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Adapalene reports
Browse community reports connected to Adapalene. These reports can show that other people are describing similar experiences, but they do not prove that Adapalene caused a symptom or reaction.
⚕️ Medicine safety note
Community reports do not prove causation, cannot be used to estimate how common a reaction is, and are not medical advice.
25 problems
Acne while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and acne appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and anxiety appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Application Site Dryness while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and application site dryness appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Burning Sensation while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and burning sensation appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Dermatitis while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and dermatitis appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and dizziness appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Eye while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and dry eye appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Skin while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and dry skin appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Eye Irritation while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and eye irritation appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Eye Pain while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and eye pain appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Hot while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and feeling hot appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and headache appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and hives appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and itching appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and nausea appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and pain appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash Erythematous while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and rash erythematous appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash Macular while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and rash macular appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash Papular while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and rash papular appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and rash appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and shortness of breath appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and skin redness appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and swelling appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Tingling or pins and needles while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and tingling or pins and needles appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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Watery eyes while using Adapalene
FDA FAERS contains adverse-event reports in which Adapalene and watery eyes appear together. This does not establish that Adapalene caused the reported reaction and cannot be used to estimate how often it occurs.
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