HappeningToo topic
Thalidomide reports
Browse community reports connected to Thalidomide. These reports can show that other people are describing similar experiences, but they do not prove that Thalidomide 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.
27 problems
Abdominal Pain while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and abdominal pain appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and anxiety appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and back pain appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and constipation appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and cough appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and decreased appetite appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and dehydration appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and diarrhea appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and dizziness appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and fatigue appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and headache appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and hypotension appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and insomnia appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and malaise appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and muscle spasms appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and nausea appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and pain appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and peripheral swelling appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and rash appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and shortness of breath appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and sleepiness appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Swelling while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and swelling appear together. This does not establish that Thalidomide 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 Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and tingling or pins and needles appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and tremor appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and vomiting appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and weakness appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Thalidomide
FDA FAERS contains adverse-event reports in which Thalidomide and weight decreased appear together. This does not establish that Thalidomide caused the reported reaction and cannot be used to estimate how often it occurs.
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