Post-Marketing Surveillance of Tetravalent Diphtheria-Tetanus-Acellular Pertussis and Inactivated Poliovirus (DTaP-IPV) Vaccine in South Korea, 2009 to 2015.

INTRODUCTION: TETRAXIM™ (Sanofi), a combined diphtheria, tetanus, acellular pertussis, and inactivated poliovirus (DTaP-IPV) vaccine, has been licensed in South Korea since 2009. In accordance with the Ministry of Food and Drug Safety regulations, this post-marketing surveillance (PMS) study evaluated the safety of the DTaP-IPV vaccine in real-world clinical practice in infants and children who received it as either a part of the three-dose primary series dose at 2, 4, and 6 months or school entry booster between 4 and 6 years of age.
METHODS: This multicenter, observational, PMS study was conducted in real-world practice in South Korea for 6 years (2009-2015) in participants aged between 2 months and 6 years. The study outcomes included solicited reactions, unsolicited adverse events (AEs)/adverse drug reactions (ADRs), unexpected AEs/ADRs, and serious AEs (SAEs)/ADRs.
RESULTS: Data from 647 participants was included in the safety analysis. Overall, 268 AEs were reported by 181 (28%) participants: 47 (17.5%) solicited reactions, 220 (82.1%) unsolicited AEs, and 1 (0.4%) unsolicited ADR. A total of 48 AEs (including 47 solicited reactions) were reported to have a causal relationship with the DTaP-IPV vaccine and were reported by 36 (5.6%) participants. A total of 212 unexpected AEs were reported by 152 (23.5%) participants, none of which had a causal relationship with the DTaP-IPV vaccine. Neither immediate AEs nor SAEs were reported during the study. Among the participants who reported AEs, 220 (34%) were on concomitant medications. Most AEs were of mild intensity, and all participants recovered.
CONCLUSION: No safety concerns related to the DTaP-IPV vaccine in a real-world setting were raised in participants aged 2-6 months for the primary series and 4-6 years for the school-entry booster dose in the Korean population. The DTaP-IPV vaccine was well tolerated and can be continued as part of routine immunization programs in infants and children. TRIAL REGISTRATION: NCT01437423.

Key Summary Points

Introduction

Diphtheria, tetanus, and pertussis are potentially severe bacterial diseases. Polio, or poliomyelitis, is a disabling and life-threatening disease caused by the poliovirus. Diphtheria causes a thick pseudomembrane covering the back of the throat, which can lead to breathing issues, paralysis, or heart failure, and tetanus causes painful tightening of the muscles, usually all over the body, and can be fatal [1]. Pertussis, also known as whooping cough, is a highly contagious bacterial infection caused by a Gram-negative coccobacillus, Bordetella pertussis (B. pertussis). It is an upper respiratory tract infection leading to severe paroxysmal coughing and post-tussive emesis [2, 3]. Infants who are too young to be vaccinated and born from pertussis-unvaccinated or incompletely vaccinated mothers are at risk of developing severe forms of pertussis. The most common sources of transmission to infants are siblings, parents, and other family members who are in close contact with them [4, 5]. Additionally, infants bear the highest disease burden due to an elevated risk for pertussis-related complications and mortality [6, 7]. Severe cases that require hospitalization and intensive care admission are most frequently observed in infants < 3 months of age [8]. Maintaining high immunity against diphtheria, tetanus, pertussis, and polio is important across the life span [9-12]. Although immunization strategies have been successfully implemented, resurgence of pertussis has been reported globally and most likely resulted from the combination of multiple factors [13, 14].

In South Korea, the disease burden of pertussis is still high, with an annual incidence rate that peaked at 24.7 per 100,000 infants per 2018 data [15]. The highest pertussis detection rates are reported in infants (< 6 months of age) and young children, followed by adolescents and adults [15, 16]. During 2010–2011, 33.8% of patients with pertussis were < 3 months old, and 29% were adolescents and adults ≥ 15 years old [17]. Despite the substantial number of cases, it may still be highly underestimated or underreported due to diagnostic challenges and lack of awareness [16].

