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Fluticasone Propionate and Salmeterol reports
Browse community reports connected to Fluticasone Propionate and Salmeterol. These reports can show that other people are describing similar experiences, but they do not prove that Fluticasone Propionate and Salmeterol 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 Pain while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and abdominal pain appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Acid reflux while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and acid reflux appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and anxiety appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and back pain appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Chest Discomfort while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and chest discomfort appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and constipation appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and cough appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and decreased appetite appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and diarrhea appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and dizziness appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Dry Mouth while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and dry mouth appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and fatigue appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and feeling abnormal appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and headache appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and heart rate increased appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and insomnia appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and itching appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and malaise appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and muscle spasms appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and nausea appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Oropharyngeal Pain while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and oropharyngeal pain appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and pain appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and palpitations appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and rash appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and shortness of breath appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and tremor appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and vision blurred appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and vomiting appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and weakness appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and weight decreased appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Fluticasone Propionate and Salmeterol
FDA FAERS contains adverse-event reports in which Fluticasone Propionate and Salmeterol and weight increased appear together. This does not establish that Fluticasone Propionate and Salmeterol caused the reported reaction and cannot be used to estimate how often it occurs.
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