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Dextromethorphan Hydrobromide; Guaifenesin Related Dizziness

Official FDA Reports165
Social Media Events4
Active Ingredients
  • Dextromethorphan Hydrobromide; Guaifenesin
Additional Drug Brands and Names
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Additional Terms for Dizziness
  • Dizzyness
  • Lightheadedness
  • Light-headed
  • Light Headedness
  • Dizzy Spells
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  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Mucinex Dm.


Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (AERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


List of Possible Side Effects Reported

Report Date Dosage Indication Outcome Country Gender Age Weight (lbs)

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


Social Media Comments From Around the Web

The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride

Mucinex Dm

Side Effects: dizziness , foggy thinking, tiredness

I accidentally got the 1200 mg by mistake (maximum strength) and couldn't drive or leave the house, I was so dizzy and out of it. I don't...


Source:" viewrating.asp

View full report on drug related dizziness

Did the author experience dizziness while taking mucinex dm?

What is this?

Dextromethorphan Hydrobromide; Guaifenesin

i took this mediciene and i was so dizzy and my pulse rate went up that i had to be rushed to the e.r. i would rather deal with the cough than go through that again


Source:" Wal-Tussin DM Oral : User Ratings cove...

View full report on drug related dizziness

Did the author experience dizziness while taking dextromethorphan hydrobromide; guaifenesin?

What is this?

Dextromethorphan Hydrobromide; Guaifenesin

... put people in trouble. POTENTIAL SIDE-EFFECTS + Can cause ulcers and bleeding in the stomach. + Can cause acidity, nausea, vomiting, diarrhoea, constipation, dizziness , rashes, and headaches. + ...


Source:" Onyival/posts/775341389185195

View full report on drug related dizziness

Did the author experience dizziness while taking dextromethorphan hydrobromide; guaifenesin?

What is this?

Tell us about your Experience with Dextromethorphan Hydrobromide; Guaifenesin Related Dizziness

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Share Your Experience

Druginformer Identified Side Effects: Fatigue, Dizziness, Lethargy, Disturbance in attention, Somnolence

Posted By Anonymous in askapatient.com on November 8, 2011 @ 12:00 am

Side Effects: dizziness, foggy thinking, tiredness I accidentally got the 1200 mg by mistake (maximum strength) and couldn't drive or leave the house, I was so dizzy and out of it. I don't...

Druginformer Identified Side Effects: Dizziness

Posted By lucylou in fdb.rxlist.com on July 1, 2009 @ 12:00 am

i took this mediciene and i was so dizzy and my pulse rate went up that i had to be rushed to the e.r. i would rather deal with the cough than go through that agai

Druginformer Identified Side Effects: Dizziness, Vision blurred

Posted By Onyival?fref=nf in facebook.com on July 3, 2014 @ 12:00 am

... put people in trouble. POTENTIAL SIDE-EFFECTS + Can cause ulcers and bleeding in the stomach. + Can cause acidity, nausea, vomiting, diarrhoea, constipation, dizziness, rashes, and headaches. + ...

Druginformer Identified Side Effects: Abdominal pain, Dizziness

Posted By punjabi.purje?ref=nf in facebook.com on November 23, 2012 @ 12:00 am

... Effects are very disturbing for everyone. Dizzy and dull. mind floats to the negative side,body hurts too. pain in legs. pain in stomache ,SleepingDisorder,constipation,people get insane,Overdose ...



* 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.