PMID- 27747566 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20200930 IS - 2199-1154 (Print) IS - 2198-9788 (Electronic) IS - 2198-9788 (Linking) VI - 2 IP - 3 DP - 2015 Sep TI - Dopamine Agonists: Time Pattern of Adverse Effects Reporting in Australia. PG - 199-203 AB - BACKGROUND: In Australia, there is voluntary reporting of suspected adverse events (AEs) of therapeutic medicines. Some dopamine agonists (DAs) have serious AEs. OBJECTIVE: We aimed to explore the pattern of DA AE reporting over two decades. METHODS: We analysed AE case line listings obtained from the Australian Committee on the Safety of Medicines (ACSOM) for bromocriptine, cabergoline, pergolide, pramipexole and ropinirole, and related these to drug utilisation data (1992-2012). We noted the AE nature, frequency, onset, novelty, severity and outcome. RESULTS: The 220 suspected AEs fell into five categories: (i) syncopal/pre-syncopal, (ii) fibrotic, (iii) psychotic, (iv) obsessive-compulsive behaviours (OCB) and (v) increased sleep. There were differential lag times between initial individual drug registration and reporting of suspected AEs, with a lag of at least one year for fibrotic reactions and OCB compared to more contemporaneous reporting of other AEs. Consistent with the published literature, ACSOM data showed that ergot DAs share fibrotic reactions as a class AE, whereas symptomatic hypotensive reactions, psychosis and OCB occurred in both ergot and non-ergot DAs, cabergoline and pramipexole, respectively. Reports of syncopal and pre-syncopal reactions seemed to diminish as ergot-based DA use declined. Levodopa was taken simultaneously with DAs in 87 instances. Of those treated, 92 % were 50 years or older. Parkinson's disease accounted for 89 % of use (119 reports). CONCLUSIONS: Exploring the temporal relationship between post-marketing AE reporting and utilisation data, as exemplified by DAs, can be a valuable pharmacovigilance tool to encourage targeted adverse event monitoring and reporting. FAU - Hollingworth, Samantha A AU - Hollingworth SA AD - School of Pharmacy, The University of Queensland, 20 Cornwall St, Woolloongabba, QLD, 4102, Australia. s.hollingworth@uq.edu.au. FAU - McGuire, Treasure M AU - McGuire TM AD - School of Pharmacy, The University of Queensland, 20 Cornwall St, Woolloongabba, QLD, 4102, Australia. AD - Mater Pharmacy Services, Mater Health Services, Raymond Tce, South Brisbane, QLD, 4101, Australia. AD - Faculty of Health, Sciences and Medicine, Bond University, Gold Coast, QLD, 4229, Australia. FAU - Pache, David AU - Pache D AD - School of Pharmacy, The University of Queensland, 20 Cornwall St, Woolloongabba, QLD, 4102, Australia. AD - Mater Pharmacy Services, Mater Health Services, Raymond Tce, South Brisbane, QLD, 4101, Australia. AD - Faculty of Health, Sciences and Medicine, Bond University, Gold Coast, QLD, 4229, Australia. FAU - Eadie, Mervyn J AU - Eadie MJ AD - School of Medicine, The University of Queensland, 288 Herston Rd, Herston, QLD, 4006, Australia. LA - eng PT - Journal Article PL - Switzerland TA - Drugs Real World Outcomes JT - Drugs - real world outcomes JID - 101658456 PMC - PMC4883210 COIS- Compliance with Ethical Standards Funding This study was funded from existing salaries. This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors. Conflict of interest The authors Dr. Hollingworth, Assoc. Prof. McGuire, Dr. Pache and Emer. Prof. Eadie declare that there were no conflicts of interest. Ethical approval No ethical approval was required as we used only secondary de-identified data sources. EDAT- 2016/10/18 06:00 MHDA- 2016/10/18 06:01 PMCR- 2015/07/16 CRDT- 2016/10/18 06:00 PHST- 2016/10/18 06:00 [entrez] PHST- 2016/10/18 06:00 [pubmed] PHST- 2016/10/18 06:01 [medline] PHST- 2015/07/16 00:00 [pmc-release] AID - 10.1007/s40801-015-0028-3 [pii] AID - 28 [pii] AID - 10.1007/s40801-015-0028-3 [doi] PST - ppublish SO - Drugs Real World Outcomes. 2015 Sep;2(3):199-203. doi: 10.1007/s40801-015-0028-3.