Levulan Prescription Drug Pharmaceutical Information

This page provides details of the prescription pharmacy drug Levulan. For further information please click one of the links below:

Pharmacy Drug Brand Name: Levulan® Kerastick
Active Ingredient(s): aminolevulinic acid HCl
Strength(s) / Dose(s): 20%
Delivery / Dosage Form(s): Topical Solution
Company Manufacturer Name: Guidelines, Incorporated
Availability / Prescription: Prescription only
FDA Approval Date *: December 3, 1999

* Approval by the FDA does not necessarily mean that this drug is available for consumers at this time.

What is Levulan used for?

The Levulan Kerastick for Topical Solution plus blue light illumination using BLU-U Blue Light Photodynamic Therapy Illuminator is a two-step (drug plus blue light) treatment used to treat pre-cancerous skin lesions of the face or scalp called actinic keratoses (AK).

Who should not be treated with Levulan?

You should not be treated with Levulan if you have:

General Precautions with Levulan:

The treated lesions are sensitive to light therefore, people being treated will need to avoid sunlight and sources of bright light for at least 40 hours after Levulan is applied.

What should I tell my doctor or health care (healthcare) provider?

There are other medications that increase sensitivity to light. Tell your doctor or health care (healthcare) provider if you are using any other medicines. These medicines include:

What are some possible side effects of Levulan? (This is not a comprehensive list of possible side effects assosciated with Levulan. Your doctor or pharmacist can provide expert advice on the possible side effects of this drug.)

Blue light treatment may cause tingling, stinging, prickling, or burning feeling of the treated areas. These feelings should improve at the end of the blue light treatment and should end within 24 hours.

Following blue light treatment, the AKs and, to some degree, the surrounding skin, will redden. Swelling may also occur. These changes should reach a maximum the day after BLU-U treatment. However, these changes are temporary, should improve markedly by the end of the first week, and should be completely gone by 4 weeks after treatment. Other side effects at the treatment sites may include:

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