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Methylphenidate reports
Browse community reports connected to Methylphenidate. These reports can show that other people are describing similar experiences, but they do not prove that Methylphenidate 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.
33 problems
Abdominal Pain Upper while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and abdominal pain upper appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and anxiety appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Application Site Irritation while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and application site irritation appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Application Site Pain while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and application site pain appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Application Site Rash while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and application site rash appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Application-site itching while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and application-site itching appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Application-site redness while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and application-site redness appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and constipation appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and decreased appetite appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and diarrhea appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and dizziness appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and excessive sweating appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and fatigue appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and feeling abnormal appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and headache appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and insomnia appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Irritability while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and irritability appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and itching appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and malaise appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and migraine appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and muscle spasms appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and nausea appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and pain appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and palpitations appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and rash appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and shortness of breath appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and sleepiness appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Tachycardia while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and tachycardia appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and tremor appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and vomiting appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and weakness appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and weight decreased appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Methylphenidate
FDA FAERS contains adverse-event reports in which Methylphenidate and weight increased appear together. This does not establish that Methylphenidate caused the reported reaction and cannot be used to estimate how often it occurs.
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