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Remdesivir Adverse Effects & Fatalities Research Study

About the Study

We are conducting a research study to examine the adverse effects and fatalities associated with Remdesivir, a widely used COVID-19 treatment. Despite being approved for emergency use, many patients and families have reported severe complications, including organ failure, worsening illness, and death following Remdesivir administration. This study aims to collect and analyze real-world data to determine the true risks of this drug.

Why This Study Matters

Many individuals were prescribed Remdesivir without fully understanding the potential dangers. Reports suggest a high incidence of kidney failure, liver damage, and respiratory distress in patients who received the drug. Yet, mainstream medical institutions have failed to acknowledge or investigate these concerns thoroughly. By gathering and analyzing patient cases, we seek to expose the truth, raise awareness, and push for medical accountability.

Who Can Participate?

We are currently collecting information from potential participants who have experienced or witnessed adverse effects related to Remdesivir. This includes family members of patients who died after receiving the drug and individuals who suffered severe complications or died. Our research team will review all submissions, and selected participants will be notified via email with further instructions. Those chosen to participate will be asked to provide a digital copy of relevant medical records and complete a follow-up questionnaire to assist in our investigation.

Remdesivir Adverse Effects & Fatalities Research Study
Participant Screening Form

Complete the form below

Patient's gender
Race (select all that apply)
Ethnicity (select one)
What is the primary language spoken by the patient?
If a language other than English was spoken, was an interpreter used during medical treatment (select all that apply)?
Pre-existing medical conditions (select all that apply)
What type of healthcare facility administered Remdesivir?
Did patient survive or are they deceased?
How many of doses of Remdesivir were administered
Reason for Remdesivir administration
Did patient or family refuse Remdesivir administration (select all that apply)?
Length of hospital stay in days
Was the patient put on a ventilator
How many doses of Remdesivir were administered before the patient required a ventilator?
How many doses of Remdesivir were administered before the patient's death?
Was patient or family made aware of Remdesivir's Emergency Use Authorization (EUA) (select all that apply)?
Was patient or family made aware of Remdesivir's side effects (select all that apply)?
Did the patient experience any of the following adverse effects of Remdesivir (selet all that apply)?
Was patient isolated from family (select all that apply)?
Did the Patient have Health Insurance
If patient had health insurance what type (select all that applies)?
Did the patient have a mental disability
Did patient recieve the COVID-19 Vaccine?
If so, which COVID-19 vaccine (select all that apply)?
Did patient also recieve the medication Baricitinib?
Was patient pregnant?
If pregnant, how far along when first dose of Remdesivir was administered?
Did the baby experience any complication due to Remdesivir?
Do you have legal right to submit medical records for this study?
Are you willing to sign a consent form to particpate?

Thanks for submitting!

Support Our Research on the Effects of Remdesivir

We are launching this critical research study to investigate the impact of Remdesivir, including severe complications and fatalities associated with its use. Too many families have been affected, and their stories deserve to be heard.

Your generous donation will help fund:


✅ Data collection and analysis
✅ Outreach to impacted individuals and families
✅ Medical record reviews and expert consultations
✅ Publication of findings to raise awareness

Every contribution, no matter the size, brings us one step closer to uncovering the truth and advocating for accountability. Together, we can make a difference.

 

Please donate and share this campaign to help us continue this vital work.

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AMERICAN FRONTLINE NURSES

PO Box 2187 Elko, Nevada 89803

American Frontline Nurses is a Nevada nonprofit corporation exempt from federal income tax under Section 501(c)(3) of the Internal Revenue Code. Federal Identification Number (EIN): 87-4046139

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