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Pomalidomide reports
Browse community reports connected to Pomalidomide. These reports can show that other people are describing similar experiences, but they do not prove that Pomalidomide 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.
34 problems
Abdominal Discomfort while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and abdominal discomfort appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and abdominal pain upper appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and alopecia appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and back pain appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and constipation appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and cough appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and decreased appetite appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and dehydration appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and diarrhea appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and dizziness appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and fatigue appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and feeling abnormal appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and headache appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and hypotension appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and insomnia appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and itching appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and malaise appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and muscle spasms appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and muscular weakness appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and nausea appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and pain appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and peripheral swelling appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and rash appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and shortness of breath appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and skin redness appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and sleepiness appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and swelling appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Tingling or pins and needles while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and tingling or pins and needles appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and tremor appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and vision blurred appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and vomiting appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and weakness appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and weight decreased appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Pomalidomide
FDA FAERS contains adverse-event reports in which Pomalidomide and weight increased appear together. This does not establish that Pomalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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