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Advice for Travelers

   
The Medical Letter on Drugs and Therapeutics • Oct 07, 2019  (Issue 1582)
-related conditions. Vaccines recommended for travelers are reviewed in a separate issue.1 TRAVELERS ...
Patients who receive pretravel advice can reduce their risk for many travel-related conditions. Vaccines recommended for travelers are reviewed in a separate issue.
Med Lett Drugs Ther. 2019 Oct 7;61(1582):153-60 | Show Introduction Hide Introduction

Expanded Table: Antibiotics for Travelers' Diarrhea (online only)

   
The Medical Letter on Drugs and Therapeutics • Oct 07, 2019  (Issue 1582)
▶ Not recommended for use in children 1.60 34.40 Levofloxacin3 – generic Levaquin (Janssen) 200, 500, 750 mg ...
View the Expanded Table: Antibiotics for Travelers' Diarrhea
Med Lett Drugs Ther. 2019 Oct 7;61(1582):e160 | Show Introduction Hide Introduction

Expanded Table: Some Drugs for Altitude Illness, Jet Lag, and Motion Sickness (online only)

   
The Medical Letter on Drugs and Therapeutics • Oct 07, 2019  (Issue 1582)
▶ Recommended for prevention of AMS in adults and children $3.00 Dexamethasone – generic 0.5, 0.75, 1, 1.5, 2 ...
View the Expanded Table: Some Drugs for Altitude Illness, Jet Lag, and Motion Sickness
Med Lett Drugs Ther. 2019 Oct 7;61(1582):e161-3 | Show Introduction Hide Introduction

Qmiiz ODT - An Orally Disintegrating Meloxicam Tablet

   
The Medical Letter on Drugs and Therapeutics • Sep 23, 2019  (Issue 1581)
. Vivlodex, a low-dose capsule formulation of meloxicam, is FDA-approved only for management of OA pain.1 ...
The FDA has approved Qmiiz ODT (TerSera), an orally disintegrating tablet formulation of the prescription NSAID meloxicam. Qmiiz ODT, like conventional oral meloxicam tablets (Mobic, and generics), is indicated for relief of the symptoms of osteoarthritis (OA) and rheumatoid arthritis (RA) in adults and of juvenile RA in children who weigh ≥60 kg. Vivlodex, a low-dose capsule formulation of meloxicam, is FDA-approved only for management of OA pain.
Med Lett Drugs Ther. 2019 Sep 23;61(1581):151-2 | Show Introduction Hide Introduction

Glucagon Nasal Powder (Baqsimi) for Severe Hypoglycemia

   
The Medical Letter on Drugs and Therapeutics • Sep 23, 2019  (Issue 1581)
see' mee SEVERE HYPOGLYCEMIA – Hypoglycemia is classified as level 1 (blood glucose ≥54 and ...
The FDA has approved glucagon nasal powder (Baqsimi – Lilly) for treatment of severe hypoglycemia in patients ≥4 years old with diabetes. Baqsimi is the first noninjectable glucagon formulation to become available in the US. Injectable glucagon emergency kits (GlucaGen Hypokit, and generic) have been available for years, but they require reconstitution of the lyophilized powder by the caregiver immediately before injection. An injectable glucagon formulation that does not require reconstitution was recently approved by the FDA (Gvoke) and is expected to become available...
Med Lett Drugs Ther. 2019 Sep 23;61(1581):148-9 | Show Introduction Hide Introduction

Lefamulin (Xenleta) for Community-Acquired Bacterial Pneumonia

   
The Medical Letter on Drugs and Therapeutics • Sep 23, 2019  (Issue 1581)
to be approved in the US; retapamulin (Altabax), a 1% topical ointment for treatment of impetigo, was approved ...
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 Introduction Hide Introduction

Duaklir Pressair: Another LAMA/LABA Inhaler for COPD

   
The Medical Letter on Drugs and Therapeutics • Sep 23, 2019  (Issue 1581)
therapy, addition of an inhaled corticosteroid is recommended.1,2 CLINICAL STUDIES — In two 24-week ...
The FDA has approved Duaklir Pressair (Circassia), a fixed-dose combination of the long-acting muscarinic antagonist (LAMA) aclidinium bromide and the longacting beta2-adrenergic agonist (LABA) formoterol fumarate, for maintenance treatment of chronic obstructive pulmonary disease (COPD). Aclidinium/formoterol is the fifth LAMA/LABA combination to be approved in the US for this indication.
Med Lett Drugs Ther. 2019 Sep 23;61(1581):149-51 | Show Introduction Hide Introduction

In Brief: Ezallor Sprinkle - A New Formulation of Rosuvastatin

   
The Medical Letter on Drugs and Therapeutics • Sep 23, 2019  (Issue 1581)
tablets (Crestor, and generics) have been available since 2003.1,2 Table 1: Rosuvastatin Products Drug ...
The lipid-lowering drug rosuvastatin is now available in a sprinkle capsule formulation (Ezallor Sprinkle – Sun Pharma). Rosuvastatin tablets (Crestor, and generics) have been available since 2003.1,2The new formulation is being marketed specifically for residents of long-term care facilities who have difficulty swallowing. Ezallor Sprinkle capsules can be swallowed whole or opened and their contents sprinkled over applesauce or mixed with water for administration via nasogastric tube.For those long-term care residents who still have a reasonable indication for a statin but have difficulty...
Med Lett Drugs Ther. 2019 Sep 23;61(1581):152 | Show Introduction Hide Introduction

Expanded Table: Statins (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 23, 2019  (Issue 1581)
The Medical Letter ® Vol. 61 (1581) September 23, 2019 Table 1. Statins Average LDL-C Drug Some ...
View the Expanded Table: Statins
Med Lett Drugs Ther. 2019 Sep 23;61(1581):e152 | Show Introduction Hide Introduction

Solriamfetol (Sunosi) for Excessive Daytime Sleepiness

   
The Medical Letter on Drugs and Therapeutics • Aug 26, 2019  (Issue 1579)
, and insomnia. ▶ A schedule IV controlled substance. ▶ A 30-day supply costs $660.00. Table 1. Pharmacology ...
The FDA has approved solriamfetol (Sunosi – Jazz), a dopamine and norepinephrine reuptake inhibitor (DNRI), to improve wakefulness in adults with excessive daytime sleepiness (EDS) associated with narcolepsy or obstructive sleep apnea (OSA). Pitolisant (Wakix), an H3-receptor antagonist/inverse agonist recently approved by the FDA for treatment of excessive daytime sleepiness in patients with narcolepsy, will be reviewed in a future issue.
Med Lett Drugs Ther. 2019 Aug 26;61(1579):132-4 | Show Introduction Hide Introduction