HappeningToo topic
Pirfenidone reports
Browse community reports connected to Pirfenidone. These reports can show that other people are describing similar experiences, but they do not prove that Pirfenidone 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 Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and abdominal discomfort appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and abdominal distension appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and abdominal pain upper appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and abdominal pain appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and acid reflux appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and anxiety appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and back pain appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and chest discomfort appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and constipation appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and cough appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and decreased appetite appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and dehydration appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and diarrhea appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and dizziness appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Skin while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and dry skin appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and dyspepsia appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and fatigue appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and feeling abnormal appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Flatulence while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and flatulence appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and headache appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and heart rate increased appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and hives appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and hypotension appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and insomnia appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and itching appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and malaise appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and myalgia appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and nausea appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Oropharyngeal Pain while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and oropharyngeal pain appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and pain appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and rash appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and shortness of breath appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and skin redness appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and sleepiness appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Taste changes while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and taste changes appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and vomiting appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and weakness appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and weight decreased appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Pirfenidone
FDA FAERS contains adverse-event reports in which Pirfenidone and weight increased appear together. This does not establish that Pirfenidone caused the reported reaction and cannot be used to estimate how often it occurs.
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