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Aflibercept reports
Browse community reports connected to Aflibercept. These reports can show that other people are describing similar experiences, but they do not prove that Aflibercept 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.
18 problems
Abdominal Pain while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and abdominal pain appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and decreased appetite appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and diarrhea appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and dizziness appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Eye while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and dry eye appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Eye Irritation while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and eye irritation appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Eye Pain while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and eye pain appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and fatigue appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and headache appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and malaise appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and nausea appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and pain appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and shortness of breath appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and vision blurred appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and vomiting appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Watery eyes while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and watery eyes appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and weakness appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Aflibercept
FDA FAERS contains adverse-event reports in which Aflibercept and weight decreased appear together. This does not establish that Aflibercept caused the reported reaction and cannot be used to estimate how often it occurs.
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