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