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