Vaccination has been the primary preventive strategy for pertussis control for several decades [18]. In 2009, the vaccination schedule recommended by the South Korean National Immunization Program (NIP) included administration of the diphtheria-tetanus-acellular pertussis (DTaP) vaccine as a three-dose primary vaccination series in infants aged 2, 4, and 6 months, with a fourth (booster) dose given at 15–18 months and a fifth (school-entry booster) dose at 4–6 years of age. At that time, the primary vaccination for polio recommended vaccinations at 2, 4, and 6 months of age, with a subsequent fourth (booster) dose at 4–6 years [19, 20]. National vaccination data for South Korea indicate successful implementation of the childhood immunization program with an estimated vaccine coverage rate of 98% for DTaP3 in 2019 [21]. Several studies reported variable vaccine coverage rates for booster immunization [16, 22, 23]. It was 95.4% (January–June 2019) and 93.5% (January–June 2020) for the fifth dose of DTaP, and 96.3% and 94.4%, respectively, for the fourth dose of inactivated poliovirus vaccine (IPV), when calculated based on the resident registration population data from the Korean Ministry of Public Administration and Security [24]. Another study that compared vaccination rates between NIP vaccines and non-NIP vaccines in Korea reported vaccination coverage rates of 56.6% for the fifth dose of DTaP and 73% for the fourth dose of IPV at school-entry age [25]. Additionally, in order to protect the infants while they are too young to be fully vaccinated, pertussis vaccination during pregnancy protects mothers from pertussis infection and disease, and reduces the likelihood of transmission to their newborn by passive transfer of maternal anti-pertussis antibodies that protect infants. Recently, vaccination against pertussis during pregnancy has been recommended as an additional strategy for protection of young infants in South Korea [26, 27].

Several tetravalent, pentavalent, and mainly hexavalent DTaP- and DTwP (diphtheria, tetanus, and whole-cell pertussis)-containing vaccines are licensed globally. The reported waning of immunity post-vaccination has been considered a possible reason for the re-emergence of some vaccine-preventable diseases [28]. Regardless of the type of pertussis vaccine or the primary series immunization schedule, they do not confer lifelong immunity against pertussis disease [29]. To increase the duration of protection after primary vaccination, the World Health Organization (WHO) recommended a pertussis booster dose for children [30]. Completion of the primary series and the first booster is expected to ensure protection against pertussis for around 4–6 years [31-36].

Multivalent vaccines that are administered as a single injection increase compliance and vaccination timeliness, improve adherence to vaccination programs, and reduce the time for vaccine preparation and the overall cost for vaccinees and national vaccination programs [37-40]. TETRAXIM™ (Sanofi) is a combined diphtheria, tetanus, acellular pertussis, and IPV (DTaP-IPV) vaccine. It has been licensed in South Korea since August 31, 2009, for active immunization against diphtheria, tetanus, pertussis, and poliomyelitis in infants and children. It has been evaluated for immunogenicity and safety in multiple randomized clinical trials including in South Korea [41]. Per the regulations from the Ministry of Food and Drug Safety (MFDS) in South Korea, data were collected in the present study in South Korea to confirm its safety profile in real-world clinical practice as a post-authorization commitment and when used per licensed indications (i.e., primary series and school-entry booster).

This post-marketing surveillance (PMS) study aimed to monitor and evaluate the safety of the DTaP-IPV vaccine over a period of 6 years in children aged between 2 months and 6 years who were given the DTaP-IPV vaccine in real-world clinical practice.

Methods

Study Design

This was a multicenter, observational PMS study, conducted in real-world practice for a duration of 6 years from the product approval date in accordance with the MFDS regulations (NCT01437423). The planned sample size was 600 participants in accordance with the MFDS notification. Participants were enrolled across eight centers from August 31, 2009, to August 30, 2015. The protocol for this study was approved by the MFDS and ethics committee before study initiation. The study was conducted in accordance with the guidelines established by the Declaration of Helsinki and MFDS Notification No. 2009-46 (basic standard for re-examination of new drug). Informed consent was obtained from all participants or their parents/legal representative before enrollment.

Study Participants

Participants aged between 2 months and 6 years were enrolled in the study. Participants were eligible if they had received ≥ 1 dose of primary vaccination as part of the primary vaccination schedule or the booster dose at 4–6 years of age with the study vaccine. Participants were not included in study analysis if they had off-label use of the vaccine.

