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The byproduct of the influenza virus, influenza vaccine is a suspension of dead or weakened virus particles in vaccine buffer solution. Influenza viruses used in the manufacturing of vaccines often are grown on chicken eggs. Influenza vaccines are then mixed with one or more types of adjuvants and stabilizers before they are distributed to the public. Influenza vaccines are classified by type and subtype, and they are manufactured in different lot sizes to meet varying demands within the United States and around the world. Some people who receive cell-attenuated influenza vaccine (CAIV) develop side effects called neuromuscular side effects, such as malaise, myalgia, and, in some patients, a temperature of greater than 100.0F (38C) over the first 24 hours of influenza vaccinations. Other side effects include headache, dizziness, sore throat, nausea, and vomiting. Many side effects of influenza vaccines are minor and subside within hours to days. But, it is reported that some fatal and serious side effects have occurred after receiving influenza vaccines. The vaccines have been associated with paralysis (para-flu-zur), Guillain-Barré Syndrome (GBS), and Transverse Myelitis (TM) and have resulted in hospitalization or death. Deaths have been reported in patients with pre-existing immunosuppression, for example, renal failure and diabetes mellitus. Neither the United States Department of Agriculture nor its Forest Service has approved cell-attenuated influenza vaccines for animals, and the widespread use of any active vaccine in animals is highly discouraged. Once a wild strain evolves that differs significantly from the vaccine strains, then the vaccine fails to generate protective immunity against the newly introduced and circulating wild strain of virus. Furthermore, if a wild influenza virus is vaccine-resistant (avirulent), then there is no efficacy of the vaccine to protect against disease. Without immunity, the vaccines cannot be effective against circulating wild strains. d2c66b5586