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Indication

Qutenza® is indicated for the management of neuropathic pain associated with postherpetic neuralgia.

About Qutenza® (capsaicin) 8% patch

Qutenza® contains capsaicin in a local dermal delivery system. The capsaicin in Qutenza® is a synthetic equivalent of the naturally occurring compound found in chili peppers.

Important Safety Information

Qutenza® is administered by a physician or a health professional under the close supervision of a physician. Qutenza® may be administered every 3 months or as warranted by the return of pain, but not more frequently than every 3 months. In clinical trials, the most common adverse reactions were application site redness, pain, itching, and papules. The majority of these reactions were transient and self limited. Among patients treated with Qutenza®, 1% discontinued prematurely due to an adverse event. Serious adverse reactions included application-site pain and increased blood pressure. Blood pressure increases during or shortly after Qutenza® treatment were on average less than 10 mm Hg, although some patients had greater increases and these changes lasted for approximately 2 hours after patch removal.

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