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