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. Author manuscript; available in PMC: 2019 May 4.
Published in final edited form as: Am J Obstet Gynecol. 2013 Dec 27;210(6):561.e1–561.e6. doi: 10.1016/j.ajog.2013.12.036

Table 1.

Characteristics of the Vaccine Adverse Event Reporting System (VAERS) reports received following hepatitis A (Hep A) or combination hepatitis A and hepatitis B (Hep AB) vaccines in pregnant women and their infants, United States, January 1, 1996-April 5, 2013 (N=134)

Characteristic Hep A (N=102) Hep AB (N=32)
Serious reports, n (%) 5 (4.9) 2 (6.3)
Maternal age in years, median (range) a 17 (13-38) 28 (19-39)
Gestational age in weeks at time of vaccination, median (range) b 4.0 (0.4-34) 5.7 (2.7-35)
Trimester of pregnancy at time of vaccination b, n (%) N=60 N=21
First (0 – 13 weeks) 50 (83.3) 18 (85.7)
Second (14 – 27 weeks) 8 (13.3) 1 (4.8)
Third (28 + weeks) 2 (3.3) 2 (9.5)
Brand name of vaccine, (n=134), n (%)
Havrix ® 55 (53.9) NA
Vaqta® 30 (29.4) NA
Twinrix® NA 31 (96.9)
Unknown 17 (16.7) 1 (3.1)
No. reports given with other vaccines c, n (%) 91 (89.2) 20 (62.5)
No. reports given with at least one live vaccine, n (%) 57 (55.9) 12 (37.5)
Type of reporter, n (%) N=102 N=32
Manufacturer 44 (43.1) 17 (53.1)
Provider 35 (34.3) 9 (28.1)
Other d 22 (21.6) 5 (15.6)
Patient/parent 1 (1.0) 1 (3.1)
a

Maternal age was missing in 3 reports after Hep A and Hep AB, each

b

Gestational age and trimester at time of vaccination was unknown for 52 Hep A and 11 Hep AB reports, respectively

c

Most common vaccine combination Hep A and Quadrivalent Human Papillomavirus Vaccine (HPV4) in 16 (11.9%) reports

d

May include office secretary,