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