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Home Court filings Klaassen v. Trustees of Indiana University Declaration of Cole Beeler, M.D. — Klaassen v. Indiana University

Court filing

Declaration of Cole Beeler, M.D. — Klaassen v. Indiana University

Record facts

CourtU.S. District Court for the Northern District of Indiana
Filed2021-07-12

U.S. District Court for the Northern District of Indiana · No. 1:21-cv-00238-DRL-SLC · Doc. 21-1 · 2021-07-12 · Docket on CourtListener

Summary

The declaration of Cole Beeler, M.D., submitted as Exhibit A in Klaassen v. The Trustees of Indiana University, Case No. 1:21-cv-00238, in the U.S. District Court for the Northern District of Indiana, stamped as document 21-1 filed July 2, 2021 and document 31-16 filed July 12, 2021. The declarant states he is an Assistant Professor of Clinical Medicine at the Indiana University School of Medicine and serves on Indiana University's Restart Committee. The declaration describes COVID-19 transmission and groups at increased risk of severe illness, and cites over 750,000 confirmed cases and over 13,000 deaths in Indiana since March 6, 2020 and almost 12,000 student positive tests at IU since July 2020. It addresses the three COVID-19 vaccines available in Indiana and variants, and responds to the plaintiffs' expert on herd immunity. The document is 38 pages and attaches the declarant's C.V.

Summary drafted by a model from the document's text below and checked by script against that text before publication. It is a navigation aid, not a reading of what the document proves. Where AI is used

Full text

______________________ 
 
EXHIBIT A 
______________________ 
 
 
 
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UNITED STATES DISTRICT COURT 
NORTHERN DISTRICT OF INDIANA 
FORT WAYNE DIVISION 
 
 
RYAN KLAASSEN, JAIME CARINI,           ) 
D.J.B., by and though his next friend and 
) 
 father, DANIEL G. BAUMGARTNER,  
) 
ASHLEE MORRIS, SETH CROWDER,  
) 
 MACEY POLICKA, MARGARET ROTH,  ) 
 and NATALIE SPERAZZA, 
) 
 
) 
 
Plaintiffs, 
) 
Case No. 1:21-cv-00238 
 
 
) 
vs. 
 
) 
 
 
) 
THE TRUSTEES OF INDIANA 
) 
UNIVERSITY, 
 
) 
 
 
) 
 
Defendant. 
) 
 
 
DECLARATION OF COLE BEELER, M.D. 
 
