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