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Searched for A-200. Results 361 to 370 of 656 total matches.
An OTC Corticosteroid Nasal Spray for Allergic Rhinitis
The Medical Letter on Drugs and Therapeutics • Nov 11, 2013 (Issue 1429)
, use of orally inhaled budesonide
200 mcg twice daily for a mean of 4.3 years in children
with asthma ...
The FDA has approved the over-the-counter (OTC)
sale of Nasacort Allergy 24HR (Sanofi), a triamcinolone
acetonide nasal spray previously available only
by prescription as Nasacort AQ. The OTC product,
which is scheduled to be marketed in the spring of
2014, will be the first corticosteroid nasal spray that
can be purchased without a prescription in the US.
Nasacort Allergy 24HR is approved for use in patients
≥2 years old with nasal allergy symptoms.
Dichlorphenamide (Keveyis) for Periodic Paralysis
The Medical Letter on Drugs and Therapeutics • Apr 11, 2016 (Issue 1492)
to a maximum of 200
mg daily. Use of dichlorphenamide in patients with
hepatic insufficiency, severe ...
Dichlorphenamide (Keveyis – Taro), an oral carbonic
anhydrase inhibitor, has been approved by the
FDA for treatment of primary hypokalemic and
hyperkalemic periodic paralysis and related variants.
Dichlorphenamide is the first drug to be approved in
the US for this indication. It was approved as Daranide
in 1958 for treatment of glaucoma, but had not been
marketed since 2002.
Pimavanserin (Nuplazid) for Parkinson's Disease Psychosis
The Medical Letter on Drugs and Therapeutics • Jun 06, 2016 (Issue 1496)
%)
Half-life ~57 hours (pimavanserin); 200 hours (active
metabolite)
CLINICAL STUDIES — FDA approval ...
The FDA has approved the atypical antipsychotic
pimavanserin (Nuplazid – Acadia) for treatment
of hallucinations and delusions associated with
Parkinson's disease. It is the first drug to be approved
in the US for this indication.
Dapagliflozin (Farxiga) - A New Indication for Heart Failure
The Medical Letter on Drugs and Therapeutics • Jun 29, 2020 (Issue 1601)
with dapagliflozin than with placebo in
patients with (20.0% vs 25.5%) and without (13.2% vs
17.7%) type 2 diabetes ...
The sodium-glucose cotransporter 2 (SGLT2)
inhibitor dapagliflozin (Farxiga), which was
initially approved by the FDA for treatment of
type 2 diabetes and then to reduce the risk of hospitalization for HF in adults who have type 2 diabetes and established cardiovascular disease
(CVD) or multiple cardiovascular risk factors, has
now been approved for a third indication: to reduce
the risk of cardiovascular death and hospitalization
for heart failure (HF) in patients with heart failure
with reduced ejection fraction (with or without
type 2 diabetes). It is the first SGLT2 inhibitor to...
Orphengesic Forte - An Old Analgesic Combination Returns
The Medical Letter on Drugs and Therapeutics • Nov 16, 2020 (Issue 1611)
pain, but it is now used mainly in low doses as a platelet inhibitor.1 Caffeine doses of 65-200 mg ...
A fixed-dose combination of orphenadrine citrate, aspirin,
and caffeine (Orphengesic Forte – Galt; previously
available as Norgesic Forte) has been approved as
a prescription drug by the FDA for treatment of mild
to moderate pain caused by acute musculoskeletal
disorders. Single-ingredient generic orphenadrine
citrate is available by prescription in oral and injectable
formulations and has been used for years as an adjunct
for treatment of acute musculoskeletal pain. Orphengesic
Forte is being marketed as a non-opioid alternative for
pain relief.
Eroxon — An OTC Gel for Erectile Dysfunction
The Medical Letter on Drugs and Therapeutics • Nov 11, 2024 (Issue 1715)
, 2024
182
1. AL Burnett et al. Erectile dysfunction: AUA guideline. J Urol
2018; 200:633.
2. PDE5 ...
The FDA has authorized over-the-counter (OTC)
sale of a nonmedicated alcohol-based gel (Eroxon –
Futura) for treatment of erectile dysfunction (ED) in
males ≥22 years old. Eroxon is the only FDA-approved
OTC and topical treatment for erectile dysfunction. It
is also available in the UK and the EU.
Med Lett Drugs Ther. 2024 Nov 11;66(1715):181-2 doi:10.58347/tml.2024.1715c | Show Introduction Hide Introduction
In Brief: New Labeling for Once-Monthly Subcutaneous Buprenorphine (Sublocade)
The Medical Letter on Drugs and Therapeutics • Apr 14, 2025 (Issue 1726)
) Brixadi (Braeburn)
Formulations 100, 300 mg 8, 16, 24, 32 mg
prefilled syringes prefilled syringes
(200 ...
The FDA has approved changes to the labeling of
Sublocade (Indivior), an extended-release formulation
of the partial opioid agonist buprenorphine, to permit
faster initiation and use of alternative injection
sites. Sublocade is indicated for once-monthly
subcutaneous treatment of moderate to severe opioid
use disorder.
Med Lett Drugs Ther. 2025 Apr 14;67(1726):63-4 doi:10.58347/tml.2025.1726e | Show Introduction Hide Introduction
Three New Drugs for Hyperlipidemia
The Medical Letter on Drugs and Therapeutics • Mar 03, 2003 (Issue 1151)
− Tricor tablets (Abbott) 160 mg once 75.60
Lofibra, micronized (Gate) 200 mg once 67.50
Niacin
Niacin ...
The FDA recently approved three new drugs for treatment of hyperlipidemia. Ezetimibe (ez et' i mibe; Zetia) is the first in a new class of drugs that inhibit intestinal absorption of cholesterol. Extended-release lovastatin (Altocor) is a new formulation of lovastatin (Mevacor, and others). Extended-release niacin plus (immediate-release) lovastatin (Advicor) is the first fixed-dose combination of lipid-lowering drugs.
Dehydroepiandrosterone (DHEA)
The Medical Letter on Drugs and Therapeutics • May 09, 2005 (Issue 1208)
) is currently under review by the FDA for
use in women with SLE. Clinical studies have shown
that DHEA 200 mg ...
Dehydroepiandrosterone (DHEA), an endogenous adrenal steroid, is marketed as a dietary supplement in the US. It is widely promoted to reverse the effects of aging (loss of muscle, memory and libido) and has been used by athletes as a substitute for anabolic steroids. DHEA is banned by the International Olympic Committee, National Collegiate Athletic Association, National Football League and other sports organizations, but it was specifically exempted from becoming a controlled substance in the Anabolic Steroid Control Act of 2004.
Retapamulin (Altabax) - A New Topical Antibiotic
The Medical Letter on Drugs and Therapeutics • Feb 25, 2008 (Issue 1280)
available as 125/31.25, 200/28.5, 250/62.5, 400/57, 600/42.9 mg/5 mL susp; 125/31.25, 200/28.5, 250/62.5 ...
Retapamulin (re-tap'-a-mue'-lin; Altabax - Glaxo SmithKline) is a topical antibiotic recently approved by the FDA for treatment of bullous and non-bullous impetigo due to Streptococcus pyogenes and methicillin-susceptible Staphylococcus aureus. It is available as a 1% ointment by prescription only.