I. 
Background 
1. 
I am over 18 years of age. This declaration is based upon my own personal and 
professional knowledge and experience. 
2. 
I am competent to testify as a medical expert to the facts and matters set forth 
herein. A true and accurate copy of my C.V. is attached hereto as Exhibit A.  
3. 
I am currently an Assistant Professor of Clinical Medicine at the Indiana 
University School of Medicine. I earned my B.S. and my M.D. from Indiana University. 
4. 
I am dual Board certified by the American Board of Internal Medicine in 
Infectious Disease and Internal Medicine. I am a member of the Infectious Diseases Society of 
America. 
5. 
I am a member of Indiana University’s Restart Committee. I serve on its 
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Modeling and Data Monitoring subgroup. 
II. 
Analysis 
A. COVID-19 
6. 
COVID-19 is an infectious disease caused by the novel coronavirus (SARS-CoV-
2) that primarily spreads through respiratory droplets and aerosol transmission.  
7. 
People of all ages can contract and transmit COVID-19.  
8. 
People who catch COVID-19 may suffer from immediate severe illness and/or 
suffer long-term ongoing health problems, extending several weeks or months. Individuals 
infected with COVID-19 can suffer these long-term negative health effects even if they were 
initially asymptomatic. COVID-19 can also be fatal. CDC, Benefits of Getting a COVID-19 Vaccine, 
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/vaccine-benefits.html. 
9. 
Certain types of individuals are at increased risk of suffering severe illness or 
death if they contract COVID-19, and thus are more likely to need more serious medical 
intervention, including hospitalization, intensive care, and a ventilator. Individuals who are at 
increased risk of suffering severe COVID-19 include:  
a. Adults over age 45; 
b. Disabled individuals; 
c. Members of many racial and ethnic minority groups; 
d. Immunocompromised individuals; 
e. Current or former smokers; 
f. Individuals who are overweight or obese; 
g. Individuals who have received organ or blood stem cell transplants; 
h. Individuals who have suffered a stroke; and 
i. Individuals with certain other underlying medical conditions, including, among 
others, cancer, chronic kidney disease, chronic lung diseases, dementia and other 
neurological conditions, diabetes (type 1 or type 2), Down syndrome, heart 
conditions, HIV infection, liver disease, sickle cell disease, cerebrovascular 
disease, and substance use disorders. 
CDC, People with Certain Medical Conditions, https://www.cdc.gov/coronavirus/2019-
ncov/need-extra-precautions/people-with-medical-conditions.html; CDC, People with 
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Underlying Medical Conditions at Increased Risk from COVID-19, 
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/recommendations/underlying-
conditions.html. 
10. 
Even though COVID-19 more often affects children less severely than adults, 
COVID-19 has also been shown to cause severe illness in children. Like adults, children with 
underlying medical conditions are at increased risk of suffering more severe illness if they 
contract COVID-19. 
11. 
Additionally, all individuals, including children, who contract COVID-19 risk 
giving it to others, including friends, family, and other individuals with whom they interact, who 
may suffer severe illness or death.  
B. Brief History of the Pandemic 
12. 
COVID-19 was first identified in Wuhan, China in late 2019.  
13. 
According to the Indiana State Department of Health (“ISDH”), Indiana’s first 
case of COVID-19 was confirmed on March 6, 2020, and Indiana’s first COVID-19-related 
death was reported on March 16, 2020. See Indiana’s Novel Coronavirus Response (last visited June 
27, 2021), available at: https://www.coronavirus.in.gov/ (“IN COVID-19 Response”). 
14. 
Since March 6, 2020, Indiana has had over 750,000 confirmed COVID-19 cases 
and over 13,000 deaths. See Indiana COVID-19 Data Report, https://www.coronavirus.in.gov/. 
According to the CDC, an estimated 25.8% of Indiana’s population has been infected with 
COVID-19. 18.4% of Indiana’s positive COVID-19 cases have been reported by individuals 
between the ages of 20 and 29. Individuals aged 20 through 29 have reported more positive 
COVID-19 cases than any other age demographic. A small number of those individuals also 
have died from the virus. 
15. 
The CDC currently estimates that there have been approximately 33.5 million 
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cases of COVID-19 in the United States and over 600,000 people have died from COVID-19 in 
the United States. See CDC, COVID Data Tracker, Nationwide Commercial Laboratory Seroprevalence 
Survey, https://covid.cdc.gov/covid-data-tracker/#national-lab. 
16. 
Nationwide, individuals aged 20-29 accounted for more than 20% of all 
confirmed COVID-19 cases between June and August of 2020. CDC, Changing Age Distribution of 
the COVID-19 Pandemic-United States, May-August 2020 (pub. Oct. 2, 2020), 
https://www.cdc.gov/mmwr/volumes/69/wr/mm6939e1.htm. 
17. 
The New York Times reports that over 700,000 cases of COVID-19 have been 
linked to colleges and universities in the U.S. since the pandemic began and more than 260,000 
COVID-19 cases have been linked to colleges and universities just since January 1, 2021. 
Tracking Coronavirus Cases at U.S. Colleges and Universities, The New York Times, 
https://www.nytimes.com/interactive/2021/us/college-covid-tracker.html. 
18. 
Since July 2020, IU has had almost 12,000 students test positive for COVID-19. 
See IU COVID-19 Testing Dashboard, https://www.iu.edu/covid/dashboard/all. 
C. COVID-19 Vaccinations 
19. 
We are likely to stop the spread of COVID-19 only when we achieve population 
immunity, also known as “herd immunity.”  
20. 
Widespread COVID-19 vaccination is a critical tool in achieving herd immunity.  
21. 
The scientific community has not yet determined the percentage of people who 
need to be protected from COVID-19 to achieve herd immunity. In fact, because the virus 
continues to mutate, which results in variants, experts remain unsure whether achieving herd 
immunity from COVID-19 is truly possible.  
22. 
Consequently, vaccinating individuals against COVID-19 currently is the leading 
prevention strategy to protect individuals from the virus and end the pandemic. CDC, Guidance 
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for [IHEs], https://www.cdc.gov/coronavirus/2019-ncov/community/colleges-universities/index.html.  
23. 
There are three COVID-19 vaccinations available in Indiana at no cost: the Pfizer-
BioNTech vaccine, the Moderna vaccine, and the Johnson & Johnson vaccine (collectively, 
“COVID-19 Vaccines”). See State of Indiana Vaccination Information and Planning, About the vaccine, 
https://www.coronavirus.in.gov/vaccine/. 
24. 
Each of the COVID-19 Vaccines has been proven safe and effective. COVID-19 
Vaccine: It’s our shot, Hoosiers (updated June 5, 2021), 
https://www.coronavirus.in.gov/files/21_IN%20Vaccine%20effectiveness_6-2.pdf at 1; see also, e.g., 
ISDH COVID-19 Vaccine FAQs at 1, 
https://www.coronavirus.in.gov/files/General%20Tool%20Kit%20Condensed%20FAQ%20and%20Links
%203.29.21.pdf  (“The vaccine has been found in trials to be 95 percent effective in preventing COVID-
19 infections . . .”). Each was developed using long-standing science and scientific techniques that 
are not experimental. Each went through all the federally mandated stages of clinical trials, 
which include extensive testing and monitoring. Each has received and continues to undergo the 
most intensive safety monitoring in U.S. history. The fact that the COVID-19 Vaccines are 
currently available under Emergency Use Authorization in no way undermines their safety or 
efficacy. 
25. 
The COVID-19 Vaccines are extremely unlikely to cause serious side effects that 
could result in long-term health problems. CDC, Safety of COVID-19 Vaccines, 
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/safety-of-vaccines.html. 
26. 
The COVID-19 Vaccines help prevent the spread of COVID-19 and are effective 
against the COVID-19 variants that have been detected in Indiana. ISDH, Variant Details, 
https://www.coronavirus.in.gov/map/VariantDetails.pdf. 
27. 
Because it takes the human body time to build antibodies to COVID-19, 
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individuals who receive a COVID-19 Vaccine are considered “fully vaccinated” two weeks after 
their second dose of a two-dose vaccine or two weeks after a one-dose vaccine.  
28. 
Fully vaccinated individuals are less likely to catch COVID-19 if exposed to it 
and less likely to spread it to others.  
29. 
The COVID-19 Vaccines also help stop mutation of COVID-19, which helps 
prevent the emergence and spreading of variants. 
30. 
The COVID-19 Vaccines provide a known level of resistance to and protection 
from COVID-19 for a sustained period of time. Conversely, while individuals who have had 
COVID-19 might have some antibodies even after their infection has passed that provide 
protection against COVID-19, the amount of protection that these individuals have against the 
virus varies from person-to-person and wanes over time. As these individuals’ natural immunity 
decreases, their risk of contracting COVID-19 increases.  
31. 
Accordingly, the CDC and the ISDH recommend that even individuals who have 
had COVID-19 receive the COVID-19 Vaccine because the vaccine will provide these 
individuals with additional protection against the virus. Frequently Asked Questions about COVID-
19 Vaccination, https://www.cdc.gov/coronavirus/2019-ncov/vaccines/faq.html. 
32. 
The CDC also recommends that children twelve and older receive the COVID-19 
Vaccine as soon as possible because vaccinating minors helps to protect the minor, their families, 
and other individuals with whom they interact.  
33. 
While the CDC has advised that it has received reports of myocarditis and 
pericarditis in adolescents and young adults after COVID-19 vaccination, it and the ISDH still 
recommend that all individuals age 12 and older receive a COVID-19 Vaccine because the 
reports of myocarditis and pericarditis are rare and the benefits of COVID-19 vaccination still far 
outweigh the known and potential risks. In fact, COVID-19 itself presents the risk of myocarditis 
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and pericarditis. CDC Children & Teens; CDC, Myocarditis and Pericarditis Following mRNA COVID-
19 Vaccination, https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/myocarditis.html. 
34. 
Additionally, people with underlying medical conditions can receive the COVID-
19 vaccine as long as they have not had an immediate or severe allergic reaction to a COVID-19 
Vaccine or its ingredients.  
D. Current COVID-19 Risks  
35. 
The COVID-19 pandemic is ongoing. Currently, the CDC advises that the risk of 
community transmission of COVID-19 in Indiana is “moderate.” Hoosiers continue to report 
hundreds of new COVID-19 cases each day.  
36. 
Additionally, variants of the COVID-19 virus continue to develop and spread 
throughout the country. These variants increase the risks associated with contracting and 
spreading COVID-19 because they spread more easily than the original strain of COVID-19 and 
can cause more severe infection.  
37. 
Indiana, specifically, has seen an increase in variants of the original COVID-19 
strain. Over 60% of the samples tested in Indiana are positive for a variant, and the most recent 
variant—the Delta variant—is confirmed to be present in Indiana. 
38. 
COVID-19 remains a particular threat to those who are unvaccinated.  
39. 
According to the ISDH, unvaccinated Hoosiers constitute 99.3% of COVID-19 
cases in Indiana, and the odds of an unvaccinated Hoosier who contracts COVID-19 being 
hospitalized are 1 in 525, as compared to 1 in 50,394 for fully vaccinated Hoosiers. 
https://www.coronavirus.in.gov/files/21_IN%20Vaccine%20effectiveness_6-2.pdf. 
40. 
IU’s ability to consistently test its students for COVID-19, particularly those 
individuals who are unvaccinated, is critical to its ability to respond quickly to COVID-19 
outbreaks and help stem the spread of the virus as we work towards herd immunity. If IU is 
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unable to regularly test its unvaccinated students for COVID-19, the risk of undetected viral 
spread on IU’s campuses and surrounding communities increases significantly and may even 
affect vaccinated or previously infected constituents via viral breakthrough.  
E. Response to Plaintiffs’ Expert 
41. 
