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Pronunciation: A fa me LAN oh tide

Brand: Scenesse

What is the most important information I should know about afamelanotide?

Afamelanotide may cause skin darkening, especially in moles or freckles. Tell your doctor about any new moles or skin lesions.

What is afamelanotide?

Afamelanotide is used in adults with erythropoietic protoporphyria (EPP). EPP is a condition that can cause severe pain or other skin reactions to sunlight or artificial light.

Afamelanotide is used to help increase the amount of pain-free time you can spend in sunlight or artificial light.

Afamelanotide may also be used for purposes not listed in this medication guide.

What should I discuss with my healthcare provider before receiving afamelanotide?

Tell your doctor if you are pregnant or breastfeeding.

Afamelanotide is not approved for use by anyone younger than 18 years old.

How is afamelanotide given?

Afamelanotide is given in a tiny implant inserted under the skin above the front of your hip. You will receive the implant in a clinic or doctor's office once every 2 months.

The implant is inserted using a special tool that pushes the implant into place under your skin. After injecting the implant, your doctor will feel the area to make sure your implant has been correctly placed.

Your skin where the implant was placed will be covered with a bandage. Leave the bandage on for 24 hours.

You may be able to feel the implant through your skin, but it should not cause pain or discomfort. The implant will dissolve in your body over time.

Call your doctor if you think it has come out of place.

Afamelanotide may cause your skin to become darker, especially any moles or freckles you have. New moles or skin lesions may appear over time. Ask your doctor about skin symptoms to watch for.

Your will need a full-body skin examination every 6 months.

What happens if I miss a dose?

Call your doctor for instructions if you miss a 2-month appointment to receive your next implant.

What happens if I overdose?

Since the afamelanotide implant contains a specific amount of the medicine, you are not likely to receive an overdose.

What should I avoid while receiving afamelanotide?

Avoid sunlight or tanning beds. Always wear protective clothing when you are outdoors and use any sunscreen your doctor recommends.

What are the possible side effects of afamelanotide?

Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have:

  • severe pain, swelling, or bleeding where the implant was placed;
  • new or worsening skin lesions;
  • a mole that has changed in size or color; or
  • if the implant sticks out of your skin or comes out by itself.

Common side effects may include:

  • pain, itching, redness, swelling, bruising, or other irritation where the implant was placed;
  • skin changes such as discoloration, scarring, or a hard lump where the implant was placed;
  • skin irritation anywhere on your body;
  • new moles or hair growth on the skin;
  • cough, pain in your mouth or throat;
  • dizziness, drowsiness, tiredness;
  • nausea; or
  • cold symptoms such as stuffy nose, sneezing, sore throat.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect afamelanotide?

Other drugs may affect afamelanotide, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell your doctor about all your current medicines and any medicine you start or stop using.

Where can I get more information?

Your doctor can provide more information about afamelanotide.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.

Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2022 Cerner Multum, Inc. Version: 1.01. Revision date: 1/21/2021.

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