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