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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).
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.
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.
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.
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 Introduction Hide 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.
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...
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.
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.
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).