HappeningToo topic
Montelukast reports
Browse community reports connected to Montelukast. These reports can show that other people are describing similar experiences, but they do not prove that Montelukast 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.
42 problems
Abdominal Discomfort while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and abdominal discomfort appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and abdominal pain upper appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and abdominal pain appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and acid reflux appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and alopecia appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and anxiety appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and back pain appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and chest discomfort appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and constipation appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and cough appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and decreased appetite appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and diarrhea appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and dizziness appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and excessive sweating appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and fatigue appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and feeling abnormal appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and headache appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and heart rate increased appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and hives appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and hypotension appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and insomnia appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and itching appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and malaise appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and migraine appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and muscle spasms appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and myalgia appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and nausea appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Oropharyngeal Pain while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and oropharyngeal pain appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and pain appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and peripheral swelling appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and rash appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and shortness of breath appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and skin redness appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and sleep disorder appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and sleepiness appear together. This does not establish that Montelukast 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 Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and tingling or pins and needles appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and tremor appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and vision blurred appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and vomiting appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and weakness appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and weight decreased appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Montelukast
FDA FAERS contains adverse-event reports in which Montelukast and weight increased appear together. This does not establish that Montelukast caused the reported reaction and cannot be used to estimate how often it occurs.
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