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Vaccine Adverse Events: Separating Myth from Reality


SANFORD R. KIMMEL, M.D., Medical College of Ohio, Toledo, Ohio

http://www.aafp.org/afp/20021201/2113.html

American Family Physician

Vaccines have turned many childhood diseases into distant memories in industrialized countries. However, questions have been raised about the safety of some vaccines because of rare but serious adverse effects that have been attributed to them. Pain, swelling, and redness at the injection site are common local reactions to vaccines. Fever and irritability may occur after some immunizations. Currently, no substantial evidence links measles-mumps-rubella vaccine to autism, or hepatitis B vaccine to multiple sclerosis. Thimerosal is being eliminated from routine childhood vaccines because of concerns that multiple immunizations with vaccines containing this preservative could exceed recommended mercury exposures. Family physicians should be knowledgeable about vaccines so that they can inform their patients of the benefits of immunization and any proven risks. If immunization rates fall, the incidence of vaccine-preventable illnesses may rise. (Am Fam Physician 2002;66:2113-20. Copyright© 2002 American Academy of Family Physicians.)

Vaccination was one of the 20th century's most successful methods of disease prevention and eradication. Smallpox was eradicated worldwide, and the Americas were declared free of wild poliovirus in 1994.1 The reported incidence of measles in the United States declined to 100 cases per year in 1999; more than one half of these cases were due to the importation of measles from other countries.2 In 1999, an outbreak of rubella occurred in Nebraska among Hispanic meatpackers who had not received rubella vaccine in childhood.3 Because vaccine-preventable diseases continue to be imported from other countries and are a threat to unimmunized persons in the United States, family physicians and other health care workers should continue to maintain high immunization rates in their patients.

 

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Investigators in several studies concluded that there is no causal relationship between MMR vaccine and autism.
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Unfortunately, maintaining high immunization rates is becoming more difficult, in part because vaccines have become victims of their own success. Diseases that are preventable by vaccination are no longer encountered by most people in this country; thus, the threat of these illnesses seems less real. In addition, vaccines are not 100 percent effective, and they can have mild or, occasionally, serious adverse effects.

Vaccine Adverse Event Reporting System

The U.S. Food and Drug Administration (FDA) established the Vaccine Adverse Event Reporting System (VAERS) as a passive surveillance system for clinical events that occur after immunization. VAERS reports are submitted by manufacturers, health care professionals, state health coordinators, and parents of vaccinated children.4

VAERS reports may be incomplete or inconsistent, and a reported adverse event may be only temporally related to a vaccine.4 However, the effectiveness of VAERS as an early warning system was demonstrated by reports of an increased incidence of intussusception after immunization with rotavirus vaccine.5 This vaccine was subsequently withdrawn from the market.

Public Perception and Tolerance of Vaccine Risks

A recent telephone survey6 demonstrated that more than 80 percent of parents supported immunizing their children to keep them well. However, 25 percent incorrectly believed that too many immunizations could weaken their child's immune system. Respondents who were women, white, or college graduates, or who had an alternative medical orientation were more likely to opt out of immunization for their children. More than 80 percent of respondents indicated that physicians were still their primary source of vaccine information.

What level of vaccine-related risk will most parents tolerate? A study7 in western Ontario found that most mothers would accept a risk ranging from one adverse event per 100,000 to 1 million vaccinations. However, 14 percent would not accept any risk of a serious adverse event. This zero-risk tolerance group tended to have a lower income and to prefer a nonnumeric statement of risk. Another study8 using a hypothetic vaccine found that 23 percent of persons would vaccinate only if the risk of a serious event was zero.

In the absence of a direct threat from disease, it is clear that some people will not undergo vaccination unless absolute safety can be assured. Although absolute vaccine safety is the optimal goal, it is difficult to achieve in the real world.

Common Adverse Events with Vaccines

Common local reactions to vaccines include pain, swelling, and redness at the injection site. Systemic reactions, including fever, irritability, drowsiness, and rash, may also occur. The administration of acetaminophen at the time of vaccination or shortly afterward may moderate these effects.

