Search Results for ""drugs for""
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Searched for "drugs for". Results 1861 to 1870 of 2581 total matches.
Vinorelbine For Treatment of Advanced Non-Small-Cell Lung Cancer
The Medical Letter on Drugs and Therapeutics • Aug 18, 1995 (Issue 955)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Vinorelbine (Navelbine - Burroughs Wellcome), a semisynthetic vinca alkaloid, has been approved by the US Food and Drug Administration for parenteral use in the treatment of advanced non-small-cell lung cancer (NSCLC). Various combinations of cisplatin (Platinol), vinblastine (Velban, and others), mitomycin (Mutamycin), ifosfamide (Ifex), etoposide (VePesid) and paclitaxel (Taxol) have been used previously for this indication.
Riluzole for Amyotrophic Lateral Sclerosis
The Medical Letter on Drugs and Therapeutics • Dec 08, 1995 (Issue 963)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
The US Food and Drug Administration (FDA) has approved 'early access' use of riluzole (Rilutek - Rh ne-Poulenc Rorer) for treatment of amyotrophic lateral sclerosis (ALS). is the first drug to become available for treatment of this condition. The premarketing supply is limited; the manufacturer (1-800-798-7425) has enough on hand to treat 3,000 of the 25,000 patients with the disease in the USA, and those 3,000 have already been selected through a lottery. Similar arrangements have been made in several European countries. Riluzole is not available commercially in any country.
Gliadel Wafers for Treatment of Brain Tumors
The Medical Letter on Drugs and Therapeutics • Sep 11, 1998 (Issue 1035)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
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).
In Brief: New Adult Immunization Recommendations
The Medical Letter on Drugs and Therapeutics • Apr 24, 2017 (Issue 1519)
-2017. Med Lett Drugs Ther 2016; 58:127.
3. Adult immunization. Treat Guidel Med Lett 2014; 12:39.
4 ...
The 2017 adult immunization schedule approved by the CDC's Advisory Committee on Immunization Practices (ACIP) includes some new or revised recommendations.1 The complete schedule is available on the CDC's website (www.cdc.gov/vaccines/schedule). New recommendations for use of influenza vaccine during the 2016-2017 season were included in a previous issue of The Medical Letter.2 Updated recommendations for other vaccines are summarized below. Recommendations for routine use of vaccines in adults were reviewed in an earlier issue.3DK Kim et al. Advisory Committee on Immunization Practices...
Turmeric Supplements
The Medical Letter on Drugs and Therapeutics • Nov 18, 2019 (Issue 1585)
Turmeric Supplements
DRUG INTERACTIONS — Curcumin inhibits CYP3A4,
1A2, and 2D6 and the efflux ...
Turmeric is a spice derived from the Curcuma longa
plant. Dietary supplements and foods containing
turmeric are widely promoted for relief of pain
and to improve joint mobility, immunity, digestion,
cardiovascular health, depression, anxiety, memory,
and cognition.
In Brief: Retifanlimab (Zynyz) for Merkel Cell Carcinoma (online only)
The Medical Letter on Drugs and Therapeutics • Apr 17, 2023 (Issue 1674)
approval of the drug was based on the response rate
and duration of response. Retifanlimab is the third ...
Retifanlimab-dlwr (Zynyz – Incyte), a programmed
death receptor-1 (PD-1) blocking antibody, has
received accelerated approval from the FDA for
treatment of metastatic or recurrent locally advanced
Merkel cell carcinoma (MCC) in adults. Accelerated
approval of the drug was based on the response rate
and duration of response. Retifanlimab is the third
drug to be approved in the US for treatment of MCC;
pembrolizumab (Keytruda), a PD-1 blocking antibody,
is approved for the same indication as retifanlimab
in patients ≥12 years old and avelumab (Bavencio),
a programmed death...
Med Lett Drugs Ther. 2023 Apr 17;65(1674):e73-4 doi:10.58347/tml.2023.1674h | Show Introduction Hide Introduction
Intravenous Immunoglobulin (IVIG)
The Medical Letter on Drugs and Therapeutics • Dec 04, 2006 (Issue 1249)
Letter
®
On Drugs and Therapeutics
Volume 48 (Issue 1249/1250)
December 4/18, 2006 ...
Intravenous immunoglobulin (IVIG) has 6 FDA approved indications and is prescribed off-label for many others. How many of these uses are justified is controversial.
Piperacillin/Tazobactam
The Medical Letter on Drugs and Therapeutics • Jan 21, 1994 (Issue 914)
The Medical Letter
On Drugs and Therapeutics
www.medletter.com
Published by The Medical ...
Piperacillin/tazobactam (Zosyn - Lederle), an antibiotic combination product, has been approved by the US Food and Drug Administration for intravenous treatment of intra-abdominal, pelvic, skin, and skin-structure infections and for community-acquired pneumonia of moderate severity.
Alirocumab (Praluent) to Lower LDL-Cholesterol
The Medical Letter on Drugs and Therapeutics • Aug 17, 2015 (Issue 1475)
(the primary endpoint)
was -61.0% with the active drug and +0.8% with placebo.
At 78 weeks of treatment ...
The FDA has approved the subcutaneously injected
PCSK9 (proprotein convertase subtilisin kexin type 9)
inhibitor alirocumab (Praluent – Sanofi/Regeneron)
as an adjunct to diet and maximally tolerated
statin therapy for adults with heterozygous familial
hypercholesterolemia (HeFH) or clinical atherosclerotic
cardiovascular disease who require additional lowering
of LDL-cholesterol (LDL-C). It was not approved for
general use in statin-intolerant patients. Alirocumab
is the first PCSK9 inhibitor to be approved in the US.
Evolocumab (Repatha – Amgen), another PCSK9
inhibitor, was...
Ibrexafungerp (Brexafemme) for Vulvovaginal Candidiasis
The Medical Letter on Drugs and Therapeutics • Sep 06, 2021 (Issue 1632)
-life 20 hours
Excretion Feces (90%; 51% as unchanged drug);
urine (1%)
CLINICAL STUDIES — FDA ...
The FDA has approved ibrexafungerp (Brexafemme –
Scynexis), a first-in-class triterpenoid antifungal
("fungerp"), for oral treatment of vulvovaginal candidiasis
in postmenarchal females.