Search Results for "days"
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Searched for days. Results 311 to 320 of 1849 total matches.

Over-the-counter Omeprazole (Prilosec OTC)

   
The Medical Letter on Drugs and Therapeutics • Aug 04, 2003  (Issue 1162)
received placebo, once daily for 14 days. On day 14, 69.7% and 73% of omeprazole-treated patients were ...
The FDA recently approved the proton pump inhibitor omeprazole magnesium (Prilosec OTC) for over-the-counter use for treatment of frequent heartburn. It will be marketed in late September or early October. Five proton pump inhibitors, including omeprazole, are available by prescription in the US (Medical Letter 2001; 43:36).
Med Lett Drugs Ther. 2003 Aug 4;45(1162):61-2 |  Show IntroductionHide Introduction

Minimed 670G: A Hybrid Closed-Loop Insulin Delivery System

   
The Medical Letter on Drugs and Therapeutics • Nov 21, 2016  (Issue 1508)
and taped in place; it is replaced every 7 days. The sensor uses interstitial fluid to take continuous ...
The FDA has approved the Minimed 670G (Medtronic), a hybrid closed-loop insulin delivery system for use in patients ≥14 years old with type 1 diabetes. The system uses an algorithm to automatically adjust basal insulin doses based on readings from a continuous glucose monitor (CGM). It fully automates basal insulin delivery in "auto" mode, but is considered a "hybrid" system (not a true "artificial pancreas") because it requires some action by the patient. The 670G system is expected to become available in Spring 2017.
Med Lett Drugs Ther. 2016 Nov 21;58(1508):147-8 |  Show IntroductionHide Introduction

Pemigatinib (Pemazyre) for Cholangiocarcinoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Dec 28, 2020  (Issue 1614)
is given once daily in 21-day treatment cycles (2 weeks on, 1 week off); one 21-day treatment cycle ...
The oral kinase inhibitor pemigatinib (Pemazyre – Incyte) has received accelerated approval from the FDA for treatment of adults with previously treated, unresectable, locally advanced or metastatic cholangiocarcinoma with fibroblast growth factor receptor 2 (FGFR2) fusions or other rearrangements. Pemigatinib is the first drug to be approved in the US for this indication.
Med Lett Drugs Ther. 2020 Dec 28;62(1614):e208-9 |  Show IntroductionHide Introduction

Varenicline Nasal Spray (Tyrvaya) for Dry Eye Disease

   
The Medical Letter on Drugs and Therapeutics • Dec 13, 2021  (Issue 1639)
was based on the results of two 28- day, double-masked trials in patients with dry eye disease (ONSET-1 ...
Tyrvaya (Oyster Point), a nasal spray formulation of the cholinergic agonist varenicline, has been approved by the FDA for treatment of dry eye disease. It is the first nasal spray to be approved in the US for this indication. An oral formulation of varenicline (Chantix, and generics) has been available for years for smoking cessation.
Med Lett Drugs Ther. 2021 Dec 13;63(1639):198-9 |  Show IntroductionHide Introduction

Glofitamab (Columvi) for Diffuse Large B-Cell Lymphoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 07, 2023  (Issue 1682)
of obinutuzumab seven days before glofitamab to mitigate cytokine release syndrome, followed by glofiamab for 12 ...
Glofitamab-gxbm (Columvi – Genentech), a bispecific CD20-directed CD3 T-cell engager, has received accelerated approval from the FDA for IV treatment of relapsed or refractory diffuse large B-cell lymphoma (DLBCL), not otherwise specified, or large B-cell lymphoma (LBCL) arising from follicular lymphoma after ≥2 lines of systemic therapy. Accelerated approval was based on response rates and durability of response. Glofitamab is the second T-cell-engaging bispecific antibody to be approved in the US for treatment of DLBCL; epcoritamab-bysp (Epkinly), which is given...
Med Lett Drugs Ther. 2023 Aug 7;65(1682):e129-30   doi:10.58347/tml.2023.1682b |  Show IntroductionHide Introduction