Compared with the first dose, the fourth dose of currently licensed diphtheria and tetanus toxoids and acellular pertussis vaccine (DTaP) has been associated with increased incidences of fever and erythema, swelling, and pain at the injection site. In a small percentage of children, swelling of the entire thigh or upper arm for about four days has been reported after the fourth or fifth dose of DTaP. This self-limited reaction has been documented for multiple products from different manufacturers.9

One comparative study10 found no significant differences in immunogenicity or reactions for a fifth-dose booster of six DTaP vaccines and one U.S.-licensed diphtheria and tetanus toxoids and whole-cell pertussis vaccine (DTwP). Redness, swelling, and pain at the injection site were increased for the fifth-dose booster compared with the fourth DTaP dose, but all common reactions occurred less frequently after DTaP than after DTwP.

Traces of antibiotics such as neomycin, which is present in varicella (chickenpox), trivalent inactivated poliovirus (IPV), and measles-mumps-rubella (MMR) vaccines, have been considered possible causes of adverse reactions. A history of anaphylactic reaction to neomycin is a contraindication to future immunization, whereas a local reaction is not.11(pp30-9)

Gelatin, which is used as a stabilizer in some live-virus vaccines (e.g., varicella and MMR vaccines), might cause a reaction. Children with a history of egg allergy may be given MMR vaccine, even though it is derived from chick embryo fibroblast tissue culture. However, influenza vaccine should not be given to a person with a history of egg allergy.11(p35)

MMR Vaccine and Autism

On November 12, 2000, the CBS television show 60 Minutes featured a story on the MMR vaccine and its alleged link to autism. In 1998, investigators published a report12(pp637-41) on 12 children referred to a London pediatric gastroenterology unit for the evaluation of gastrointestinal diseases associated with developmental regression. The parents of eight of these children associated the onset of behavioral symptoms with the administration of MMR vaccine. The investigators identified lymphoid nodular hyperplasia in 10 children and postulated that "the consequences of an inflamed or dysfunctional intestine may play a part in behavioural changes in some children."12(p639) However, behavioural symptoms preceded bowel symptoms in four of the six children for whom the onset of bowel symptoms was known. The investigators stated, "We did not prove an association between measles, mumps, and rubella vaccine and the syndrome described."12(p641)

In 1999, other investigators published the findings of a much larger population-based study conducted in North London.13(pp2026-9) The study identified 498 children with autism but found no temporal association between onset of the disorder and receipt of MMR vaccine in the previous one to two years. Cases of developmental regression were not clustered in the months after vaccination. The investigators concluded, "Our analyses do not support a causal association between MMR vaccine and autism. If such an association occurs, it is so rare that it could not be identified in this large regional sample."13(p2026)

Another set of investigators found no vaccine-associated cases of inflammatory bowel disease or autism in 1.8 million Finnish children who received almost 3 million doses of MMR vaccine over 14 years.14 In California, retrospective analyses15 of MMR immunization coverage and children with autism also did not suggest an association between MMR vaccine and an increased incidence of autism.

The Institute of Medicine (IOM) recently concluded that "the evidence favors rejection of a causal relationship at the population level between MMR vaccine and ASD (autistic spectrum disorders)."16(p9) However, the IOM could "not exclude the possibility that MMR vaccine could contribute to ASD in a small number of children."16(p9)

Data on measles, mumps, and rubella disease and MMR vaccine11,14,17-23 are summarized in Table 1.24

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TABLE 1
Measles, Mumps, and Rubella Disease and Vaccine Fact Sheet*


Disease factor/
risk of sequelae
Measles Mumps Rubella MMR vaccine
Disease factor        
Highest number of U.S. cases 894,134 cases in 194117 152,209 cases in 196818 12 million cases in 1964-1965; 57,686 cases in 196919
Congenital rubella: 20,000 cases in 1964-196519
Highly efficacious in preventing disease†
Recent number of U.S. cases 86 cases in 200020 338 cases in 200020 176 cases in 200020 Congenital rubella: 9 cases in 200020 No cases of congenital rubella reported after immunization of pregnant women, but theoretic risk is 2%21
Transmission route Droplets Direct contact, airborne droplets, fomites bysaliva Oral droplets
Congenital rubella: transplacental passage
--
Transmission risk in susceptible household contacts 90% in susceptible household contacts17 Rate not available, because 30% to 40% of infections are subclinical18 50% to 60% in susceptible family members and almost 100% in closed populations19 Incidence of defects in congenital rubella: >=50% with infection during first month of pregnancy; 20% to 30% with infection during second month; 5% with infection during third or fourth month11(pp495-500) --
Risk of sequelae        
Mortality 1 to 2 deaths per 1,000 measles cases11(pp385-96),17 2.5 to 50 deaths per 1 million mumps cases, because of 1.4% to 2% fatality rate from encephalitis18,22 1 death per 30,000 rubella cases, because of 20% fatality rate from encephalitis19
Congenital rubella: no data available
1 death, but not attributed to vaccine14
Fatal measles pneumonitis in a 21-year-old man with advanced HIV infection23
Encephalitis 1 to 2 cases per 1,000 measles cases17 1 case per 400 to 6,000 mumps cases22 1 case per 5,000 to 6,000 rubella cases19 1 case per 1 million doses14
Subacute sclerosing panencephalitis 8.5 cases per 1 million measles cases17 -- 20 reported cases of progressive rubella panencephalitis19 0 to 0.7 cases per 1 million doses14,17
Pneumonia 3% of young adultswith measles23 -- -- 2 cases per 1 million doses14
Thrombocytopenia   Rare22 1 case per 3,000 rubella cases19 0.5 to 33 cases per 1 milliondoses11(pp385-96),14
Orchitis -- 14% to 35% of adolescent and adult men with mumps14,18 -- 0.3 cases per 1 million doses14
Anaphylaxis -- -- -- 5 cases per 1 million doses (none fatal)14

