Eversense 365 is the world’s first and only one year CGM, which was approved by the United States (US) Food and Drug Administration in September of 2024 and launched across the country in October of ...

These days, many devices are programmed through apps on patients’ phones. But the FDA warns that certain phone settings, such ...

The US Food and Drug Administration (FDA) is cautioning patients and caregivers about the potential for not receiving blood ...

Patients who use smartphone apps to manage their diabetes could face serious health problems if they miss notifications ...

Health care providers are urged to inform patients to periodically check their smartphone settings and to confirm that they are able to receive alerts.

The Phase 1b/2a study will assess the safety of CNP-103 in adults (aged 18-35) and pediatrics (aged 12-17) who have Stage III or newly diagnosed (within the last 6 months) T1D as well as C-peptide ...

Approximately 15.5 million Americans have been or currently are on injectable diabetes or weight-loss medications known as ...

Although Mounjaro and insulin have different effects on ... This is the most serious warning from the Food and Drug Administration (FDA). It alerts doctors and patients about drug effects that ...

The first is by having an insulin-like effect in the body—in other words ... it should be noted that supplements are not regulated by the U.S. Food and Drug Administration. Moridpour AH, Kavyani Z, ...

Wetherill to lead the Division of Chemistry, which would become the Bureau of Chemistry in 1901 and the Food and Drug Administration in 1906. 1906 – Pure Food and Drug Act and Federal Meal Inspection ...

The Food and Drug Administration (FDA or we) is amending the color additive regulations to provide for the safe use of myoglobin as a color additive in ground meat and ground poultry analogue products ...