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Searched for rapid. Results 471 to 480 of 545 total matches.

Drugs for Vomiting Caused by Cancer Chemotherapy

   
The Medical Letter on Drugs and Therapeutics • Dec 24, 1993  (Issue 912)
cause no adverse effects, although rapid injection can cause intense genital or perineal pain. Mild ...
Several currently available antiemetic drugs can prevent vomiting caused by cancer chemotherapy. Anticancer drugs that cause vomiting are listed in the table below.
Med Lett Drugs Ther. 1993 Dec 24;35(912):124-6 |  Show IntroductionHide Introduction

Three New Drugs for Hyperlipidemia

   
The Medical Letter on Drugs and Therapeutics • Mar 03, 2003  (Issue 1151)
absorbed and metabolized, and both niacin and its metabolites are rapidly excreted in urine. CLINICAL ...
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

Atazanavir (Reyataz) and Emtricitabine (Emtriva) for HIV Infection

   
The Medical Letter on Drugs and Therapeutics • Nov 10, 2003  (Issue 1169)
mean elimination half-life is 7 hours. Emtricitabine is rapidly absorbed regardless of food intake ...
Atazanavir (Reyataz - Bristol-Myers Squibb), a new protease inhibitor (PI), and emtricitabine (Emtriva - Gilead), a nucleoside analogue reverse transcriptase inhibitor (NRTI) chemically similar to lamivudine, have been approved by the FDA for treatment of HIV-1 infection. Both are taken once daily, unlike most anti-HIV drugs.
Med Lett Drugs Ther. 2003 Nov 10;45(1169):90-2 |  Show IntroductionHide Introduction

Two New Drugs for Colon Cancer

   
The Medical Letter on Drugs and Therapeutics • Jun 07, 2004  (Issue 1184)
the drug more rapidly. There is no evidence that the speed of clearance affects the drug’s efficacy ...
Cetuximab (Erbitux - ImClone Systems/Bristol-Myers Squibb), an epidermal growth factor receptor (EGFR) inhibitor, and bevacizumab (Avastin - Genentech), the first vascular endothelial growth factor angiogenesis inhibitor, have recently been approved by the FDA for treatment of patients with metastatic colorectal cancer. Cetuximab is approved for treatment of patients with EGFR-expressing tumors, either in combination regimens with irinotecan (Camptosar)when the cancer has progressed on irinotecan-based therapy, or as monotherapy for those who cannot tolerate irinotecan. Bevacizumab is approved...
Med Lett Drugs Ther. 2004 Jun 7;46(1184):46-8 |  Show IntroductionHide Introduction

Tinidazole (Tindamax) - A New Anti-Protozoal Drug

   
The Medical Letter on Drugs and Therapeutics • Aug 30, 2004  (Issue 1190)
with tinidazole achieved a rapid clinical cure (81% vs. 33%) (S Mendis et al, Ceylon Med J 1984; 29:97 ...
Tinidazole (Tindamax - Presutti Labs), an oral antiprotozoal drug similar to metronidazole (Flagyl, and others), has been approved by the FDA for treatment of trichomoniasis in adults and for treatment of giardiasis, intestinal amebiasis and amebic liver abcess in adults and children more than 3 years old. Tinidazole has been widely used outside of the US for decades under the trade name Fasigyn (Pfizer).
Med Lett Drugs Ther. 2004 Aug 30;46(1190):70-2 |  Show IntroductionHide Introduction

Menactra: A Meningococcal Conjugate Vaccine

   
The Medical Letter on Drugs and Therapeutics • Apr 11, 2005  (Issue 1206)
of age, have found that children have little protective antibody left at age 4, but show a rapid ...
The FDA has approved a conjugated polysaccharide vaccine, Menactra (Sanofi-Pasteur), for protection against disease caused by Neisseria meningitidis in people 11-55 years old, and the manufacturer has applied for approval for use in children 2 to 10 years old. An unconjugated meningoccocal polysaccharide vaccine (Menomune - Sanofi-Pasteur) has been licensed in the US since 1981.
Med Lett Drugs Ther. 2005 Apr 11;47(1206):29-31 |  Show IntroductionHide Introduction

Removable Permanent Tattoo Ink

   
The Medical Letter on Drugs and Therapeutics • Sep 10, 2007  (Issue 1269)
rapidly after exposure to Qswitched lasers and were removed much more effectively than India ink tattoos ...
In the US, over one third of adults under the age of 35 and about one quarter of those aged 18-50 now have at least one tattoo. In later life, some people come to regret their tattoos, but tattoo inks can be difficult and expensive to remove.2 Recently, some new tattoo inks have been designed for improved safety and ease of removal.
Med Lett Drugs Ther. 2007 Sep 10;49(1269):75-6 |  Show IntroductionHide Introduction

Retapamulin (Altabax) - A New Topical Antibiotic

   
The Medical Letter on Drugs and Therapeutics • Feb 25, 2008  (Issue 1280)
progressing rapidly to vesicles, pustules, and exudative crusts. It occurs most frequently in children ...
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

A Rivastigmine Patch for Dementia

   
The Medical Letter on Drugs and Therapeutics • Mar 24, 2008  (Issue 1282)
has been available in the US since 2000, 2 but gastrointestinal adverse effects possibly related to rapidly rising ...
Cholinesterase inhibitors are now used routinely in patients with dementia. Rivastigmine transdermal system (Exelon Patch - Novartis), a patch formulation of the cholinesterase inhibitor rivastigmine tartrate, has been approved by the FDA for treatment of mild to moderate dementia associated with Alzheimer's or Parkinson's disease. An oral formulation of rivastigmine tartrate has been available in the US since 2000,2 but gastrointestinal adverse effects possibly related to rapidly rising serum concentrations have limited its use.
Med Lett Drugs Ther. 2008 Mar 24;50(1282):21-2 |  Show IntroductionHide Introduction

Fesoterodine (Toviaz) for Overactive Bladder

   
The Medical Letter on Drugs and Therapeutics • May 04, 2009  (Issue 1311)
, with or without food, and rapidly hydrolyzed to its active moiety 5-hydroxymethyl tolterodine, which is also ...
The FDA has approved the marketing of fesoterodine (Toviaz - Pfizer), a muscarinic receptor antagonist, for treatment of overactive bladder. It is the sixth antimuscarinic drug approved for this indication.
Med Lett Drugs Ther. 2009 May 4;51(1311):34-5 |  Show IntroductionHide Introduction