Search Results for "lateral"
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 lateral. Results 191 to 200 of 278 total matches.

Choice of Benzodiazepines

   
The Medical Letter on Drugs and Therapeutics • Feb 26, 1988  (Issue 760)
effects after discontinuing long half-life compounds usually begin later and are less intense (MM Mitler ...
Since The Medical Letter last reviewed the choice of benzodiazepines (Volume 23, page 41, 1981), several new drugs have been marketed and some old ones are now available generically. Most of the benzodiazepines available for oral use in the USA are listed in the table on page 28.
Med Lett Drugs Ther. 1988 Feb 26;30(760):26-8 |  Show IntroductionHide Introduction

Ketorolac Tromethamine

   
The Medical Letter on Drugs and Therapeutics • Aug 24, 1990  (Issue 825)
was comparable to that with morphine, but the peak effect occurred later (about two hours after injection ...
Ketorolac (kee'; toe role ak) tromethamine (Toradol), manufactured by Syntex but also marketed by Roche, is the first parenteral nonsteroidal anti-inflammatory drug (NSAID) to become available for analgesic use in the USA. Parenteral indomethacin (Indocin I.V.) has been marketed here since 1985, but only for treatment of patent ductus arteriosus in newborn infants. Other parenteral NSAIDs are available in other parts of the world, but low potency, poor aqueous solubility, and substantial tissue irritation on injection have limited their usefulness. Ketorolac has been approved by the US ...
Med Lett Drugs Ther. 1990 Aug 24;32(825):79-80 |  Show IntroductionHide Introduction

High Altitude Sickness

   
The Medical Letter on Drugs and Therapeutics • Sep 04, 1992  (Issue 878)
’’ malaise may begin during ascent to high altitudes, but more characteristically occur 6 to 48 hours later ...
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

Aspirin for Prevention of Myocardial Infarction

   
The Medical Letter on Drugs and Therapeutics • Feb 17, 1995  (Issue 942)
placebo. One year later, a total of 78 patients taking aspirin and 145 taking placebo had died ...
Aspirin is now widely used for antithrombotic prophylaxis in patients who have had angina pectoris or a myocardial infarction and has also been tried in healthy people to prevent myocardial infarction. Recent studies have focused on increasingly lower doses of the drug. The use of aspirin in patients who have had transient ischemic attacks or strokes will not be discussed here.
Med Lett Drugs Ther. 1995 Feb 17;37(942):14-6 |  Show IntroductionHide Introduction

Tenecteplase (TNKase) for Thrombolysis

   
The Medical Letter on Drugs and Therapeutics • Nov 13, 2000  (Issue 1092)
, repeated 2,750.00 30 minutes later Streptokinase − Streptase (AstraZeneca) 1.5 MU IV over 60 minutes ...
Tenecteplase, a recombinant variant of human tissue plasminogen activator, is now available for thrombolysis in patients with acute myocardial infarction.
Med Lett Drugs Ther. 2000 Nov 13;42(1092):106-8 |  Show IntroductionHide Introduction

Insulin Glargine (Lantus), A New Long-acting Insulin

   
The Medical Letter on Drugs and Therapeutics • Aug 06, 2001  (Issue 1110)
onset of action was later with glargine (1.5 hr) than with continuous infusion (0.5 hr), NPH (0.8 hr ...
Insulin Glargine (Lantus) is a new long-acting human insulin analog approved by the FDA for treatment of both type 1 and type 2 diabetes. Synthesized by recombinant DNA technology, it differs from human insulin at position 21 in the A-chain where asparagine is replaced by glycine and at the C-terminus of the B-chain where two arginines are added.
Med Lett Drugs Ther. 2001 Aug 6;43(1110):65-6 |  Show IntroductionHide Introduction

In Brief: Anaphylaxis with Omalizumab (Xolair)

   
The Medical Letter on Drugs and Therapeutics • Jul 16, 2007  (Issue 1265)
of the injection, but 32% occurred later, up to 4 days after the injection. No deaths have been reported ...
The FDA has received new reports of serious and life-threatening hypersensitivity reactions to omalizumab (Xolair – Genentech), a monoclonal anti-IgE antibody injected subcutaneously for treatment of asthma (Med Lett Drugs Ther 2003; 45:67), and has added a black-box warning to the package insert.Postmarketing reports submitted to the FDA included 124 reports of anaphylaxis among an estimated 57,300 patients (0.2%) who might have been treated with the drug between June 2003 and December 2006. Anaphylaxis occurred after the first dose of Xolair in 39% of cases, after a 2nd dose in 19%, after...
Med Lett Drugs Ther. 2007 Jul 16;49(1265):59 |  Show IntroductionHide Introduction

Abuse-Deterrent Opioid Formulations

   
The Medical Letter on Drugs and Therapeutics • Aug 31, 2015  (Issue 1476)
deterrence in the labeling later this year.7 Abuse-Deterrent Opioid Formulations Table 1. Some Mechanisms ...
Development of abuse-deterrent opioid products, including reformulation of existing products, has become a priority for drug manufacturers and public health advocates. Three available opioid formulations, OxyContin (Purdue), Embeda (Pfizer), and Hysingla ER (Purdue), now include claims of abuse deterrence in their package inserts.
Med Lett Drugs Ther. 2015 Aug 31;57(1476):119-21 |  Show IntroductionHide Introduction

A New Subcutaneous Immune Globulin (HyQvia) for Primary Immunodeficiency

   
The Medical Letter on Drugs and Therapeutics • Aug 31, 2015  (Issue 1476)
, but may also develop later in life. TREATMENT — Immunoglobulin replacement is the standard treatment for many ...
Immune globulin (IgG) has been available for administration intravenously once every 3-4 weeks or subcutaneously once daily, once weekly, or every 2 weeks for treatment of primary immunodeficiencies. Now the FDA has approved human immune globulin 10% with recombinant human hyaluronidase (HyQvia – Baxter) for subcutaneous administration only every 3-4 weeks in adults with these disorders. The IgG component of HyQvia is identical to Gammagard Liquid, which was approved in 2005 for IV administration and in 2011 for SC administration.
Med Lett Drugs Ther. 2015 Aug 31;57(1476):121-2 |  Show IntroductionHide Introduction

Evolocumab (Repatha) - A Second PCSK9 Inhibitor to Lower LDL-Cholesterol

   
The Medical Letter on Drugs and Therapeutics • Oct 12, 2015  (Issue 1479)
to be given at least 7 days later. LDL-C levels should be measured 4-8 weeks after starting evolocumab ...
Evolocumab (Repatha – Amgen), a subcutaneously injected PCSK9 inhibitor, has been approved by the FDA as an adjunct to diet and maximally tolerated statin therapy for adults with heterozygous familial hypercholesterolemia (HeFH) or clinical atherosclerotic cardiovascular disease who require additional lowering of LDL-cholesterol (LDL-C). It was also approved as an adjunct to diet and other LDL-lowering therapies in patients with homozygous familial hypercholesterolemia (HoFH) who require additional lowering of LDL-C. Evolocumab is the second PCSK9 inhibitor to be approved in the...
Med Lett Drugs Ther. 2015 Oct 12;57(1479):140-1 |  Show IntroductionHide Introduction