Search Results for "days"
Search again or select article below to purchase. Single article price: $45. Order 3 or more at one time and receive a 10% discount.
Sort by relevance | Sort by date
Searched for days. Results 781 to 790 of 1849 total matches.

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

An ACE inhibitor after a Myocardial Infarction

   
The Medical Letter on Drugs and Therapeutics • Aug 05, 1994  (Issue 928)
). CLINICAL TRIALS — A three-year double-blind trial begun 3 to 16 days after a myocardial infarction in 2,231 ...
The US Food and Drug Administration has approved use of the angiotensin-converting enzyme (ACE) inhibitor captopril (Capoten) for patients with left ventricular dysfunction after a myocardial infarction. ACE inhibitors, widely used for treatment of hypertension, in recent years have also been used for treatment of heart failure (Medical Letter, 35:40, 1993).
Med Lett Drugs Ther. 1994 Aug 5;36(928):69-70 |  Show IntroductionHide Introduction

New Uses of Thalidomide

   
The Medical Letter on Drugs and Therapeutics • Feb 16, 1996  (Issue 968)
in dosage of 50 to 200 mg per day for periods ranging from three days to two months or longer ...
Thalidomide is now available as an investigational drug in the USA. A synthetic derivative of glutamic acid, it was marketed in Europe in 1957 as a sedative but withdrawn four years later after being associated with severe human teratogenicity (PF DArcy and JP Griffin, Adverse Drug React Toxicol Rev, 13:65, 1994). The drug has since been found effective for several different indications.
Med Lett Drugs Ther. 1996 Feb 16;38(968):15-6 |  Show IntroductionHide Introduction

Anastrozole for Metastatic Breast Cancer

   
The Medical Letter on Drugs and Therapeutics • Jul 05, 1996  (Issue 978)
AND COST — The recommended dosage of anastrozole is one 1-mg tablet per day. No dose modification ...
Anastrozole (Arimidex - Zeneca), a selective nonsteroidal aromatase inhibitor, has been approved by the US Food and Drug Administration (FDA) for treatment of postmenopausal women with advanced breast cancer that has progressed during treatment with tamoxifen (Nolvadex, and others).
Med Lett Drugs Ther. 1996 Jul 5;38(978):61-2 |  Show IntroductionHide Introduction

Samarium-153 Lexidronam for Painful Bone Metastases

   
The Medical Letter on Drugs and Therapeutics • Aug 29, 1997  (Issue 1008)
that emits beta-particles and a gamma photon. It has a half-life of 1.9 days. 153 Sm chelated ...
Samarium-153 lexidronam (Quadramet - Dupont Pharma) has been approved by the FDA for relief of pain in patients with osteoblastic bone metastases. Strontium-89 (Metastron) has been available for several years for this indication (Medical Letter, 35:102, 1993).
Med Lett Drugs Ther. 1997 Aug 29;39(1008):83-4 |  Show IntroductionHide Introduction