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Ceftriaxone Sodium reports
Browse community reports connected to Ceftriaxone Sodium. These reports can show that other people are describing similar experiences, but they do not prove that Ceftriaxone Sodium 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.
26 problems
Abdominal Distension while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and abdominal distension appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and abdominal pain appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and chest discomfort appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Chills while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and chills appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and constipation appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and cough appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and decreased appetite appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and diarrhea appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and dizziness appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and fatigue appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and headache appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and hives appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and hypotension appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and itching appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and malaise appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and nausea appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and pain appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and peripheral swelling appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash Maculo-papular while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and rash maculo-papular appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and rash appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and shortness of breath appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and skin redness appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and sleepiness appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Tachycardia while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and tachycardia appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and vomiting appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Ceftriaxone Sodium
FDA FAERS contains adverse-event reports in which Ceftriaxone Sodium and weakness appear together. This does not establish that Ceftriaxone Sodium caused the reported reaction and cannot be used to estimate how often it occurs.
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