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Apremilast reports
Browse community reports connected to Apremilast. These reports can show that other people are describing similar experiences, but they do not prove that Apremilast 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.
28 problems
Abdominal Discomfort while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and abdominal discomfort appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and abdominal pain upper appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and abdominal pain appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and alopecia appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and anxiety appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and decreased appetite appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and diarrhea appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and dizziness appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and dry mouth appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and dyspepsia appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and fatigue appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and headache appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and hives appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and insomnia appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and itching appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and malaise appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and migraine appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and muscle spasms appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and nausea appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and pain appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and rash appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and shortness of breath appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and sleep disorder appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and swelling appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and vomiting appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and weakness appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and weight decreased appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Apremilast
FDA FAERS contains adverse-event reports in which Apremilast and weight increased appear together. This does not establish that Apremilast caused the reported reaction and cannot be used to estimate how often it occurs.
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