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