WYDUR Board Meeting Minutes
Ramada Inn
Members Present: Kay Kohler, Becky Drnas, Kendra Grande,
Antoinette Brown, Dawn Ford, Scott Johnston, Mike Carpenter, Richard Johnson,
George Zaharas, Bill Harrison, Lenny Kosirog, Deb Devereaux
Members Excused: Steve Brown
Guests: Bobbie Cesko, John Vandel, Justin Woods (VA
resident), Laura Miller, Lori Howarth (Berlex), Dennis Sagendorf (Purdue
Pharma), Paul Pereira (TAP), Linda Pryor (Pfizer), Larry Bridger (Pfizer), Joan
Solem (Lilly), Betty Iverson (Wyeth), Kelly Steiner (Merck), Jeff Jenkins
(Merck), Angela McCoy (Janssen), Bob Schultz (BCBS), Michelle Simmons (Ortho
McNeil), Allison Kaelberer (Ortho McNeil), Mike Ross (Takeda), Bill Thomson
(Pharma Counsel)
The meeting was called to
order by Chair Kay Kohler at
I. Retrospective and Prospective DUR
Alert Changes: (a.) suppress alert for progesterone
contraceptives/migraine because estrogen component is associated with headaches
(b) suppress oral contraceptive/antibiotic alert because data surrounding the
interaction is weak (c) add alert for acetaminophen maximum dose per day
>4gm.
Provider response forms were
reviewed.
Other: Data regarding Somatropin (human growth
hormone) was reviewed. Most patients are
under 17 years old but a few are greater than 18 yo.
The Board discussed the
evaluation of drugs for off label use.
There are difficulties in identifying those cases purely by data
analysis. Dr. Johnston suggested that a
review of Viagra, Cialis and Levitra be conducted to ensure that there is no
utilization by females. If that use
exists, it was suggested that a hard edit would be appropriate.
A special celebration and
awards were presented to Dawn Ford for her 12 years of service to the Wyoming
Drug Utilization Review Board and program.
The minutes of the
Antoinette presented prior
authorization statistics. The next PDL
Advisory Group meeting is Thursday April 15 from 10-2 in
Newsletter suggestions: ACEI equivalency chart, atypical antipsychotics
Dr. Johnston presented data
on the utilization of Marinol-delta 9 thc which is the schedule III drug
indicated for HIV induced anorexia and cancer induced nausea. There were 29 patients who received the drug
at a cost of $105,000. Five patients had
an HIV diagnosis, 1 had cancer and 11 had MS.
In MS studies, there is no objective improvement in spasticity although
subjectively patients reported feeling better.
The side effect profile is problematic for non-prior users: heavy sedation with a 30-40% dropout
rate. Other states policies regarding
this drug will be looked at with a possible hard edit for dosage.
A utilization review report
of Mimenda was discussed. There were 20
patients currently utilizing the medication-16 had Alzheimers and 4 had a pain
diagnosis. This medication will continue
to be monitored.
There being no further
business the meeting was adjourned at
Respectfully Submitted,
Debra S. Devereaux MBA,
R.Ph.
Manager,