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Levonorgestrel reports
Browse community reports connected to Levonorgestrel. These reports can show that other people are describing similar experiences, but they do not prove that Levonorgestrel 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.
31 problems
Abdominal Discomfort while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and abdominal discomfort appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Distension while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and abdominal distension appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Lower while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and abdominal pain lower appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and abdominal pain upper appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and abdominal pain appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Acne while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and acne appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Alopecia while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and alopecia appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and anxiety appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and back pain appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and diarrhea appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and dizziness appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and fatigue appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and feeling abnormal appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and headache appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and insomnia appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Irritability while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and irritability appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and itching appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Libido Decreased while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and libido decreased appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and malaise appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and migraine appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and muscle spasms appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and nausea appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and pain appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and palpitations appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and rash appear together. This does not establish that Levonorgestrel 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 Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and tingling or pins and needles appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Vertigo while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and vertigo appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and vision blurred appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and vomiting appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and weakness appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Levonorgestrel
FDA FAERS contains adverse-event reports in which Levonorgestrel and weight increased appear together. This does not establish that Levonorgestrel caused the reported reaction and cannot be used to estimate how often it occurs.
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