MMR = measles, mumps, rubella; HIV = human immunodeficiency virus.

*--Data on measles, mumps, and rubella disease represent reported or estimated disease and sequelae; data on vaccine represent estimated risks.

†--A single dose of vaccine given at 12 to 15 months of age has an efficacy of 95%; efficacy is further improved by a second dose given at 4 to 6 years of age.11(pp385-96)

Adapted from Kimmel SR. Communicating the benefits and risks of vaccines. J Fam Pract 2001;50(10 suppl):S52-7. Adapted with permission from Society of Teachers of Family Medicine. Copyright© 2001 Society of Teachers of Family Medicine.

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Thimerosal in Vaccines

Thimerosal, a preservative containing ethyl mercury, has been used to prevent bacterial and fungal contamination of vaccines since the 1930s. In 1999, the FDA determined that infants who received multiple thimerosal-containing vaccines might be exposed to more mercury than is recommended. As a result, initial hepatitis B immunization was deferred until two to six months of age in infants of hepatitis B surface antigen (HBsAg)­negative mothers.25 However, birth immunization continued to be recommended for the infants of HBsAg­positive mothers and the infants of mothers whose hepatitis B status was unknown.25 Unfortunately, some unimmunized infants contracted hepatitis B, and at least one unimmunized infant born to an HBsAg­positive mother died of fulminant hepatitis B.26 Routine hospital immunization of newborns with currently available thimerosal-free hepatitis B vaccines is now recommended.

Except for local hypersensitivity reactions, a recent review27 found no evidence of harm from thimerosal in vaccines. Thimerosal-free vaccines are now available for all routine childhood immunizations. The American Academy of Family Physicians (AAFP), American Academy of Pediatrics (AAP), and Public Health Service (PHS) continue to recommend the reduction or removal of thimerosal from vaccines and note substantial progress in this effort.28

Vaccines and Multiple Sclerosis

Allegations have been raised that hepatitis B (HepB) vaccine can cause chronic fatigue syndrome, multiple sclerosis, and other autoimmune disorders.29 However, the National Multiple Sclerosis Society30 cited a French report that found a lower frequency of neurologic disease among recipients of 60 million doses of HepB vaccine. The fact that genetic sequencing has not demonstrated a similarity between HepB vaccine and myelin basic protein casts doubt on a theory proposing that immunization provokes the formation of antimyelin antibodies (molecular mimicry).31

A recent report32 from the Nurses' Health Study, which included more than 200,000 women, found no association between HepB vaccine and the development of multiple sclerosis. A study from the European Database for Multiple Sclerosis33 found that vaccination against tetanus, hepatitis B, and influenza did not increase the risk of short-term relapse in patients with multiple sclerosis.

