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Searched for days. Results 781 to 790 of 1874 total matches.

Osilodrostat (Isturisa) for Cushing's Disease

   
The Medical Letter on Drugs and Therapeutics • Feb 08, 2021  (Issue 1617)
. The wholesale acquisition cost of a 30-day supply at the lowest usual maintenance dosage is $14,388. 22 ...
The FDA has approved osilodrostat (Isturisa – Recordati), a cortisol synthesis inhibitor, for oral treatment of adults with Cushing's disease when surgical resection of the pituitary adenoma is not an option or has not been curative. Osilodrostat is the first cortisol synthesis inhibitor to be approved in the US for this indication. Other oral steroidogenesis inhibitors such as ketoconazole and metyrapone have been used off-label for this indication for many years.
Med Lett Drugs Ther. 2021 Feb 8;63(1617):21-3 |  Show IntroductionHide Introduction

Oliceridine (Olinvyk) - A New Opioid for Severe Pain

   
The Medical Letter on Drugs and Therapeutics • Mar 08, 2021  (Issue 1619)
regimen should be used until oliceridine can be administered the next day. In the clinical trials ...
Oliceridine (Olinvyk - Trevena), an IV opioid agonist, has been approved by the FDA for management of acute pain severe enough to require an opioid and for which alternative treatment options are inadequate.
Med Lett Drugs Ther. 2021 Mar 8;63(1619):37-9 |  Show IntroductionHide Introduction

Zavegepant (Zavzpret) for Acute Treatment of Migraine

   
The Medical Letter on Drugs and Therapeutics • Jul 24, 2023  (Issue 1681)
orally disintegrating tabs3 75 mg PO (max 75 mg/day) $118.90 Ubrogepant – Ubrelvy (Abbvie) 50, 100 mg ...
The FDA has approved zavegepant nasal spray (Zavzpret – Pfizer) for acute treatment of migraine with or without aura in adults. Zavzpret is the first nasal spray formulation of a calcitonin gene-related peptide (CGRP) receptor antagonist ("gepant") to become available in the US.
Med Lett Drugs Ther. 2023 Jul 24;65(1681):116-8   doi:10.58347/tml.2023.1681c |  Show IntroductionHide Introduction

Drugs for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022  (Issue 1663)
mg tabs 1500-2550 mg/day PO divided bid-tid4 $2.70 Riomet (Sun) 500 mg/5 mL soln (4, 16 oz) 665.205 ...
Diet, exercise, and weight loss can improve glycemic control, but almost all patients with type 2 diabetes require antihyperglycemic drug therapy. Treating to a target A1C of <7% while minimizing hypoglycemia is recommended to prevent microvascular complications of diabetes (retinopathy, nephropathy, and neuropathy). An A1C target of <8% may be appropriate for some older patients.
Med Lett Drugs Ther. 2022 Nov 14;64(1663):177-84 |  Show IntroductionHide Introduction

Lemborexant (Dayvigo) for Insomnia

   
The Medical Letter on Drugs and Therapeutics • Jun 29, 2020  (Issue 1601)
5 mg was not significantly different from placebo in next-day postural stability, memory ...
The FDA has approved lemborexant (Dayvigo – Eisai), an orexin receptor antagonist, for treatment of sleep-onset and/or sleep-maintenance insomnia in adults. It is the second orexin receptor antagonist to be approved for this indication; suvorexant (Belsomra) was the first.
Med Lett Drugs Ther. 2020 Jun 29;62(1601):97-100 |  Show IntroductionHide Introduction

Drugs for Psychotic Disorders

   
The Medical Letter on Drugs and Therapeutics • Dec 19, 2016  (Issue 1510)
for renal or hepatic impairment. 2. Approximate WAC for 30 days’ treatment with the lowest usual adult ...
Oral antipsychotic drugs used for treatment of schizophrenia, schizoaffective disorder, delusional disorder, and other manifestations of psychosis or mania are listed in Table 1. Parenteral antipsychotic drugs used for treatment of these disorders are listed in Table 2.
Med Lett Drugs Ther. 2016 Dec 19;58(1510):160-4 |  Show IntroductionHide Introduction

Methylphenidate Revisited

   
The Medical Letter on Drugs and Therapeutics • May 06, 1988  (Issue 765)
be started with a 5-mg methylphenidate tablet at breakfast. Dosage can be increased at three- to seven-day ...
Methylphenidate (Ritalin and others), a Schedule II controlled substance in the USA, is a short-acting central-nervous-system stimulant widely used for treatment of children with school performance or behavior problems, or what is now called Attention Deficit-Hyperactivity Disorder, or AD-HD (American Psychiatric Association, Diagnostic and Statistical Manual of Mental Disorders, third ed., revised [DSM-III R], Washington, DC:authors, 1987, p 50). Some studies have estimated that more than 3% of elementary school students are taking methylphenidate, and one parents' group has brought a...
Med Lett Drugs Ther. 1988 May 6;30(765):51-2 |  Show IntroductionHide Introduction

Altretamine For Ovarian Cancer

   
The Medical Letter on Drugs and Therapeutics • Aug 09, 1991  (Issue 850)
is usually given in cycles of 260 mg/m 2 /d for 14 to 21 days, followed by seven days’ rest. In concurrent ...
Altretamine (Hexalen - US Bioscience; Hexastat - Rh ne-Poulenc in Canada), formerly known only by its chemical name, hexamethylmelamine, was recently approved by the US Food and Drug Administration as a single agent for palliative oral treatment of persistent or recurrent ovarian cancer.
Med Lett Drugs Ther. 1991 Aug 9;33(850):76-7 |  Show IntroductionHide Introduction

Fludarabine

   
The Medical Letter on Drugs and Therapeutics • Sep 20, 1991  (Issue 853)
fludarabine (25 to 30 mg/m 2 for five days per month) had a response rate of 57%, with 13% complete ...
Fludarabine phosphate (Fludara - Berlex), an analog of vidarabine (Vira-A), was recently approved by the U.S. Food and Drug Administration for treatment of patients with refractory chronic lymphocytic leukemia (CLL). The drug has not yet been marketed but is still available, as it has been for two years, through the National Cancer Institute.
Med Lett Drugs Ther. 1991 Sep 20;33(853):89-90 |  Show IntroductionHide Introduction

Podofilox For Genital Warts

   
The Medical Letter on Drugs and Therapeutics • Dec 13, 1991  (Issue 859)
for three days, followed by a four-day drug-free period; this cycle may be repeated up to four times ...
Podofilox 0.5% solution (Condylox - Oclassen) was recently approved by the US Food and Drug Administration for treatment of (condylomata acuminata). The drug requires a prescription, but is labeled for application by the patient. Similar topical solutions previously available for this indication are approved only for application by the physician.
Med Lett Drugs Ther. 1991 Dec 13;33(859):117-8 |  Show IntroductionHide Introduction