The FDA asks health care professionals and patients to report side effects from the use of Xolair to the FDA's MedWatch Adverse Effects Reporting program.

On Oct. 9, 1997, Gov. Pete Wilson signed into law a bill that gave state education officials five weeks to choose and adopt a statewide achievement test, called the Standardized Testing and Reporting program.

Report serious adverse reactions or product quality problems to FDA's MedWatch Adverse Event Reporting program at http://www.fda.gov/Safety/MedWatch/default.htm.

Consumers and health care professionals should report adverse events to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax:

Consumers should report serious adverse events (side effects) with the device to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail, fax, or phone.

Health care professionals and consumers should report serious adverse events (side effects) or product quality problems to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail, fax or phone.

Adverse reactions or quality issues can also be reported to the FDA's MedWatch Adverse Event Reporting program.

Report any side effects with Xenical or Alli to FDA's MedWatch Adverse Event Reporting program either online, by regular mail, by fax, or by phone.

Health care professionals and patients may report serious side effects online to the FDA's MedWatch Adverse Event Reporting program, by regular mail, phone, or fax.

Consumers or health care professionals may report any side effects or product quality problems with Toviaz to the FDA's MedWatch Adverse Event Reporting program.