VaxFact.net
🟠

Hepatitis A Vaccine

Hepatitis A

Hepatitis A virus (HAV) is a self-limiting liver infection. Unlike HepB, it does not cause chronic disease. However, it causes acute liver failure in ~0.5% of cases, with fatality rates rising sharply in adults and those with pre-existing liver disease. Large outbreaks have swept through homeless communities and produce/restaurant supply chains.

📅
30+ yrs
Years in Use
💉
Over 100 million doses in the US since 1995
Doses Administered
🛡️
99% vs severe disease
Effectiveness
👶
12–23 months (2-dose series); catch-up at any age
Age Window

Overall Benefit Score

59/ 100
Moderate Recommendation

Default scenario · 12-month-old · US community (92% vax rate)

Score for your child →
Moderate Recommendation

The evidence moderately supports this vaccine for your child's situation. Benefits outweigh risks but some factors in your scenario lower the urgency.

📊 Evidence Scores

Scores computed from peer-reviewed data using VaxFact's evidence model. Based on default scenario (12-month-old, standard US community).

Net BenefitBenefit minus risk, weighted by exposure probability
59
Exposure RiskLikelihood of encountering the disease
39
Disease ConsequenceSeverity of outcomes if disease is acquired
100
Vaccine BenefitProtection provided against disease and death
99
Vaccine HarmRisk from the vaccine itself (adverse events)
11
Evidence ConfidenceQuality and consensus of the scientific evidence
90

🦠 Disease Burden

Hepatitis A virus (HAV) is a self-limiting liver infection. Unlike HepB, it does not cause chronic disease. However, it causes acute liver failure in ~0.5% of cases, with fatality rates rising sharply in adults and those with pre-existing liver disease. Large outbreaks have swept through homeless communities and produce/restaurant supply chains.

🔄
Fecal-oral route — contaminated food, water, or close contact. Very stable in environment; resistant to freezing and chlorination at standard levels.
Transmission
high
Outbreak Potential
🏥
22% of infected
Hospitalization Rate
⏱️
0% of infected
Long-term Complications
📈
75 per 100,000/yr
Incidence (unvaccinated)
📉
0.4 per 100,000/yr
Incidence (vaccinated)
Quality of Life Impact

Jaundice, profound fatigue, nausea, and abdominal pain lasting 2–6 weeks. Most working-age adults miss 2–4 weeks of work. A prolonged relapsing form affects ~10–15% and extends illness for months. Full hepatic failure requiring transplant occurs rarely but is devastating.

🛡️ Vaccine Effectiveness

🦠
99%
Against Infection
🏥
99%
Against Severe Disease
💚
99%
Against Death
Waning Immunity

Mathematical models project protection lasting at least 25–40 years based on antibody decay rates. Booster not currently recommended for immunocompetent individuals after primary series. Some immunocompromised patients may need booster.

Breakthrough Infections

Breakthrough infections are exceptionally rare — fewer than 1 per 100,000 vaccinated per year in surveillance data.

⚠️ Adverse Events & Side Effects

All probabilities are per 100,000 doses administered, sourced from VAERS, Vaccine Safety Datalink, and post-licensure surveillance studies.

Common Side Effects

Injection site pain
Most common AE; resolves in 1–2 days
50,000 / 100k
per dose
Headache/fatigue
Mild, transient
15,000 / 100k
per dose
Fever
Low-grade; uncommon
5,000 / 100k
per dose

Rare Serious Events

Anaphylaxis
~1 per million doses; among the lowest anaphylaxis rates of any vaccine
1 / 100k
per dose

📅 Vaccine Schedule

Dosing Schedule
112–23 months
26–18 months after dose 1
Key Info
Minimum interval
6 months between dose 1 and dose 2
Can co-administer with
MMR, Varicella, DTaP, IPV
Catch-Up Notes

Unvaccinated children through age 18 should receive 2-dose catch-up series. Adults traveling to endemic areas should receive dose 1 at least 2 weeks before departure.

⚖️ Benefits vs. Considerations

✓ Benefits

  • 99% effective — among the highest efficacy of any vaccine
  • 30 years of post-licensure safety data with an exceptionally clean adverse event profile
  • Prevents a miserable weeks-long illness that causes major work/school disruption
  • Critical protection for international travel to most of the developing world
  • Eliminates disease in communities once herd immunity is achieved — demonstrated in Israel and US states that introduced universal vaccination
  • Single dose provides protection within 2 weeks — useful for pre-travel

↕ Considerations

  • HepA rarely causes death in children — benefit is largest in adults and those with liver disease
  • Requires 2 doses 6 months apart for full protection
  • Significant injection site pain (~50% of recipients)
  • Not on routine schedule in many high-income countries with low endemic risk

🔬 What Some Researchers Question

These are legitimate scientific debates — not fringe claims. They represent areas of ongoing research or policy disagreement among credentialed experts.

  • Some health economists and infectious disease physicians argue that universal toddler vaccination is poorly targeted — the disease burden in children is mild, whereas the vaccine's greatest impact is in adults and those with liver disease. Targeted vaccination of high-risk populations may achieve similar public health outcomes at lower cost (Arguedas et al., 2004).
  • The 2-dose schedule separated by 6 months creates access challenges in mobile or underserved populations — single-dose programs have been evaluated in some countries with acceptable outcomes, but the US continues to recommend the 2-dose series.

🌫️ Scientific Uncertainties

Honest acknowledgment of what we don't yet know with confidence.

  • Exact duration of immunity — models predict 25–40 years but real-world cohort data beyond 25 years is limited
  • Whether single-dose schedules provide sufficient community protection (some countries use 1 dose)
  • Optimal timing in immunocompromised children where antibody responses may be suboptimal

💉 Related Vaccines

Vaccines often given together or covering related diseases.

🌍 International Policy Comparison

How different countries approach this vaccine — revealing where global consensus is strong vs. where policy diverges.

US
United States✓ Recommended
12–23m, then 6–18m later
Universal childhood vaccination since 2006; previously targeted only high-risk groups.
IL
Israel✓ Recommended
18m, 24m
First country to introduce universal HepA vaccination (1999); incidence fell 95%.
GB
United KingdomVaries / Optional
Risk groups and travelers only
Not on routine schedule; UK strategy relies on targeted vaccination of risk groups.
DE
GermanyVaries / Optional
Travel and risk groups only
Low endemic risk in Germany; STIKO recommends for specific risk groups.
AU
AustraliaVaries / Optional
Aboriginal children 12–24m; travelers
Universal only in Aboriginal and Torres Strait Islander populations due to higher endemic burden.

Brand Names

HavrixVaqtaTwinrix (HepA+HepB combo)

Evidence Quality

Years of Study78/100
Long-Term Safety80/100
Evidence Confidence90/100
In use since1996

Key Sources

Fiore et al. — Prevention of Hepatitis A Through Active or Passive Immunization (MMWR)
REVIEW · 2006 · USA · high confidence
WHO Position Paper on Hepatitis A Vaccines
REVIEW · 2012 · Global · high confidence
CDC MMWR — Hepatitis A Outbreaks in Homeless Populations
SURVEILLANCE · 2019 · USA · high confidence
🎯

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