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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...
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.
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.
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.
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.
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.
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.
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.
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.
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.