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Ritonavir reports
Browse community reports connected to Ritonavir. These reports can show that other people are describing similar experiences, but they do not prove that 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.
23 problems
Abdominal Pain while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and abdominal pain appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and anxiety appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and back pain appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and cough appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and decreased appetite appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Dehydration while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and dehydration appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and diarrhea appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and dizziness appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and fatigue appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and headache appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and hypotension appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and insomnia appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and itching appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and malaise appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Myalgia while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and myalgia appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and nausea appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and pain appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and rash appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and shortness of breath appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and vomiting appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and weakness appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and weight decreased appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Ritonavir
FDA FAERS contains adverse-event reports in which Ritonavir and weight increased appear together. This does not establish that Ritonavir caused the reported reaction and cannot be used to estimate how often it occurs.
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