Although COVID rates are declining, the etiology behind this is potentially 
obscured by improved weather (temperature, humidity, UV all favorable for blunting 
transmission). SARS-2 is a respiratory virus and will likely have seasonality like other 
respiratory viruses. Murray, Piot, The Potential Future of the COVID-19 Pandemic:  Will SARS-
CoV-2 Become a Recurrent Seasonal Infection, https://jamanetwork.com/journals/jama/article-
abstract/2777343. Coupled with an unknown fraction of the population that has neither been 
infected or vaccinated, uncertain durations of clinical immunity after natural infection, and the 
potential for breakthrough variants (e.g. B 1617-2), the state of the pandemic over the coming 
winter is still very uncertain. 
42. 
In my expert opinion, the degree of unknowns associated with all of Dr. 
McCullough’s statements as well as significant risks to the collegiate and county communities 
that can be effectively avoided with use of the vaccine, make a mandate the safest way to protect 
our constituents, their families, and their counties from a second inevitable rise in cases over the 
winter. 
Herd Immunity 
43. 
Indiana has not reached herd immunity.  
44. 
Herd immunity is based on the infectivity and R0 of the virus.  The herd immunity 
threshold is still unknown for this virus.  In fact, many authors do not believe herd immunity is 
possible with this virus. Kadkhoda, Herd Immunity to COVID-19:  Alluring and Elusive, 
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https://academic.oup.com/ajcp/article/155/4/471/6063411?login=true; Taylor, COVID-19:  Is 
Manaus the final nail in the coffin for natural herd immunity?) 
https://www.bmj.com/content/372/bmj.n394.short; Tkachenko et al, Time-Dependent 
Heterogeneity leads to transient suppression of the COVID-19 epidemic, not herd immunity, 
https://www.pnas.org/content/118/17/e2015972118.short; Burki, Herd Immunity for COVID-19, 
https://www.thelancet.com/journals/lanres/article/PIIS2213-2600(20)30555-
5/fulltext?utm_content=buffer6eaeb&utm_medium=social&utm_source=twitter.com&utm_cam
paign=buffer.  The current director of the CDC mentions similar concerns:  
https://www.foxnews.com/health/no-magic-target-herd-immunity-walensky. In total, calculations 
like those set forth by Dr. McCullough are highly error prone because of uncertainly related to 
the included variables. See https://www.nature.com/articles/d41586-021-00728-2. 
College Aged Individuals and COVID-19 
45. 
Although the mortality rate for college aged students is lower than other age 
groups, I disagree that there could be “no risk” of infection. The purpose of mass vaccination is 
also to protect individuals who are at higher risk of poor outcome or unable to mount an effective 
immune response. Older individuals, those with problems with their immune system, and those 
on certain medications that interfere with the development of an immune response may not have 
the same protections as a typical college-aged student when vaccinated or infected naturally with 
the virus.   
46. 
We have learned over the last year that our students, faculty, and staff are very 
much members of their communities; they interact and engage consistently within the counties in 
which they live. In any epidemic, infections spread through vulnerable links in the chain until 
eventually resulting in morbidity and mortality in hosts that are less protected. Indeed, our 
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constituency also includes a number of vulnerable individuals for both bad outcomes from 
COVID as well as inability to mount a strong response to the vaccine.   
47. 
The goal of universal vaccination is not limited to individual protection (even 
though there is very strong evidence for this), but includes community-wide protection — to 
reduce the total amount of all exposures to COVID-19, not just infections. Each exposure is 
potential for transmission to a vulnerable individual, and these vulnerable individuals may be 
vulnerable by choice or despite their best efforts to be immune.   
48. 
In addition, the long-term consequences of natural COVID-19 infection are still 
unknown. Even “long COVID” can affect young adults at high levels and lead to long term 
debility. https://health.ucdavis.edu/health-news/newsroom/studies-show-long-haul-covid-19-
afflicts-1-in-4-covid-19-patients-regardless-of-severity/2021/03; 
https://healthblog.uofmhealth.org/childrens-health/long-haul-covid-kids; 
https://www.usnews.com/news/health-news/articles/2021-02-23/whats-wrong-with-me-young-
covid-survivors-battle-long-haul-symptoms. There is still much unknown here. Compared with 
the Covid-19 Vaccines whose platforms have now been used for decades, the uncertainty around 
the consequences of infection with a novel virus, especially in relation to long term side effects 
and sequellae, presents an undue risk. Pardi et al, mRNA vaccines- a new era in vaccinology, 
https://www.nature.com/articles/nrd.2017.243.   
49. 
In summary, though the morbidity and mortality rate in the college age group is 
low, it is not zero. It is coupled with many unknowns, and infections in this population 
potentially drive infections in the community. 
50. 
Moreover, not all studies exonerate students for contribution of spread in their 
surrounding county. Bosslet, et al, The effect of in-person primary and secondary school 
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instruction on county-level SARS-COV-2 spread in Indiana, 
https://www.medrxiv.org/content/10.1101/2021.03.17.21250449v1; Courtemanche et al, School 
Reopenings, Mobility, and COVID-19 spread:  Evidence from Texas, 
https://www.nber.org/papers/w28753; Andersen et al, College Openings, Mobility, and the 
Incidence of COVID-19, https://www.medrxiv.org/content/10.1101/2020.09.22.20196048v1; Lu 
et al, Are College Campuses Superspreaders? A data-driven modeling study, 
https://www.tandfonline.com/doi/full/10.1080/10255842.2020.1869221.   
51. 
Regional differences in county “spill-over” from campus epidemics are likely 
related to variations in infection prevention strategies employed at the campuses with more 
robust strategies leading to less “spill-over.” The most robust strategy is having as many people 
immune as possible and this is best (and most safely) achieved by vaccination.   
52. 
All individuals are equally likely to catch COVID-19. There is no protection from 
infectivity or infectiousness in the college age group. This group may be more likely to be 
asymptomatic, but spread is certainly still very possible as IU and many other colleges across the 
nation, experienced firsthand over the last year. https://www.nytimes.com/interactive/2020/us 
/covid-college-cases-tracker.html. 
Asymptomatic Spread 
53. 
Very quickly in the pandemic, the medical community learned that ignoring 
asymptomatic spread of this virus leads to propagation. As many as 30% of patients with 
COVID-19 never develop symptoms. Johansson et al, SARS-COV-2 Transmission from people 
without COVID-19 symptoms and it is estimated that more than half of all transmissions are 
from individuals who are asymptomatic; Johansson et al, 
https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2774707. This assessment has 
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been supported by the CDC. Bender et al, https://wwwnc.cdc.gov/eid/article/27/4/20-
4576_article; Infectious viral loads start increasing before symptom development; Sakurai, et al, 
Natural History of Asymptomatic SARS-COV-2 Infection, 
https://www.nejm.org/doi/full/10.1056/NEJMc2013020; The Natural History and Transmission 
Potential of Asymptomatic Severe Acute Respiratory Syndrome Coronavirus 2 Infection, 
https://academic.oup.com/cid/article/71/10/2679/5851471.   
54. 
Isolation by symptoms alone is not the consensus opinion of medical experts, 
which is why most states in the U.S. as well as around the world recommend quarantine of 
exposed individuals. This is because symptoms do not predict infectivity and it is safer to stay 
home through the duration of an infectivity window after an exposure in order to protect the 
community.   
55. 
Masking is also an effective and evidence-based intervention to help stem the 
spread of COVID-19, even in asymptomatic individuals. Although this protection is significantly 
less potent than immunity by vaccination, ongoing masking of unvaccinated individuals is a 
potential stopgap for those unable to be vaccinated.  Unmasked and unvaccinated individuals put 
themselves at additive risk of infection as well as those around them that are unable to be 
vaccinated or mount a sufficient immune response.   
COVID Treatments 
56. 
Reliable data on treatment for COVID-19 is still lacking. Most of the regimens 
listed in Table 5 of Dr. McCullough’s Report (p. 16) have been proven to be ineffective in 
clinical trials despite hypothesized benefit. Indeed, some have even caused patient harm. 
57. 
Vitamins and medications like: 
Zinc (Yao, et al, The minimal effect of Zinc on the survival of hospitalized patients with 
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COVID-19:  An observational study, Chest 2021); 
Hydroxychloroquine (Lewis et al, The efficacy and safety of hydroxychloroquine for 
COVID-19 prophylaxis:  A systematic review and meta-analysis of randomized trials 
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0244778; Kashour et 
al, Efficacy of Chloroquine or hydroxychloroquine in COVID-19 patients: a systematic 
review and meta-analysis, 
https://academic.oup.com/jac/article/76/1/30/5919602?login=true);  
Ivermectin (Schmith, et al, The Approved Dose of Ivermectin Alone is not the Ideal 
Dose for the Treatment of COVID-19, 
https://ascpt.onlinelibrary.wiley.com/doi/full/10.1002/cpt.1889); 
Azithromycin (Escheverria-Esnal et al, Azithromycin in the treatment of COVID-19:  a 
review, https://www.tandfonline.com/doi/full/10.1080/14787210.2020.1813024); 
Doxycycline (Narendrakumar et al, Potential effectiveness and adverse implications of 
repurposing doxycycline in COVID-19 treatment, 
https://www.tandfonline.com/doi/full/10.1080/14787210.2021.1865803); 
Inhaled Budesonide (Agusti et al, Early Treatment with Inhaled Budesonide to prevent 
clinical deterioration in patients with COVID-19, 
https://www.thelancet.com/journals/lanres/article/PIIS2213-2600(21)00171-5/fulltext);  
have not been studied in rigorous head-to-head trials to determine actual benefit, have negative 
consequences, or have been associated with patient harm. Their use has been thoroughly 
discredited and discouraged by the CDC/NIH. https://www.covid19treatmentguidelines.nih.gov/ 
about-the-guidelines/whats-new/.   
58. 
At IU Health and many other centers, the adult treatment regimen for COVID-19 
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includes Dexamethasone, Remdesivir, Tocilizumab, and Baricitinib. All of these agents are 
restricted to patients who have moderate to severe disease (minimal requirement of supplemental 
oxygen). Dexamethasone, Tocilizumab and Baricitinib are for patients with severe 
manifestations for disease (high flow oxygenations, non-invasive mechanical ventilation, and 
mechanical ventilation). These recommendations in the hospital are based on the high-quality 
studies showing benefit in these populations; however, there is still back-and-forth data even 
with these agents.   
59. 
The evidence base for treatment is still very uncertain as evidenced by the lack of 
primary literature support for each individual regimen by Dr. McCullough. Successful outpatient 
management of COVID in some patients can be very challenging, and even if an individual is 
able to avoid hospitalization with investigational therapies, this does not speak to the 
consequences of infectious spread in the people who they live with, their vulnerabilities, and 
their ability to obtain care. Prevention still remains the key driver for avoiding morbidity and 
mortality from COVID-19 of which the vaccines are our most potent tool. 
COVID Vaccines 
60. 
All three COVID-19 Vaccines have been studied in robust multi-centered, 
international, randomized-controlled trials and proven both effective and safe in millions of 
people.   
61. 
All three COVID-19 Vaccines have demonstrated a very high rate of efficacy 
(Pfizer 95%, Moderna 94.1%, Johnson & Johnson 72%). 
https://www.yalemedicine.org/news/covid-19-vaccine-comparison. These rates are much higher 
than annual influenza vaccination (30-60% effective depending on the year), which is a 
mandated annual vaccine at many universities. Breakthrough infections are possible with any 
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15 
 
