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