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Persons using assistive technology might not be able to fully access information in this file. For assistance, please send e-mail to: mmwrq@cdc.gov. Type 508 Accommodation and the title of the report in the subject line of e-mail. Notice to Readers Recall of Tripedia(TM) VaccineOn January 27, 1999, the Food and Drug Administration initiated a voluntary recall of Tripedia(TM) diphtheria and tetanus toxoids and acellular pertussis vaccine (DTaP), lot number 0916490, manufactured by Pasteur Merieux Connaught USA. * Routine post-release stability testing completed in January 1999 indicated that the potency of the diphtheria toxoid component of this lot was below specification. The potency of the tetanus and pertussis components of this lot was acceptable. The lot was distributed during February-June 1998. All lots of Tripedia(TM) met potency specifications before release. Previously tested lots of Tripedia(TM) met diphtheria potency specifications in routine stability testing after release; stability testing of additional lots is in progress. A primary series (three doses) of fully potent diphtheria toxoid-containing vaccine is required to reliably induce protective antibody levels. Five doses of diphtheria toxoid-containing vaccine are recommended for preschool-aged children in the United States and provide optimal protection against diphtheria. The risk for exposure to toxigenic strains of Corynebacterium diphtheriae in the United States is low; however, diphtheria remains endemic in many countries. Additional doses of diphtheria toxoid-containing vaccine beyond those recommended in the childhood immunization schedule are associated with an increase in local reactions and should be considered only for children vaccinated with Tripedia(TM) lot number 0916490 who may be at increased risk for exposure to toxigenic strains of C. diphtheriae. CDC, the American Academy of Pediatrics, and the American Academy of Family Physicians have developed recommendations for children who received one or more doses of Tripedia(TM) lot number 0916490. The complete text of the recommendations is available on CDC's National Immunization Program World-Wide Web site, http://www.cdc.gov/nip/news/recall.htm; in summary, the recommendations are as follows:
* Use of trade names and commercial sources is for identification only and does not imply endorsement by CDC or the U.S. Department of Health and Human Services. ** Travelers may be at substantial risk for exposure to toxigenic strains of C. diphtheriae, especially with prolonged travel, extensive contact with children, or exposure to poor hygiene. Countries comprise the following: Africa -- Algeria, Egypt, and sub-Saharan Africa; Americas -- Brazil, Dominican Republic, Ecuador, and Haiti; Asia/Oceania -- Afghanistan, Bangladesh, Cambodia, China, India, Indonesia, Iran, Iraq, Laos, Mongolia, Myanmar, Nepal, Pakistan, Philippines, Syria, Thailand, Turkey, Vietnam, and Yemen; and Europe -- Albania and all countries of the former Soviet Union. Table_1 Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size.
TABLE 1. Recommendations for children who travel to areas where the risk for
diphtheria is high* and who received Tripedia(TM) diphtheria and tetanus toxoids and
acellular pertussis vaccine (DTaP) lot number 0916490+
=======================================================================================================
Total doses received
of any diphtheria No. doses of
toxoid-containing Tripedia(TM) from lot
Age (mos) vaccine no. 0916490 Recommendation&
-----------------------------------------------------------------------------------------------
2-11 1-2 1-2 Complete primary series with DTaP@
3 1 Administer fourth dose of DTaP at
age 15-18 mos
3 2-3 Administer supplemental dose of DT,
followed by fourth dose of DTaP at
age 15-18 mos
-----------------------------------------------------------------------------------------------
>=12 3 1 Administer fourth dose of DTaP at
age 15-18 mos
3 2-3 Administer supplemental dose of DT
if <6 months have elapsed since
third dose of DTaP, followed by
fourth dose of DTaP at age
15-18 mos
OR
Administer fourth dose of DTaP as
early as age 12 mos if >=6 months
have elapsed since third dose of
DTaP
4 1-3 Administer fifth dose of DTaP at age
4 to 6 yrs
5 1 Administer routine tetanus and
diphtheria toxoids (for adolescent
and adult use) boosters
-----------------------------------------------------------------------------------------------
* Travelers may be at substantial risk for exposure to toxigenic strains of Corynebacterium
diphtheriae, especially with prolonged travel, extensive contact with children, or exposure to
poor hygiene conditions. Countries comprise the following: Africa--Algeria, Egypt, and sub-Saharan
Africa; Americas--Brazil, Dominican Republic, Ecuador, and Haiti; Asia/Oceania--
Afghanistan, Bangladesh, Cambodia, China, India, Indonesia, Iran, Iraq, Laos, Mongolia,
Myanmar, Nepal, Pakistan, Philippines, Syria, Thailand, Turkey, Vietnam, and Yemen; and
Europe--Albania and all countries of the former Soviet Union.
+ Manufactured by Pasteur Mórieux Connaught USA. Use of trade names and commercial
sources is for identification only and does not imply endorsement by CDC or the U.S. Depart-
ment of Health and Human Services.
& The minimum interval is 4 weeks between a dose of diphtheria and tetanus toxoids (for
pediatric use) (DT) and any other dose of diphtheria toxoid-containing vaccine. The minimum
interval is 6 months between the third dose of DTaP (including doses of Tripedia(TM) lot number
0916490) and the fourth dose of DTaP.
@ If time is sufficient before travel, children who received two doses of Tripedia(TM) lot number
0916490 should receive their third dose of DTaP (as early as 4 weeks after the previous dose
of DTaP) and a supplemental dose of DT (as early as 4 weeks after the third dose of DTaP).
=======================================================================================================
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