HappeningToo topic
Ribociclib reports
Browse community reports connected to Ribociclib. These reports can show that other people are describing similar experiences, but they do not prove that Ribociclib 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.
33 problems
Abdominal Discomfort while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and abdominal discomfort appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Pain Upper while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and abdominal pain upper appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Pain while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and abdominal pain appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Alopecia while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and alopecia appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Anxiety while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and anxiety appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Back Pain while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and back pain appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Chills while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and chills appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Constipation while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and constipation appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Cough while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and cough appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Decreased Appetite while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and decreased appetite appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dehydration while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and dehydration appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Diarrhea while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and diarrhea appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dizziness while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and dizziness appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dry Skin while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and dry skin appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dyspepsia while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and dyspepsia appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Fatigue while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and fatigue appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Feeling Abnormal while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and feeling abnormal appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Headache while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and headache appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Hot Flush while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and hot flush appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Insomnia while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and insomnia appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Itching while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and itching appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Malaise while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and malaise appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Nausea while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and nausea appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Pain while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and pain appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Peripheral swelling while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and peripheral swelling appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Rash while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and rash appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Shortness of breath while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and shortness of breath appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Skin redness while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and skin redness appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Sleepiness while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and sleepiness appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Vomiting while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and vomiting appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weakness while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and weakness appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weight Decreased while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and weight decreased appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weight Increased while using Ribociclib
FDA FAERS contains adverse-event reports in which Ribociclib and weight increased appear together. This does not establish that Ribociclib caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →