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Searched for moderate concentrate. Results 361 to 370 of 512 total matches.

Safety of Testosterone Replacement Therapy

   
The Medical Letter on Drugs and Therapeutics • Mar 14, 2016  (Issue 1490)
, and vitality in a total of 790 men ≥65 years old with moderately low serum testosterone concentrations ...
Three coordinated double-blind, placebo-controlled clinical trials have evaluated the efficacy of one year of testosterone replacement therapy in improving sexual function, physical function, and vitality in a total of 790 men ≥65 years old with moderately low serum testosterone concentrations and symptoms suggesting hypoandrogenism. Sexual function improved modestly, and there appeared to be marginal benefits in some areas of physical function and vitality as well. The trials were not designed to evaluate the safety of testosterone replacement therapy.
Med Lett Drugs Ther. 2016 Mar 14;58(1490):33-4 |  Show IntroductionHide Introduction

A Fixed-Dose Combination of Finasteride and Tadalafil (Entadfi) for BPH (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 05, 2022  (Issue 1658)
— Pharmacologic treatment is recommended for men with bothersome, moderate to severe BPH. An alpha-1 antagonist ...
The FDA has approved Entadfi (Veru), a fixed-dose combination of the 5α-reductase inhibitor finasteride and the phosphodiesterase type 5 (PDE5) inhibitor tadalafil, for initial treatment of benign prostatic hyperplasia (BPH) in men with an enlarged prostate; use of the drug is limited to 26 weeks. Entadfi is the first 5α-reductase inhibitor/PDE5 inhibitor combination to become available in the US. Finasteride (Proscar, and generics) and tadalafil (Cialis, and generics) are also available separately.
Med Lett Drugs Ther. 2022 Sep 5;64(1658):e1-2 |  Show IntroductionHide Introduction

Topical Metronidazole For Rosacea

   
The Medical Letter on Drugs and Therapeutics • Aug 11, 1989  (Issue 798)
concentration in the other seven patients, according to the manufacturer, was about 100 times less than with one ...
A topical formulation of 0.75% metronidazole gel (MetroGel - Curatek), an antibacterial, antiparasitic agent, was recently approved by the US Food and Drug Administration for treatment of rosacea.
Med Lett Drugs Ther. 1989 Aug 11;31(798):75-6 |  Show IntroductionHide Introduction

Pentostatin and 2-Chlorodeoxyadenosine for Hairy-Cell Leukemia

   
The Medical Letter on Drugs and Therapeutics • Sep 18, 1992  (Issue 879)
inhibits adenosine deaminase, an important enzyme in purine metabolism found in high concentrations ...
Pentostatin (2'-deoxycoformycin; DCF; - Parke-Davis), a purine analog, was recently approved by the US Food and Drug Administration (FDA) for treatment of hairy-cell leukemia resistant to interferon alfa (Intron A; Roferon-A). is a rare (500 cases/year in the USA) form of chronic lymphocytic leukemia. Acutely ill patients may respond rapidly to interferon, but the drug is rarely curative. Another purine analog, 2-chlorodeoxyadenosine (CdA; Leustatin - Ortho Biotech), may also be approved soon for treatment of hairy-cell leukemia (JD Piro, Blood, 79:843, 1992). Fludarabine (Fludara...
Med Lett Drugs Ther. 1992 Sep 18;34(879):89-90 |  Show IntroductionHide Introduction

Choice of an Antidepressant

   
The Medical Letter on Drugs and Therapeutics • Mar 19, 1993  (Issue 892)
, increasing concentrations of the neurotransmitter at synapses in the central nervous system, and have little ...
Since the introduction of fluoxetine (Prozac - Medical Letter, 30:45, 1988), bupropion (Wellbutrin - Medical Letter, 31:97, 1989), sertraline (Zoloft - Medical Letter, 34:47, 1992) and paroxetine (Paxil - this issue), the choice of an antidepressant has become more difficult. Should these widely prescribed new drugs replace tricyclic antidepressants such as amitriptyline (Elavil, and others), imipramine (Tofranil, and others), or nortriptyline (Aventyl, and others) for treatment of most patients with depression?
Med Lett Drugs Ther. 1993 Mar 19;35(892):25-6 |  Show IntroductionHide Introduction

Ziac for Hypertension

   
The Medical Letter on Drugs and Therapeutics • Mar 18, 1994  (Issue 918)
) in patients with mild to moderate hypertension compared once-daily treatment with hydrochlorothiazide alone ...
Ziac (Lederle), a combination of the beta-blocker bisoprolol fumarate and a very low dose (6.25 mg) of the diuretic hydrochlorothiazide, has been approved for treatment of hypertension by the US Food and Drug Administration (FDA). Bisoprolol, a new cardioselective beta-blocker with no intrinsic sympathomimetic activity, has also been marketed as a single drug (Zebeta - Lederle). The manufacturer is promoting the combination for initial treatment of hypertension with the claim that the low doses of the two drugs used together are effective in lowering blood pressure, but are each too low ...
Med Lett Drugs Ther. 1994 Mar 18;36(918):23-4 |  Show IntroductionHide Introduction

Moexipril: Another ACE Inhibitor For Hypertension

   
The Medical Letter on Drugs and Therapeutics • Sep 01, 1995  (Issue 956)
of the drug, moexipril should be taken in a fasting state. Plasma concentrations of moexiprilat reach a peak ...
Moexipril hydrochloride (Univasc - Schwarz Pharma), an angiotensin-converting enzyme (ACE) inhibitor, was recently approved by the US Food and Drug Administration (FDA) for treatment of. It is the eighth ACE inhibitor to be marketed in the USA.
Med Lett Drugs Ther. 1995 Sep 1;37(956):75-6 |  Show IntroductionHide Introduction

Candesartan for Hypertension

   
The Medical Letter on Drugs and Therapeutics • Nov 20, 1998  (Issue 1040)
hydrolyzed to its active metabolite candesartan, reaching peak plasma concentrations in three to four hours ...
Candesartan cilexetil (Atacand - Astra) is the fourth angiotensin II receptor antagonist to become available in the USA for oral treatment of hypertension.
Med Lett Drugs Ther. 1998 Nov 20;40(1040):109-10 |  Show IntroductionHide Introduction

A New Conjugated Estrogen

   
The Medical Letter on Drugs and Therapeutics • Jul 30, 1999  (Issue 1058)
concentration in plasma within 4 to 16 hours. Conjugated estrogens, like endogenous estrogens, are metabolized ...
A new synthetic conjugated estrogen product (Cenestin - Duramed) was recently approved by the US Food and Drug Administration for treatment of vasomotor symptoms due to estrogen deficiency.
Med Lett Drugs Ther. 1999 Jul 30;41(1058):67-70 |  Show IntroductionHide Introduction

Anakinra (Kineret) For Rheumatoid Arthritis

   
The Medical Letter on Drugs and Therapeutics • Feb 18, 2002  (Issue 1124)
of moderately to severely active rheumatoid arthritis in adults who have failed at least one disease-modifying ...
Anakinra (Kineret - Amgen), an interleuken-1 (IL-1) receptor antagonist, has been approved by the FDA for treatment of moderately to severly active rheumatoid arthritis in adults who have failed at least one disease-modifying anti-rheumatic drug(DMARD) such as methotrexate (Medical Letter 2000; 24:57).
Med Lett Drugs Ther. 2002 Feb 18;44(1124):18-9 |  Show IntroductionHide Introduction