
- May 2015 Skin & Eye Health
- Volume 81
- Issue 5
Rx Product News (May 2015)
Read about the new Rx Products featured in May.
Boehringer Ingelheim Pharmaceuticals, Inc
Indication: The FDA has approved Glyxambi (empagliflozin and linagliptin) as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus when treatment with both empagliflozin and linagliptin is appropriate. The recommended dose is 10 mg empagliflozin/5 mg linagliptin once daily, taken in the morning, with or without food. Glyxambi should not be used for the treatment of type 1 diabetes mellitus or diabetic ketoacidosis.
Dosage Form: Tablets: 10 mg/5 mg and 25 mg/5 mg
For More Information: www.glyxambi.com
EyleaMarketed by: Regeneron Pharmaceuticals, Inc
Indication: The FDA has expanded the approved use of Eylea (aflibercept) to include the treatment of diabetic retinopathy in patients with diabetic macular edema. The recommended dosage for this indication is 2 mg (0.05 mL) administered by intravitreal injection every 4 weeks for the first 5 injections, followed by 2 mg (0.05 mL) via intravitreal injection once every 8 weeks. Eylea is also indicated for treating (1) neovascular (wet) age-related macular degeneration, (2) macular edema following central retinal vein occlusion, and (3) diabetic macular edema.
Dosage Form: Single-use vial: 40 mg/ mL solution for intravitreal injection
For More Information: www.eylea.us
JadenuMarketed by: Novartis Pharmaceuticals Corporation
Indication: The FDA has approved Jadenu (deferasirox), an iron chelator, for the treatment of (1) chronic iron overload due to blood transfusions in patients 2 years and older and (2) chronic iron overload in nontransfusion-dependent thalassemia syndromes in patients 10 years and older. For the dosing guidelines, see the full prescribing information, which includes a black box warning for renal failure, hepatic failure, and gastrointestinal hemorrhage.
Dosage Form: Tablets: 90, 180, and 360 mg
For More Information: www.jadenu.com
SaphrisMarketed by: Actavis, Inc
Indication: The FDA has approved Saphris (asenapine) sublingual tablets as monotherapy for the acute treatment of manic or mixed episodes associated with bipolar I disorder for patients aged 10 to 17 years. For the dosing guidelines, see the full prescribing information, which includes a black box warning for increased mortality in elderly patients with dementia-related psychosis. Saphris is also approved for the treatment of schizophrenia.
Dosage Form: Sublingual tablets: 2.5, 5, and 10 mg
For More Information: www.saphris.com
Articles in this issue
over 10 years ago
Alpha-Gal (Mammalian Meat) Allergy: Implications for Pharmacistsover 10 years ago
Altruism and Educationover 10 years ago
Pet Peeves (May 2015)over 10 years ago
Can You Read These Rxs? (May 2015)over 10 years ago
Case Studies (May 2015)over 10 years ago
Statin Use May Increase Cataracts Riskover 10 years ago
Poor Hygiene Habits Increase Contamination of Contact Lens Casesover 10 years ago
Ranibizumab Found to Reverse Diabetes-Related Vision LossNewsletter
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