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. 2020 May 5;3(5):e204079. doi: 10.1001/jamanetworkopen.2020.4079

Table 4. Rates of Any Adverse Event and Medical Attention for Any Influenza Vaccine Stratified by Vaccine Type and According to Whether Influenza Vaccine Was Administered With a Concomitant Vaccine.

Outcome Respondents, No./Total (%)
Overall Only influenza vaccine Concomitant vaccinea
Any PPSV23 Zoster
Any influenza vaccine
Any adverse event 3684/50 134 (7.4) 2778/43 958 (6.3) 906/6176 (14.7) 761/4229 (18.0) 112/1370 (8.2)
Medical attention 141/49 493 (0.3) 95/43 434 (0.2) 46/6059 (0.8) 40/4140 (1.0) 6/1355 (0.5)
aIIV3
Any adverse event 1796/28 003 (6.4) 1340/24 762 (5.4) 456/3241 (14.1) 378/2178 (17.4) 54/742 (7.3)
Medical attention 80/27 665 (0.3) 55/24 486 (0.2) 25/3179 (0.8) 23/2133 (1.1) 1/732 (0.1)
HD-IIV3
Any adverse event 1716/19 306 (8.9) 1318/16 754 (7.9) 398/2552 (15.6) 341/1799 (19.0) 50/565 (8.9)
Medical attention 56/19 030 (0.3) 38/16 525 (0.2) 18/2505 (0.7) 14/1760 (0.8) 5/560 (0.9)

Abbreviations: aIIV3, adjuvanted trivalent inactivated influenza vaccine; HD-IIV3, high-dose trivalent inactivated influenza vaccine; PPSV23, 23-valent pneumococcal polysaccharide vaccine.

a

Participants may have received one or more concomitant vaccines. PPSV23 vaccine was the most commonly administered concomitant vaccine among those 65 years or older, administered to 68.5% of participants. Zoster vaccine was the second most commonly administered concomitant vaccine, administered to 22.2% of participants.