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