Search Results for "rapid"
Search again or select article below to purchase. Single article price: $45. Order 3 or more at one time and receive a 10% discount.
Sort by relevance | Sort by date
Searched for rapid. Results 391 to 400 of 541 total matches.

Adalimumab (Humira) For Rheumatoid Arthritis

   
The Medical Letter on Drugs and Therapeutics • Mar 31, 2003  (Issue 1153)
signs and symptoms of RA and retard progression of joint damage, with a more rapid onset than ...
Adalimumab (Humira - Abbott), a tumor necrosis factor alpha (TNF-α) inhibitor, has been approved by the FDA for treatment of moderate to severe rheumatoid arthritis (RA). A genetically engineered human IgG1 monoclonal antibody, adalimumab is approved for subcutaneous (SC) injection in adults who have failed at least one disease-modifying anti-rheumatic drug (DMARD), for use either alone or with other DMARDs such as methotrexate (Rheumatrex, and others). Two other TNF-α antagonists, etanercept (Enbrel) and infliximab (Remicade), are already on the market for treatment of RA (Treatment...
Med Lett Drugs Ther. 2003 Mar 31;45(1153):25-7 |  Show IntroductionHide Introduction

Tiotropium (Spiriva) for COPD

   
The Medical Letter on Drugs and Therapeutics • May 24, 2004  (Issue 1183)
, inhibiting the bronchoconstrictive and secretory effects of acetylcholine. Tiotropium dissociates rapidly ...
Tiotropium bromide inhalation powder (Spiriva HandiHaler - Boehringer Ingelheim), a long-acting anticholinergic agent, has been approved by the FDA for once-daily maintenance treatment of bronchospasm associated with chronic obstructive pulmonary disease (COPD). Available in Europe since 2002, it is the first long-acting inhaled anticholinergic drug for treatment of COPD. Ipratropium bromide (Atrovent), an anticholinergic used four times daily, has been available in the US for many years.
Med Lett Drugs Ther. 2004 May 24;46(1183):41-2 |  Show IntroductionHide Introduction

Rituximab (Rituxan) for Rheumatoid Arthritis

   
The Medical Letter on Drugs and Therapeutics • Apr 24, 2006  (Issue 1233)
%). In addition, patients treated with rituximab experienced a rapid decrease in rheumatoid factor levels ...
Rituximab (Rituxan - Genentech), an anti-CD20 monoclonal antibody already marketed for treatment of B-cell non-Hodgkin's lymphoma, is now FDA-approved for use concurrently with methotrexate to treat moderate to severe rheumatoid arthritis in patients who have had an inadequate response to one or more tumor necrosis factor (TNF) inhibitors. Rituximab selectively depletes CD20+ B cells, which apparently play a role in the autoimmune response and in the chronic synovitis associated with rheumatoid arthritis.
Med Lett Drugs Ther. 2006 Apr 24;48(1233):34-5 |  Show IntroductionHide Introduction

Invader UGT1A1 Molecular Assay for Irinotecan Toxicity

   
The Medical Letter on Drugs and Therapeutics • May 08, 2006  (Issue 1234)
colorectal cancer. J Clin Oncol 2004; 22:1439. 14. Y Hasegawa et al. Rapid detection of UGT1A1 gene ...
The FDA has approved a new genetic test to identify patients who may be at increased risk of severe toxicity when treated with the cancer chemotherapy drug irinotecan (Camptosar). The Invader UGT1A1 Molecular Assay (Third Wave Technologies) detects the UGT1A1*28 allele, a variation in the uridine diphosphate glucuronosyltranferase 1A1 (UGT1A1) gene. The FDA recently revised the safety labeling for irinotecan, recommending that the dosing of irinotecan be reduced for patients who are homozygous for the UGT1A1*28 allele.
Med Lett Drugs Ther. 2006 May 8;48(1234):40 |  Show IntroductionHide Introduction