Acrivastine/Pseudoephedrine (Semprex-D) for Seasonal Allergic Rhinitis

   
The Medical Letter on Drugs and Therapeutics • Sep 02, 1994  (Issue 930)
)* 10 mg once/day 10-mg tablets $ 24.78 Brompheniramine maleate 4 mg q4-6h 4-mg tablets, liquid ...
Acrivastine/Pseudoephedrine (Semprex-D) for Seasonal Allergic Rhinitis (Burroughs-Wellcome), a combination of acrivastine with pseudoephedrine hydrochloride, has been approved by the US Food and Drug Administration for treatment of seasonal allergic rhinitis. Acrivastine is a new H 1 -receptor antagonist with a chemical structure similar to that of triprolidine (Actidil, and others) (RN Brogden and D McTavish, Drugs, 41:927, 1991). Pseudoephedrine is an α -adrenergic agonist. The combination is available only by prescription.
Med Lett Drugs Ther. 1994 Sep 2;36(930):78-80 |  Show IntroductionHide Introduction

Two New Antiplatelet Drugs for Angioplasty and Acute Coronary Syndromes

   
The Medical Letter on Drugs and Therapeutics • Sep 11, 1998  (Issue 1035)
infarction at 30 days was 15.7% with placebo and 14.2% with the drug (PURSUIT, N Engl J Med, 339:436, August ...
Two new platelet glycoprotein IIb/IIIa receptor antagonists have been approved for marketing by the US Food and Drug Administration (FDA). Eptifibatide (ep ti fi' ba tyde; Integrilin - Cor, Key) is approved for use in acute coronary syndromes (unstable angina or non-Q-wave myocardial infarction) or percutaneous coronary intervention (angioplasty or atherectomy). Tirofiban (tye roe fye' ban; Aggrastat - Merck) is approved for acute coronary syndromes, but not for angioplasty without an acute coronary syndrome. Abciximab (ReoPro), a monoclonal antibody glycoprotein IIb/IIIa receptor...
Med Lett Drugs Ther. 1998 Sep 11;40(1035):89-90 |  Show IntroductionHide Introduction

Rofecoxib for Osteoarthritis and Pain

   
The Medical Letter on Drugs and Therapeutics • Jul 02, 1999  (Issue 1056)
and 25 mg per day as effective for osteoarthritis as ibuprofen (Motrin, and others) 800 mg t.i.d. Two one ...
Rofecoxib, a selective COX-2 inhibitor, has been approved by the FDA for treatment of osteoarthritis, acute pain and menstrual pain.
Med Lett Drugs Ther. 1999 Jul 2;41(1056):59-62 |  Show IntroductionHide Introduction

Beta-blockers For Heart Failure

   
The Medical Letter on Drugs and Therapeutics • Jun 26, 2000  (Issue 1081)
Starting dosage Target dosage Cost 1 Bisoprolol 2 − Zebeta (Wyeth-Ayerst) 1.25 mg once/day 10 mg once ...
Standard treatment for patients with heart failure has included a diuretic, digitalis and an ACE inhibitor. In recent years carvedilol, a nonselective beta-blocker with alpha-1 blocking activity, and the beta-selective blockers bisoprolol and metroprolol have also been used for this indication.
Med Lett Drugs Ther. 2000 Jun 26;42(1081):54-5 |  Show IntroductionHide Introduction

Dapagliflozin/Saxagliptin (Qtern) for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • Mar 26, 2018  (Issue 1543)
) of 7-10.5% who were stabilized on open-label treatment with metformin and saxagliptin 5 mg/day for 8 ...
The FDA has approved Qtern (AstraZeneca), a fixed-dose combination of the sodium-glucose co-transporter 2 (SGLT2) inhibitor dapagliflozin (Farxiga) and the dipeptidyl peptidase-4 (DPP-4) inhibitor saxagliptin (Onglyza), for oral treatment of adults with type 2 diabetes. Dapagliflozin and saxagliptin have each been available for years alone and in combination with extended-release metformin (Xigduo XR; Kombiglyze XR). Three SGLT2/DPP-4 inhibitor combinations are now available in the US (see Table 2).
Med Lett Drugs Ther. 2018 Mar 26;60(1543):55-6 |  Show IntroductionHide Introduction