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