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0 0.5 1 1.5 2+ Symp. case 22% Improvement Relative Risk Recovery time 37% Famotidine for COVID-19  Balouch et al.  Prophylaxis Is prophylaxis with famotidine beneficial for COVID-19? Retrospective 307 patients in the USA Fewer symptomatic cases (p=0.49) and faster recovery (p=0.32), not sig. Balouch et al., J. Voice, January 2021 Favors famotidine Favors control

Role of Famotidine and Other Acid Reflux Medications for SARS-CoV-2: A Pilot Study

Balouch et al., Journal of Voice, doi:10.1016/j.jvoice.2021.01.007
Jan 2021  
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Famotidine for COVID-19
26th treatment shown to reduce risk in October 2021
*, now known with p = 0.00026 from 30 studies.
No treatment is 100% effective. Protocols combine complementary and synergistic treatments. * >10% efficacy in meta analysis with ≥3 clinical studies.
3,800+ studies for 60+ treatments.
Survey of 307 patients in the USA, showing no significant difference in COVID-19 cases with famotidine use.
risk of symptomatic case, 22.0% lower, RR 0.78, p = 0.49, treatment 18 of 80 (22.5%), control 49 of 227 (21.6%), adjusted per study, odds ratio converted to relative risk, multivariable.
recovery time, 36.9% lower, relative time 0.63, p = 0.32, treatment 80, control 227.
Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates
Balouch et al., 20 Jan 2021, retrospective, USA, peer-reviewed, 5 authors.
This PaperFamotidineAll
Role of Famotidine and Other Acid Reflux Medications for SARS-CoV-2: A Pilot Study
Bailey Balouch, Swetha Vontela, Heather Yeakel, Ghiath Alnouri, Robert T Sataloff
Journal of Voice, doi:10.1016/j.jvoice.2021.01.007
Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the coronavirus-19 disease (COVID-19) pandemic. The H-2 blocker famotidine has been suggested as an FDAapproved drug that could potentially be repurposed for treatment of COVID-19. Famotidine has since been shown to improve patient outcomes and reduce symptom severity in patients acutely ill with COVID-19. Other studies have suggested that proton pump inhibitors (PPIs) might have an association with COVID-19. Objective. The purpose of the present study was to determine whether famotidine or any other antireflux medications have a prophylactic or detrimental effect for SARS-CoV-2 infection when taken regularly for the management of acid reflux. Methods. An anonymous, web-based survey was distributed via email to adult otolaryngology patients to collect demographic data, past medical history, medication history, incidence of symptoms associated with COVID-19, potential exposure to SARS-CoV-2, and results of any PCR or serological testing. Associations between reflux medications and incidence of COVID-19 cases were analyzed. Statistical analysis was performed using SPSS. Chisquare with Fisher's exact test, Point-Biserial correlation, Kendall's-tau-b, independent samples t test, and the Mann-Whitney U test were used as appropriate. A binary logistic regression model was fit to determine probability of COVID-19 cases after adjustment for other risk factors. Results. There were 307 patients who responded to the survey. The average age of respondents was 52.63 § 17.03. Famotidine use was not associated with incidence of laboratory-confirmed (P= 0.717) or symptomatically suspected (P= 0.876) COVID-19. No other reflux medications were found to be significant predictors for laboratory-confirmed or suspected COVID-19 (P> 0.05). Younger age (odds ratio [OR] = 1.043, 95% CI: 1.020−1.065, P< 0.001), high risk obesity (OR = 4.005, 95% CI: 1.449−11.069, P= 0.007), and use of a corticosteroid nasal spray (OR = 3.529, 95% CI: 1.352−9.211, P= 0.010) were significant predictors for symptomatically suspected COVID-19 cases. Conclusions. There was no association between incidence of COVID-19 and use of reflux medications, including famotidine at doses used orally to manage reflux and high dose PPIs. Reflux medications did not protect against or increase the risk of COVID-19.
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