Few patients who are prescribed varenicline to assist in smoking cessation remain on the therapy, according to retrospective data presented during the 45th midyear meeting of the American Society of Health Systems Pharmacists, in Anaheim, Calif.
Few patients who are prescribed varenicline to assist in smoking cessation remain on the therapy, according to retrospective data presented during the 45th midyear meeting of the American Society of Health-Systems Pharmacists, in Anaheim, Calif.
A retrospective review of the Blue Cross and Blue Shield (BCBS) of Vermont pharmacy database was conducted for members who were prescribed varenicline, yielding 3,758 members who filled 7,911 prescriptions. The mean duration of therapy was approximately 2 months (59.2 days).
About half (47.7%) of members received only 1 prescription for varenicline, and 24.6% received 2 prescriptions.
The recommended initial treatment duration for varenicline is 12 weeks, and for patients who successfully quit smoking, an additional 12 weeks of therapy is recommended to increase the likelihood of long-term abstinence. Allowing for a 7-day grace period, only 8.1% of members completed the recommended continuous 84-day treatment, reported John Grossomanides, PharmD, director of pharmacy at BCBS of Vermont, Montpelier.
Some 39.1% completed 28 days or fewer of therapy. Only 3% completed 2 full 84-day courses.
The proportion of days covered, defined as the number of days with drug divided by the number of days in the specific time interval (maximum of 84 days), was greater than 80% for only 13% of the varenicline courses, indicating low adherence.
The reason for the low duration of treatment and low adherence needs to be explored, said Dr Grossomanides.
Navitus to Offer Unbranded Stelara Biosimilar, Remove Stelara from Formulary
March 13th 2025Lumicera Health Services, Navitus’ specialty pharmacy, has made a deal with Teva to offer an unbranded biosimilar that they estimate will save $112,000 and $336,000 per patient per year. Navitus will remove Stelara from formulary on July 1, 2025.
Read More
FDA Approves Neffy 1 mg Nasal Spray for Pediatric Patients
March 6th 2025Neffy 1 mg is now approved by the FDA to treat pediatric patients who weigh 33 to 65 lbs. Neffy was first FDA-approved as a 2 mg dose in August 2024 for the emergency treatment of anaphylaxis in children and adults weighing at least 66 lbs.
Read More