FDA Approves Longest Lasting Continuous Glucose Monitor for Diabetes

It is expected to be available for adult patients this spring 2022. Previously, the longest approved sensor lasted for 90 days. This was also an Eversense product, and was approved in 2018. Senseonics What is a CGM? How Long Do Most CGM Sensors Last? A sensor that can be changed at home will typically last between one and two weeks. How Does The Eversense E3 Work? While the sensor collects data, the transmitter interprets it and displays it to the wearer....

April 18, 2025 · 1 min · 148 words · Bryce Jordan

FDA Approves Mounjaro, a Novel Type 2 Diabetes Medication

Targeting GLP-1 and GIP can help patients lose weight and manage glucose levels. Unlike insulin, which often requires two shots per day, Mounjaro can be self-administered once a week. In clinical trials, participants treated with Mounjarolost between 12 and 25 pounds on average. Lara Antal / Verywell Whether Mounjaro will be prescribed alone or with insulin may depend on specific patient profiles, according to Ayuk. The treatment should be used in addition to a balanced diet and exercise routine, according to the FDA....

April 18, 2025 · 1 min · 140 words · Travis Carter

FDA Approves Saphnelo to Treat Lupus

Saphnelo is a prescription intravenous medication, administered once every four weeks over 30 minutes. What Is Lupus? Lupusis an autoimmune disorder that causes the immune system to overreact and attack healthy body cells. Lara Antal / Verywell It tends to impact young women between 15 and 45, as well as women of color. Lupus can be triggered by high levels of bang out 1 interferon. How Is It Administered? Saphnelo is given in an outpatient setting....

April 18, 2025 · 2 min · 260 words · Susan Forbes

FDA Approves the First New Type of High Blood Pressure Drug In Decades

Uncontrolled high blood pressure, or resistant hypertension, is hard to manage. A new way to treat hypertension has been a long time coming. Blocking receptors to endothelin produces vasodilatation. Illustration by Julie Bang for Verywell Health Researchers evaluated Tryvio in the PRECISION trial, which was conducted from 2018 to 2022. Is Tryvio Safe? Some people might experience liver problems, fluid retention, decreased sperm count, or anemia while taking Tryvio. The reason why Im cautious is we dont have long-term data from this medication, Cingolani said....

April 18, 2025 · 2 min · 297 words · Laura Bradshaw

FDA Authorizes COVID-19 Booster Shots for People Who Are Immunocompromised

Preliminary data should be available in September, an NIH spokesperson tells Verywell. Who Is Considered Immunocompromised? Its important to remember that boosters are not the only protection people who are immunocompromised need to prevent COVID-19. JurgaR/E+/Getty Images According to the FDA, masks and social distancing continue to be necessary. [Immunocompromised] patients should be counseled to maintain physical precautions to help prevent COVID-19, Woodcock says. This allows healthcare providers to be reimbursed for administering the shots....

April 18, 2025 · 1 min · 114 words · Danielle Delgado

FDA Authorizes New Drug for Emergency Use on Hospitalized COVID-19 Patients

In clinical trials, Actemra helped reduce mechanical ventilation and shorten hospitalization time. It lowered risks of death by about 5%. Its best utilized if patients are sick enough to require an ICU admission or who are close to one. Getty Images How Does Actemra Work? Actemra is infused into a patients bloodstream as a fluid. By blocking theinterleukin-6 receptor, Actemra fights against a hyperactive immune system to reduce inflammation. To avoid contracting COVID-19, the CDC recommends that eligible people get an FDA-approved COVID-19 vaccination....

April 18, 2025 · 1 min · 160 words · Robert Butler

FDA Authorizes Pfizer As First COVID-19 Vaccine

The vaccine, developed byPfizer Inc.and the German company BioNTech, will begin distribution shortly. The emergency use authorization (EUA) applies to people age 16 and older. The panel advises more people of color be added to ongoing clinical trials. Pool / Pool / Getty Images Offit recommended that studies also be conducted on the vaccine in people with common allergies. Distribution could begin very soon after that. The first doses of the vaccine are expected to be administered to healthcare workers and nursing home residents....

April 18, 2025 · 1 min · 166 words · Emily Johnson

FDA Authorizes Pfizer Booster for Seniors and High Risk Groups. What's Next?

The predicted risk of myocarditis associated with the third shot is acting like very low, the panelists said. Why Are Boosters Only Recommended for Certain Groups? Those with waning antibodies will be more in need of a boosters. Tara Croser - Pool / Getty Images What About People Who Received a Moderna or Johnson & Johnson Vaccine? The panelists said more data is needed before authorizing Moderna or Johnson & Johnson boosters....

April 18, 2025 · 1 min · 194 words · Wesley Ray

FDA Clears a New Patch for Excessive Armpit Sweating

One software can last up to four months. Brella requires a prescription, and it must be administered by a healthcare provider. This non-invasive treatment takes about three minutes. Illustration by Lara Antal for Verywell Health Its expected to be available in the United States later this summer. How Does Brella SweatControl Patch Work? Brella is the first clinical utility of this technology called targeted alkali thermolysis (TAT), she added. Who Is the Brella SweatControl Patch for?...

April 18, 2025 · 1 min · 152 words · Timothy Francis

FDA Clears Breast Cancer Vaccine For Clinical Trials

The vaccine, Tuohy tells Verywell, essentially works by nipping tumor development in the bud. Most triple-negative breast cancers express alpha-lactalbumin," Tuohy says. He describes the vaccine mechanism as simply taking advantage of this mistake. PhotoAlto/Michele Constantini / Getty Images What Happens Next? The FDAs approval clears the way for the Cleveland Clinic to start Phase I clinical trials of the vaccine. But it is hard to know exactly when the results might arrive....

April 18, 2025 · 1 min · 209 words · Ronald Clark

FDA Greenlights ‘Mixing and Matching’ COVID-19 Vaccine Boosters

(A booster for Pfizer vaccine recipientswas previously authorized.) The FDAs decision on booster doses, while important, was actually an interim step. The CDC director reviews the ACIP committees recommendations but can modify them. Aitor Diago / Getty Images But CDC director Rochelle Walensky, MD, MPH, allowed it. But Glatt says its very difficult to make any prediction on this right now. For the most recent updates on COVID-19, visit ourcoronavirus news page....

April 18, 2025 · 1 min · 81 words · Bethany Case

FDA Orders Juul to Remove Its E-Cigarette Products Over Safety Concerns

It was one of the most sweeping actions the FDA has taken against vaping products in recent years. And studies have linked e-cigarette use to increased odds of asthma and chronic obstructive pulmonary disease (COPD). Still, more than 2 million U.S. youth currently use e-cigarettes. Mario Tama / Getty Images Many students also cite feeling anxious, stressed, or depressed as reasons for using e-cigarettes. The FDA has been making bold attempts to reduce nicotine use and addiction....

April 18, 2025 · 1 min · 109 words · Elizabeth Cooper

FDA Panel Endorses Johnson & Johnson COVID-19 Booster Shot

The FDA also said COVID booster shots do not have to match a recipient’s initial vaccine series. In other words, vaccines can be “mixed and matched.” Both decisions will need to be backed up by an official FDA authorization before people can receive those boosters. Jessica Olah / Verywell This is not even a question of waning immunity and needing a booster. But Wen says the optimism shouldnt take away the importance of protecting people from getting infected by the virus....

April 18, 2025 · 1 min · 104 words · Logan Mercer