Vaccines and Type 1 Diabetes

Concerns have been expressed that vaccines could be linked to type 1 diabetes. A Swedish study34 found that children with type 1 diabetes were less likely to have received measles vaccine than children without diabetes. No connection was reported between type 1 diabetes and tetanus toxoid or pertussis, rubella, mumps, and bacille Calmette-Guérin vaccines.34 A Vaccine Safety Datalink project of the Centers for Disease Control and Prevention (CDC) did not find an increased risk of type 1 diabetes with whole-cell or acellular pertussis­containing vaccines, MMR vaccine, HepB vaccine, and varicella vaccine.35 Similarly, there has been no association between type 1 diabetes and Haemophilus influenzae type b conjugate vaccine.36

Influenza Vaccine and Guillain-Barré Syndrome

The 1976 swine influenza vaccine was associated with an increased risk of Guillain-Barré syndrome (slightly less than 10 cases per 1 million persons vaccinated) compared with the background risk.37 Later studies found either no statistically significant increase in risk or an increase of about one additional case of Guillain-Barré syndrome per 1 million persons vaccinated.37 This risk is significantly less than that for severe influenza and its complications. However, influenza vaccine may be avoided or antiviral chemoprophylaxis may be used in patients who are not at high risk and who developed this syndrome within six weeks after receiving influenza vaccine. Inactivated influenza vaccine contains noninfectious killed viruses and cannot cause influenza.37

Varicella Vaccine and VAERS

The use of varicella vaccine is increasing in the United States because of state mandates and reports of secondary infection with invasive group A streptococcal disease in children with varicella-zoster virus infection.38 Deaths from varicella pneumonia, encephalitis, and disseminated disease have also occurred in adults exposed to children with varicella.39

Significant risks of varicella disease and adverse events attributed to varicella vaccine11,38,40-43 (many of them reported from VAERS) are listed in Table 2.24 Although events reported to VAERS may be temporally related to vaccination, this relationship does not establish causation. Adverse events such as anaphylaxis may be related to a sensitivity to vaccine components (e.g., gelatin) rather than to the attenuated vaccine virus itself.

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TABLE 2
Varicella Disease and Vaccine Fact Sheet*


Disease factor/risk of sequelae Varicella Varicella vaccine
Disease    
Average annual number of U.S. cases 3.7 million cases per year in 1980-199040 Efficacious in preventing disease†
Transmission route Direct contact or airborne spread of respiratory tract secretions; transplacental passage  
Transmission rate to susceptible contacts 90% in susceptible household contacts40
<= 30% in classroom contacts41
3 confirmed cases secondary to transmission in immunocompetent persons42
Risk of sequelae    
Mortality 94 deaths per year in 1987-199240 14 deaths in 1995-1998‡; vaccine not implicated or confirmed as cause42
Localized rash   3% to 5% of vaccine recipients11(pp624-38)
Generalized varicella-like rash 100% of persons with varicella 3% to 5% of vaccine recipients11(pp624-38)
Invasive group A streptococcal disease 5.2 cases per 100,000 varicella cases38§ 1 case42
Anaphylaxis -- 30 nonfatal cases42ý
Herpes zoster (children under 20 years of age) 68 cases per 100,000 person-years11(pp624-38) 2.6 cases per 100,000 doses11(pp624-38),42
Thrombocytopenia 1% to 2% of persons with varicella41 0.3 cases per 100,000 doses42
Arthropathy -- 0.5 cases per 100,000 doses42
Cerebellar ataxia 1 case per 4,000 varicella cases43 0.4 cases per 100,000 doses41
Encephalitis 0.1% to 0.2% of persons with varicella43 0.3 cases per 100,000 doses42
Pneumonia 1 case per 400 varicella cases in adults43 0.2 cases per 100,000 doses42
Congenital varicella syndrome 0.4% of infants zero to 12 weeks of gestational age who have varicella11(pp624-38),40 2% of infants 13 to 20 weeks of gestational age who have varicella11(pp624-38),40 No cases in 87 women who received vaccine before or during pregnancy42

*--Data on varicella disease represent reported or estimated disease and sequelae; data on varicella vaccine represent estimated risks.

--The vaccine has an efficacy of 70% to 90%40; it is 95% to 100% effective in preventing moderate to severe disease.11(pp624-38),42

--Based on reports to the Vaccine Adverse Event Reporting System (VAERS) from March 17, 1995, through July 25, 1998. Data from VAERS do not prove association of an adverse event with a vaccine, but may prompt further investigation. The VAERS reporting rate is the number of adverse events per estimated vaccine doses sold.42

§--In children without varicella, the incidence of invasive group A streptococcal disease is 0.09 cases per 100,000.

Adapted from Kimmel SR. Communicating the benefits and risks of vaccines. J Fam Pract 2001;50(10 suppl):S52-7. Adapted with permission from Society of Teachers of Family Medicine. Copyright© 2001 Society of Teachers of Family Medicine.

