Received: 29 April 2022
Accepted: 23 June 2022
First Online: 7 July 2022
: The study was conducted in accordance with the principles of the Declaration of Helsinki, the Good Pharmacoepidemiology Practice (GPP) and the Spanish laws and regulations. It was classified into the Observational Post-Authorization Study-Other Designs (EPA-OD) category by the Spanish Agency of Medicine and Sanitary Products (AEMPS) and approved by the Ethics Committee of the Consorci Sanitari de Terrassa (Terrassa, Spain) on 27/01/2020. The study also complied with the current General Data Protection Regulation (EU) 2016/679 (GPDR) of the European Parliament and of the Council of 27 April 2016 and with the Spanish Organic Law 3/2018 of 5 December 2018 on Data Protection and Guarantee of Digital Rights. Written informed consent was not requested from patients as information obtained from medical records was dissociated from the personal identification data and used anonymously.
: Not applicable.
: PI received honoraria from Eli Lilly, Novartis, TEVA, Abbvie and Chiesi for educational activities; DGA received honoraria from Allergan, Lundbeck, Eli Lilly, Novartis, Chiesi and Teva for educational activities. MN, SD, PGP, TP and AC are Eli Lilly employees. ASN and ASM provided independent consultant expertise.