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Searched for days. Results 81 to 90 of 1849 total matches.

Methotrexate and Misoprostol for Abortion

   
The Medical Letter on Drugs and Therapeutics • Apr 26, 1996  (Issue 973)
for 63 days or less (two thirds for less than 45 days) received an IM dose of methotrexate, 50 mg/m 2 ...
Recent articles in the press have suggested that in early pregnancy, an intramuscular (IM) injection of methotrexate (Folex, and others), a folic acid antagonist, and oral or vaginal administration of misoprostol (Cytotec), a prostaglandin, offers a medical alternative to a surgically induced abortion. Methotrexate is approved by the US Food and Drug Administration for use in rheumatoid arthritis, psoriasis and various types of cancer, including choriocarcinoma, and has also been used to terminate ectopic pregnancies. Misoprostol is approved for prevention of gastric ulcers induced by...
Med Lett Drugs Ther. 1996 Apr 26;38(973):39-40 |  Show IntroductionHide Introduction

Netupitant/Palonosetron (Akynzeo) for Chemotherapy-Induced Nausea and Vomiting

   
The Medical Letter on Drugs and Therapeutics • Apr 27, 2015  (Issue 1467)
extent by by CYP2C9 and 2D6 CYP3A4 and 1A2 Tmax 5 hours 5 hours Excretion Feces (~71% in 14 days ...
The FDA has approved Akynzeo (Helsinn/Eisai), an oral fixed-dose combination of the substance P/neurokinin 1 (NK1) receptor antagonist netupitant and the serotonin-3 (5-HT3) receptor antagonist palonosetron, for prevention of acute and delayed nausea and vomiting associated with cancer chemotherapy in adults. Akynzeo is the first product to combine drugs from these two classes. Palonosetron (Aloxi) is also available as a single agent for prevention of chemotherapy-induced and postoperative nausea and vomiting. Netupitant is the second substance P/NK1 receptor antagonist to be...
Med Lett Drugs Ther. 2015 Apr 27;57(1467):61-3 |  Show IntroductionHide Introduction

Lefamulin (Xenleta) for Community-Acquired Bacterial Pneumonia

   
The Medical Letter on Drugs and Therapeutics • Sep 23, 2019  (Issue 1581)
lefamulin treatment and for 2 days after the last dose. CABP — CABP is a leading cause of hospitalization ...
Lefamulin (Xenleta – Nabriva), a semisynthetic pleuromutilin antibiotic, has been approved by the FDA for IV and oral treatment of community-acquired bacterial pneumonia (CABP) in adults. It is the first systemic pleuromutilin antibiotic to be approved in the US; retapamulin (Altabax), a 1% topical ointment for treatment of impetigo, was approved in 2007.
Med Lett Drugs Ther. 2019 Sep 23;61(1581):145-8 |  Show IntroductionHide Introduction

Lumateperone (Caplyta) for Schizophrenia

   
The Medical Letter on Drugs and Therapeutics • Jul 27, 2020  (Issue 1603)
mg/mL soln 10-15 mg once/day 10-30 mg once/day $2.10 Abilify (Otsuka) 2, 5, 10, 15, 20, 30 mg tabs ...
The FDA has approved lumateperone (Caplyta — Intracellular Therapies), an oral second-generation antipsychotic, for once-daily treatment of schizophrenia in adults. It is the 13th second-generation antipsychotic drug to be approved by the FDA for this indication.
Med Lett Drugs Ther. 2020 Jul 27;62(1603):113-6 |  Show IntroductionHide Introduction

Ganaxolone (Ztalmy) for CDKL5 Deficiency Disorder (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024  (Issue 1709)
/day titrated to 63 mg/kg/day; >28 kg: 450 mg/day titrated to 1800 mg/day. ▶ Cost: 30 days ...
The FDA has approved ganaxolone (Ztalmy – Marinus) for oral treatment of seizures associated with cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder in patients ≥2 years old. It is the first drug to be approved in the US for this indication.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):e139-40   doi:10.58347/tml.2024.1709g |  Show IntroductionHide Introduction

Drugs for Hypertension

   
The Medical Letter on Drugs and Therapeutics • May 27, 2024  (Issue 1703)
such as the Dietary Approaches to Stop Hypertension (DASH) diet,2 limiting intake of sodium (ideally ...
American College of Cardiology/American Heart Association (ACC/AHA) guidelines for treatment of hypertension were last published in 2018. Treatment of hypertensive urgencies and emergencies is not discussed here.
Med Lett Drugs Ther. 2024 May 27;66(1703):81-8   doi:10.58347/tml.2024.1703a |  Show IntroductionHide Introduction

Drugs for Urinary Tract Infections

   
The Medical Letter on Drugs and Therapeutics • Jul 23, 2012  (Issue 1395)
, the drug of choice for non-pregnant women is trimethoprim/sulfamethoxazole (TMP/SMX) for 3 days, as long ...
The most recent guidelines from the Infectious Diseases Society of America (IDSA) and its European counterpart on the choice of antimicrobials for treatment of uncomplicated urinary tract infections (UTIs) in non-pregnant women focus on the unnecessary use of fluoroquinolones to treat uropathogens that are increasingly becoming resistant to them. Resistance of Escherichia coli to ciprofloxacin in the US has increased from 3% in 2000 to 17.1% in 2010.
Med Lett Drugs Ther. 2012 Jul 23;54(1395):57-8 |  Show IntroductionHide Introduction

Comparison Chart: Some Drugs for Irritable Bowel Syndrome with Diarrhea (IBS-D) (online only)

   
The Medical Letter on Drugs and Therapeutics • Feb 03, 2025  (Issue 1721)
) 5.8 g/teaspoon powder; 5.8 g packets; 1.8 g caps; 2 g wafers $29.00 10-35 g/day in 2-3 divided ...
View the Comparison Chart: Some Drugs for Irritable Bowel Syndrome with Diarrhea (IBS-D)
Med Lett Drugs Ther. 2025 Feb 3;67(1721):e1-3   doi:10.58347/tml.2025.1721f |  Show IntroductionHide Introduction

Citalopram for Depression

   
The Medical Letter on Drugs and Therapeutics • Dec 04, 1998  (Issue 1041)
− Celexa (Forest/Parke-Davis) 40 mg once/day $60.48 Fluoxetine − Prozac (Lilly/Dista) 20 mg once/day 75.04 ...
Citalopram hydrobromide (Celexa - Forest/Parke-Davis), a selective serotonin reuptake inhibitor (SSRI) available in Europe since 1989, has now been approved by the US Food and Drug Administration (FDA) for treatment of depression. It is being advertised as having a 'favorable side-effect profile.'
Med Lett Drugs Ther. 1998 Dec 4;40(1041):113-4 |  Show IntroductionHide Introduction

OTC loratadine (Claritin)

   
The Medical Letter on Drugs and Therapeutics • Jan 06, 2003  (Issue 1147)
/day 2-5 years: 2.5 or 5 mg once/day or 2.5 mg bid 6 months-2 years: 2.5 mg once/day 5 or 10 mg ...
The FDA has approved the marketing of loratadine (Claritin - Schering), a second-generation H1-antihistamine, without a prescription. The drug was also recently approved for OTC use as Alavert (Wyeth) and other generics are expected.
Med Lett Drugs Ther. 2003 Jan 6;45(1147):3-4 |  Show IntroductionHide Introduction