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Searched for days. Results 1211 to 1220 of 1911 total matches.

Extended-Release Hydrocodone (Hysingla ER) for Pain

   
The Medical Letter on Drugs and Therapeutics • May 11, 2015  (Issue 1468)
. 2. Approximate WAC for 30 days’ treatment at the starting dosage. WAC = wholesaler acquisition cost ...
The FDA has approved a second extended-release (ER) formulation of the oral opioid agonist hydrocodone (Hysingla ER – Purdue) for management of pain severe enough to require continuous long-term therapy and for which alternative treatment options are inadequate. Hysingla ER tablets have abuse-deterrent properties to discourage their misuse.
Med Lett Drugs Ther. 2015 May 11;57(1468):71-2 |  Show IntroductionHide Introduction

Intravenous Diclofenac (Dyloject)

   
The Medical Letter on Drugs and Therapeutics • Dec 21, 2015  (Issue 1484)
30 minutes. Use of ketorolac is limited to 5 days because of an increased risk of GI bleeding ...
The FDA has approved Dyloject (Hospira), an IV formulation of the NSAID diclofenac sodium, for use in adults. It can be administered alone for treatment of mild to moderate pain or in combination with opioid analgesics for moderate to severe pain. Dyloject is the first injectable formulation of diclofenac to become available in the US.
Med Lett Drugs Ther. 2015 Dec 21;57(1484):171-2 |  Show IntroductionHide Introduction

Selexipag (Uptravi) for Pulmonary Arterial Hypertension

   
The Medical Letter on Drugs and Therapeutics • Feb 15, 2016  (Issue 1488)
days’ treatment at the lowest usual adult dosage or for a 70-kg patient. WAC = wholesaler acquisition ...
The FDA has approved selexipag (Uptravi – Actelion), an oral selective prostacyclin IP receptor agonist, for treatment of pulmonary arterial hypertension (PAH). Treprostinil (Orenitram), an oral prostacyclin analog, was approved earlier for this indication.
Med Lett Drugs Ther. 2016 Feb 15;58(1488):21-3 |  Show IntroductionHide Introduction

A Two-Dose Hepatitis B Vaccine for Adults (Heplisav-B)

   
The Medical Letter on Drugs and Therapeutics • Jan 29, 2018  (Issue 1539)
schedule, with doses given on day 0, day 7, and day 21-30, and a booster dose given at month 12. HB ...
The FDA has approved a two-dose hepatitis B virus (HBV) vaccine (Heplisav-B – Dynavax) for use in adults ≥18 years old. The three other HBV vaccines marketed in the US are usually administered in 3 doses. Engerix-B and Recombivax HB are licensed for use in persons of all ages. A combination hepatitis A/B vaccine (Twinrix) contains the same hepatitis B component as Engerix-B and is licensed for use only in adults.
Med Lett Drugs Ther. 2018 Jan 29;60(1539):17-8 |  Show IntroductionHide Introduction

Desmopressin (Nocdurna and Noctiva) for Nocturnal Polyuria

   
The Medical Letter on Drugs and Therapeutics • Mar 25, 2019  (Issue 1568)
hour before to 8 hours after taking the drug. The cost of 30 days’ treatment with either strength ...
The FDA has approved a sublingual tablet (Nocdurna – Ferring) and a nasal spray (Noctiva – Avadel) formulation of desmopressin acetate for treatment of nocturia due to nocturnal polyuria in adults who wake up ≥2 times per night to void. Nocdurna and Noctiva are the first two products to be approved in the US for this indication. Higher-strength nasal spray and oral tablet formulations of desmopressin (DDAVP, and others) have been available for years for treatment of diabetes insipidus and primary nocturnal enuresis (bedwetting in children). In 2007, the indication for primary...
Med Lett Drugs Ther. 2019 Mar 25;61(1568):46-8 |  Show IntroductionHide Introduction

