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Searched for days. Results 171 to 180 of 1856 total matches.

Felbamate

   
The Medical Letter on Drugs and Therapeutics • Nov 26, 1993  (Issue 910)
trials, felbamate (3600 mg/day) was more effective than a placebo (a low dose of valproate) in 155 ...
Felbamate (Felbatol - Wallace Laboratories), a phenyl dicarbamate structurally similar to meprobamate (Equanil, and others), was recently approved by the US Food and Drug Administration for use alone or with other drugs in adults with partial seizures with or without secondary generalization. It was also approved for use in addition to other drugs in children with the multiple types of seizures associated with the Lennox-Gastaut syndrome, a severe epileptic encephalopathy.
Med Lett Drugs Ther. 1993 Nov 26;35(910):107-8 |  Show IntroductionHide Introduction

Two Neuraminidase Inhibitors for Treatment of Influenza

   
The Medical Letter on Drugs and Therapeutics • Oct 08, 1999  (Issue 1063)
that inhaled zanamivir 10 mg twice daily for five days decreased the time to improvement in symptoms ...
Zanamivir, a neuraminidase inhibitor taken by inhalation, has been approved by the FDA for treatment of influenza. Oseltamivir phosphate, an oral neuraminidase inhibitor, will probably be approved soon.
Med Lett Drugs Ther. 1999 Oct 8;41(1063):91-3 |  Show IntroductionHide Introduction

High Altitude Sickness

   
The Medical Letter on Drugs and Therapeutics • Sep 04, 1992  (Issue 878)
subside in one to seven days even when staying at the same altitude. Prevention — Physical conditioning ...
Rapid exposure to altitudes more than 8,000 feet above sea level can cause serious medical problems. Since the last Medical Letter article on this subject (Vol. 30, page 89, 1988), some new information on prevention and treatment of these disorders has been reported.
Med Lett Drugs Ther. 1992 Sep 4;34(878):84-6 |  Show IntroductionHide Introduction

Sparfloxacin and Levofloxacin

   
The Medical Letter on Drugs and Therapeutics • Apr 25, 1997  (Issue 999)
-acquired pneumonia; high-dose parenteral penicillin (≥10 million units/day) is an effective alternative ...
Sparfloxacin (Zagam - Rh ne-Poulenc Rorer) and levofloxacin (Levaquin - Ortho-McNeil) are the newest fluoroquinolone antimicrobials to be approved by the US Food and Drug Administration. Sparfloxacin in a once-daily oral preparation is being marketed for treatment of community-acquired pneumonia and acute bacterial exacerbations of chronic bronchitis. Levofloxacin, which is the active stereoisomer of ofloxacin (Floxin), is available for either oral or parenteral use; it is approved for oncedaily treatment of community-acquired pneumonia, acute exacerbations of chronic bronchitis,...
Med Lett Drugs Ther. 1997 Apr 25;39(999):41-3 |  Show IntroductionHide Introduction

Esomeprazole (Nexium)

   
The Medical Letter on Drugs and Therapeutics • Apr 30, 2001  (Issue 1103)
or 40 mg/day capsule $119.90 Lansoprazole − Prevacid (Tap) 30 mg/day capsule 119.90 Omeprazole ...
Esomeprazole magnesium (Nexium - AstraZeneca), the S-isomer of omeprazole (Prilosec), is the fifth benzimidazole proton pump inhibitor to become available in the United States. Omeprazole, which was the first, is going off patent this year.
Med Lett Drugs Ther. 2001 Apr 30;43(1103):36-7 |  Show IntroductionHide Introduction

Desloratadine (Clarinex)

   
The Medical Letter on Drugs and Therapeutics • Mar 18, 2002  (Issue 1126)
hours. The usual daily dose of 5 mg achieves steady-state plasma concentrations within 7 days ...
Desloratadine (des lor at' a deen; Clarinex - Schering), an active metabolite of the H1-receptor antagonist loratadine (Claritin), has been approved by the FDA for oral treatment of allergic rhinitis and chronic urticaria in patients at least 12 years old. The patent for loratadine expires in December 2002, and generic or over-the-counter versions are expected.
Med Lett Drugs Ther. 2002 Mar 18;44(1126):27-8 |  Show IntroductionHide Introduction

Gemifloxacin (Factive)

   
The Medical Letter on Drugs and Therapeutics • Sep 20, 2004  (Issue 1192)
days’ treatment of acute bacterial exacerbations of chronic bronchitis (ABECB) and 7 days’ treatment ...
Gemifloxacin (Factive - Oscient), a new oral fluoroquinolone antibiotic, has been approved by the FDA for 5 days' treatment of acute bacterial exacerbations of chronic bronchitis (ABECB) and 7 days' treatment of mild to moderate community-acquired pneumonia (CAP) in adults. For the next 6-8 months it will only be available, presumably for commercial reasons, in states east of the Rocky Mountains.
Med Lett Drugs Ther. 2004 Sep 20;46(1192):78-9 |  Show IntroductionHide Introduction

Seasonale

   
The Medical Letter on Drugs and Therapeutics • Feb 02, 2004  (Issue 1175)
are taken for 84 consecutive days, followed by 7 days of inactive tablets, allowing for withdrawal bleeding ...
Seasonale (Barr), the first "extended-cycle" oral contraceptive, is now available in the US for pregnancy prevention. Active tablets containing 30 ╡g of ethinyl estradiol and 0.15 mg of levonorgestrel are taken for 84 consecutive days, followed by 7 days of inactive tablets, allowing for withdrawal bleeding only four times a year. Other combination oral contraceptives are dispensed as 21 days of active tablets and 7 days of placebo or no tablets, resulting in 13 withdrawal bleeding episodes each year.
Med Lett Drugs Ther. 2004 Feb 2;46(1175):9 |  Show IntroductionHide Introduction

Tramadol Oral Solution (Qdolo) for Pain

   
The Medical Letter on Drugs and Therapeutics • May 31, 2021  (Issue 1625)
Dosage Rapid onset of analgesia not required: 25 mg/day Rapid onset of analgesia required: 50-100 mg q4 ...
The opioid agonist tramadol is now available in an oral solution (Qdolo – Athena Bioscience) for management of pain severe enough to require an opioid and for which alternative treatment options are inadequate. Tramadol has been available for years in immediate-release tablets and capsules, extended-release capsules (Ultram, and others), and in a fixed-dose combination tablet with acetaminophen (Ultracet, and generics).
Med Lett Drugs Ther. 2021 May 31;63(1625):83-4 |  Show IntroductionHide Introduction

Edoxaban (Savaysa) - The Fourth New Oral Anticoagulant

   
The Medical Letter on Drugs and Therapeutics • Mar 30, 2015  (Issue 1465)
— Edoxaban 60 mg/day (or 30 mg/ day in patients with CrCl 30-50 mL/min, weight ≤60 kg, or concomitant use ...
The FDA has approved edoxaban (Savaysa – Daiichi Sankyo), a once-daily, oral, direct factor Xa inhibitor, for treatment of venous thromoboembolism (VTE) and for prevention of stroke and systemic embolism in patients with nonvalvular atrial fibrillation. It is the fourth new oral anticoagulant to be approved for VTE and nonvalvular atrial fibrillation.
Med Lett Drugs Ther. 2015 Mar 30;57(1465):43-5 |  Show IntroductionHide Introduction