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