Study Vaccine

The DTaP-IPV vaccine (TETRAXIM™) is available as a sterile suspension in a single-dose prefilled syringe. Each 0.5 mL dose of the vaccine contains antigens against four target pathogens, ≥ 30 international units (IU) of diphtheria toxoids, ≥ 40 IU of tetanus toxoids, two purified antigens of B. pertussis (25 μg of pertussis toxoid [PT] and 25 μg of filamentous hemagglutinin [FHA], each adsorbed onto aluminum salt), and three distinct poliovirus antigens (40 D-antigen units of type 1 poliovirus, 8 D-antigen units of type 2 poliovirus, and 32 D-antigen units of type 3 poliovirus; each produced on Vero cells). It is a licensed vaccine in South Korea for immunization against diphtheria, tetanus, pertussis, and poliomyelitis in infants and children. It was administered intramuscularly per local product labeling. It was administered as primary vaccination (at least one of the three successive doses at 2-month interval starting from 2 months of age) or as school-entry booster vaccination (children aged 4–6 years).

Data Collection

Demographic and other baseline data were collected on a case report form (CRF). Immediate events, within 30 min of the observation period after the vaccination, were also collected on a CRF on the day of vaccination. Participants and/or parents were given a diary card to record safety information on all pre-listed solicited injection site and systemic reactions and all adverse events (AEs), including unsolicited AEs/adverse drug reactions (ADRs) and serious AEs (SAEs) occurring up to 30 days after vaccination.

Study Outcomes

The study outcomes included occurrence of solicited ADRs (pre-listed injection site reactions and systemic reactions), unsolicited AEs/ADRs, unexpected AEs/ADRs, and SAEs/serious ADRs. Adverse drug reactions were defined as the AEs reported to be related to the study vaccine. By definition, all the solicited AEs were considered to have a causal relationship with the DTaP-IPV vaccine. Unsolicited AEs were defined as observed AEs that did not fulfil the conditions of solicited reactions, i.e., not pre-listed in the CRF in terms of diagnosis and onset window post-vaccination. Unsolicited ADRs were defined as unsolicited AEs that were considered related to the study vaccine. Unexpected ADRs were defined as the ADRs that were not reflected in the AE section of the local product label. SAEs were defined as any event that is fatal or life-threatening or causes hospitalization or the prolongation of hospitalization, or persistent or significant disabilities/incapacity, congenital anomalies, or birth defect, or other medically significant events that jeopardize the participant or require medical or surgical intervention to prevent one of the outcomes.

Per the summary of product characteristics, the safety profile of the study vaccine does not differ significantly between the different age groups. However, some AEs such as myalgia, malaise, and headache are specific to children ≥ 2 years of age [42]. The solicited (pre-listed) injection site AEs for participants for all age groups were tenderness/pain, erythema, and swelling. The solicited (pre-listed) systemic AEs were fever, vomiting, abnormal crying, drowsiness, appetite loss, and irritability for participants aged ≤ 23 months, and myalgia, malaise, and headache for participants aged 4–6 years old.

The intensity of the solicited and unsolicited AEs was measured by the participant’s parent/legal representative based on an intensity scale provided on the CRF. Solicited injection site reactions and systemic reactions were classified as grade 1 (mild), grade 2 (moderate), or grade 3 (severe). Unsolicited AEs were classified as grade 1 (mild—did not interfere with daily activities), grade 2 (moderate—interfered with daily activities), or grade 3 (severe—prevented daily activities).

The causality of each AE was assessed for all events occurring up to 30 days post-vaccination. It was assessed by the investigator as certain (valid time relationship to vaccine administration and cannot be explained by other concomitant drugs or other disorders), probable/likely (pertinent time relationship to vaccine administration and was not likely to be caused by other concomitant drugs or disorders), possible (pertinent time relationship to vaccine administration, but could be caused by other concomitant drugs or disorders), unlikely (not likely to have causal relationship with vaccine administration; temporary cases), conditional/unclassified (requires more data for proper assessment), or unassessable/unclassifiable (insufficient information exists).

