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EVENTS
E-Cigarette Use Among U.S. Youth Continues to Decline in 2024
EVENTS
August 2025

E-Cigarette Use Among U.S. Youth Continues to Decline in 2024

In 2024, the National Youth Tobacco Survey revealed a significant decrease in e-cigarette use among U.S. middle and high school students, with current use dropping from 2.13 million (7.7%) in 2023 to 1.63 million (5.9%) in 2024.

This reduction is mainly due to a decline in high school e-cigarette use, while middle school usage remained stable. The number of youth using e- cigarettes is now about one-third of the peak level in 2019. The survey also noted a decrease in the use of Elf Bar products, attributed to FDA enforcement actions. Despite these positive trends, concerns remain about any youth tobacco use, including nicotine pouches, and ongoing public health efforts are essential.

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Stay Aware of Common High-Alert Medications
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August 2025

Stay Aware of Common High-Alert Medications

High-alert medications are those with a high risk of causing significant harm if used incorrectly. They often have narrow therapeutic indices, complex dosing requirements, and similar names or packaging to other drugs.

Common examples include:

  1. Acetaminophen
  2. Chemotherapy Agents
  3. Insulin
  4. Oral Methotrexate
  5. Neuromuscular Blocking Agents
  6. Opioid Analgesics
  7. Intravenous Potassium

Prevention strategies include robust error identification, limiting access to these medications, staff and patient education, and ensuring rapid access to antidotes or reversal agents in case of errors. Vigilance and adherence to protocols are essential to mitigate risks associated with these medications.

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Fall Vaccine Updates
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August 2025

Fall Vaccine Updates

As we enter mid-fall and illnesses such as the influenza virus are on the rise, it is important to review the available vaccines, guidelines, and changes that have occurred. This guide will help consolidate key vaccine information into a single document for your reference and convenience as well as provide access to VIS and consent forms. Though this provides some general information, it is important to look at individualized patient needs and prescriber specific recommendations.

Flu Vaccine Recommendations

  • Everyone over the age of 6 months should receive a dose to be up to date.
  • Best time for vaccination is September/October.
  • All flu vaccines are trivalent formulation this year, inactivated, recombinant, live attenuated, along with High-Dose.
  • ACIP made a special off-label recommendation for people 18-64 with immunosuppression from organ transplant can now be given the High- Dose or adjuvanted flu vaccine which is typically indicated for ages 65+.

Flu (VIS)

Flu CPT/CVS Codes Product List

Respiratory Syncytial Virus (RSV)
Vaccine Recommendations

  • There are three currently available products.
  • This vaccine is not an annual vaccine like flu – it's a once single lifetime dose.
  • The newest vaccine Mresvia by Moderna is an mRNA vaccine, while the other two are recombinant.
  • The general recommendation is to give a single dose to all adults 60+.
  • A monoclonal antibody, Nirsevimab, is available for pediatric use for infants up to 8 months old going into their first RSV season.

RSV (VIS)

Pneumococcal Vaccine Recommendations

  • The age for routine vaccination has been lowered from 65 to 50 (PCV only).
  • Risk based recommendation still applies for individuals ages 19-49.
  • CDC approved use of the new PCV21 vaccine (Capvaxive) to be officially added to all pneumococcal recommendations.

Pneumococcal Conjugate Vaccine (VIS)
Pneumococcal Polysaccharide Vaccine (VIS)
Pneumococcal Vaccine Timing for Adults


COVID-19 Vaccine Recommendations

  • All individuals over the age of 6 months are eligible to receive a dose of the 2024-25 COVID-19 vaccine (pediatrics have more specific dosing based on prior vaccine history).
  • Adults over the age of 65, or individuals that are moderate to severely immunocompromised are now eligible to receive a 2nd dose of the 2024-25 formulation 6 months after the previous dose to be considered up to date.
  • An additional third dose can be considered based on shared clinical decision making for severely immunocompromised individuals with at least a two-month interval from last dose.
  • Reminder – moderate to severely compromised individuals dosing guidelines suggest that the initial dose series should be completed with the 2024-25 vaccine, meaning they will need the initial three-dose series and then the additional 4th dose after 6 months.
EVENTS
FDA New Drug Approvals and Updates
EVENTS
August 2025

FDA New Drug Approvals and Updates

Embecta is a new fully disposable insulin patch pump for patients with Type 1 and Type 2 Diabetes. This patch pump has a larger reservoir holding 300 units of insulin allowing for extended use for up to 3 days to better accommodate higher insulin needs as seen with Type 2 Diabetes. The pump patch also is great for individuals who are doing multiple daily injections to manage their diabetes therefore improving compliance and convenience for individuals.

Bezisterim is an investigation drug being studied for "potential ability to reduce the neurological symptoms associated with long Covid” Though there is not exact definition of what "long Covid" is, common symptoms are extreme fatigue, brain fog, light headedness, dizziness, and loss of taste and smell. Bezasterim is being investigated for Alzheimer’s and Parkinsons Disease since results showed patients experienced improved cognition and biomarker levels in Alzheimer’s disease. This drug can potentially be an added benefit in LTC if it shows meaningful improvement in motor control and cognition.

Novavax just received Emergency use authorization from the FDA for its new 2024-25 formula of the Covid-19 vaccine. Novavax is different from the other MRNA technology-based vaccines, as this on is protein based and targets the JN.1 strain but effectively covers the KP strains. Authorization of the updated Novavax, gives an additional option of another Covid-19 vaccine meeting FDA standards.

Neffy is the first ever needle-free Epinephrine Nasal spray that received approval from the FDA. Neffy is approved for type 1 allergic reactions, including anaphylaxis in adults and pediatrics that weigh over 66 pounds. This is a breakthrough treatment because up until now EpiPen/epinephrine has only been available as an injectable and can be challenging to self- administer for some individuals who fear needles that are going through an anaphylactic reaction. That delay in administering a needle can be life threatening with anaphylaxis. Neffy will be a safe and accessible therapeutic option and is easy to carry/store - beneficial to the long-term care and community.

References:

https://www.drugtopics.com/fda-updates

CMS Survey Process Changes and Modernization to "Targeted Survey"

September 2024

All nursing homes that participate in the Medicare program must go through an annual recertification inspection, known as standard survey. These surprise visits conducted by the State can last days and is an intense process. Covid-19 and other factors resulted in state surveyors falling months to years behind on the annual survey process. Delayed surveys affect the CMS compliance and five - star quality rating of a nursing home as well and cause some facilities to fall out of compliance due to lack of consistent surveys. CMS finally decided to pilot a new "risk- based survey" as of April 2024. The goal is to use a more focused survey that will take less time for facilities that were consistently "higher- quality". The goal is that shorter quality surveys for these facilities will free up the time and resources for the higher-risk nursing homes and help all facilities to be up to date with annual surveys and their CMS ratings. "Higher quality nursing homes" are considered those that had few to no citations of non-compliance, better higher staffing, and fewer hospitalizations as well as other characteristics related to resident harm, abuse, investigations etc. If this survey pilot is successful, it will be the first change in the survey process in a long time and a potential benefit for all.