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