HappeningToo topic
Mirtazapine reports
Browse community reports connected to Mirtazapine. These reports can show that other people are describing similar experiences, but they do not prove that Mirtazapine 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.
42 problems
Abdominal Discomfort while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and abdominal discomfort appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Pain Upper while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and abdominal pain upper appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Abdominal Pain while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and abdominal pain appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Anxiety while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and anxiety appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Back Pain while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and back pain appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Chills while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and chills appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Constipation while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and constipation appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Cough while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and cough appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Decreased Appetite while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and decreased appetite appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dehydration while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and dehydration appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Diarrhea while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and diarrhea appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dizziness while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and dizziness appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Dry Mouth while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and dry mouth appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Excessive sweating while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and excessive sweating appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Fatigue while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and fatigue appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Feeling Abnormal while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and feeling abnormal appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Headache while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and headache appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Heart Rate Increased while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and heart rate increased appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Hypotension while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and hypotension appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Insomnia while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and insomnia appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Itching while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and itching appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Malaise while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and malaise appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Muscle Spasms while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and muscle spasms appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Muscular Weakness while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and muscular weakness appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Myalgia while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and myalgia appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Nausea while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and nausea appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Pain while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and pain appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Palpitations while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and palpitations appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Peripheral swelling while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and peripheral swelling appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Rash while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and rash appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Restlessness while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and restlessness appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Shortness of breath while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and shortness of breath appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Sleep Disorder while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and sleep disorder appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Sleepiness while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and sleepiness appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Tachycardia while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and tachycardia appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Tingling or pins and needles while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and tingling or pins and needles appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Tremor while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and tremor appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Vision Blurred while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and vision blurred appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Vomiting while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and vomiting appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weakness while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and weakness appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weight Decreased while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and weight decreased appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →
Weight Increased while using Mirtazapine
FDA FAERS contains adverse-event reports in which Mirtazapine and weight increased appear together. This does not establish that Mirtazapine caused the reported reaction and cannot be used to estimate how often it occurs.
View reports →