The information sourced from the pragmatic review of the literature was combined with a questionnaire survey among community pharmacies (
For this rapid analysis, we selected via purposive sampling representation of pharmacies from across India. This included Ahmedabad, Jodhpur, and Pune as part of Western India, West Singhbhum and Kolkata as part of Eastern India, and Delhi in northern India. Convenience sampling in these cities was used to select pharmacists through emails, telephone contact, personal contacts and other mechanisms. There was no sample size calculation as there was no previous data in India to base calculations upon. However, the intention was to undertake the research among an appreciable number of community pharmacies across India to gain good insights and provide a basis for future studies if needed.
Key questions were to assess patterns of demand, availability, and price changes of selected medicines and equipment, as well as the potential future role of pharmacists to reduce misinformation. These are contained in
The pharmacists were briefed on the objectives of the study with the option to participate or not, with confidentiality maintained throughout. Our hypothesis, based on findings in other countries, was that there would be shortages of some of the medicines, although countered in India as a chief producer of medicines with export bans in place certainly initially (Duffy & Hussain, 2020 ) Price rises especially for medicines potentially tempered though by the Ministry of Pharma and Consumer Affairs being instructed to take necessary action to regulate these for PPE and other health related materials alongside existing regulations for (
We subsequently combined the data collected using the experience of the co-authors regarding key issues including pharmaceutical care, health policy and self-purchasing in LMICs to provide future direction, building on comments from the interviewed pharmacists. We have previously successfully used this approach to provide future direction in LMICs (Godman et al., 2018 (link); Godman et al., 2019a (link); Godman et al., 2020a (link); Godman et al., 2020b (link); Godman et al., 2020c (link); Godman et al., 2020d (link)).
Ethical approval for this study was not required according to national legislation and institutional guidelines. However, all pharmacists freely provided the requested information having been given the opportunity to refuse to participate if wished. This is in line with previous studies undertaken by the co-authors in related areas including analysis of policies to enhance the rationale use of medicines and biosimilars, pricing policies and issues surrounding generics, which involved direct contact with health authority personnel and other key stakeholders (Moorkens et al., 2017 (link); Godman et al., 2019b ; Gad et al., 2020 (link); Godman et al., 2020a (link); Godman et al., 2020c (link); Miljković et al., 2020 (link)).