 months
after last dose
5-11 years 10 mcg/0.3 mL; light blue cap and
label
1 dose 1 ...
A new 2023-2024 formulation of the adjuvanted
protein subunit COVID-19 vaccine manufactured by
Novavax that was developed to more closely target
currently circulating SARS-CoV-2 variants has been
made available in the US under an FDA Emergency Use Authorization (EUA) for use in persons ≥12
years old. The original formulation of the Novavax
vaccine is no longer authorized for use in the US.
In September, updated formulations of the mRNA
COVID-19 vaccines manufactured by Pfizer/BioNTech (Comirnaty) and Moderna (Spikevax) were
licensed by the FDA for use in persons ≥12 years old
and...
Med Lett Drugs Ther. 2023 Nov 13;65(1689):182-3 doi:10.58347/tml.2023.1689b | Show Introduction Hide Introduction
COVID-19 Update: Pfizer/BioNTech and Moderna Vaccines Authorized for Children ≥6 Months Old
The Medical Letter on Drugs and Therapeutics • Jul 11, 2022 (Issue 1654)
No 50 mcg/0.5 mL 5
12-17 yrs Light blue No 100 mcg/0.5 mL 10-11 or
13-152
1. A low dead-weight ...
The FDA has expanded its Emergency Use Authorizations
(EUAs) for the mRNA COVID-19 vaccines
manufactured by Pfizer/BioNTech (Comirnaty) and
Moderna (Spikevax) to allow for their use in children
as young as 6 months old. The Pfizer vaccine was
previously authorized for use in persons ≥5 years old,
and the Moderna vaccine was authorized for use in
adults ≥18 years old.
Drugs for Open-Angle Glaucoma
The Medical Letter on Drugs and Therapeutics • Apr 28, 2025 (Issue 1727)
, yellow-brown,
or blue/gray-brown), increases in the length,
thickness, and darkness of eyelashes ...
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