 
vaccine, but when you look at the amount vaccinated, these numbers are very low (0.05% in 
Indiana). https://www.whas11.com/article/news/health/coronavirus/indiana-covid-breakthrough-
case-vaccine-differences/417-e62d4d8a-a044-4816-a50b-aceddd6741e8). I would note that we 
also have breakthrough cases after natural infection (0.65%). 
https://www.eurekalert.org/pub_releases/2021-03/l-tls031821.php.   
62. 
Overall, these are some of the most effective vaccines that have ever been 
developed. 
63. 
There is currently no evidence of genotoxicity, mutagenicity, teratogenicity and 
oncogenicity in any of the EUA-approved COVID vaccines.   
64. 
A formal FDA approval for safety requires 6 months of data. These outcomes 
would require decades of research (Kostoff et al, COVID-19 vaccine safety, 
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521561/) and are unnecessary based on the 
mechanism of vaccine action. In the cell, DNA in the nucleus encodes for a messenger (RNA) 
that leaves the nucleus and utilizes the cellular machinery in the cytoplasm to make proteins that 
do the work of the cell. The RNA vaccines utilize cellular machinery to make a protein that looks 
like the main target of our natural immune system to the SARS2 virus.  The current lay public 
suspicions regarding mutagenesis take a backwards view of how RNA works in the cell and are 
not currently supported by consensus opinion. Since the vaccines do not interact with DNA, they 
do not lead to mutations, gene damage, or the development of cancers. Cimolai et al, Do RNA 
vaccines obviate the need for genotoxicity studies? 
https://academic.oup.com/mutage/article/35/6/509/5995048?login=true;  
https://www.mskcc.org/coronavirus/myths-about-covid-19-vaccines; https://news.llu.edu/health-
wellness/expert-debunks-5-covid-19-vaccine-misconceptions. 
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16 
 
