<p>(A) Placebo, (B) M01ZH09, and (C) Ty21a vaccine recipient groups. Maximum severity score per participant for each symptom was used; grade 1: symptom reported but no interference with daily activity; grade 2: some interference with normal daily activities; grade 3: significant symptoms preventing normal daily activity; grade 4: potentially life-threatening (see <b><a href="http://www.plosntds.org/article/info:doi/10.1371/journal.pntd.0004926#pntd.0004926.s003" target="_blank">S1 Protocol</a></b>).</p
BACKGROUND: The rapid authorization and widespread rollout of COVID-19 vaccines in the United States...
BACKGROUND: The rapid authorization and widespread rollout of COVID-19 vaccines in the United States...
BACKGROUND: The rapid authorization and widespread rollout of COVID-19 vaccines in the United States...
Frequency of related solicited adverse events experienced at least once; recorded at peak severity g...
<p>Bars represent the maximum severity per volunteers within 28 days after either 2 vaccinations in ...
(A) Frequency of possibly, probably and definitely related (“Related”) unsolicited adverse events fr...
<p>The Y-axis of <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0041936#pone-...
Background/Aim: Vaccines are said to be associated with side effects. The aim of the study was to sh...
<p>Solicited reactogenicity was collected for 7 days after each vaccination for 21 days total after ...
a<p>total number of participants who received: MVA = 382; placebo = 43.</p>b<p>expressed in mean ± s...
<p>Data are reported as: Number of participants with a serious adverse event (% [95% confidence inte...
There are various methods to collect adverse events (AEs) in clinical trials. The methods how AEs ar...
<p>Comparison of solicited adverse events following the first and second doses of vaccine (n = 44) a...
There are various methods to collect adverse events (AEs) in clinical trials. The methods how AEs ar...
This study aimed to compare the occurrence and nuisance of adverse events following administration o...
BACKGROUND: The rapid authorization and widespread rollout of COVID-19 vaccines in the United States...
BACKGROUND: The rapid authorization and widespread rollout of COVID-19 vaccines in the United States...
BACKGROUND: The rapid authorization and widespread rollout of COVID-19 vaccines in the United States...
Frequency of related solicited adverse events experienced at least once; recorded at peak severity g...
<p>Bars represent the maximum severity per volunteers within 28 days after either 2 vaccinations in ...
(A) Frequency of possibly, probably and definitely related (“Related”) unsolicited adverse events fr...
<p>The Y-axis of <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0041936#pone-...
Background/Aim: Vaccines are said to be associated with side effects. The aim of the study was to sh...
<p>Solicited reactogenicity was collected for 7 days after each vaccination for 21 days total after ...
a<p>total number of participants who received: MVA = 382; placebo = 43.</p>b<p>expressed in mean ± s...
<p>Data are reported as: Number of participants with a serious adverse event (% [95% confidence inte...
There are various methods to collect adverse events (AEs) in clinical trials. The methods how AEs ar...
<p>Comparison of solicited adverse events following the first and second doses of vaccine (n = 44) a...
There are various methods to collect adverse events (AEs) in clinical trials. The methods how AEs ar...
This study aimed to compare the occurrence and nuisance of adverse events following administration o...
BACKGROUND: The rapid authorization and widespread rollout of COVID-19 vaccines in the United States...
BACKGROUND: The rapid authorization and widespread rollout of COVID-19 vaccines in the United States...
BACKGROUND: The rapid authorization and widespread rollout of COVID-19 vaccines in the United States...