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