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Metformin Hydrochloride reports
Browse community reports connected to Metformin Hydrochloride. These reports can show that other people are describing similar experiences, but they do not prove that Metformin 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.
39 problems
Abdominal Discomfort while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and abdominal discomfort appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and abdominal distension appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and abdominal pain upper appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and abdominal pain appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and acid reflux appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and alopecia appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and anxiety appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and back pain appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and constipation appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and cough appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and decreased appetite appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and dehydration appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and diarrhea appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and dizziness appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dyspepsia while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and dyspepsia appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and excessive sweating appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and fatigue appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and feeling abnormal appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and headache appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Hives while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and hives appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and hypotension appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and insomnia appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and itching appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and malaise appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and muscle spasms appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscular Weakness while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and muscular weakness appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and myalgia appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and nausea appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and pain appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Peripheral swelling while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and peripheral swelling appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and rash appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and shortness of breath appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Skin redness while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and skin redness appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and sleepiness appear together. This does not establish that Metformin 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 Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and tingling or pins and needles appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and vomiting appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and weakness appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and weight decreased appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Metformin Hydrochloride
FDA FAERS contains adverse-event reports in which Metformin Hydrochloride and weight increased appear together. This does not establish that Metformin Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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