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On October 20, 2005, the Food and Drug Administration (FDA) along with the Centers for Disease Control and Prevention (CDC) updated a previous alert which announced that they are investigating the possibility of a link between Menactra Meningococcal Vaccine and Guillain Barre Syndrome (GBS). The investigation has found 15 confirmed cases of GBS in patients who had received the Menactra Meningococcal Vaccine manufactured by Sanofi Pasteur.
The 15 cases reported to the FDA that could possibly link GBS to the meningitis vaccine occurred in individuals who were between the ages of 11-19. Two additional cases were confirmed in adults over the age of 20.
These individuals developed symptoms within six weeks of receiving Menactra vaccine. All have recovered or are in the process of recovery.
These cases suggest a small increase risk of GBS following immunization with Menactra. However, officials cannot say with certainty that the reports of GBS were caused by the vaccine. Currently, there are no changes in recommendations for vaccination.
Because many vaccine adverse effects are not reported, the FDA suspects that there may be additional cases.
Note - Do not change medications without first consulting your doctor.
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