Statistical Analysis

Primary analyses were descriptive in nature. Safety evaluation population was defined as all participants who received the DTaP-IPV vaccine. AEs were summarized using the WHO Adverse Reaction Terminology. Summary statistics were presented for AEs (MedDRA [Medical Dictionary for Regulatory Activities] preferred term). As required by the MFDS in South Korea, in order to determine the factors that may affect the incidence of AEs, univariate analysis (chi-square test or Fisher’s exact test) was conducted on the demographic and medical factors of participants. Gender distribution, current medical history, past medical history, previous vaccination history, simultaneous vaccination, and concomitant medication were assessed using the chi-square test, and age, renal disease (current medical history), and allergic history were assessed using Fisher’s exact test.

Results

Demographic and Baseline Characteristics

Among the 662 participants enrolled in the study, data from 647 outpatient participants were included in the safety analysis (Fig. 1). Overall, 602 participants had received ≥ 1 dose of the primary vaccination series, and 45 participants had received the school-entry booster dose. The exclusion criteria included failure to follow up (n = 12) and off-label vaccine usage (n = 3). The demographic and baseline characteristics are presented in Table 1. Overall, 50.5% of the participants were female. A total of 14.4% of participants had ongoing medical conditions at the time of vaccination. The most frequently reported current medical condition was bronchitis (3.9%), followed by upper respiratory tract infection (1.9%) and otitis media (1.4%). Overall, 34% of participants were on concomitant medications at the time of vaccination or during the safety follow-up (30-days period post-vaccination). The most frequently reported concomitant medications were for the treatment of cough and cold episodes (17.9%), followed by anti-asthmatics and other respiratory disease medications (16.1%), and nasal decongestant or other nasal preparations (15.9%). None of the study participants experienced diphtheria, tetanus, pertussis, or poliomyelitis during the study. Among 647 participants, 477 (73.7%) were vaccinated simultaneously with at least one other vaccine. The most frequent simultaneous vaccines were Haemophilus influenzae type b (37.9%), rotavirus (33.1%), hepatitis B (26.1%), and Streptococcus pneumoniae (16.2%) vaccines. Additionally, 58 (9%) participants were vaccinated with other vaccines within 4 weeks prior to the study vaccine. The most frequent vaccines administered within the past 4 weeks were hepatitis B (7%), H. influenzae type b (1.6%), and S. pneumoniae (1.2%) vaccines.

Fig. 1

Disposition of participants

Table 1

Demographics and baseline characteristics of participants

Characteristics	Participants (%)N = 647
Gender
Male, n (%)	320 (49.5)
Female, n (%)	327 (50.5)
Age (years), mean ± SD	8.2 ± 13.4
Primary vaccination series
< 1 year old	602 (93)
≤ 1 to < 2 years old	0
≤ 2 to < 4 years old	0
School-entry booster dose
≤ 4 to < 5 years old	35 (5.4)
≤ 5 to < 6 years old	7 (1.1)
≥ 6 years old	3 (0.5)
Weight (kg)—primary series (n = 595), mean ± SD	7.6 ± 1.3
Weight (kg)—school-entry booster dose (n = 44), mean ± SD	19.2 ± 4.1
Participants with term delivery, n (%)	642 (99.2)
Participants with current medical conditions, n (%)	93 (14.4)
Participants on concomitant medicationa, n (%)	220 (34)

aConcomitant medication(s), if any: taken at the time of vaccine administration or during the 30-day post-vaccination period

Safety Analysis

Overall, 268 AEs were reported by 181 (28%) participants (Table 2), of which 47 (17.5%) were solicited reactions, 220 (82.1%) were unsolicited AEs, and 1 (0.4%) was an unsolicited ADR. The most frequently reported AE was bronchitis (11.8%), followed by upper respiratory tract infection (4.6%), enteritis (3.1%), injection site tenderness (3.1%), and contact dermatitis (2.3%).

Table 2

Overall incidence of adverse events and adverse drug reactions

	Adverse events			Adverse drug reactions
	Participants with AEs, n (%)N = 647	No. of AEs	95% CI	Participants with ADRs, n (%)N = 647	No. of ADRs	95% CI
AEs	181 (28)	268	24.6–31.6	36 (5.6)	48	3.9–7.6
Serious AEs	0	0	0–0.6	0	0	0–0.6
Unexpected AEs	152 (23.5)	212	20.3–27	0	0	0–0.6

ADR adverse drug reaction; AE adverse event; CI confidence interval

Immediate Adverse Events

No immediate (occurring within 30 min after vaccination) AEs were reported during this study.

