HappeningToo topic
Rituximab reports
Browse community reports connected to Rituximab. These reports can show that other people are describing similar experiences, but they do not prove that Rituximab 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.
24 problems
Abdominal Discomfort while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and abdominal discomfort appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Pain Upper while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and abdominal pain upper appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Pain while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and abdominal pain appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Alopecia while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and alopecia appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Cough while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and cough appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Decreased Appetite while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and decreased appetite appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Diarrhea while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and diarrhea appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dizziness while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and dizziness appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Fatigue while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and fatigue appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Headache while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and headache appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Hives while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and hives appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Hypotension while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and hypotension appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Insomnia while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and insomnia appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Itching while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and itching appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Malaise while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and malaise appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Nausea while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and nausea appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Pain while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and pain appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Rash while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and rash appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Shortness of breath while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and shortness of breath appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Swelling while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and swelling appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Vomiting while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and vomiting appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weakness while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and weakness appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weight Decreased while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and weight decreased appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weight Increased while using Rituximab
FDA FAERS contains adverse-event reports in which Rituximab and weight increased appear together. This does not establish that Rituximab caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →