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Drug Interactions with St. John's Wort
The Medical Letter on Drugs and Therapeutics • Jun 26, 2000 (Issue 1081)
of hypericum and
has many biologically active constituents. The hypericins (hypericin and pseudohypericin ...
Even though its effectiveness has not been established, many patients take St. John's Wort (Hypericum perforatum), an over-the-counter herbal extract, to treat symptoms of depression, often without the knowledge of their physicians. Recent reports indicate that St. John's wort interacts adversely with a number of drugs.
Gemtuzumab for Relapsed Acute Myeloid Leukemia
The Medical Letter on Drugs and Therapeutics • Jul 24, 2000 (Issue 1083)
patients treated with gemtuzumab had hyperbilirubinemia or increased aminotransferase activity, and one ...
Gemtuzumab ozogamicin, a monoclonal antibody bound to a cytotoxic antibiotic, has been approved by the FDA for treatment of patients with CD33-positive acute myeloid leukemia (AML) in first relapse who are more than 60 years old and may not be able to tolerate cytotoxic chemotherapy
Topical Tacrolimus For Treatment of Atopic Dermatitis
The Medical Letter on Drugs and Therapeutics • Apr 16, 2001 (Issue 1102)
similar to cyclosporine. It decreases activation of T-lymphocytes, suppresses humoral
and cell-mediated ...
Tacrolimus ointment (Protopic) has been approved by the FDA in 0.03% and 0.1% formulations for treatment of atopic dermatitis. Tacrolimus is used systemically (Prograf) to prevent rejection of organ transplants.
Neotame - a new artificial sweetener
The Medical Letter on Drugs and Therapeutics • Aug 19, 2002 (Issue 1137)
that the
offspring of rats fed neotame 1000 mg/kg daily had reduced motor activity and ability to swim
through ...
Neotame (Neotame - NutraSweet Co.), an analog of aspartame (NutraSweet, and others), has been approved by the FDA for use as a nonnutritive sweetener and "flavor enhancer" in foods and beverages. Other non-caloric sweeteners available in the US include saccharin (Sweet'N Low, and others), acesulfame potassium (Sunette - Medical Letter, 1988; 30:116) and sucralose (Splenda - Medical Letter, 1998; 40:67). Neotame was approved for use in Australia and New Zealand in 2001.
Once-a-week Risedronate (Actonel)
The Medical Letter on Drugs and Therapeutics • Oct 14, 2002 (Issue 1141)
and decrease osteoclast
activity, inhibiting the resorption phase of the bone turnover cycle. These drugs ...
A once-weekly 35-mg oral formulation of the bisphosphonate risedronate (Actonel) has been approved by the FDA for prevention and treatment of postmenopausal osteoporosis. A once-weekly formulation of alendronate (Fosamax) was approved last year (Medical Letter 2001; 43:26). Bisphosphonates bind to the mineral surface of bone and decrease osteoclast activity, inhibiting the resorption phase of the bone turnover cycle. These drugs are not metabolized and remain bound to bone for several weeks.
Memantine for Alzheimer's Disease
The Medical Letter on Drugs and Therapeutics • Sep 15, 2003 (Issue 1165)
Input (CIBIC-Plus) and the Alzheimer’s Disease Cooperative
Study Activities of Daily Living Inventory ...
Memantine hydrochloride, which has been used to treat dementia in Germany (Axura Merz) since 1982, has become the latest word-of-mouth miracle drug for Alzheimer's disease in the US (G Kolata, NY Times, June 15, 2003). Forest Laboratories has submitted a New Drug Application to the FDA for memantine. This review describes the standard treatment for Alzheimer's Disease, mechanism of action, clinical studies, adverse effects and dosage. Also included are sections on availability of the drug and how some people are obtaining memantine from abroad.
In Brief: Tamoxifen and SSRI Interactions
The Medical Letter on Drugs and Therapeutics • Jun 15, 2009 (Issue 1314)
, tamoxifen must be
metabolized by CYP2D6 to become pharmacologically
fully active (MJ Higgins et al. J Natl ...
Use of a selective serotonin reuptake inhibitor (SSRI) is common in women taking tamoxifen (Nolvadex, and others) for breast cancer, both to treat depression and to decrease hot flashes. However, tamoxifen must be metabolized by CYP2D6 to become pharmacologically fully active (MJ Higgins et al. J Natl Compr Canc Netw 2009; 7:203), and the SSRIs fluoxetine (Prozac, and others) and paroxetine (Paxil, and others) are strong inhibitors of CYP2D6. Sertraline (Zoloft, and others) inhibits CYP2D6 to a lesser extent. Citalopram (Celexa, and others) and escitalopram (Lexapro), the 2 other SSRIs...
In Brief: Only The Name Remains The Same
The Medical Letter on Drugs and Therapeutics • Jun 28, 2010 (Issue 1341)
surprises among their ingredients, as shown in the
table below.
IN BRIEF
Name Formulation Active ...
A Medical Letter subscriber was surprised to discover that a new Citracal product contained not only calcium citrate, but also calcium carbonate. Citracal Plus Bone Density Builder actually contains more calcium carbonate per tablet than calcium citrate (240 mg vs. 60 mg). Another Citracal product, Citracal Plus Heart Health, also contains more calcium carbonate than calcium citrate. Many clinicians prefer calcium citrate because it can be taken with or without food, while calcium carbonate must be taken with food for optimal absorption. Other familiar over-the-counter (OTC) names also contain...
Dabigatran Etexilate (Pradaxa) - A New Oral Anticoagulant
The Medical Letter on Drugs and Therapeutics • Nov 15, 2010 (Issue 1351)
is the active form. Serum concentrations
of dabigatran reach a peak about 1 hour after
oral administration ...
The FDA has approved the oral direct thrombin
inhibitor dabigatran (da big’ a tran) etexilate (Pradaxa –
Boehringer Ingelheim) for prevention of thromboembolic
stroke in patients with non-valvular atrial fibrillation.
It has been available in Canada (Pradax) since
2008 for prevention of thromboembolism in patients
undergoing knee or hip replacement surgery and was
recently approved there for use in atrial fibrillation.
Rilpivirine (Edurant) - A New Drug for HIV Infection
The Medical Letter on Drugs and Therapeutics • Aug 22, 2011 (Issue 1371)
randomised double-blind active-controlled
trial. Lancet 2011; 378:238.
4. R Schrijvers et al. Rilpivirine ...
The FDA has approved rilpivirine (Edurant –
Janssen), a non-nucleoside reverse transcriptase
inhibitor (NNRTI), for use with other antiretroviral
agents for treatment of HIV-1 infection in treatment-naive
adults. Rilpivirine is also available in a fixed-dose
combination with emtricitabine and tenofovir
(Complera – Gilead).