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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.
Med Lett Drugs Ther. 2013 Nov 11;55(1429):90-1 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 2016 Apr 11;58(1492):50 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 2016 Jun 6;58(1496):74-5 |  Show IntroductionHide Introduction

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...
Med Lett Drugs Ther. 2020 Jun 29;62(1601):102-3 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 2020 Nov 16;62(1611):180-1 |  Show IntroductionHide Introduction

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 IntroductionHide 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 IntroductionHide 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.
Med Lett Drugs Ther. 2003 Mar 3;45(1151):17-9 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 2005 May 9;47(1208):37-8 |  Show IntroductionHide Introduction

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.
Med Lett Drugs Ther. 2008 Feb 25;50(1280):13-4 |  Show IntroductionHide Introduction