Search Results for "Skin"
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Searched for Skin. Results 171 to 180 of 438 total matches.
Miltefosine (Impavido) for Leishmaniasis
The Medical Letter on Drugs and Therapeutics • Sep 15, 2014 (Issue 1451)
. Cutaneous leishmaniasis usually
presents as an ulcerative skin lesion at the site
of the sand fly bite ...
The FDA has approved miltefosine (Impavido – Knight
Therapeutics), an oral alkylphosphocholine analog,
for treatment of visceral, cutaneous, and mucosal
leishmaniasis caused by some Leishmania species.
It is the first drug to be approved by the FDA for
treatment of cutaneous and mucosal leishmaniasis
and the first oral drug to be approved for treatment of
visceral leishmaniasis.
Comparison Table: Some Parenteral Anticoagulants for VTE (online only)
The Medical Letter on Drugs and Therapeutics • Jul 25, 2022 (Issue 1655)
-12h Adverse Effects: Heparininduced
thrombocytopenia, skin
necrosis, urticaria, increased liver ...
View the Comparison Table: Some Parenteral Anticoagulants for VTE
Adagrasib (Krazati) for Colorectal Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024 (Issue 1709)
, hepatotoxicity, headache, dry skin, abdominal
pain, decreased appetite, edema, anemia, and cough.
QTc-interval ...
The RAS GTPase family inhibitor adagrasib (Krazati –
BMS), which received accelerated approval for
treatment of KRAS G12C (glycine-to-cysteine mutation
at codon 12)-mutated locally advanced or metastatic
non-small cell lung cancer (NSCLC) in 2022, has now
received accelerated approval from the FDA for use
with cetuximab for treatment of KRAS G12C-mutated
locally advanced or metastatic colorectal cancer
(CRC) in adults who received prior fluoropyrimidine-,
oxaliplatin-, and irinotecan-based chemotherapy.
Adagrasib is the first KRAS inhibitor to be approved in
the US for treatment...
Med Lett Drugs Ther. 2024 Aug 19;66(1709):e137-8 doi:10.58347/tml.2024.1709f | Show Introduction Hide Introduction
Three Drugs for Atopic Dermatitis (Adbry, Cibinqo, and Rinvoq)
The Medical Letter on Drugs and Therapeutics • Apr 03, 2023 (Issue 1673)
known as eczema) is a highly pruritic, chronic
inflammatory skin disorder that commonly presents ...
The subcutaneously injected interleukin-13 (IL-13)
antagonist tralokinumab-ldrm (Adbry – Leo) and
the oral Janus kinase (JAK) inhibitors abrocitinib
(Cibinqo – Pfizer) and upadacitinib (Rinvoq – Abbvie)
have been approved by the FDA for treatment of
moderate to severe atopic dermatitis.
Med Lett Drugs Ther. 2023 Apr 3;65(1673):51-5 doi:10.58347/tml.2023.1673b | Show Introduction Hide Introduction
Transdermal Methylphenidates (Daytrana) for ADHD
The Medical Letter on Drugs and Therapeutics • Jun 19, 2006 (Issue 1237)
should be alternated each day to minimize skin irritation. Using the patch on inflamed skin or
applying ...
A transdermal patch formulation of methylphenidate (Daytrana - Noven/Shire) has been approved by the FDA for treatment of attention-deficit/hyperactivity disorder (ADHD) in patients ≥ 6 years old. Like other methylphenidate products, the patch is a schedule II controlled substance. According to the manufacturer, it will be available in pharmacies by the end of June.
Daclizumab (Zinbryta) for Multiple Sclerosis
The Medical Letter on Drugs and Therapeutics • Sep 12, 2016 (Issue 1503)
SC once/mo Autoimmune disorders (skin reactions, 82,000.00
(Biogen/Abbvie) lymphadenopathy ...
The FDA has approved daclizumab (Zinbryta – Biogen/Abbvie), an interleukin-2 (IL-2) receptor blocking
monoclonal antibody, for treatment of adults with
relapsing forms of multiple sclerosis (MS). It is the
first subcutaneously injected monoclonal antibody to
be approved for treatment of MS.
In Brief: An Over-the-Counter Retinoid for Acne
The Medical Letter on Drugs and Therapeutics • Sep 26, 2016 (Issue 1504)
, particularly for patients with
inflammatory lesions.1
Adverse effects of topical retinoids include dry skin ...
Differin Gel 0.1% (Galderma), a topical formulation of the retinoid adapalene, will soon be available over the counter (OTC) for once-daily treatment of acne in patients ≥12 years old. It is the first topical retinoid to be approved for sale over the counter.All topical retinoids normalize keratinization and appear to have anti-inflammatory effects; whether any one topical retinoid is more effective than any other is not clear. Many dermatologists now recommend topical retinoids for first-line treatment of acne; they can be used alone or in combination with antibiotics to treat both inflamed...
Intravenous Ciprofloxacin
The Medical Letter on Drugs and Therapeutics • Aug 09, 1991 (Issue 850)
, bronchial secretions, sputum, lymph, peritoneal fluid, lung, skin, bone,
and prostate. CSF and eye ...
Ciprofloxacin, previously available orally (Cipro - Medical Letter, 30:11, 1988) and for ophthalmic use (Ciloxan - Medical Letter, 33:52, May 31, 1991), is now the first fluoroquinolone antibiotic to become available in the USA in an intravenous (IV) formulation. Cipro I.V. (Miles) is being promoted as an alternative to third-generation cephalosporins, aminoglycosides, and other drugs used for treatment of serious infections.
Dutasteride (Avodart) for Benign Prostatic Hyperplasia
The Medical Letter on Drugs and Therapeutics • Dec 23, 2002 (Issue 1146)
in the prostate, dutasteride inhibits a
second isoform as well, reducing DHT formation in the skin and liver. 5α ...
Dutasteride (Avodart - GlaxoSmithKline) is now available in the US for oral treatment of benign prostatic hyperplasia (BPH). It is similar to finasteride (Proscar - Merck), which has been marketed for this indication since 1992 and also, since 1998, for alopecia (Propecia - Medical Letter 1998; 40:25).
Low-Voltage Electronic Diagnostic Devices
The Medical Letter on Drugs and Therapeutics • Dec 01, 2008 (Issue 1300)
are
galvanometers that measure skin resistance to an
electric current. The FDA classifies “devices that use ...
Health care professionals may be asked about lowvoltage electronic devices now being used to diagnose and/or treat a number of health problems. Most are galvanometers that measure skin resistance to an electric current. The FDA classifies "devices that use resistance measurements to diagnose and treat various diseases" as Class III devices that require FDA approval prior to marketing. None of the devices reviewed here has such approval.