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