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