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Searched for lateral. Results 61 to 70 of 278 total matches.
In Brief: Anktiva for Bladder Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Jun 24, 2024 (Issue 1705)
complete
response at month 25 and later can receive the drug
with BCG once weekly for 3 weeks at months ...
Nogapendekin alfa inbakicept-pmln (Anktiva –
ImmunityBio), a first-in-class interleukin-15 (IL15)
receptor agonist, has been approved by the FDA for
use with Bacillus Calmette-Guérin (BCG) for treatment
of patients with BCG-unresponsive nonmuscle
invasive bladder cancer (NMIBC) with carcinoma in
situ with or without papillary tumors. Such patients
generally undergo bladder tumor resection, followed
by intravesical BCG treatment, but treatment failure
and cancer recurrence are common. The adenoviral
vector-based intravesical gene therapy nadofaragene
firadenovec-vncg (Adstiladrin)...
Med Lett Drugs Ther. 2024 Jun 24;66(1705):e105-6 doi:10.58347/tml.2024.1705e | Show Introduction Hide Introduction
New Ways To Scan The Myocardium
The Medical Letter on Drugs and Therapeutics • Sep 20, 1991 (Issue 853)
in the image. If
a defect is present, another image is obtained several hours later. Delayed redistribution ...
Myocardial images produced by injections of radioactive thallium chloride (201Tl), usually during exercise, have been used for many years for diagnosis of coronary artery disease (Medical Letter, 21:49, 1979). Recently, some new techniques and radiopharmaceuticals have become available for myocardial imaging.
Gamma Hydroxybutyrate (Xyrem) for Narcolepsy
The Medical Letter on Drugs and Therapeutics • Dec 09, 2002 (Issue 1145)
. Patients
took one dose of GHB at bedtime and a second dose 2.5 to 4 hours later, even if they had ...
The FDA has approved use of gamma hydroxybutyrate (sodium oxybate is the official generic name; Xyrem - Orphan Medical) for oral treatment of cataplexy in patients with narcolepsy. Gamma hydroxybutyrate (GHB), a metabolite of gamma-aminobutyric acid (GABA), is a central-nervous-system depressant marketed in Europe for use in general anesthesia. In recent years it has been notorious for its use in "date-rape" (Medical Letter 2002; 44:21). Xyrem is a Schedule III controlled substance.
Drugs for Ovulation Induction
The Medical Letter on Drugs and Therapeutics • Oct 31, 2011 (Issue 1376)
.
Intrauterine insemination and/or natural intercourse
should follow 24-36 hours later.
INTRAUTERINE ...
Infertility occurs in about 15% of couples. About one-third
of cases are due to problems with ovulation or other
female factors, another third are due to a male infertility
factor, and the remaining third are unexplained. In older
women, unexplained infertility is probably caused by
diminished quality and quantity of oocytes. The first
approach to treatment of female-factor infertility generally
is the use of drugs that stimulate oocyte production.
Bellafill for Acne Scars
The Medical Letter on Drugs and Therapeutics • Jun 22, 2015 (Issue 1471)
) or
saline, with a touch-up injection 4 weeks later if needed.
The primary endpoint, at least a 2-point ...
Bellafill (Suneva), a dermal filler approved earlier for
correction of nasolabial folds, has now also been
approved by the FDA for correction of moderate to
severe, atrophic, distensible facial acne scars on the
cheek in adults ≥21 years old. It is the only dermal filler
approved in the US for correction of facial acne scars.
Fluad - An Adjuvanted Seasonal Influenza Vaccine for Older Adults
The Medical Letter on Drugs and Therapeutics • Jan 18, 2016 (Issue 1486)
, for immunization
of adults >65 years old. It will become available later
this year for use during the 2016-2017 ...
The FDA has approved Fluad (Seqirus), an adjuvanted
trivalent seasonal influenza vaccine, for immunization
of adults ≥65 years old. It will become available later
this year for use during the 2016-2017 influenza
season. Fluad is the second influenza vaccine to be
approved in the US specifically for older adults; Fluzone
High-Dose was the first. Fluad has been available in
other countries for many years.
Gliadel Wafers for Treatment of Brain Tumors
The Medical Letter on Drugs and Therapeutics • Sep 11, 1998 (Issue 1035)
over a
period of about 2 to 3 weeks. Wafer remnants may still be visible months later on brain imaging ...
A biodegradable polymer 'wafer' (Gliadel - Rh ne-Poulenc Rorer) impregnated with the alkylating agent carmustine (BCNU; Bicnu) has been marketed in the USA for local treatment of recurrent glioblastoma multiforme that requires re-operation. The dime-sized polyanhydride wafers are implanted into the surgical cavity left behind after resection. Release of the alkylating agent directly into the area of the tumor bypasses the blood-brain barrier (H Brem and R Langer, Sci Med, 3:1, 1996).
Ustekinumab (Stelara) for Psoriasis
The Medical Letter on Drugs and Therapeutics • Jan 25, 2010 (Issue 1330)
, the recommended dose is 45 mg initially and
4 weeks later, followed by 45 mg every 12 weeks. For
patients ...
The FDA has approved the use of ustekinumab (Stelara - Centocor Ortho Biotech), an interleukin antagonist given by subcutaneous (SC) injection for treatment of adults with moderate to severe plaque psoriasis. It is the first agent in its class for this indication; the other biologic agents for psoriasis are Tcell or tumor necrosis factor (TNF) inhibitors.
A New Dihydroergotamine Nasal Spray (Trudhesa) for Migraine
The Medical Letter on Drugs and Therapeutics • Dec 27, 2021 (Issue 1640)
dose of Migranal requires 4 sprays (1 spray
per nostril, repeated 15 minutes later).
One dose ...
The FDA has approved Trudhesa (Impel Neuropharma),
a new dihydroergotamine nasal spray
product, for acute treatment of migraine with or
without aura in adults. Another dihydroergotamine
nasal spray (Migranal, and generics) has been
available for many years for the same indication.
A Drug Prevention of Anthracycline-Induced Cardiac Toxicity
The Medical Letter on Drugs and Therapeutics • Sep 06, 1991 (Issue 852)
treatment, five had a recurrence of failure four to ten years later, and two
of these required heart ...
Recent studies have caused concern about cardiomyopathy associated with doxorubicin (Adriamycin, and others), daunorubicin (Cerubidine, and others), idarubicin (Idamycin), mitoxantrone (Novantrone), and related anthracycline or anthraquinone anticancer drugs. Dexrazoxane (ADR-529, ICRF-187 - Adria), a piperazine derivative of ethylenediaminetetraacetic acid (EDTA), is now under investigation for prevention of this drug-induced cardiomyopathy.