Clarithromycin reports

Abdominal Discomfort while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and abdominal discomfort appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain Upper while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and abdominal pain upper appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Abdominal Pain while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and abdominal pain appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Anxiety while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and anxiety appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Back Pain while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and back pain appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Chest Discomfort while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and chest discomfort appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Constipation while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and constipation appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Cough while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and cough appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Decreased Appetite while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and decreased appetite appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Dehydration while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and dehydration appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Diarrhea while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and diarrhea appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Dizziness while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and dizziness appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Dyspepsia while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and dyspepsia appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Excessive sweating while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and excessive sweating appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Fatigue while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and fatigue appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Feeling Abnormal while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and feeling abnormal appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Headache while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and headache appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Heart Rate Increased while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and heart rate increased appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Hives while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and hives appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Hypotension while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and hypotension appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Insomnia while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and insomnia appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Itching while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and itching appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Malaise while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and malaise appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscle Spasms while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and muscle spasms appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Muscular Weakness while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and muscular weakness appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Myalgia while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and myalgia appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Nausea while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and nausea appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Pain while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and pain appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Palpitations while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and palpitations appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Peripheral swelling while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and peripheral swelling appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Rash while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and rash appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Shortness of breath while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and shortness of breath appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Skin redness while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and skin redness appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Sleepiness while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and sleepiness appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Tachycardia while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and tachycardia appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Taste changes while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and taste changes appear together. This does not establish that Clarithromycin 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 Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and tingling or pins and needles appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Tinnitus while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and tinnitus appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Tremor while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and tremor appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Vision Blurred while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and vision blurred appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Vomiting while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and vomiting appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Weakness while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and weakness appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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Weight Decreased while using Clarithromycin

FDA FAERS contains adverse-event reports in which Clarithromycin and weight decreased appear together. This does not establish that Clarithromycin caused the reported reaction and cannot be used to estimate how often it occurs.

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