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Aripiprazole Oral reports
Browse community reports connected to Aripiprazole Oral. These reports can show that other people are describing similar experiences, but they do not prove that Aripiprazole Oral 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.
24 problems
Anxiety while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and anxiety appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and constipation appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and diarrhea appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and dizziness appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and excessive sweating appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and fatigue appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and feeling abnormal appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and headache appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Hypotension while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and hypotension appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and insomnia appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Irritability while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and irritability appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and malaise appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and nausea appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and pain appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and rash appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Restlessness while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and restlessness appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and shortness of breath appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and sleepiness appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Tachycardia while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and tachycardia appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and tremor appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and vomiting appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and weakness appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and weight decreased appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Aripiprazole Oral
FDA FAERS contains adverse-event reports in which Aripiprazole Oral and weight increased appear together. This does not establish that Aripiprazole Oral caused the reported reaction and cannot be used to estimate how often it occurs.
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