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Rosiglitazone (Avandia) Revisited
The Medical Letter on Drugs and Therapeutics • Mar 08, 2010 (Issue 1333)
(Amaryl,
and others).
1
Both rosiglitazone and pioglitazone can
cause edema and weight gain ...
The cardiovascular safety of the thiazolidinedione rosiglitazone (Avandia – GlaxoSmithKline) is in the news again, with some authorities calling for its removal from the market (New York Times, February 19, 2010).
Dutasteride (Avodart) for Prevention of Prostate Cancer
The Medical Letter on Drugs and Therapeutics • Apr 19, 2010 (Issue 1336)
, reduced the risk of prostate cancer over a 4year period.
1
5-REDUCTASE INHIBITORS — Dutasteride is one ...
A study recently published in the New England Journal of Medicine concluded that dutasteride (Avodart –
GlaxoSmithKline), a 5α-reductase inhibitor marketed for treatment of symptomatic benign prostatic hyperplasia, reduced the risk of prostate cancer over a 4-year period.
In Brief: Herpes Zoster Vaccine (Zostavax) Revisited
The Medical Letter on Drugs and Therapeutics • May 31, 2010 (Issue 1339)
neuralgia, especially in reducing the severity and duration of the disease.
1
Some new information ...
The 2006 Medical Letter article on the then-new varicella-zoster vaccine concluded that Zostavax appears to be safe and effective in protecting patients ≥60 years old against herpes zoster and postherpetic neuralgia, especially in reducing the severity and duration of the disease.1 Some new information has recently become available.CLINICAL STUDIES — A Veterans Administration randomized, double-blind trial enrolled more than 38,000 patients ≥60 years old and followed them for a mean of 3.4 years after administration of Zostavax or placebo. Since the efficacy of the vaccine had been...
Bioidentical Hormones
The Medical Letter on Drugs and Therapeutics • May 31, 2010 (Issue 1339)
and are
structurally identical to hormones produced by the
ovary.
1
Route of
Drug Source Delivery
Estriol Soy Oral ...
In recent years, many women have become concerned about the safety of pharmaceutical replacement
hormones for treatment of menopausal symptoms. “Bioidentical” hormone preparations, which are not approved by the FDA, are heavily promoted in popular books and on TV as alternatives; these are
derivatives of soy or plant extracts, chemically modified to be structurally identical to endogenous hormones.
Most FDA-approved single-entity hormones are also derivatives of soy or plant extracts and are
structurally identical to hormones produced by the ovary.
Cologuard Plus — An At-Home Stool DNA Test for Colorectal Cancer Screening
The Medical Letter on Drugs and Therapeutics • May 12, 2025 (Issue 1728)
FDA-approved
multitarget stool DNA test, has been available
since 2014.1
COLORECTAL CANCER ...
The FDA has approved Cologuard Plus (Exact
Sciences), a new at-home multitarget stool DNA test,
for colorectal cancer (CRC) screening in average-risk
adults ≥45 years old. Cologuard, the first FDA-approved
multitarget stool DNA test, has been available
since 2014.
Med Lett Drugs Ther. 2025 May 12;67(1728):73-5 doi:10.58347/tml.2025.1728a | Show Introduction Hide Introduction
Drugs for Female Sexual Dysfunction
The Medical Letter on Drugs and Therapeutics • Dec 13, 2010 (Issue 1353)
, orgasm
and painful intercourse are common in women.1 Since
the last Medical Letter article ...
Sexual complaints related to desire, arousal, orgasm
and painful intercourse are common in women. Since
the last Medical Letter article on this subject, some
new information has become available.
Drugs for Cognitive Loss and Dementia
The Medical Letter on Drugs and Therapeutics • Aug 22, 2022 (Issue 1657)
; it may be a transitional state between the
cognitive changes of normal aging and dementia.1
Treatment of reversible ...
Alzheimer's disease (AD) is the most common
cause of dementia, but cognitive decline is also
associated with other neurological conditions such
as Parkinson's disease, dementia with Lewy bodies,
vascular dementia, and frontotemporal dementia.
Treatment of Clostridium difficile-Associated Disease (CDAD)
The Medical Letter on Drugs and Therapeutics • Nov 06, 2006 (Issue 1247)
- and thirdgeneration cephalosporins, clindamycin and fluoroquinolones.
1
The emergence in recent years of a new ...
The gram-positive anaerobic bacillus Clostridium difficile is the most common identifiable cause of antibiotic-associated diarrhea. The antibiotics most often implicated have been ampicillin, second and third generation cephalosporins, clindamycin and fluoroquinolones. The emergence in recent years of a new, more toxic epidemic strain (BI/NAP1), possibly related to widespread use of fluoroquinolones, has caused a marked increase in the incidence and severity of C. difficile-associated disease (CDAD).
In Brief: Clopidogrel and Omeprazole
The Medical Letter on Drugs and Therapeutics • Nov 29, 2010 (Issue 1352)
.1 A
randomized, placebo-controlled trial (COGENT) has
found that use of the PPI omeprazole ...
Use of a proton pump inhibitor (PPI) to protect against gastrointestinal (GI) bleeding in patients taking the antiplatelet agent clopidogrel (Plavix) may interfere with the activation of clopidogrel and diminish its antiplatelet effect, increasing the risk of cardiovascular events.1 A randomized, placebo-controlled trial (COGENT) has found that use of the PPI omeprazole in patients taking clopidogrel in addition to aspirin decreased the incidence of GI bleeding without increasing the risk of a cardiovascular event, but the number of cardiovascular events was small and the formulation of...
In Brief: Delayed-Release Risedronate (Atelvia)
The Medical Letter on Drugs and Therapeutics • Mar 21, 2011 (Issue 1360)
daily (8.8% vs. 4.9% and
5.2% vs. 2.9%, respectively).1
DOSAGE AND COST — Atelvia is available as a 35 ...
A new enteric-coated delayed-release formulation of risedronate (Atelvia – Warner Chilcott) has been approved by the FDA for treatment of postmenopausal osteoporosis. Unlike immediate-release risedronate (Actonel) and all other oral bisphosphonates, which must be taken after an overnight fast and at least 30 minutes before eating breakfast, the new formulation is taken immediately after breakfast with at least 4 ounces of water. Then the patient must remain upright for at least 30 minutes.CLINICAL TRIAL — Approval of Atelvia was based on a 52-week non-inferiority study in more than 900...