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Consequences of Failure to Vaccinate

A recent study44 in Colorado demonstrated that children who were exempted from immunization were 22 times more likely to develop measles and almost six times more likely to acquire pertussis than vaccinated children. School was the site of infection in more than 20 percent of the children who developed measles or pertussis. In this study, each 1 percent increase in children exempted from immunization increased the risk of a pertussis outbreak by 12 percent.44 Because immunizations against measles and pertussis are not 100 percent effective, there was a 60 percent and a 90 percent annual increased risk of measles and pertussis among vaccinated children three to 18 years of age for each 1 percent increase in the proportion of unimmunized children (exemptors) by county.44,45

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One study found that children who were exempted from immunization were 22 times more likely to develop measles and almost six times more likely to develop pertussis than vaccinated children.
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Consequently, the choice of some parents not to immunize their children increases the risk for children who are immunized. These parents may not realize that the individual choice not to vaccinate a child has public health consequences.

National Vaccine Injury Compensation Program

The National Childhood Vaccine Injury Act of 1986 established the National Vaccine Injury Compensation Program (VICP) as a federal no-fault system to compensate persons (or families of persons) who are injured by covered childhood vaccines. This act also requires physicians and other health care providers who administer VICP-covered vaccines or vaccines purchased under CDC contract to record the date of administration, the vaccine manufacturer, the lot number, and their name, business address, and title in the patient's permanent medical record.46

Health care providers must also give the vaccine recipient or the recipient's legal guardian the corresponding and most up-to-date Vaccine Information Statement (VIS) each time a VICP-covered vaccine is administered. The VIS for a non­VICP-covered vaccine must also be given if the vaccine is purchased through a CDC contract. The CDC requires that the VIS version date and the date the VIS is provided be documented in the patient's medical record.46

The VIS for each vaccine may be obtained from the CDC (www.cdc.gov/nip/publications/vis/default.htm), the state health department, or the Immunization Action Coalition (www.immunize.org/vis). VIS translations in different languages are available on the Immunization Action Coalition Web site.

Manufacturers, state health coordinators, health care professionals, and parents may submit reports of adverse events following immunization. The table of reportable events is available at www.vaers.org/pdf/reportable.pdf. VAERS reporting forms can be obtained from the VAERS Web site (www.vaers.org) or by telephone (800-822-7967). A written form is available at the end of the Physicians' Desk Reference. Definitions of possibly compensable injuries and further information regarding eligibility and documentation of claims may be obtained from the VICP (www.hrsa.gov/bhpr/vicp) or by telephone (800-338-2382).

The author indicates that he does not have any conflicts of interest. Sources of funding: Work on the manuscript was supported by funding from the Centers for Disease Control and Prevention National Immunization Program, through Cooperative Agreement U66/CCU719217-01 to the Society of Teachers of Family Medicine Foundation. Dr. Kimmel is a member of the speaker's bureau (immunizations) for GlaxoSmithKline and serves on the Adult Vaccine Advisory Board for Merck & Co., Inc.


The Author

SANFORD R. KIMMEL, M.D., is professor of clinical family medicine at the Medical College of Ohio, Toledo. After graduating from Ohio State University College of Medicine, Columbus, he completed a family practice residency at St. Elizabeth Medical Center, Dayton, Ohio, and pediatric training at Children's Hospital, Columbus, Ohio. Dr. Kimmel is the author of multiple articles on immunizations and book chapters on various pediatric topics. Previously, he chaired the Group on Immunization Education of the Society of Teachers of Family Medicine.

Address correspondence to Sanford R. Kimmel, M.D., Department of Family Medicine, Medical College of Ohio, 1015 Garden Lake Pkwy., Toledo, OH 43614 (e-mail: skimmel@mco.edu). Reprints are not available from the author.

