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Methylphenidate Hydrochloride reports
Browse community reports connected to Methylphenidate Hydrochloride. These reports can show that other people are describing similar experiences, but they do not prove that Methylphenidate Hydrochloride 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.
36 problems
Abdominal Discomfort while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and abdominal discomfort appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain Upper while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and abdominal pain upper appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Abdominal Pain while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and abdominal pain appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Anxiety while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and anxiety appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Back Pain while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and back pain appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Constipation while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and constipation appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Cough while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and cough appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Decreased Appetite while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and decreased appetite appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Diarrhea while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and diarrhea appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Dizziness while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and dizziness appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Excessive sweating while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and excessive sweating appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Fatigue while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and fatigue appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Feeling Abnormal while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and feeling abnormal appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Headache while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and headache appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Heart Rate Increased while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and heart rate increased appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Insomnia while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and insomnia appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Irritability while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and irritability appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Itching while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and itching appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Malaise while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and malaise appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Migraine while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and migraine appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Muscle Spasms while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and muscle spasms appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Nausea while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and nausea appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Pain while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and pain appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Palpitations while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and palpitations appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Rash while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and rash appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Shortness of breath while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and shortness of breath appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleep Disorder while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and sleep disorder appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Sleepiness while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and sleepiness appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Tachycardia while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and tachycardia appear together. This does not establish that Methylphenidate Hydrochloride 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 Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and tingling or pins and needles appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Tremor while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and tremor appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Vision Blurred while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and vision blurred appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Vomiting while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and vomiting appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weakness while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and weakness appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Decreased while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and weight decreased appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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Weight Increased while using Methylphenidate Hydrochloride
FDA FAERS contains adverse-event reports in which Methylphenidate Hydrochloride and weight increased appear together. This does not establish that Methylphenidate Hydrochloride caused the reported reaction and cannot be used to estimate how often it occurs.
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