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FDA Approves Label Update for PREZISTA® to Include 192-Week Data in HIV-1-Infected Adult Patients Starting Treatment
Date:10/21/2011

e of PREZISTA/ritonavir.Please see accompanying full Prescribing Information for more details. Full prescribing information is also available at http://prezista.com/sites/default/files/pdf/us_package_insert.pdf

You are encouraged to report negative side effects of prescription drugs to the FDA.  Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

About Janssen Therapeutics At Janssen, we are dedicated to addressing and solving some of the most important unmet medical needs of our time in HIV and other infectious diseases.  Driven by our commitment to patients, we develop innovative products, services and healthcare solutions to help people throughout the world.  Headquartered in Titusville, New Jersey, Janssen Therapeutics, Division of Janssen Products, LP, is one of the Janssen Pharmaceutical Companies.  Please visit JanssenTherapeutics.com for more information. Media Contact:

Pamela Van HoutenOffice: 609-730-7902Mobile: 908-295-7367Email: pvanhou5@its.jnj.com Investor Contacts:

Louise Mehrotra, 732-524-6491Stan Panasewicz, 732-524-2524
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SOURCE Janssen Therapeutics, Division of Janssen Products, LP
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