(410 ILCS 235/8)
(from Ch. 111 1/2, par. 7508)
(a) If, within 30 days of administering a pertussis vaccine,
the health care provider has reason to believe that the recipient of the
vaccine has had a major adverse reaction, the health care provider shall
record all relevant information in the child's permanent medical record and
report the information, including the manufacturer and the lot number, to the Department.
(b) Upon receipt of the information, the Department shall immediately
notify the manufacturer of the vaccine and the Center for Disease Control
of the adverse reaction.
(Source: P.A. 85-898.)