DrugInformer Search

Dextromethorphan Hydrobromide; Guaifenesin

Official FDA Reports4,351
Social Media Events22
Total Posts334
Avg. Review Score2.74/ 5
Active Ingredients
  • Dextromethorphan Hydrobromide; Guaifenesin
Approved Uses *

* Extracted from Drug Label

Brands and Other Names
  • Mucinex Dm
  • Cough Syrup
  • Tussin Dm
  • Guiatuss Dm
  • Robitussin Cough And Chest Congestion Dm
Show more brands
Manufacturers
  • A-s Medication Solutions Llc
  • Aaron Industries, Inc.
  • Access Business Group Llc
  • Accudial Pharmaceutical, Inc.
  • Advanced Generic Corporation
Show more manufacturers

  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.

* Extracted from FDA Adverse Event Report

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.


The proportion of people completing user reviews who complained about a side effect.

The proportion of social media adverse event complaints for each adverse event type.

The proportion of FAERS (FDA) adverse event complaints for each adverse event type.


Dextromethorphan Hydrobromide; Guaifenesin Side Effects

  Social Media
(Online Comments)
FAERS
(Reports Submitted to FDA)
Side Effect On Drug
Label
Overall
Alarm
Reports % of
Reports
Alarm Reports % of
Reports
Alarm

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


User Voices

The following are comments from users that experienced side effects while taking Dextromethorphan Hydrobromide; Guaifenesin

Fatigue

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...


View Original Source

View full report on Dextromethorphan Hydrobromide; Guaifenesin related fatigue

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

What is this?

Lethargy

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...


View Original Source

View full report on Dextromethorphan Hydrobromide; Guaifenesin related lethargy

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

What is this?

Dizziness

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...


View Original Source

View full report on Dextromethorphan Hydrobromide; Guaifenesin related dizziness

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

What is this?

Additional Drug Information


* 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.