A Progestin Implant (Implanon) for Long-Term Contraception

   
The Medical Letter on Drugs and Therapeutics • Oct 09, 2006  (Issue 1245)
and fertility returns rapidly upon removal. It appears to be easier to insert and remove than Norplant ...
Implanon (Organon), an implantable contraceptive containing the progestin etonogestrel, has been approved by the FDA. Two other implantable contraceptives, Norplant and Jadelle, which both contain levonorgestrel, are FDA-approved but not marketed in the US.
Med Lett Drugs Ther. 2006 Oct 9;48(1245):83-4 |  Show IntroductionHide Introduction

Decitabine (Dacogen) for Myelodysplastic Syndromes

   
The Medical Letter on Drugs and Therapeutics • Nov 06, 2006  (Issue 1247)
of DNA, which may restore normal gene expression 1 ; cytotoxic effect on rapidly dividing cells ...
Decitabine (Dacogen - MGI Pharma), a pyrimidine nucleoside analog of cytidine, was approved by the FDA as an orphan drug for treatment of myelodysplastic syndromes (MDS), a heterogeneous group of clonal hemopathies that decrease production of normal blood elements (red cells, white cells and platelets) and are associated with a risk of progression to acute leukemia.
Med Lett Drugs Ther. 2006 Nov 6;48(1247):91-2 |  Show IntroductionHide Introduction

CT Colonography (Virtual Colonoscopy) Revisited

   
The Medical Letter on Drugs and Therapeutics • Dec 01, 2008  (Issue 1300)
have become available on colonography. TECHNIQUE — Rapid helical CT scanners are used to generate both ...
Options in screening for colon cancer include fecal occult blood tests, flexible sigmoidoscopy, colonoscopy, computed tomography (CT) colonography and fecal DNA tests. Since the last Medical Letter article on this subject, more data have become available on colonography.
Med Lett Drugs Ther. 2008 Dec 1;50(1300):94-5 |  Show IntroductionHide Introduction

Vancomycin Dosing and Monitoring

   
The Medical Letter on Drugs and Therapeutics • Apr 06, 2009  (Issue 1309)
recommended. In seriously ill patients, a loading dose of 25-30 mg/kg could be considered to rapidly achieve ...
Consensus recommendations for dosing and therapeutic monitoring of intravenous (IV) vancomycin (Vancocin, and others) were recently published. IV vancomycin has been used for decades as an alternative to penicillins for treatment of serious infections due to gram-positive cocci. In recent years, the widest use of the drug has been for treatment of serious methicillin-resistant Staphylococcus aureus (MRSA) infections.
Med Lett Drugs Ther. 2009 Apr 6;51(1309):25 |  Show IntroductionHide Introduction

Artemether-Lumefantrine (Coartem) for Treatment of Malaria

   
The Medical Letter on Drugs and Therapeutics • Sep 21, 2009  (Issue 1321)
. In the erythrocytic stages of P. falciparum, artemether acts rapidly to reduce the number of parasites. Lumefantrine ...
The FDA has approved artemether-lumefantrine (Coartem - Novartis) for oral treatment of uncomplicated Plasmodium falciparum malaria. It is not approved for prophylaxis. Artemether-lumefantrine is the first artemisinin-based drug approved for use in the US. Artemisinins are Chinese herbal products used worldwide to treat malaria. The intravenous formulation of artesunate, another artemisinin, is available in the US through the CDC.
Med Lett Drugs Ther. 2009 Sep 21;51(1321):75-6 |  Show IntroductionHide Introduction

Which TNF Inhibitor for Rheumatoid Arthritis?

   
The Medical Letter on Drugs and Therapeutics • May 17, 2010  (Issue 1338)
it has a rapid onset of action and a short half-life that makes toxicity, if it occurs, relatively short-lived ...
The FDA has approved five tumor necrosis factor (TNF) inhibitors for treatment of moderately to severely active rheumatoid arthritis (RA). TNF-α is a pro-inflammatory cytokine involved in the pathogenesis of many systemic inflammatory disorders.
Med Lett Drugs Ther. 2010 May 17;52(1338):38-9 |  Show IntroductionHide Introduction