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