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