Overactive Bladder Agents
Indications for Prior Authorization
Gelnique (oxybutynin chloride)
-
For diagnosis of Overactive Bladder Symptoms
Indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency.
Criteria
Gelnique
Step Therapy
Length of Approval: 12 Month(s)
- Requested drug is being used for a Food and Drug Administration (FDA)-approved indication AND
- Trial and failure (of a minimum 30-day supply), contraindication, or intolerance to two of the following: [2]
- Myrbetriq tablets
- generic darifenacin ER
- generic oxybutynin immediate-release (IR)/extended-release (ER)
- generic solifenacin
- generic tolterodine IR/ER
- generic trospium IR/ER
- generic fesoterodine ER
P & T Revisions
2024-02-19, 2023-03-15, 2022-08-04, 2022-03-03, 2021-09-17, 2021-06-28, 2021-05-20, 2021-03-04, 2020-01-31, 2019-12-10, 2019-11-18
References
- Gelnique prescribing information. Allergan USA, Inc. Madison. NJ. March 2019.
- American Urological Association. Guideline on Diagnosis and Treatment of Non-Neurogenic Overactive Bladder (OAB) in Adults (2019). https://www.auanet.org/guidelines/overactive-bladder-(oab)-guideline. Accessed February 14, 2022.
Revision History
- 2024-02-19: 2024 Annual review. No changes to clinical criteria. Updated GPIs.
- 2023-03-15: Annual review - added FDA approved indication criterion.
- 2022-08-04: Updated ST to include generic fesoterodine as ST1 alt.
- 2022-03-03: Annual review - updated references.
- 2021-09-17: Criteria update to state Myrbetriq "tablets".
- 2021-06-28: Updated prerequisite options to include Myrbetriq, generic darifenacin ER and generic solifenacin.
- 2021-05-20: EHB specific guideline, added to EHB formulary, removed from ORx standard formulary. no changes to criteria
- 2021-03-04: Annual review - added "minimum 30-day supply" language to T/F requirement. Added trospium ER and tolterodine ER as additional T/F options. Updated references.
- 2020-01-31: Annual review - updated references.
- 2019-12-10: EHB guideline that only targets Gelnique.
- 2019-11-18: Removed Vesicare as target from existing guideline as it will be managed via the Generic-first Program.