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1.
J Epidemiol Glob Health ; 6(2): 105-18, 2016 06.
Article in English | MEDLINE | ID: mdl-26166425

ABSTRACT

Epidemiological evidence suggests a link between mercury (Hg) exposure from Thimerosal-containing vaccines and specific delays in development. A hypothesis-testing longitudinal cohort study (n=49,835) using medical records in the Vaccine Safety Datalink (VSD) was undertaken to evaluate the relationship between exposure to Hg from Thimerosal-containing hepatitis B vaccines (T-HBVs) administered at specific intervals in the first 6months of life and specific delays in development [International Classification of Disease, 9th revision (ICD-9): 315.xx] among children born between 1991 and 1994 and continuously enrolled from birth for at least 5.81years. Infants receiving increased Hg doses from T-HBVs administered within the first month, the first 2months, and the first 6months of life were significantly more likely to be diagnosed with specific delays in development than infants receiving no Hg doses from T-HBVs. During the decade in which T-HBVs were routinely recommended and administered to US infants (1991-2001), an estimated 0.5-1million additional US children were diagnosed with specific delays in development as a consequence of 25µg or 37.5µg organic Hg from T-HBVs administered within the first 6months of life. The resulting lifetime costs to the United States may exceed $1 trillion.


Subject(s)
Hepatitis B Vaccines/adverse effects , Hepatitis B Vaccines/economics , Hepatitis B/drug therapy , Hepatitis B/economics , Mercury/adverse effects , Thimerosal/adverse effects , Thimerosal/economics , Antiviral Agents/adverse effects , Antiviral Agents/economics , Antiviral Agents/therapeutic use , Child , Child Development/drug effects , Child, Preschool , Cohort Studies , Female , Hepatitis B Vaccines/therapeutic use , Humans , Infant , Infant, Newborn , Longitudinal Studies , Male , Risk Factors , Thimerosal/therapeutic use , United States
2.
J Emerg Med ; 33(2): 199-211, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17692778

ABSTRACT

The National Childhood Vaccine Injury Act of 1986, as amended, established the Vaccine Injury Compensation Program (VICP). The VICP went into effect on October 1, 1988 and is a Federal "no-fault" system designed to compensate individuals, or families of individuals, who have been injured by covered vaccines. From 1988 until July 2006, a total of 2531 non-autism/thimerosal and 5030 autism/thimerosal claims were made to the VICP. The compensation paid for the non-autism/thimerosal claims from 1988 until 2006 was $902,519,103.37 for 2542 awards. There was no compensation for any of the autism/thimerosal claims. On the basis of the deaths and extensive suffering to patients and families from the adverse reactions to vaccines, all physicians must provide detailed information in the Vaccine Information Statement to the patient or the parent or legal guardian of the child about the potential dangers of vaccines as well as the VICP.


Subject(s)
Compensation and Redress/legislation & jurisprudence , Preservatives, Pharmaceutical/adverse effects , Thimerosal/adverse effects , Vaccines/adverse effects , Adolescent , Autistic Disorder/chemically induced , Autistic Disorder/economics , Child , Child, Preschool , Humans , Infant , Mandatory Programs/legislation & jurisprudence , Mass Vaccination/adverse effects , Mass Vaccination/legislation & jurisprudence , Patient Education as Topic/legislation & jurisprudence , Patient Rights , Thimerosal/economics , Truth Disclosure , United States , Vaccines/economics
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