Onabotulinumtoxina reports

Abdominal Pain Upper while using Onabotulinumtoxina

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

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Alopecia while using Onabotulinumtoxina

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

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Anxiety while using Onabotulinumtoxina

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

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Back Pain while using Onabotulinumtoxina

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

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Burning Sensation while using Onabotulinumtoxina

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

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Constipation while using Onabotulinumtoxina

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

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Cough while using Onabotulinumtoxina

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

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Diarrhea while using Onabotulinumtoxina

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

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Dizziness while using Onabotulinumtoxina

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

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Dry Eye while using Onabotulinumtoxina

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

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Dry Mouth while using Onabotulinumtoxina

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

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Excessive sweating while using Onabotulinumtoxina

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

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Eye Pain while using Onabotulinumtoxina

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

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Fatigue while using Onabotulinumtoxina

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

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Feeling Abnormal while using Onabotulinumtoxina

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

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Headache while using Onabotulinumtoxina

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

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Hives while using Onabotulinumtoxina

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

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Influenza Like Illness while using Onabotulinumtoxina

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

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Insomnia while using Onabotulinumtoxina

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

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Itching while using Onabotulinumtoxina

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

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Malaise while using Onabotulinumtoxina

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

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Migraine while using Onabotulinumtoxina

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

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Muscle Spasms while using Onabotulinumtoxina

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

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Muscular Weakness while using Onabotulinumtoxina

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

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Myalgia while using Onabotulinumtoxina

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

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Nausea while using Onabotulinumtoxina

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

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Neck Pain while using Onabotulinumtoxina

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

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Pain while using Onabotulinumtoxina

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

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Palpitations while using Onabotulinumtoxina

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

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Rash while using Onabotulinumtoxina

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

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Shortness of breath while using Onabotulinumtoxina

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

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Skin redness while using Onabotulinumtoxina

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

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Sleepiness while using Onabotulinumtoxina

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

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Swelling while using Onabotulinumtoxina

FDA FAERS contains adverse-event reports in which Onabotulinumtoxina and swelling appear together. This does not establish that Onabotulinumtoxina 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 Onabotulinumtoxina

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

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Tremor while using Onabotulinumtoxina

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

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Vertigo while using Onabotulinumtoxina

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

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Vision Blurred while using Onabotulinumtoxina

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

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Vomiting while using Onabotulinumtoxina

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

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Weakness while using Onabotulinumtoxina

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

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Weight Decreased while using Onabotulinumtoxina

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

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