Solicited Reactions

Overall, 47 solicited reactions were reported by 47 (7.3%) participants (Table 3), all of which were reported to have a causal relationship with the DTaP-IPV vaccine, by definition. All solicited reactions were mild in intensity, except fever. Two cases of fever were of moderate intensity (> 38.5 to ≤ 39.5 °C). Injection site tenderness was the most frequently observed solicited reaction, reported by 3.1% of participants (n = 20). All participants with solicited reactions recovered.

Table 3

Overall incidence of solicited reactions

Solicited reactiona	Participants with adverse events n (%)N = 647	No. of adverse events
Solicited injection site reactions
Injection site tenderness/pain	20 (3.1)	20
Injection site erythema	10 (1.6)	10
Injection site swelling	10 (1.6)	10
Solicited systemic reactions
Fever	6 (0.9)	6
Abnormal crying	1 (0.2)	1
Vomiting	0	0
Drowsiness	0	0
Appetite loss	0	0
Irritability	0	0
Headache	0	0
Malaise	0	0
Myalgia	0	0
Total	47 (7.3)	47

aSolicited reactions for participants aged < 23 months were injection site tenderness, erythema, and swelling, and fever, vomiting, abnormal crying, drowsiness, appetite loss, and irritability; solicited reactions for participants aged 4–6 years were injection site pain, erythema, and swelling, and fever, headache, malaise, and myalgia

Unsolicited Adverse Events

Overall, 221 unsolicited AEs were reported (Table 4). The most frequently observed unsolicited AE was bronchitis (11.8% [n = 79]), followed by upper respiratory tract infection (4.6% [n = 32]), enteritis (3.1% [n = 20]), and contact dermatitis (2.3% [n = 15]). Only one case of irritability of mild intensity in one (0.2%) participant was reported to have a possible causal relationship with the DTaP-IPV vaccine. All other unsolicited AEs were reported to have no causal relationship with the study vaccine.

Table 4

Overall incidence of unsolicited adverse events and unexpected adverse events reported in ≥ 0.5% of participants

Unsolicited adverse eventa	Participants with adverse events n (%)N = 647	No. of adverse events
Bronchitisb	76 (11.8)	79
Upper respiratory tract infectionb	30 (4.6)	32
Enteritisb	20 (3.1)	20
Contact dermatitisb	15 (2.3)	15
Coryzab	10 (1.6)	10
Bronchiolitisb	6 (0.9)	6
Gastroenteritisb	5 (0.8)	5
Otitis mediab	5 (0.8)	6
Coughingb	4 (0.6)	4
Rhinitisb	4 (0.6)	4
Diarrhea	4 (0.6)	4
Atopic dermatitisb	4 (0.6)	4
Fever	3 (0.5)	3
Common coldb	3 (0.5)	3
Tonsillitisb	3 (0.5)	3
Diaper dermatitisb	3 (0.5)	3
Impetigo rashb	3 (0.5)	3

aOverlapping numbers, i.e., one participant could have experienced > 1 AE

bUnexpected AE

Most (91.4%) of the AEs were of mild intensity, and none of the unsolicited AEs were severe in intensity. Among the most frequently reported unsolicited AEs, 66/79 cases of bronchitis, 30/32 cases of upper respiratory tract infection, 19/20 cases of enteritis, and all 15 cases of contact dermatitis were of mild intensity. Thirteen cases of bronchitis were of moderate intensity, followed by four cases of otitis media, two of upper respiratory tract infection, two of fever, and one case each for bronchiolitis, enteritis, and diarrhea (Table 5). Participants with moderate-intensity AEs recovered within a few days. Overall, all participants with unsolicited AEs recovered.