Rimegepant (Nurtec ODT) for Acute Treatment of Migraine

   
The Medical Letter on Drugs and Therapeutics • May 04, 2020  (Issue 1597)
). The safety of treating >15 migraine attacks in a 30-day period with rimegepant has not been established ...
The FDA has approved an orally disintegrating tablet (ODT) formulation of rimegepant (Nurtec ODT – Biohaven), a small-molecule calcitonin gene-related peptide (CGRP) receptor antagonist ("gepant"), for acute treatment of migraine with or without aura in adults. Rimegepant is the second oral gepant to become available in the US; ubrogepant (Ubrelvy), which is approved for the same indication, was the first. Four parenteral CGRP antagonists, erenumab (Aimovig), fremanezumab (Ajovy), galcanezumab (Emgality), and eptinezumab (Vyepti), are approved for prevention of...
Med Lett Drugs Ther. 2020 May 4;62(1597):70-2 |  Show IntroductionHide Introduction

MenQuadfi - A New Meningococcal (A, C, W, and Y) Vaccine

   
The Medical Letter on Drugs and Therapeutics • May 17, 2021  (Issue 1624)
) to ≥1:16 (day 30; ≥1:8 in Chang et al), or a ≥4-fold increase at day 30 from a baseline of ≥1:8 ...
The FDA has licensed MenQuadfi (Sanofi Pasteur), a quadrivalent polysaccharide conjugate vaccine that uses tetanus toxoid as a protein carrier, for prevention of invasive meningococcal disease caused by Neisseria meningitidis serogroups A, C, W, and Y (MenACWY) in persons ≥2 years old.
Med Lett Drugs Ther. 2021 May 17;63(1624):78-80 |  Show IntroductionHide Introduction

Azstarys (Serdexmethylphenidate/Dexmethylphenidate) for ADHD

   
The Medical Letter on Drugs and Therapeutics • Oct 04, 2021  (Issue 1634)
days. They were evaluated at 8 time points over a 13-hour period using the SKAMP rating scale, a 13 ...
The FDA has approved a long-acting fixed-dose combination of the stimulant dexmethylphenidate and the prodrug serdexmethylphenidate (Azstarys – Corium) for once-daily treatment of attention-deficit/hyperactivity disorder (ADHD) in patients ≥6 years old. Azstarys is the first product containing serdexmethylphenidate to become available in the US.
Med Lett Drugs Ther. 2021 Oct 4;63(1634):157-9 |  Show IntroductionHide Introduction

Tramadol/Celecoxib (Seglentis) for Pain

   
The Medical Letter on Drugs and Therapeutics • Apr 18, 2022  (Issue 1648)
in additive effects. Use of a monoamine oxidase (MAO) inhibitor with or within 14 days of tramadol ...
The FDA has approved Seglentis (Esteve/Kowa), an oral combination of tramadol hydrochloride, a weak opioid agonist and weak serotonin and norepinephrine reuptake inhibitor (SNRI), and celecoxib, a COX-2 selective nonsteroidal anti-inflammatory drug (NSAID), for use in adults with acute pain that is severe enough to require an opioid and for which alternative treatment options are inadequate.
Med Lett Drugs Ther. 2022 Apr 18;64(1648):58-60 |  Show IntroductionHide Introduction

Rosiglitazone/Glimepiride (Avandaryl) for Diabetes

   
The Medical Letter on Drugs and Therapeutics • Mar 13, 2006  (Issue 1230)
mg once 29.10 Amaryl (Aventis) (max 8 mg) 38.70 1. Cost of 30 days’ treatment (8 mg/d ...
Avandaryl, a new fixed-dose tablet combining the thiazolidinedione rosiglitazone (Avandia) and the sulfonylurea glimepiride (Amaryl, and others), was recently approved by the FDA for treatment of type 2 diabetes. It is approved for patients already taking a combination of rosiglitazone and a sulfonylurea or those not adequately controlled on rosiglitazone or sulfonylurea monotherapy. Rosiglitazone is also available in a fixed-dose combination with metformin (Avandamet). Most patients with type 2 diabetes eventually require 2 drugs with different mechanisms to control...
Med Lett Drugs Ther. 2006 Mar 13;48(1230):22-4 |  Show IntroductionHide Introduction