FDA Requires New Warning for Testosterone Products
The FDA now requires a general warning in the drug labeling of all approved testosterone products regarding the risk of venous blood clots.
The FDA now requires a general warning in the drug labeling of all approved testosterone products regarding the risk of venous blood clots.
Boehringer Ingelheim and Eli Lilly and Company announced the resubmission of the empagliflozin NDA to the FDA for the treatment of adults with type 2 diabetes.
Many patients with adrenal incidentaloma may not receive the necessary care for their condition.
Romosozumab significantly increased bone mineral density and bone content in postmenopausal women.
Levels of parathyroid hormone (PTH) should be considered when evaluating the effect of vitamin D status on glucose metabolism.
Lenvatinib, a new TKI inhibitor, delays disease progression and shows promising clinical efficacy against differentiated radioiodine-resistant thyroid cancer.
Primarily used in food and drink packaging, ingestion of bisphenol A has been linked to obesity, diabetes and reproductive disorders.
Novartis announced results from a phase 3 trial for Signifor LAR (pasireotide LAR; SOM230) in patients with acromegaly for whom current standard of care provides inadequate disease control.
The FDA has approved Tanzeum (albiglutide) subcutaneous injection for type 2 diabetes.
Despite adhering to lifestyle modifications, a woman’s glycemic control remains inadequate.
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