Table 5

Severity of adverse events in ≥ 0.5% of participants

	Adverse events		Intensity
	Participants with adverse eventsn (%)N = 647	No. of adverse events	Mild	Moderate	Severe
Bronchitis	76 (11.8)	79	66	13	0
Upper respiratory tract infection	30 (4.6)	32	30	2	0
Enteritis	20 (3.1)	20	19	1	0
Injection site tenderness	20 (3.1)	20	20	0	0
Contact dermatitis	15 (2.3)	15	15	0	0
Coryza	10 (1.6)	10	10	0	0
Injection site erythema	10 (1.6)	10	10	0	0
Injection site swelling	10 (1.6)	10	10	0	0
Fever	9 (1.4)	9	7	2	0
Bronchiolitis	6 (0.9)	6	5	1	0
Gastroenteritis	5 (0.8)	5	5	0	0
Otitis media	5 (0.8)	6	2	4	0
Coughing	4 (0.6)	4	4	0	0
Rhinitis	4 (0.6)	4	4	0	0
Diarrhea	4 (0.6)	4	3	1	0
Atopic dermatitis	4 (0.6)	4	4	0	0
Common cold	3 (0.5)	3	3	0	0
Tonsillitis	3 (0.5)	3	3	0	0
Diaper dermatitis	3 (0.5)	3	3	0	0
Impetigo rash	3 (0.5)	3	3	0	0

Unexpected Adverse Events

Among 268 reported AEs, a total of 212 unexpected AEs were reported by 152 (23.5%) participants. The most frequently reported unexpected AE was bronchitis (11.8%), followed by upper respiratory tract infection (4.6%), enteritis (3.1%), and contact dermatitis (2.3%). None of the unexpected AEs were reported to have a causal relationship with the DTaP-IPV vaccine.

Serious Adverse Events

No SAEs were reported during the study.

Occurrence of Adverse Events by Demographic or Medical Characteristics

Demographic and medical factors, including gender, age, current medical history, past medical history, allergic history, previous vaccination history, simultaneous vaccination, and concomitant medications, were assessed for their effect on the incidence of AEs. Among the participants who reported AEs, 34% (n = 220) were on concomitant medications. Although results indicated that the incidence of AEs was higher among participants on concomitant medications (odds ratio [OR], 59.98; 95% confidence interval, 34.64–103.87; p < 0.0001), data from participants receiving the medication in response to an AE post-vaccination with DTaP-IPV were also included in the analysis. Other medical characteristics did not have a significant effect on the incidence of AEs (p > 0.05).

Discussion

This PMS study evaluated the safety of the DTaP-IPV vaccine in South Korea, after its approval, in participants aged between 2 and 6 months for the primary series and between 4 and 6 years for the school-entry booster dose. Results demonstrated an acceptable safety profile, although the sample size, which was driven by local regulatory requirements, would not necessarily allow the detection of rare AEs. All the solicited and unsolicited AEs were mild or moderate in intensity, and all participants recovered. No unexpected AEs were reported to have a causal relationship with the DTaP-IPV vaccine. There were no deaths or SAEs reported during the study, and no participant discontinued due to AEs.

The findings from this study are consistent with the information present on the local product label. They are also in line with the good safety profile of other DTaP-IPV vaccines reported from real-word use [19, 43]. Injection site AEs/ADRs are commonly reported for vaccines administered via the intramuscular route [44]. By definition, all the solicited injection site reactions, including injection site tenderness, erythema, and swelling, were considered related to the DTaP-IPV vaccine in this study. The occurrence of solicited reactions in this study was consistent with the information on the product label, where redness, pain, and swelling at the injection site were considered to be very common (≥ 1/10) AEs [42]. Fever was reported as the most common AE (11.9%) in another PMS study that assessed the safety profile of another DTaP-IPV in South Korea [19]. In contrast to this other PMS study and the product label of the study vaccine, which considers a fever ≥ 38 °C as a very common AE, the rate of fever was substantially lower in the current study (1.4%). The overall incidence of solicited reactions in this study was lower than that observed in a randomized clinical trial assessing the immunogenicity and safety of DTaP-IPV (primary vaccination series) in infants from South Korea [41], possibly because this PMS study evaluated the safety of the DTaP-IPV vaccine in real-world clinical practice.

Some unsolicited AEs were reported in this study. All were considered not related to the study vaccine, except one case of irritability. The majority of the other unsolicited AEs were diseases or conditions occurring commonly in infants and children.

