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Lenvatinib reports
Browse community reports connected to Lenvatinib. These reports can show that other people are describing similar experiences, but they do not prove that Lenvatinib 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.
32 problems
Abdominal Discomfort while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and abdominal discomfort appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and abdominal distension appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and abdominal pain upper appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and abdominal pain appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and back pain appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and constipation appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and cough appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and decreased appetite appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and dehydration appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and diarrhea appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and dizziness appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and dry mouth appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Skin while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and dry skin appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and fatigue appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and headache appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and hypotension appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and insomnia appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and itching appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and malaise appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and muscle spasms appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and muscular weakness appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and myalgia appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and nausea appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Oropharyngeal Pain while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and oropharyngeal pain appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and pain appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and peripheral swelling appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and rash appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and shortness of breath appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and sleepiness appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and vomiting appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and weakness appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Lenvatinib
FDA FAERS contains adverse-event reports in which Lenvatinib and weight decreased appear together. This does not establish that Lenvatinib caused the reported reaction and cannot be used to estimate how often it occurs.
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