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