 
65. 
There are many medications and vaccines that we use today that have not had 
these studies. Investigation into these areas should be based on clinical suspicion and 
hypothesized links of which there are neither currently for the three COVID-19 Vaccines.  
Further hypothesized risks of the vaccine are dwarfed by the very real risk of actual COVID-19 
infection among the college constituency and in their communities.    
66. 
While the three currently available vaccines are made of the building blocks of 
RNA, they are not genes, but are messenger scripts for making a protein. Their safety has been 
repeatedly confirmed in randomized controlled trials with no difference in adverse outcomes 
between vaccinated and unvaccinated individuals. There is no evidence that the spike protein 
itself injures our body’s organs. The spike is an entry receptor for the virus to get into cells and 
the major target of our immune system. The spike protein itself cannot damage tissues, cause 
infections, or lead to complications. The immune response to the spike protein may be associated 
with some adverse outcomes like clotting and myocarditis; however, the risks of these outcomes 
associated with the vaccine are dwarfed by the risks of these outcomes associated with COVID-
19 infection itself. Torjesen, COVID-19:  Risk of cerebral blood clots from disease is 10 times 
than from vaccination, study finds, https://www.bmj.com/content/373/bmj.n1005.full; Wise et al, 
COVID-19:  Should we be worried about reports of myocarditis and pericarditis after mRNA 
vaccines?, https://www.bmj.com/content/373/bmj.n1635).   
67. 
As an example, the rate of myocarditis in all recipients is 13/1,000,000 vaccines 
administered (32/1,000,000 in males aged 12-39). 
https://www.cdc.gov/vaccines/acip/meetings/downloads/slides-2021-06/03-COVID-
Shimabukuro-508.pdf. In contrast, 2.3% of collegiate athletes who had recovered from COVID-
19 had evidence of myocarditis on heart imaging. Daniels et al, Prevalence of Clinical and 
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Subclinical Myocarditis in Competitive Athletes with Recent Sars-CoV-2 Infection:  Results 
from the Big Ten Covid-19 Cardiac Registry, 
https://jamanetwork.com/journals/jamacardiology/fullarticle/2780548.   
68. 
The infection of COVID-19 itself puts college-aged students at higher risk for 
myocarditis than the vaccine. In addition, all vaccine associated myocarditis patients have 
survived and were treated effectively. https://whyy.org/articles/myocarditis-and-the-covid-19-
vaccine-what-to-know-about-rare-heart-inflammation/. Because of all of this, the CDC continues 
to recommend COVID vaccination for this younger age group.  
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/myocarditis.html.  
69. 
Although the risk of cerebral sinus thrombosis after the Johnson & Johnson 
vaccine is significant, it occurs with incredibly low probability and there is no proof of causation 
between the vaccination and myocarditis. 
https://www.cdc.gov/vaccines/acip/meetings/downloads/slides-2021-04/03-COVID-
Shimabukuro-508.pdf. While the vaccines may have statistics that support an association of 
adverse outcomes, it is important not to imply causality until we are sure. The Johnson & 
Johnson vaccine provides very meaningful benefit to a college-aged population given its ease of 
administration as one dose.  Additionally, IU students are able to receive whichever of the three 
COVID-19 vaccines they prefer if they are personally concerned about this potential association. 
Vaccination after COVID-19 infections     
70. 
The CDC continues to recommend vaccination for those who have been infected 
naturally with COVID-19 and there is emerging evidence that vaccination may provide a broader 
spectrum of protection to variants than natural infection 
(https://directorsblog.nih.gov/2021/06/22/how-immunity-generated-from-covid-19-vaccines-
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differs-from-an-infection/).   
71. 
There is no strong data for or against vaccination after natural infection 
https://www.nature.com/articles/d41586-021-01609-4. We may have this data in the future, but 
right now, we do not have accurate ways to diagnose prior infection. This leads to huge 
challenges with trying to figure out who does and does not need the vaccine. Until this data is 
looked at in a systematic and controlled fashion, more “boosters” to immunity in the form of a 
COVID-19 Vaccine are likely beneficial to avoiding infection even despite mild side effects that 
are transient and benign.   
72. 
Another major concern will be availability of data. There will consistently be new 
variants of COVID that will be selected out by vaccination and natural infection. These will be 
allowed to continue to mutate as long as there is susceptible population available. We have much 
better data for efficacy of vaccines against variants than we do for efficacy of natural immunity 
against variants. This is because we know exactly when immunity is established and the 
trajectory over time. Without vaccination, there will be lingering concerns about breakthrough 
variants leading to reinfection that will be more difficult to study internationally and provide 
guidance to the cohort of our population that has not gotten the vaccine. 
73. 
It is entirely possible that the vaccine provides a broader immunity than natural 
infection. It may be that people who were previously infected have a higher rate of vaccination 
side effects after the first dose of the vaccine, but these symptoms are generally mild and not 
dangerous. There are no reports of serious, life-threatening safety concerns for previously 
infected individuals.   
74. 
The preprint article from Raw et al referenced in paragraph 63 of Dr. 
McCullough’s declaration references “severe side effects” which include fever, fatigue, myalgia, 
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arthralgia, and lymphadenopathy. From a clinical perspective, these are easily managed at home 
with over-the-counter medications and do not require an escalation in care. This is a misleading 
way to bucket side effect profiles, and even the most “severe” cited are mild in contrast to the 
viral infection itself.  
75. 
We may learn that those previously infected do not need both shots of the 
vaccine, but currently the CDC still recommends both doses even after natural infection. These 
mild symptoms are acceptable from a public health perspective when weighed against the risks 
of repeat natural infection (which can be truly severe, resulting in hospitalization or death).   
76. 
Additionally, we still have no reliable way to confirm previous exposure to 
COVID. Serologic tests for COVID-19 “antibodies” have a wide range of specificity (and vary 
across platform).  
77. 
Using a serologic test to equate to immunity is not evidence-based and not 
recommended by the CDC. https://www.cdc.gov/coronavirus/2019-ncov/testing/serology-
overview.html. 
78. 
COVID also has syndromic overlap with many other respiratory infections and 
previous consistent symptoms alone cannot be grounds for proof of immunity. Even if using the 
gold standard PCR test, there is a wide range in duration of immunity after PCR positivity, and 
PCRs can be positive for months after natural infection. This can make it very challenging to set 
the onset of immunity for an individual. Pragmatically, the only surefire way to assure effective 
immunity is vaccination.  
Potential Adverse Events 
79. 
The Vaccine Adverse Event Reporting System (VAERS) is a passive reporting 
system. This means anyone can report any symptom they want after vaccination. These are each 
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combed through in order to identify trends, but the majority of symptoms are mild and are a 
result of the normal immune response to the vaccine.   
80. 
VAERS reports and percentages have to be taken into context with prevalence of 
the disease. If there was a meningococcal pandemic and we were vaccinating individuals at 
higher rates, we may see higher percentages of adverse events reported due to heightened public 
awareness. It is not a fair comparison from a rare disease to a hyper-prevalent novel disease with 
a new vaccine that has a lot of entrenched (and, in my opinion, inappropriate and unfounded) 
public uncertainty.   
81. 
Additionally, it is important to distinguish between association and causation. 
Adverse effects are possible with any vaccine, but the decision to administer the vaccine is based 
on the assessment of benefit over that risk. Regarding the risk of adverse events in those 18 to 29 
years old, it is not surprising they are reporting more given their more robust immune responses. 
Again, most of these reports are of mild generalized symptoms.  
82. 
The literature referenced in paragraph 48 of Dr. McCullough’s declaration, cited 
in support of the medical community acknowledging the adverse effects of vaccines, links to a 
study in mice, not humans. Additionally, while the CDC does acknowledge these side effects, 
they still continue to strongly encourage vaccination of all those eligible given the benefit to the 
entire population. 
83. 
The British health regulator has also reviewed the data requested and concluded 
the benefits outweigh the risks. https://healthfeedback.org/claimreview/yellow-card-scheme-for-
adverse-events-does-not-suggest-any-new-side-effects-of-covid-19-vaccines-tess-lawrie/. 
IU’s Policies 
84. 
Indiana University will not be performing research on students or constituents 
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getting the COVID vaccine without their express consent and in alignment with the local IRB 
policies and procedures. All studies proving efficacy and safety of the vaccine were done with 
critical event committees, data safety monitoring boards, and ethics committees in place.   
85. 
IU only plans to mandate the vaccine in age groups approved by the FDA.  While 
the WHO recommended that vaccinating children was less urgent than adults, WHO still 
recommended vaccination. https://healthfeedback.org/claimreview/the-world-health-
organization-states-that-covid-19-vaccination-for-children-is-less-urgent-but-doesnt-
recommend-against-it/. The CDC continues to recommend children 12 years and older get the 
vaccine. https://www.cdc.gov/coronavirus/2019-
ncov/vaccines/recommendations/adolescents.html. 
86. 
IU’s COVID-19 Vaccine Policy allows exemptions for pregnant women. IU 
follows the recommended CDC list for vaccine exemptions. https://www.cdc.gov/vaccines/covid-
19/clinical-considerations/covid-19-vaccines-us.html.   
F. Conclusion 
87. 
In my expert opinion, a COVID-19 vaccine mandate is the only safe and reliable 
way to assure lack of spread of COVID among our students and our communities and prevent 
morbidity and mortality. While COVID does not necessarily cause disproportionate bad 
outcomes in our constituency, any bad outcome from COVID is potentially avoidable with the 
vaccines where the benefit dwarfs the potential rare risks that may not be causally linked. The 
vaccines used for COVID are based on technology that has been developed over decades and 
have repeatedly been shown to be safe when given to millions of patients. This is not 
experimentation.  This is application of known science to a novel pathogen with uncertain and 
threatening immediate and long-term consequences to our students, faculty, staff, and 
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communities at large.  Given that this virus can be infectious despite an asymptomatic host and 
that not everyone can mount an immune response after vaccination, an individual’s choice to 
remain unvaccinated puts others around them in the community at risk.  Ultimately, the benefit 
to multiple college students being vaccinated has far-reaching benefits for the community as it 
relates to reduction in spread, avoidance of variant selection, and reductions in morbidity and 
mortality going into an uncertain season. 
III. 
Selected List of Additional Materials Reviewed 
1. 
See, e.g., Centers for Disease Control & Prevention (“CDC”), COVID-19 
Vaccines for Children and Teens (last visited June 27, 2021), available at: 
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/recommendations/adolescents.html  
2. 
CDC, Benefits of Getting a COVID-19 Vaccine (last visited June 27, 2021), 
available at: https://www.cdc.gov/coronavirus/2019-ncov/vaccines/vaccine-benefits.html.  
3. 
CDC, People with Certain Medical Conditions (last visited June 27, 2021), 
available at: https://www.cdc.gov/coronavirus/2019-ncov/need-extra-precautions/people-with-
medical-conditions.html  
4. 
CDC, People with Underlying Medical Conditions at Increased Risk from 
COVID-19 (last visited June 27, 2021), available at: https://www.cdc.gov/coronavirus/2019-
ncov/vaccines/recommendations/underlying-conditions.html  
5. 
Indiana’s Novel Coronavirus Response (last visited June 27, 2021), available at: 
https://www.coronavirus.in.gov/. 
6. 
CDC, Changing Age Distribution of the COVID-19 Pandemic-United States, 
May-August 2020 (pub. Oct. 2, 2020), available at: 
https://www.cdc.gov/mmwr/volumes/69/wr/mm6939e1.htm 
7. 
Tracking Coronavirus Cases at U.S. Colleges and Universities, The New York 
Times (last updated May 26, 2021), available at: 
https://www.nytimes.com/interactive/2021/us/college-covid-tracker.html 
8. 
CDC, COVID Data Tracker, Nationwide Commercial Laboratory Seroprevalence 
Survey (last visited June 27, 2021), available at: https://covid.cdc.gov/covid-data-
tracker/#national-lab. 
9. 
Indiana COVID-19 Data Report (last visited June 27, 2021), available at: 
https://www.coronavirus.in.gov/  
10. 
IU COVID-19 Testing Dashboard (last visited June 27, 2021), available at: 
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https://www.iu.edu/covid/dashboard/all. 
11. 
CDC, COVID-19 Vaccines Are Free to the Public (last visited June 27, 2021), 
available at: https://www.cdc.gov/coronavirus/2019-ncov/vaccines/no-cost.html 
12. 
CDC, Key Things to Know about COVID-19 Vaccines (last visited June 27, 
2021), available at: https://www.cdc.gov/coronavirus/2019-ncov/vaccines/keythingstoknow.html 
13. 
Harvard School of Public Health, Can herd immunity stop COVID-19? (last 
visited June 27, 2021), available at: https://www.hsph.harvard.edu/news/hsph-in-the-news/can-
herd-immunity-stop-covid-19/. 
14. 
CDC, Guidance for [IHEs] (last visited June 27, 2021), available at: 
https://www.cdc.gov/coronavirus/2019-ncov/community/colleges-universities/index.html 
15. 
State of Indiana Vaccination Information and Planning, About the vaccine, 
available at: https://www.coronavirus.in.gov/vaccine/ 
16. 
COVID-19 Vaccine: It’s our shot, Hoosiers (updated June 5, 2021), available at: 
https://www.coronavirus.in.gov/files/21_IN%20Vaccine%20effectiveness_6-2.pdf  
17. 
ISDH COVID-19 Vaccine FAQs (last updated Mar. 31, 2021), at 1, available at: 
https://www.coronavirus.in.gov/files/General%20Tool%20Kit%20Condensed%20FAQ%20and
%20Links%203.29.21.pdf 
18. 
ISDH COVID-19 Vaccine Fact Sheet (pub. Jan. 2021), available at: 
https://www.coronavirus.in.gov/files/Fact%20Sheet.pdf 
19. 
CDC, Safety of COVID-19 Vaccines (last visited June 27, 2021), available at: 
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/safety-of-vaccines.html 
20. 
ISDH, Variant Details (last visited June 27, 2021), available at: 
https://www.coronavirus.in.gov/map/VariantDetails.pdf 
21. 
CDC COVID-19 Info., Frequently Asked Questions about COVID-19 Vaccination 
(last visited June 27, 2021), available at: https://www.cdc.gov/coronavirus/2019-
ncov/vaccines/faq.html 
22. 
CDC, Myocarditis and Pericarditis Following mRNA COVID-19 Vaccination 
(last visited June 27, 2021), available at: https://www.cdc.gov/coronavirus/2019-
ncov/vaccines/safety/myocarditis.html 
23. 
Declaration of Peter A. McCullough, MD, MPH (June 28, 2021) 
IV. 
Other Testimony & Compensation 
I have not previously provided expert testimony in litigation.  
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This declaration is being provided in addition to my duties of teaching, patient care, and service 
on the Restart Committee. I am being compensated for my work in this matter at a rate of $500 
per hour. 
 
