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Searched for days. Results 581 to 590 of 1850 total matches.
Relyvrio for ALS
The Medical Letter on Drugs and Therapeutics • Nov 28, 2022 (Issue 1664)
Tanabe) 30 mg/100 mL single-dose 60 mg IV once/day in 4-week cycles3 12,230.00
infusion bags
Radicava ...
The FDA has approved Relyvrio (Amylyx), a fixed-dose
combination of sodium phenylbutyrate and
taurursodiol, for treatment of amyotrophic lateral
sclerosis (ALS). Sodium phenylbutyrate (Buphenyl,
and others) has been available by prescription
for years for treatment of urea cycle disorders.
Taurursodiol (tauroursodeoxycholic acid), a derivative
of ursodiol, is an over-the-counter bile acid
supplement claimed to have neuroprotective
benefits. Relyvrio is the third drug to be approved
in the US for treatment of ALS; riluzole (Rilutek, and
others) and edaravone (Radicava, Radicava...
Xanomeline/Trospium (Cobenfy) for Schizophrenia
The Medical Letter on Drugs and Therapeutics • Nov 11, 2024 (Issue 1715)
for at least 2 days, then 100
mg/20 mg twice daily for at least 5 days; can be increased to
a maximum of 125 ...
The FDA has approved Cobenfy (BMS), an oral
fixed-dose combination of the muscarinic agonist
xanomeline and the peripheral muscarinic antagonist
trospium chloride, for treatment of schizophrenia in
adults. It is the first antipsychotic drug to be approved
in the US for treatment of schizophrenia that does not
block dopamine receptors. This is the first approval
for xanomeline; trospium has been available for many
years for treatment of overactive bladder.
Med Lett Drugs Ther. 2024 Nov 11;66(1715):177-9 doi:10.58347/tml.2024.1715a | Show Introduction Hide Introduction
Drugs for Multiple Sclerosis
The Medical Letter on Drugs and Therapeutics • Mar 22, 2021 (Issue 1620)
and
tolerability to older interferon formulations that must
be injected SC every other day or IM weekly.3 ...
Most patients with multiple sclerosis (MS) present
with the relapsing-remitting form of the disease.
Pharmacologic treatment usually includes a
disease-modifying drug, corticosteroids for acute
exacerbations, and other drugs for managing
symptoms such as fatigue, depression, and pain.
Early use of disease-modifying therapy has improved
clinical outcomes.
Finasteride and Minoxidil for Alopecia Revisited
The Medical Letter on Drugs and Therapeutics • Nov 21, 2005 (Issue 1222)
conducted in 1879 men 18-41 years old, finasteride 1
mg/day for up to 5 years increased hair counts ...
Finasteride and minoxidil continue to be the only drugs approved by the FDA to treat alopecia. Since these agents have different mechanisms of action, some clinicians have used both to treat hair loss in men.
Tinidazole (Tindamax) - A New Option for Treatment of Bacterial Vaginosis
The Medical Letter on Drugs and Therapeutics • Sep 10, 2007 (Issue 1269)
vaginosis is 2 g once daily for 2 days or 1 g
once daily for 5 days. Each dose should be taken with
food ...
Tinidazole (Tindamax - Mission Pharmacal), an oral antiprotozoal drug available in the US since 2004 for treatment of trichomoniasis, giardiasis, amebiasis and amebic liver abscess, was recently approved by the FDA for treatment of bacterial vaginosis.
Tetrabenazine (Xenazine) for Huntington's Chorea
The Medical Letter on Drugs and Therapeutics • Jan 26, 2009 (Issue 1304)
escalating doses to a maximum dose of 100
mg/day. TBZ treatment produced a significant 23.5%
improvement ...
Tetrabenazine (Xenazine - Ovation Pharmaceuticals), an old drug first synthesized 50 years ago for treatment of schizophrenia, was recently approved by the FDA for the treatment of chorea associated with Huntington's disease. It has been available in other countries for decades.
Alemtuzumab (Campath) Off-Label for Relapsing Multiple Sclerosis
The Medical Letter on Drugs and Therapeutics • Mar 09, 2009 (Issue 1307)
1
Alemtuzumab
2
– 12 mg IV x 5d initially $ 8,190.90
3
Campath (Bayer) then 3 days annually ...
Alemtuzumab (Campath), a genetically engineered, humanized monoclonal antibody currently approved to treat B-cell chronic lymphocytic leukemia (BCLL) and used off-label for induction therapy in solid organ transplants, is now also being tried off-label for treatment of relapsing multiple sclerosis (MS).
Benzyl Alcohol Lotion for Head Lice
The Medical Letter on Drugs and Therapeutics • Jul 27, 2009 (Issue 1317)
days after the
final treatment, compared to 4.8% and 26.2% with the
vehicle alone. Resistance ...
The FDA has approved benzyl alcohol lotion, 5% (Ulesfia Lotion - Sciele) for treatment of head lice in patients ≥6 months old. The active ingredient is 5% benzyl alcohol; the vehicle is 5% mineral oil.
Alirocumab (Praluent) to Lower LDL-Cholesterol
The Medical Letter on Drugs and Therapeutics • Aug 17, 2015 (Issue 1475)
75-150 mg injected subcutaneously every 2 weeks
to oral ezetimibe 10 mg/day or placebo in patients ...
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...
A New Dihydroergotamine Nasal Spray (Trudhesa) for Migraine
The Medical Letter on Drugs and Therapeutics • Dec 27, 2021 (Issue 1640)
dihydroergotamine 1 mg, or Migranal 2 mg over 3
treatment periods with a 7-day washout between
treatments.4 ...
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.