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Remeron Related Gait disturbance

Official Government Database Reports185
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Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients. To view the active ingredient report, please click here.


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Druginformer Identified Side Effects: Lethargy, Dysarthria, Confusional state, Depression, Gait disturbance, Muscular weakness, Somnolence

Posted By Anonymous in askapatient.com on June 27, 2011 @ 12:00 am

Side Effects: Extreme tiredness, extreme weakness (mostly in legs), slurred speech, more depressed, lethargic, confusion, hard time making decisions, slowed down and doped up (not in a good way).

Druginformer Identified Side Effects: Fatigue, Gait disturbance

Posted By lowcoal in fdb.rxlist.com on March 31, 2009 @ 12:00 am

... when he was admitted to a rehab center. i can see it given to someone who is terminal but not someone in rehab. he is not upset about being away from home anymore, but he is exhausted and cannot walk ...

Druginformer Identified Side Effects: Fatigue, Gait disturbance

Posted By lowcoal in fdb.rxlist.com on March 31, 2009 @ 12:00 am

... when he was admitted to a rehab center. i can see it given to someone who is terminal but not someone in rehab. he is not upset about being away from home anymore, but he is exhausted and cannot walk ...

Druginformer Identified Side Effects: Dizziness, Nausea, Abnormal dreams, Gait disturbance

Posted By Anonymous in askapatient.com on August 13, 2004 @ 12:00 am

Side Effects: After 5 days taking one 30 Mg tab at night, I became so dizzy that I could hardly walk. Had to stay at home for 2 days to recover. Felt nauseous. BAD dreams. Shouldn't be lega...


* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.