Use of azilsartan medoxomil in the primary-care setting in Germany: A real-world evidence study
Birgit Ehlken1, Margarita Shlaen1, Maria del Pilar Lopez Fuensalida de Torres1, Michie Hisada2, Dimitri Bennett3
1 IQVIA, Real World & Analytics Solutions, Munich, Germany, 2 Takeda Development Center Americas, Inc., Pharmacovigilance, One Takeda Parkway, Deerfield, IL, and 3 Takeda Pharmaceuticals International Co., Epidemiology, Cambridge, MA, USA
DOI 10.5414/CP203359
Abstract
Objective: To evaluate azilsartan medoxomil (AZM) (Edarbi®) utilization patterns in the primary-care setting in Germany. Materials and methods: This is a retrospective cohort study among patients receiving AZM in the primary-care setting in Germany. Prescription patterns – including patient demographics, off-label use, use in specific populations, concomitant use of other antihypertensive drugs, and drugs potentially causing interactions with AZM – were analyzed in two periods (01/2012 – 12/2013 and 01/2014 – 11/2016) using the primary-care physician panel of German IMS® Disease Analyzer, a patient-level electronic medical records database. Results: In total, 852 of 1,159 (74%) and 696 of 811 (86%) patients met the inclusion criteria for both periods, respectively. Approximately 25% of patients were aged ≥ 75 years; 1 patient was < 18 years old; ~ 50% were females. AZM was prescribed for the approved indication of essential hypertension in 83% and 68% of patients in the first and second period, while indication was missing in 12% and 26% of patients, respectively. AZM was coprescribed on the same day with other antihypertensive drugs in 23% (first period) and 37% (second period) of patients. Drugs that might cause an interaction with AZM were coprescribed on the same day in 3% of patients in both periods; overlapping prescription periods were detected in 14% (first period) and 8% (second period) of patients. Coprescription of AZM with angiotensin-converting enzyme (ACE) inhibitors (2%) or aliskiren (< 1%) on the same day was rare in both periods. Overlapping prescription periods with AZM decreased from 20 to 6% for ACE inhibitors and from 8 to 1% for aliskiren. Conclusion: Findings from this real-world evidence study demonstrate that AZM was generally utilized for approved indication and in accordance with the summary of product characteristics recommendations.
Author Details
Authors
Departments
- 1 IQVIA, Real World & Analytics Solutions, Munich, Germany,
- 2 Takeda Development Center Americas, Inc., Pharmacovigilance, One Takeda Parkway, Deerfield, IL, and
- 3 Takeda Pharmaceuticals International Co., Epidemiology, Cambridge, MA, USA
Address
Birgit Ehlken, MSc
IQVIA, Real World & Analytics Solutions
Landshuter Allee 10, 80637 Munich, Germany
Email:
[email protected]
Citation
Birgit Ehlken, Margarita Shlaen, Maria del Pilar Lopez Fuensalida de Torres, Michie Hisada, Dimitri Bennett.Use of azilsartan medoxomil in the primary-care setting in Germany: A real-world evidence study
. 2019; 57: 275-283. doi: 10.5414/CP203359.