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Exhibit A
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1 
CURRICULUM VITAE 
 
NAME:  Cole Beeler 
Contact Information:  
Emerson Hall, Rm 445 
Indianapolis, IN, 46202 
T: 317-274-7943 
F: 317-944-8660 
 
EDUCATION:  
 
POSTDOCTORAL 
 
 
Institution 
Degree 
Date 
Awarded 
Indiana University School of Medicine 
Internship, Internal Medicine 
2012 
Indianapolis, IN 
Residency, Internal Medicine 
2015 
 
Fellowship, Infectious Diseases 
2017 
GRADUATE 
 
 
Institution 
Degree 
Date 
Awarded 
Indiana University School of Medicine 
M.D. 
2011 
Indianapolis, IN 
 
 
 
 
 
UNDERGRADUATE 
 
 
Institution 
Degree 
Date 
Awarded 
Indiana University 
B.S. Biology 
2007 
Bloomington, IN 
 
 
 
 
 
 
APPOINTMENTS: 
 
ACADEMIC 
 
 
Institution 
Rank 
Inclusion dates 
Indiana University School of Medicine 
Assistant Clinical Professor 
7/2017 to 
current 
Indiana University School of Medicine 
Associate Fellowship Director 
12/2018 to 
current 
Indiana University School of Medicine 
Key Clinical Educator for Division of Infectious 
Diseases 
12/2018 to 
current 
Indiana University School of Medicine 
Director of Symptomatic Testing, COVID Medical 
Response Team 
5/2020 to 
current 
 
 
 
NON-ACADEMIC 
 
 
Institution 
Rank 
Inclusion dates 
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2 
Indiana University Health 
University Hospital Medical Director of Infection 
Prevention and Control 
7/2017 to 
current 
 
 
 
LICENSURE, CERTIFICATION, SPECIALTY BOARD STATUS 
 
Credential 
Number 
Inclusion dates 
Indiana Medical License 
01074103a 
5/30/2014 to 
10/31/2021 
Certification in Internal Medicine 
354639 
2014-2024 
Certification in Infectious Diseases 
354639 
2017-2027 
 
 
PROFESSIONAL ORGANIZATION MEMBERSHIPS:  
 
Organization 
Inclusive Dates 
Infectious Disease Society of America 
2015 to current 
 
    
PROFESSIONAL HONORS AND AWARDS:  
 
SERVICE 
 
 
Award Name 
Granted By 
Date Awarded 
Outstanding Intern- Internal Medicine 
Internal Medicine Residency 
2012 
Outstanding 3rd year Resident- Internal Medicine 
Internal Medicine Residency 
2015 
Resident's Choice Fellow of the Year 
Internal Medicine Residency 
2016 
Outstanding Young Clinician Award 
Indiana University School of Medicine 
2020 
IU Bicentennial Medal Award 
Indiana University 
2020 
System Services Values Leadership Award 
Indiana University Health 
2020 
 
 
 
OVERALL/OTHER 
 
 
Award Name 
Granted By 
Date Awarded 
Jay Thomas Memorial Award in Physiology 
Indiana University School of Medicine 
2008 
John Van Nuys Memorial Fellowship 
Indiana University School of Medicine 
2008 
Class of 1978 R.C. Powell Scholarship 
Indiana University School of Medicine 
2009 
Charles C. Odya Award in Pharmacology 
Indiana University School of Medicine 
2009 
Ronald H. Doneff Scholarship 
Indiana University School of Medicine 
2010 
Gold Humanism Honor Society 
Indiana University School of Medicine 
2012 
 
PROFESSIONAL DEVELOPMENT:   
 
Course/Workship Title 
Provider 
Date 
 
 
 
Eskenazi Hospital Chief Residency 
Indiana Unversity School of Medicine 
2015-2016 
Clinical Education Teaching Program 
Indiana University School of Medicine 
2017 
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3 
Sailing the High Seas Leadership Development 
Indiana University Health 
2017 
IU Talk Session 
Indiana University Health 
2017 
Redcap Training 
Indiana Unversity School of Medicine 
2018 
The Value of Social Media 
Indiana Unversity School of Medicine 
2018 
Medical Education Combinator 
Indiana Unversity School of Medicine 
2018 
 
 
TEACHING:  
 
TEACHING ASSIGNMENTS:   
 
POSTGRADUATE 
 
 
 
 
Course # 
Short Title 
Format 
Role 
Term 
93MD700 
Clinical Infectious 
Disease 
Clinical 
Director 
2018 to current 
93MD710 
Infectious Disease 
Research Elective 
Research 
Director 
2018 to current 
93MI690 
MS3 Medicine 
Clerkship- ID 
Clinical 
Sub-Director 
2019 to current 
 
 
MENTORING 
 
Individual 
Role 
Inclusive Dates 
Zahir Sheikh 
Medical School Research Mentor 
2018-2019 
Brenna McElderry 
Medical School Mentor 
2018-2019 
Kishan Shah 
Medical School Mentor 
2018-2019 
Braden Sciarra 
Medical School Mentor 
2018-2019 
Arefin Chowdhury 
Residency Research Mentor 
2018-2019 
Madhu Reddy 
Fellowship Research Mentor 
2017-2019 
Madiha Tahir 
Fellowship Mentor 
2017-2019 
Jonathan Ryder 
Residency Research Mentor 
2018-2020 
Jaewon Jung 
Medical School Mentor 
2018-2019 
Junstin Hendrix 
Medical School Mentor 
2019-2020 
Nick Litchin 
Medical School Mentor 
2019-2020 
Wiaam Elkhatib 
Medical School Mentor 
2019-2020 
Chizelle Onochie 
Medical School Mentor 
2018-2020 
Amanda Agard 
Fellowship Mentor 
2018 to current 
Humaira Khan 
Medical School Mentor 
2020 to current 
Matthew Stack 
Residency Research Mentor 
2020 to current 
Yebon Oh 
Medical School Mentor 
2020 to current 
Taylor Munsch 
Medical School Mentor 
2020 to current 
Aaron Smith 
Medical School Mentor 
2020 to current 
Omar Elsheikh 
Fellowship Research Mentor 
2021 to current 
Beth Nagel 
Residency Research Mentor 
2021 to current 
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TEACHING ADMINISTRATION AND CURRICULUM DEVELOPMENT:   
 
Associate Fellowship Director
Fellowship in Infectious Diseases
2018 to current
ID Clinical Track Development
System for structure of ID Fellowship
2018 to current
Infection Prevention Curriculum
Curriculum for Infectious Disease 
Fellows
2018 to current
Antibiotic Stewardship Curriculum
Implementation and Development of 
IDSA curriculum to fellows
2019 to current
Advanced Antibiotic Stewardship 
Curriculum
Implementation and Development of 
IDSA curriculum to fellows
2021 to current
VIPER:  YouTube Channel 
(https://www.youtube.com/channel
/UC3HwM1yj5nhPOjWffgGrM9Q/vid
eos)
Videos for training and education in 
Infection Prevention for IU Health
2019 to current
eRVU educational development
Training for the Division of Infectious 
Diseases
2019 to current
Special Elective in ID
"Build your own elective" 
implementation with the Internal 
2019 to current
Delivering Appropriate Feedback
Training for the Division of Infectious 
Diseases
2020 to current
ID Clinical Conference Director
Weekly Lecture with attendees from 
across the state and country
2019 to current
 
 
 
INVITED PRESENTATIONS- TEACHING 
 
 
LOCAL 
 
 
Title 
Organization 
Date 
Intern Core Lecture Series 
Indiana University School of Medicine 
2014 to 2016 (yearly) 
University ID Clinical Conference 
Indiana University School of Medicine 
2015 to current (monthly) 
Eskenazi ID Clinical Conference 
Indiana University School of Medicine 
2015 to 2020 (monthly) 
Methodist ID Clinical Conference 
Indiana University School of Medicine 
2015 to 2020 (monthly) 
Infectious Disease Curriculum Session:  
Endocarditis 
Indiana University School of Medicine 
2015 to current (monthly) 
Quality Minute:  3 Arm Gowns 
Indiana University Health 
2017 
Host Defense Medical Student Lecture 
Indiana University School of Medicine 
2017 
C diff Guideline Update 
Indiana University School of Medicine 
2018 
Let me see that 1,2 Step VIPER 
Indiana University Health 
2018 
Osteomyelitis for the Nurse 
Practitioner 
Eskenazi Health 
2018 
Your Foley is Contaminated VIPER 
Indiana University Health 
2018 
Empiric Antibiotics 
Eskenazi Health 
2018 
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 21-1   filed 07/02/21   page 31 of 38
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 31-16   filed 07/12/21   page 31 of 38

