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