In this study, all the unexpected AEs were determined to be unrelated to vaccination. Most of them were mild in severity, and all participants recovered.

Participants who had concomitant medications (any medication being taken at the time of study vaccination and/or within the 30-day post-vaccination period) reported a higher incidence of AEs in this study. However, this data should be interpreted with extreme caution as the data from these participants receiving the medication in response to an AE following vaccination were not excluded from the analysis, and therefore, introduced a bias in the analysis.

Clinical trials have demonstrated the safety of the DTaP-IPV combination vaccine in South Korea [41] and other countries [45-53], and their results were based on data obtained through selective inclusion and exclusion criteria and mainly included healthy participants. On the other hand, real-world post-licensure safety studies can complement knowledge regarding vaccine safety in the general population. Hence, such studies have important implications for the formation and implementation of national immunization policies. The data from this study support the overall assessment of the safety of the DTaP-IPV vaccine in real-world practice in South Korea in addition to the existing clinical trial data. The findings from this PMS study are consistent with the known safety profile of DTaP-IPV.

Combination vaccines simplify vaccine administration, permit inclusion of new vaccines to the childhood schedules, help in achieving higher vaccination coverage, and reduce vaccination costs. A clinical trial previously demonstrated no clinically significant difference between the reactogenicity of the DTaP-IPV vaccine versus the DTaP and IPV vaccines administered separately. The incidence of solicited injection site reactions (tenderness, erythema, and swelling) was 27.0–36.9% in participants who received DTaP–IPV, 11.6–23.9% for DTaP, and 6.0–20.2% for IPV. The incidence of severe injection site reactions was low and was similar between the combined and separate vaccine groups (0.2–0.6% in the DTaP-IPV group vs. 0.2–0.6% in the DTaP + IPV group). Overall, the proportion of solicited systemic reactions was similar between the two groups. Fever (≥ 37.4 °C, axillary) was observed in 9.5% and 7.1% of participants in the DTaP-IPV and DTaP + IPV groups, respectively. Other solicited systemic AEs were observed in 20.6–27.0% of participants in the DTaP-IPV group and in 19.1–24.5% in the DTaP + IPV group. Unsolicited AEs were reported in 72.8% and 73.9% of participants who received the DTaP-IPV and separate vaccines, respectively [41], indicating a similar safety profile between the two groups.

Vaccine safety in real-life practice is key for vaccine acceptance and adherence to vaccination programs. This will contribute to the achievement and maintenance of optimal vaccination coverage in the entire targeted populations to sustain high immunity against diphtheria, tetanus, pertussis, and polio. Vaccinating school-entry children who are a source of infection for younger infants, too young to be vaccinated or incompletely vaccinated, also confers herd protection. Monitoring of the safety of the DTaP-IPV vaccine will be continued through voluntary reporting of post-vaccination AEs and collection of safety information.

This study had some limitations. As the sample size was based on the regulatory requirement in South Korea, it was limited (approximately 600 participants), which would not necessarily allow the detection of rare AEs. Furthermore, the AEs were self-reported by parents, and this might have led to reporting bias. However, the vaccine safety management system in South Korea includes a rapid response system to ensure the documentation of rare or serious AEs post-vaccination [54].

Conclusion

No safety concerns related to the use of the DTaP-IPV vaccine in the real world were raised in participants 2–6 months old for the primary series and 4–6 years old for the school-entry booster dose in the Korean population. The review of safety results in this local PMS study reaffirms that the DTaP-IPV vaccine was well tolerated and can be given as part of routine immunization programs for active immunization against diphtheria, tetanus, pertussis, and poliomyelitis in infants and children.

Post-marketing surveillance of the combined diphtheria, tetanus, acellular pertussis, and inactivated poliovirus (DTaP-IPV) vaccine provides the safety profile of this vaccine in a real-life setting in South Korea.

No safety concerns related to the DTaP-IPV vaccine in real-world use were raised in participants aged 2–6 months for the primary series and 4–6 years for the school-entry booster dose in the Korean population.

A combined diphtheria, tetanus, acellular pertussis, and inactivated poliovirus vaccine was well tolerated and can be given as part of routine immunization programs for protection against diphtheria, tetanus, pertussis, and poliomyelitis in infants and children.