REFERENCES

  1. Centers for Disease Control and Prevention. Poliomyelitis prevention in the United States: updated recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep 2000;49(RR-5):1-22.
  2. Measles, rubella, and congenital rubella syndrome--United States and Mexico, 1997-1999. MMWR Morb Mortal Wkly Rep 2000;49:1048-50,1059.
  3. Danovaro-Holliday MC, LeBaron CW, Allensworth C, Raymond R, Borden TG, Murray AB, et al. A large rubella outbreak with spread from the workplace to the community. JAMA 2000;284:2733-9.
  4. Varricchio F. The Vaccine Adverse Event Reporting System. J Toxicol Clin Toxicol 1998;36:765-8.
  5. Intussusception among recipients of rotavirus vaccine--United States, 1998-1999. MMWR Morb Mortal Wkly Rep 1999;48:577-81.
  6. Gellin BG, Maibach EW, Marcuse EK. Do parents understand immunizations? A national telephone survey. Pediatrics 2000;106:1097-1102.
  7. Freeman TR, Bass MJ. Determinants of maternal tolerance of vaccine-related risks. Fam Pract 1992; 9:36-41.
  8. Ritov I, Baron J. Reluctance to vaccinate: omission bias and ambiguity. J Behav Decis Making 1990;3:263-77.
  9. Use of diphtheria toxoid­tetanus toxoid­acellular pertussis vaccine as a five-dose series. Supplemental recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep 2000;49(RR-13):1-8.
  10. Pichichero ME, Edwards KM, Anderson EL, Rennels MB, Englund JA, Yerg DE, et al. Safety and immunogenicity of six acellular pertussis vaccines and one whole-cell pertussis vaccine given as a fifth dose in four- to six-year-old children. Pediatrics 2000;105:e11.
  11. Pickering LK, ed. 2000 Red book: report of the Committee on Infectious Diseases. 25th ed. Elk Grove Village, Ill.: American Academy of Pediatrics, 2000.
  12. Wakefield AJ, Murch SH, Anthony A, Linnell J, Casson DM, Malik M, et al. Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children. Lancet 1998; 351.
  13. Taylor B, Miller E, Farrington CP, Petropoulos MC, Favot-Mayaud I, Li J, et al. Autism and measles, mumps, and rubella vaccine: no epidemiological evidence for a causal association. Lancet 1999; 353.
  14. Patja A, Davidkin I, Kurki T, Kallio MJ, Valle M, Peltola H. Serious adverse events after measles-mumps-rubella vaccination during a fourteen-year prospective follow-up. Pediatr Infect Dis J 2000; 19:1127-34.
  15. Dales L, Hammer SJ, Smith NJ. Time trends in autism and in MMR immunization coverage in California. JAMA 2001;285:1183-5.
  16. Stratton K, Gable A, Shetty P, McCormick M, eds. Immunization safety review: measles-mumps-rubella vaccine and autism. Washington, D.C.: National Academy Press, 2001.
  17. Maldonado Y. Measles. In: Behrman RE, Kliegman RM, Jenson HB, eds. Nelson Textbook of pediatrics. 16th ed. Philadelphia: Saunders, 2000:946-51.
  18. Maldonado Y. Mumps. In: Behrman RE, Kliegman RM, Jenson HB, eds. Nelson Textbook of pediatrics. 16th ed. Philadelphia: Saunders, 2000:954-5.
  19. Maldonado Y. Rubella. In: Behrman RE, Kliegman RM, Jenson HB, eds. Nelson Textbook of pediatrics. 16th ed. Philadelphia: Saunders, 2000:951-4.
  20. Notice to readers: final 2000 reports of notifiable diseases. MMWR Morb Mortal Wkly Rep 2001; 50:712. Retrieved September 9, 2002, from www.cdc.gov/mmwr/preview/mmwrhtml/mm5033a5.htm.
  21. Gershon A. Rubella virus. In: Mandell GL, Douglas RG, Bennett JE, Dolin R, eds. Mandell, Douglas, and Bennett's Principles and practice of infectious diseases. 5th ed. Philadelphia: Churchill Livingstone, 2000:1708-14.
  22. Baum SG, Litman N. Mumps virus. In: Mandell GL, Douglas RG, Bennett JE, Dolin R, eds. Mandell, Douglas, and Bennett's Principles and practice of infectious diseases. 5th ed. Philadelphia: Churchill Livingstone, 2000:1776-81.
  23. Gershon A. Measles virus (rubeola). In: Mandell GL, Douglas RG, Bennett JE, Dolin R, eds. Mandell, Douglas, and Bennett's Principles and practice of infectious diseases. 5th ed. Philadelphia: Churchill Livingstone, 2000:1801-8.
