
Articles
-
3 weeks ago |
healio.com | Carol L. DiBerardino
Key takeaways: FDA warned of potential serious risks when using compounded topical finasteride. There are no FDA-approved topical formulations of the drug. The FDA issued an alert warning of potential serious risks associated with the use of compounded topical finasteride, which is marketed to treat hair loss but does not have agency-approved labeling.
-
3 weeks ago |
dental.einnews.com | Sara Kellner |Carol L. DiBerardino
Offering HPV vaccines at dental visits improved uptake among children Added to email alerts You've successfully added Pediatric Vaccine-Preventable Diseases to your alerts. You will receive an email when new content is published. You've successfully added Pediatric Vaccine-Preventable Diseases to your alerts. You will receive an email when new content is published. We were unable to process your request. Please try again later.
-
4 weeks ago |
healio.com | Raj Chovatiya |Erin Michael |Carol L. DiBerardino
In this video, Raj Chovatiya, MD, PhD, discusses updates on oral therapies in psoriasis from the American Academy of Dermatology Annual Meeting. “We saw updates largely in the oral therapeutic realm, even more so than the biologic therapeutic realm,” Chovatiya, who is a clinical associate professor for Chicago Medical School at Rosalind Franklin University and assistant clinical professor at George Washington University School of Health Sciences, said.
-
4 weeks ago |
healio.com | Regina Schaffer |Kameelah Phillips |Carol L. DiBerardino
Key takeaways:About one in nine people who present with vaginitis symptoms also have at least one STI. CDC recommends co-testing for STIs when women are diagnosed with vaginitis, particularly bacterial vaginosis. Vaginitis, including yeast infections and bacterial vaginosis, affects up to 75% of women at least once in their lives, yet many women are unaware that a sexually transmitted infection, or STI, could be the cause.
-
4 weeks ago |
healio.com | Gabrielle Capaldo |Carol L. DiBerardino |Heather Rogers |Susan Taylor
Key takeaways: The U.S. has not seen the approval of a new sunscreen ingredient since the 1990s. The FDA’s plan to phase out animal testing removes one of the obstacles standing between Americans and new sunscreens. The FDA announced it will be reducing, refining and potentially replacing the animal testing requirement for the approval of certain drugs, which could have implications for the approval of new sunscreen ingredients in the United States.
Try JournoFinder For Free
Search and contact over 1M+ journalist profiles, browse 100M+ articles, and unlock powerful PR tools.
Start Your 7-Day Free Trial →