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Ixekizumab reports
Browse community reports connected to Ixekizumab. These reports can show that other people are describing similar experiences, but they do not prove that Ixekizumab 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.
29 problems
Abdominal Discomfort while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and abdominal discomfort appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and abdominal pain upper appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and abdominal pain appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and alopecia appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and anxiety appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and back pain appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and cough appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and diarrhea appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and dizziness appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and fatigue appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and feeling abnormal appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and headache appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and hives appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Influenza Like Illness while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and influenza like illness appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and insomnia appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and itching appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and malaise appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and myalgia appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and nausea appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Oropharyngeal Pain while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and oropharyngeal pain appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and pain appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and rash appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and shortness of breath appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and skin redness appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and swelling appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and vomiting appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and weakness appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and weight decreased appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Ixekizumab
FDA FAERS contains adverse-event reports in which Ixekizumab and weight increased appear together. This does not establish that Ixekizumab caused the reported reaction and cannot be used to estimate how often it occurs.
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