  24. Kimmel SR. Communicating the benefits and risks of vaccines. J Fam Pract 2001;50(10 suppl):S52-7.
  25. Thimerosal in vaccines--an interim report to clinicians. American Academy of Pediatrics. Committee on Infectious Diseases and Committee on Environmental Health. Pediatrics 1999;104(3 pt 1):570-4.
  26. Fasano N. Infant dies of fulminant hepatitis B, 1999. Needle Tips 2000;10:12. Retrieved September 9, 2002, from www.immunize.org/nslt.d/n23/n23.pdf.
  27. Ball LK, Ball R, Pratt RD. An assessment of thimerosal use in childhood vaccines. Pediatrics 2001;107:1147-54.
  28. Joint statement of AAFP, AAP, ACIP, and the USPHS on thimerosal in childhood vaccines (Approved by AAFP, AAP, ACIP, and PHS on June 22, 2000). Retrieved September 9, 2002, from www.vaccinesafety.edu/AAFP-AAP-ACIP-thimerosal.htm.
  29. National Vaccine Information Center. Hepatitis B vaccine: the untold story. Retrieved September 9, 2002, from www.909shot.com/Diseases/hepbnlr. htm.
  30. Hepatitis B vaccine and multiple sclerosis. Retrieved September 9, 2002, from www.nationalmssociety. org/Research-1998Aug.asp.
  31. Multiple sclerosis and the hepatitis B vaccine. Rerieved September 9, 2002, from www.cdc.gov/nip/vacsafe/concerns/MS/default.htm.
  32. Ascherio A, Zhang SM, Hernan MA, Olek MJ, Coplan PM, Brodovicz K, et al. Hepatitis B vaccination and the risk of multiple sclerosis. N Engl J Med 2001;344:327-32.
  33. Confavreux C, Suissa S, Saddier P, Bourdes V, Vukusic S. Vaccinations and the risk of relapse in multiple sclerosis. Vaccines in Multiple Sclerosis Study Group. N Engl J Med 2001;344:319-26.
  34. Blom L, Nystrom L, Dahlquist G. The Swedish childhood diabetes study. Vaccinations and infections as risk determinants for diabetes in childhood. Diabetologia 1991;34:176-81.
  35. DeStefano F, Mullooly JP, Okoro CA, Chen RT, Marcy SM, Ward JI, et al. Childhood vaccinations, vaccination timing, and risk of type 1 diabetes mellitus. Pediatrics 2001;108:E112. Retrieved September 9, 2002, from www.pediatrics.org/cgi/content/full/108/6/e112.
  36. Karvonen M, Cepaitis Z, Tuomilehto J. Association between type 1 diabetes and Haemophilus influenzae type b vaccination: birth cohort study. BMJ 1999;318:1169-72.
  37. Bridges CB, Fukuda K, Uyeki TM, Cox NJ, Singleton JA. Prevention and control of influenza. Recommendations of the Advisory Committee on Immunization Practices. MMWR Recomm Rep 2002; 51(RR-3):1-31.
  38. Laupland KB, Davies HD, Low DE, Schwartz B, Green K, McGeer A. Invasive group A streptococcal disease in children and association with varicella-zoster virus infection. Ontario Group A Streptococcal Study Group. Pediatrics 2000;105:E60.
  39. Varicella-related deaths among adults--United States, 1997. MMWR Morb Mortal Wkly Rep 1997;46:409-12.
  40. Prevention of varicella: recommendations of the Advisory Committee on Immunization Practices (ACIP). Centers for Disease Control and Prevention. MMWR Recomm Rep 1996;45(RR-11):1-36.
  41. Myers MG, Stanberry LR. Varicella-zoster virus. In: Behrman RE, Kliegman RM, Jenson HB, eds. Nelson Textbook of pediatrics. 16th ed. Philadelphia: Saunders, 2000:973-7.
  42. Wise RP, Salive ME, Braun MM, Mootrey GT, Seward JF, Rider LG, et al. Postlicensure safety surveillance for varicella vaccine. JAMA 2000;284:1271-9.
  43. Whiteley RJ. Varicella-zoster virus. In: Mandell GL, Douglas RG, Bennett JE, Dolin R, eds. Mandell, Douglas, and Bennett's Principles and practice of infectious diseases. 5th ed. Philadelphia: Churchill Livingstone, 2000:1580-6.
  44. Feikin DR, Lezotte DC, Hamman RF, Salmon DA, Chen RT, Hoffman RE. Individual and community risks of measles and pertussis associated with personal exemptions to immunization. JAMA 2000; 284:3145-50.
  45. Edwards KM. State mandates and childhood immunization. JAMA 2000;284:3171-3.
  46. Evans G. Pediatricians must use official Vaccine Information Statements. AAP News April 2000;16:14.

 

 

 

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