News
Stay up to date on topics that are important to Nurse Practitioners.
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CDC Updates Recommendation for Pfizer Booster to 5 Months After Primary Series
The CDC has updated its recommendation for when many people can receive a booster shot after the primary…
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FDA Authorizes Merck’s Oral Antiviral for Treatment of COVID-19 in Certain Adults
The FDA issued an emergency use authorization (EUA) for Merck’s molnupiravir for the treatment of mild-to-moderate COVID-19 in…
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FDA Authorizes Pfizer’s Oral Antiviral for COVID-19 in Adults, Pediatric Patients 12 Years and Older
The FDA issued an emergency use authorization (EUA) for Pfizer’s oral antiviral nirmatrelvir/ritonavir tablets, co-packaged for oral use…
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Add-On Therapy Approved to Lower LDL Cholesterol in High-Risk Patients
The FDA approved inclisiran (Leqvio) injection as an adjunct to diet and maximally tolerated statin therapy for the…
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New Biologic Drug Approved for Moderate to Severe Atopic Dermatitis
The FDA approved tralokinumab-ldrm (Adbry), a biologic for the treatment of moderate-to-severe atopic dermatitis in adults 18 years…
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FDA Approves New Drug for Insomnia in Adults
The FDA has approved daridorexant (Quviviq) 25 mg and 50 mg for the treatment of adult patients with…
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AAN Updated Guideline for Treatment of Painful Diabetic Neuropathy: Top Takeaways
Painful diabetic neuropathy (PDN) is a highly prevalent condition that greatly affects quality of life. The American Academy…
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Nurse Practitioner Ranked as Top Healthcare Job in 2022
U.S. News & World Report ranked the nurse practitioner role: First on its 2022 Best Health Care Jobs…
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Monoclonal Antibody Therapy for COVID-19 Authorized for Pediatric Patients, Including Newborns
The FDA issued an emergency use authorization (EUA) of bamlanivimab and etesevimab—previously authorized for pediatric patients 12 year…
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FDA Expands Eligibility for Pfizer-BioNTech COVID-19 Booster to 16- and 17-Year-Olds
The FDA amended the emergency use authorization (EUA) for the Pfizer-BioNTech COVID-19 Vaccine, authorizing a single booster dose…
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CDC Recommends Other COVID-19 Vaccines Be Preferred Over Janssen/J&J
Based on concerns about the increased incidence of thrombosis with thrombocytopenia (TTS) in people who received the Janssen/Johnson…
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FDA Approves New Combo Long-acting Monoclonal Antibodies for Pre-exposure Prevention
The FDA issued an emergency use authorization (EUA) for tixagevimab co-packaged with cilgavimab (Evusheld), administered together, for pre-exposure…
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