5 
HIV for Residents 
Indiana University School of Medicine 
2018 
IMPACT:  GI Infections 
Indiana University School of Medicine 
2018 
Immunodeficiency for Residents 
Indiana University School of Medicine 
2018 to current (monthly) 
Procalcitonin for Hospitalists 
Indiana University Health 
2018 
UTI for Hospitalists 
Indiana University Health 
2018 
Quality Minute:  Two Step C diff 
Testing 
Indiana University Health 
2018 
Urology C Diff Lecture 
Indiana University Health 
2018 
Quality Minute:  Influenza 
Indiana University Health 
2018 
Transplant Quality Review 
Indiana University Health 
2018 to current (monthly) 
Grand Rounds- Oyez Lectures 
Indiana University School of Medicine 
2019 
Seeing a Difference in C diff 
Indiana University Health 
2019 
STD Lecture for Clinical Therepeutics 
Indiana University School of Medicine 
2019 
Procalcitonin VIPER 
Indiana University Health 
2019 
Isolation 2.0 VIPER 
Indiana University Health 
2019 
CHG VIPER 
Indiana University Health 
2019 
Winter is Coming VIPER 
Indiana University Health 
2019 
IMPACT:  Pneumonia 
Indiana University School of Medicine 
2019, 2020 
Aint' Nothin but a CHG Thang VIPER 
Indiana University Health 
2019 
MICU Residen Orientation 
Indiana University Health 
2019 to current (monthly) 
SICU Resident Orientation 
Indiana University Health 
2019 to current (monthly) 
IMPACT:  Antibiotic Stewardship 
Indiana University School of Medicine 
2019 
Chest Conference:  MICU HAI Review 
Indiana University Health 
2019 
Is a Foley ever Indicated 
Eskenazi Health 
2019 
Critical Care Grand Rounds- Is a Foley 
Ever Indicated 
Indiana University School of Medicine 
2019 
Chest Conference:  PPE Use 
Indiana University School of Medicine 
2020 
C diff Lecture for GI Fellows 
Indiana University School of Medicine 
2020 to current (yearly) 
Dermatology Grand Rounds- 
Ectoparasites 
Indiana University School of Medicine 
2020 
Ophthalmology Grand Rounds- COVID 
Indiana University School of Medicine 
2020 
Chaplaincy Department lecture- COVID 
Indiana University Health 
2020 
GME PPE Training Video for new 
resident orientation 
Indiana University School of Medicine 
2020 
EMS Lecture- COVID 
Indiana University Health 
2020 
HIV Lecture for GI Fellows 
Indiana University School of Medicine 
2021 
Diagnostic Stewardship for General 
Surgery 
Indiana University School of Medicine 
2021 
Chest Conference:  COVID 
Indiana University School of Medicine 
2021 
 
 
 
REGIONAL 
 
 
Title 
Organization 
Date 
HIV Update for Family Practice 
Indiana Academy of Family Physicians 
2018 
Community Acquired Pneumonia 
Union Hospital 
2018-2020 (yearly) 
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 21-1   filed 07/02/21   page 32 of 38
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 31-16   filed 07/12/21   page 32 of 38

6 
Is a Foley Ever Indicated? 
APIC Regional Meeting 
2019 
Everyone's Infectious 
Union Hospital 
2019 
Influenza Update 
IUH E. Washington Clinic 
2019 
COVID Update 
One America 
2020 
COVID Town Hall 
IUPUI 
2021 (x3) 
 
 
 
NATIONAL 
 
 
Title 
Organization 
Date 
Teaching During COVID 
ID Week (IDSA) 
2020 
 
 
 
SERVICE:   
 
 
UNIVERSITY SERVICE 
 
 
DEPARTMENT 
 
 
Acitivity 
Role 
Inclusive Dates 
Infectious Diseases Fellowship 
Associate Fellowship Director 
2018 to current 
Key Clinical Educator 
Division Representative 
2018 to current 
 
 
 
SCHOOL 
 
 
Acitivity 
Role 
Inclusive Dates 
Teaching Awards Committee 
Member 
2019 to current 
Curriculum Council Clinical 
Component Committee 
Member 
2019 to 2020 
Faculty Commnity Relations 
Committee 
Member 
2019 to 2020 
Faculty Steering Committee  
FCRC representative 
2019 to 2020 
 
 
 
CAMPUS 
 
 
Acitivity 
Role 
Inclusive Dates 
 
 
 
UNIVERSITY 
 
 
Acitivity 
Role 
Inclusive Dates 
COVID Medical Response 
Team 
Director of Symptomatic Testing 
2020 to current 
COVID Outbreak Investigation 
and Response Team 
Member/Reviewer 
2020 to current 
COVID Symptomatic testing 
Transition Team 
Member 
2020 to current 
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 21-1   filed 07/02/21   page 33 of 38
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 31-16   filed 07/12/21   page 33 of 38

7 
EALC Meetings- COVID 
Updates for President 
McRobbie 
Presenter 
2020 to current (weekly) 
President's Cabinet Meetings- 
COVID updates 
Presenter 
2020 to current 
(biweekly) 
IU Regional Dean's Meetings- 
COVID updates 
Presenter 
2020 to current 
(biweekly) 
IU COVID Restart Committee 
Member 
2020 to current 
IU Education Restart 
Committee 
Member 
2020 to current 
GME Coronavirus Rapid 
Response Team 
Member 
2020 to current 
 
 
 
PROFESSIONAL SERVICE 
 
 
LOCAL 
 
 
Organization 
Activity 
Inclusive Dates 
Indiana University Health 
Infection Control Research Committee 
2017 to current 
Indiana University Health 
System Infection Control Committee 
2017 to current 
Indiana University Health 
IP/MD System Dyad Committee 
2017 to current 
Indiana University Health 
Quality Improvement Committee 
2017 to current 
Indiana University Health 
Hand hygiene committee 
2017 to 2020 
Indiana University Health 
CLABSI Harm Team 
2017 to 2020 
Indiana University Health 
C diff Harm Team 
2017 to 2020 
Indiana University Health 
Antibiotic Stewardship Committee 
2017 to current 
Indiana University Health 
AIM Pathology Laboratory Committee 
2017 to current 
Indiana University Health 
MICU end of life culturing QI project 
2018 
Indiana University Health 
CLABSI Harm Team Toolkit Development 
2018 
Indiana University Health 
Poor Peripheral Access Algorithm 
2018 
Indiana University Health 
Foley Point Prevalence Survey 
2018 
Indiana University Health 
3E CLABSI Project 
2018 
Indiana University Health 
Device Round Standardization 
2018 
Indiana University Health 
Abdominal Transplant Quality Committee 
2018 to current 
Indiana University Health 
CAUTI Harm Team 
2018 to 2019 
Indiana University Health 
Influenza Incident Command 
2018 to 2020 
Indiana University Health 
IP orientation for ICU residents 
2018 to current 
Indiana University School of 
Medicine 
Residency Applicant Inverviewer 
2018 to current 
Indiana Univeristy School of 
Medicine 
Faculty Awards Committee 
2018 to current 
Indiana University Health 
Isolation 2.0 Curriculum Development 
2019 
Indiana University Health 
MPCU CAUTI/C diff Harm pilot 
2019 to current 
Indiana University Health 
Transplant CLABSI harm reduction QI 
project 
2019 to current 
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 21-1   filed 07/02/21   page 34 of 38
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 31-16   filed 07/12/21   page 34 of 38

8 
Indiana University Health 
BMT C diff reduction QI project 
2019 to current 
Indiana University Health 
The "Basics" Team for Harm Reduction 
2019 to current 
Indiana University Health 
Augmented C diff response development 
2019 
Indiana University Health 
Device Indication Standardization Project 
2019 
Indiana University School of 
Medicine 
Medical Response Team 
2020 to current 
Indiana University Health 
COVID Incident Command 
2020 to current 
Indiana University Health 
Diagnostic Stewardship System 
Development 
2020 to current 
Indiana University Health 
Epidural Foley Project with Surgery 
2020 
 
 
 
REGIONAL 
 
 
Organization 
Activity 
Inclusive Dates 
Indianapolis patient safety 
coalition 
Member 
2017 to current 
Orange Theory COVID Advisor 
Advisor 
2020 to current 
College Park Church COVID 
Advisor 
Advisor 
2020 to current 
 
 
 
NATIONAL 
 
 
Organization 
Activity 
Inclusive Dates 
Infectious Disease Society of 
America 
Antibiotic Stewardship Education 
Committee 
2017 to current 
 
 
 
INVITED PRESENTATIONS – SERVICE 
LOCAL 
Title 
Organization 
Date 
  Don’t trust the Pus                              University Hospital                               9/27/2017 
  Brace for Impact:  The Flu and You    University Hospital                               1/18/2018 
  Interview for Flu                                   WTHR                                                  1/9/2018 
  Interview for MRSA                              RTV6                                                   11/3/2017 
  Interview for Flu                                   WTHR                                                  10/12/2017 
 
1. http://app.criticalmention.com/app/#clip/view/32671017?token=2642c46b-6c16-444b-88e7-
f830ee2a1d45 (WISH) 
2. http://wishtv.com/2018/03/22/flu-cases-declining-but-still-as-dangerous-doctors-say/ (WISH) 
3. http://wishtv.com/2018/02/13/indiana-flu-deaths-nearly-seventeen-times-higher-than-this-time-
last-season/ (WISH) 
4. http://wishtv.com/2018/02/13/a-chilling-look-at-this-years-flu-season/ (WISH) 
5. https://www.theindychannel.com/news/local-news/indianapolis/indianas-244-flu-related-deaths-
include-3-kids-4-or-younger (WRTV) 
6. http://app.criticalmention.com/app/#clip/view/32245731?token=f9de2a1d-7441-40b0-83c0-
9072090b0ccf (WTHR) 
7. http://app.criticalmention.com/app/#clip/view/33752168?token=4df7120b-76f4-4dc9-b29d-
e0f54b00ba40 (WISH) 
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 21-1   filed 07/02/21   page 35 of 38
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 31-16   filed 07/12/21   page 35 of 38

