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Pegfilgrastim reports

Browse community reports connected to Pegfilgrastim. These reports can show that other people are describing similar experiences, but they do not prove that Pegfilgrastim 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.

30 problems

Abdominal Pain Upper while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and abdominal pain upper appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and abdominal pain appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Alopecia while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and alopecia appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and anxiety appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Application Site Discomfort while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and application site discomfort appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Application Site Pain while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and application site pain appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and back pain appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and constipation appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and cough appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and decreased appetite appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Dehydration while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and dehydration appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and diarrhea appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and dizziness appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Excessive sweating while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and excessive sweating appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and fatigue appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Feeling Abnormal while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and feeling abnormal appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and headache appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Hypotension while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and hypotension appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Insomnia while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and insomnia appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and malaise appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Myalgia while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and myalgia appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and nausea appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and pain appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and rash appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and shortness of breath appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Skin redness while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and skin redness appear together. This does not establish that Pegfilgrastim 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 Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and tingling or pins and needles appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and vomiting appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and weakness appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Pegfilgrastim

FDA FAERS contains adverse-event reports in which Pegfilgrastim and weight decreased appear together. This does not establish that Pegfilgrastim caused the reported reaction and cannot be used to estimate how often it occurs.

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