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  5. Gefitinib (marketed as Iressa) Information
  1. Postmarket Drug Safety Information for Patients and Providers

Gefitinib (marketed as Iressa) Information


Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax, using the contact information at the bottom of this page.

Related Information

Regulatory History and Labeling from Drugs@FDA