Loratadine Oral reports

Abdominal Discomfort while using Loratadine Oral

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

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Abdominal Distension while using Loratadine Oral

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

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Abdominal Pain Upper while using Loratadine Oral

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

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Abdominal Pain while using Loratadine Oral

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

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Acid reflux while using Loratadine Oral

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

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Alopecia while using Loratadine Oral

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

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Anxiety while using Loratadine Oral

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

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Back Pain while using Loratadine Oral

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

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Chest Discomfort while using Loratadine Oral

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

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Chills while using Loratadine Oral

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

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Constipation while using Loratadine Oral

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

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Cough while using Loratadine Oral

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

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Decreased Appetite while using Loratadine Oral

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

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Dehydration while using Loratadine Oral

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

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Diarrhea while using Loratadine Oral

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

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Dizziness while using Loratadine Oral

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

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Dry Mouth while using Loratadine Oral

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

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Dyspepsia while using Loratadine Oral

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

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Excessive sweating while using Loratadine Oral

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

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Fatigue while using Loratadine Oral

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

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Feeling Abnormal while using Loratadine Oral

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

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Flushing while using Loratadine Oral

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

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Headache while using Loratadine Oral

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

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Heart Rate Increased while using Loratadine Oral

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

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Hives while using Loratadine Oral

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

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Hypotension while using Loratadine Oral

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

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Insomnia while using Loratadine Oral

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

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Itching while using Loratadine Oral

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

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Malaise while using Loratadine Oral

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

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Migraine while using Loratadine Oral

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

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Muscle Spasms while using Loratadine Oral

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

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Myalgia while using Loratadine Oral

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

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Nausea while using Loratadine Oral

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

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Oropharyngeal Pain while using Loratadine Oral

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

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Pain while using Loratadine Oral

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

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Palpitations while using Loratadine Oral

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

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Peripheral swelling while using Loratadine Oral

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

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Rash while using Loratadine Oral

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

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Shortness of breath while using Loratadine Oral

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

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Skin redness while using Loratadine Oral

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

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Sleepiness while using Loratadine Oral

FDA FAERS contains adverse-event reports in which Loratadine Oral and sleepiness appear together. This does not establish that Loratadine Oral 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 Loratadine Oral

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

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Tremor while using Loratadine Oral

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

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Vision Blurred while using Loratadine Oral

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

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Vomiting while using Loratadine Oral

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

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Weakness while using Loratadine Oral

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

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Weight Decreased while using Loratadine Oral

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

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Weight Increased while using Loratadine Oral

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

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