The researches find that the a real advance for Americans with diabetes, the U.S. Food and Drug Administration on Wednesday gave the nod to a needle-free method of helping people recover from an episode of dangerous low blood sugar. Therefore The new formulation, called Baqsimi, contains the rescue medication glucagon; but is instead give as a nasally inhale powder, the FDA said. But “Until now, people suffering from a severe hypoglycemic episode had to be treat with a glucagon injection that first had to be mix in a several-step process;” explained Dr. Janet Woodcock, who directs the FDA’s Center for Drug Evaluation and Research.

Dangerous low blood sugar

Baqsimi “may simplify the process, which can be critical during an episode;” she said in an agency news release. One diabetes expert agreed. Because The new drug’s approval is “a great boon for people with diabetes at risk for low blood glucose [hypoglycemia], as well as for their families and their health care providers;” said Dr. Minisha Sood. She’s an endocrinologist at Lenox Hill Hospital in New York City. Sood noted that very often; a diabetic person is incapacitate by hypoglycemia meaning that a friend, family member or other bystander must administer inject glucagon.

That means “training friends and family of patients” on how to inject the drug intra muscularly; which can be a real “limitation,” she said. Having a more “straightforward” option of administering glucagon “is a game-changer when it comes to treating severe hypoglycemia outside of a hospital or doctor’s office;” Sood said. “I look forward to using this for my patients.” As the FDA explained; “severe hypoglycemia occurs when a patient’s blood sugar levels fall to a level where he or she becomes confused or unconscious or suffers from other symptoms that require assistance from another person to treat.

Treating severe hypoglycemia

Typically, severe hypoglycemia occurs in people with diabetes who are using insulin treatment.” Baqsimi will come in a single-use dispenser easily administered to deliver glucagon-containing powder into the nose. But The drug “increases blood sugar levels in the body by stimulating the liver to release stored glucose into the bloodstream,” the FDA said. Wednesday’s approval was based on findings from two studies involving 83 and 70 adults with diabetes. Baqsimi is find to work as well as injected glucagon to raise blood sugar levels.

Similar results were found in a study involving 48 children with type 1 diabetes, the FDA added. Baqsimi, made by Eli Lilly and Co., does have some restrictions. But According to the FDA; it shouldn’t be used by people with a rare condition known as pheochromocytoma, a tumor of the adrenal gland; or people with a pancreatic tumor known as an insulinoma.