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