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