9 
8. http://app.criticalmention.com/app/#clip/view/33764096?token=4df7120b-76f4-4dc9-b29d-
e0f54b00ba40 (WISH) 
9. http://app.criticalmention.com/app/#clip/view/32671015?token=2642c46b-6c16-444b-88e7-
f830ee2a1d45 (WRTV) 
10. http://indianapublicmedia.tumblr.com/post/172040087114/hospitals-lift-visitor-restrictions-as-
flu-season (WFIU) 
Interview for Flu                                        WTHR/NPR                                                   10/18/2018 
Interview for Chagas                           WTHR                                                     6/201/2019 
 
REGIONAL 
Title 
Organization 
Date 
  Community-Acquired Pneumonia        Union Hospital Terra Haute                 1/17/2018     
 
NATIONAL 
Title 
Organization 
Date 
 
 
INTERNATIONAL 
Title 
Organization 
Date 
 
 
 
PUBLICATIONS:   
 
TEACHING 
Refereed 
Luther VP, Shnekendorf R, Abbo LM, Advani S, Armstrong WS, Barsoumian AE, Beeler CB, 
Bystritsky R, Cherabuddi K, Cohen S, Hamilton KW, Ince D, Justo JA, Logan A, Lynch JB 3rd, 
Nori P, Ohl CA, Patel PK, Pottinger PS, Schwartz BS, Stack C, Zhou Y.  Antimicrobial 
Stewardship Training for Infectious Diseases Fellows:  Program Directors Identify a Curriculum 
Need.  Clin Infect Dis. 2018 Apr 16. doi: 10.1093/cid/ciy332. 
Contribution- Curriculum development, manuscript editing 
 
Non-refereed 
 
RESEARCH/CREATIVE ACTIVITY 
Refereed 
 
Non-Refereed 
 
SERVICE 
Refereed 
 
Chung, EK, Beeler, CB, Muloma, EW, Osterholzer, D, Damer, KM, Erdman, SM.  Development 
and implementation of a pharmacist-managed outpatient parenteral antimicrobial therapy 
program.  American Journal of Health-System Pharmacy.  January 1, 2016 Vol. 73 no. 1 e24-
e33. 
Contribution- Manuscript development, editing 
 
Beeler C, Dbeibo L, Kelley K, Thatcher L, Webb D, Bah A, Monahan P, Fowler NR, Nicol S, 
Judy-Malcolm A, Azar J.  Assessing patient risk of central line-associated bacteremia via 
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 21-1   filed 07/02/21   page 36 of 38
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 31-16   filed 07/12/21   page 36 of 38

10 
machine learning.  Am J Infect Control. 2018 Apr 13. pii: S0196-6553(18)30143-3. doi: 
10.1016/j.ajic.2018.02.021. 
Contribution- Project conception, implementation training, data collection, data analysis, 
manuscript writing, editing 
 
Azar J, Kelley K, Dunscomb J, Perkins A, Wang Y, Beeler C, Dbeibo L, Webb D, Stevens L, 
Luektemey M, Kara, A, Nagy R, Solid CA, Boustani, M. Using the agile implementation model 
to reduce central line-associated bloodstream infections.  Am J Infect Control. 2019 
Jan;47(1):33-37. Doi:  10.1016/j.ajic.2018.07.008. 
Contribution- Manuscript editing 
 
Dbeibo L, Kelley K, Beeler C, Kara A, Monahan P, Perkins AJ, Wang Y, Brinkman A, 
Snyderman W, Hatfield N, Wrin J, Miller J, Webb D, Azar J. Achieving Clostridioides difficile 
infection Health and Human Services 2020 goals:  Using agile implementation to bring 
evidence to the bedside.  Infect Control Hosp Epidemiol. 2019. Dec 5:1-3. doi: 
10.1017/ice.2019.337 
Contribution- Manuscript editing 
 
Beeler C, Kerley D, Davis C, Hazen D, Snyderman W, Lyons K, Sadowski J, Sweeney J, 
Debibo L, Kelley K, Webb DH. Strategies for the successful implementation of disinfecting port 
protectors to reduce CLABSI in a large tertiary care teaching hospital. Am J Infect Control. 
2019 Dec;47(12): 1505-1507. doi: 10.1016/j.ajic.2019.05.016 
Contribution- Project conception, implementation training, data collection, data analysis, 
manuscript writing, editing 
 
Dbeibo, L., Brinkman, A., Beeler, C., Fadel, W., Snyderman, W., Hatfield, N., Sadowski, J, 
Wang Y, Kelley K, Webb D, Azar J, Kara, A. (2020). Utilizing a real-time discussion approach 
to improve the appropriateness of Clostridioides difficile testing and the potential unintended 
consequences of this strategy. Infection Control & Hospital Epidemiology, 41(10), 1215-1218. 
doi:10.1017/ice.2020.276 
Contribution- Manuscript editing, scripting review 
 
Dbeibo, L., Brinkman, A., Beeler, C., Kelley, K., Fadel, W., Wang, Y., Snyderman, W, Hatfield 
N, Sadowski J, Kara, A. (2020). Assessing the Efficacy and Unintended Consequences of 
Utilizing a Behavioral Approach to Reduce Inappropriate Clostridioides difficile 
Testing. Infection Control & Hospital Epidemiology, 41(S1), S58-S59. doi:10.1017/ice.2020.543 
Contribution- Manuscript editing 
 
Valinetz, Ethan MD; Beeler, Cole MD; Erdman, Sharon M. PharmD, FIDP. Outcomes of 
Orthopedic Hardware-Related Infection Treated Via a Public Teaching Hospital Outpatient 
Parenteral Antimicrobial Therapy Program, Infectious Diseases in Clinical Practice: December 
28, 2020 - Volume Publish Ahead of Print - Issue - 
Contribution- Case review, data analysis, resident mentoring, manuscript development and 
editing 
 
Gavin W, Campbell E, Zaidi S, Dbeibo L, Beeler C, Kuebler K, Abdel-Rahman A, Luetkemeyer 
M, Kara A. Clinical characteristics, outcomes, and prognosticators in adult patients hospitalized 
with COVID-19.  Am J Infect Control. Volume 49, Issue 2, February 2021, Pages 158-165. 
Contribution- Study Design, Manuscript editing 
 
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 21-1   filed 07/02/21   page 37 of 38
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 31-16   filed 07/12/21   page 37 of 38

11 
Shannon Page, Dana Hazen, Kristen Kelley, Ranjeet Singh, Richard B. Rodgers, Brian Brewer, 
Joshua Sadowski, Armisha Desai, Cole Beeler, Douglas Webb, Jose Azar, Lana Dbeibo, 
Changing the culture of urine culturing: Utilizing Agile Implementation to improve diagnostic 
stewardship in the ICU, American Journal of Infection Control, Volume 48, Issue 11, 2020, 
Pages 1375-1380, ISSN 0196-6553, https://doi.org/10.1016/j.ajic.2020.01.022. 
Contribution- Manuscript editing 
 
Dbeibo, L., Kuebler, K., Keen, A., George, A., Kelley, K., Sadowski, J., Basham, L, Beeson T, 
Schmidt CM, Beeler C, Webb, D. (2021). Assessment of a Universal Preprocedural Screening 
Program for COVID-19. Infection Control & Hospital Epidemiology, 1-9. 
doi:10.1017/ice.2021.40 
Contribution- Manuscript editing 
 
Barros, N, Sharfuddin, AA, Powelson, J, Yaqub M, Adebiyi O, Beeler C, Lutz A, Fridell 
J. Rabbit anti‐thymocyte globulin administration to treat rejection in simultaneous pancreas and 
kidney transplant recipients with recent COVID‐19 infection. Clin 
Transplant. 2021; 35:e14149. https://doi.org/10.1111/ctr.14149 
Contribution- Manuscript editing 
 
Andrew M. Peseski, Mitchell McClean, Steven D. Green, Cole Beeler & Heiko 
Konig (2021) Management of fever and neutropenia in the adult patient with acute myeloid 
leukemia, Expert Review of Anti-infective Therapy, 19:3, 359-
378, DOI: 10.1080/14787210.2020.1820863 
Contribution- Literature search, Joint presentation with Heme/Onc, Resident mentorship, 
manuscript editing 
 
 
Non-refereed 
 
 
 
 
 
(Date) 
 
 
(Signature of Candidate) 
 
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 21-1   filed 07/02/21   page 38 of 38
USDC IN/ND case 1:21-cv-00238-DRL-SLC   document 31-16   filed 07/12/21   page 38 of 38

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