<p>*reported as possibly related.</p><p>Adverse events (AEs) during trial period (day 0–182) by vaccination group.</p
<p>Studies reporting quantitative data for adverse events (AEs) after ivermectin-albendazole co-admi...
Live viral vectors that express heterologous antigens of the target pathogen are being investigated ...
BACKGROUND:Influenza contributes significantly to the burden of disease worldwide; the United Kingdo...
<p>N = number of subjects in the specified group; n = number of subjects in the specified category (...
<p>Local adverse events that were reported twice by individual subjects (8 adverse events) in the se...
<p>Solicited adverse events following booster vaccination or in case of clade 2 primary vaccination ...
<p>Adverse events related to vaccination description and proportion of volunteers suffering any side...
<p>(a) Post ChAd63 CS 5×10<sup>9</sup> vp; (b) Post ChAd63 CS 5×10<sup>10</sup> vp; (c) Post MVA CS ...
<p>Adverse events deemed possibly, probably or definitely related to vaccination are shown. ‘Other s...
Frequency of related solicited adverse events experienced at least once; recorded at peak severity g...
<p>Serious adverse events (SAE) reported for the period 1–5 months after the 2009 AS03-adjuvanted mo...
AE: Adverse Events; 1 AstraZeneca includes the vaccines ChAdOx1 nCoV-19 and BBV152; *AE reported as ...
<p>The AE experienced during the study are listed.</p><p><sup>*</sup>Frequency: 1 = Intermittent, 2...
<p><b>Panel A</b> is for screening prior to enrolment; <b>Panels B</b> and <b>C</b> are for vaccinat...
<p>LAIV = live attenuated influenza vaccine; IIV = inactivated influenza vaccination; AE = adverse e...
<p>Studies reporting quantitative data for adverse events (AEs) after ivermectin-albendazole co-admi...
Live viral vectors that express heterologous antigens of the target pathogen are being investigated ...
BACKGROUND:Influenza contributes significantly to the burden of disease worldwide; the United Kingdo...
<p>N = number of subjects in the specified group; n = number of subjects in the specified category (...
<p>Local adverse events that were reported twice by individual subjects (8 adverse events) in the se...
<p>Solicited adverse events following booster vaccination or in case of clade 2 primary vaccination ...
<p>Adverse events related to vaccination description and proportion of volunteers suffering any side...
<p>(a) Post ChAd63 CS 5×10<sup>9</sup> vp; (b) Post ChAd63 CS 5×10<sup>10</sup> vp; (c) Post MVA CS ...
<p>Adverse events deemed possibly, probably or definitely related to vaccination are shown. ‘Other s...
Frequency of related solicited adverse events experienced at least once; recorded at peak severity g...
<p>Serious adverse events (SAE) reported for the period 1–5 months after the 2009 AS03-adjuvanted mo...
AE: Adverse Events; 1 AstraZeneca includes the vaccines ChAdOx1 nCoV-19 and BBV152; *AE reported as ...
<p>The AE experienced during the study are listed.</p><p><sup>*</sup>Frequency: 1 = Intermittent, 2...
<p><b>Panel A</b> is for screening prior to enrolment; <b>Panels B</b> and <b>C</b> are for vaccinat...
<p>LAIV = live attenuated influenza vaccine; IIV = inactivated influenza vaccination; AE = adverse e...
<p>Studies reporting quantitative data for adverse events (AEs) after ivermectin-albendazole co-admi...
Live viral vectors that express heterologous antigens of the target pathogen are being investigated ...
BACKGROUND:Influenza contributes significantly to the burden of disease worldwide; the United Kingdo...