HappeningToo topic
Bimatoprost reports
Browse community reports connected to Bimatoprost. These reports can show that other people are describing similar experiences, but they do not prove that Bimatoprost 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.
33 problems
Abdominal Discomfort while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and abdominal discomfort appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and alopecia appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and anxiety appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and back pain appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and constipation appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and cough appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and decreased appetite appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and diarrhea appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and dizziness appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Eye while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and dry eye appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Eye Irritation while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and eye irritation appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Eye Pain while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and eye pain appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and fatigue appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and feeling abnormal appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and headache appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and hypotension appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and insomnia appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and itching appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and malaise appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and myalgia appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and nausea appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and pain appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and peripheral swelling appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and rash appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and shortness of breath appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and skin redness appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and sleepiness appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and vision blurred appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and vomiting appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Watery eyes while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and watery eyes appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and weakness appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and weight decreased appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Bimatoprost
FDA FAERS contains adverse-event reports in which Bimatoprost and weight increased appear together. This does not establish that Bimatoprost caused the reported reaction and cannot be used to estimate how often it occurs.
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