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User Voices for Dextromethorphan Hydrobromide; Guaifenesin

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

Somnolence

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

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Did the author experience somnolence while taking mucinex dm?

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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...


Source: viewrating.asp

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Did the author experience fatigue while taking mucinex dm?

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...


Source: viewrating.asp

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Did the author experience dizziness while taking mucinex dm?

What is this?

Disturbance In Attention

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

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Did the author experience disturbance in attention while taking mucinex dm?

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...


Source: viewrating.asp

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Did the author experience lethargy while taking mucinex dm?

What is this?

Drug Ineffective

I took this medication for 4 straight days with absolutely zero results. It did not help relieve congestion and had no effect on my cold and cough.


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

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Did the author experience drug ineffective while taking dextromethorphan hydrobromide; guaifenesin?

What is this?

Cough

I took this medication for 4 straight days with absolutely zero results. It did not help relieve congestion and had no effect on my cold and cough .


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

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

What is this?

Dizziness

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...

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

What is this?

Insomnia

kept me awake , caused breathing problems


Source: Broncotron-D Oral : User Ratings cover...

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

What is this?

Respiration Abnormal

kept me awake, caused breathing problems


Source: Broncotron-D Oral : User Ratings cover...

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Did the author experience respiration abnormal while taking dextromethorphan hydrobromide; guaifenesin?

What is this?

Fear

i ended up in the ER after taking this medication while in Florida on vacation. I was unable to stop vomiting and had a terrible feeling of impending doom come over me several times.....a terrible exp...


Source: Wal-Tussin Cough Oral : User Ratings c...

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

What is this?

Vomiting

i ended up in the ER after taking this medication while in Florida on vacation. I was unable to stop vomiting and had a terrible feeling of impending doom come over me several times.....a terrible exp...


Source: Wal-Tussin Cough Oral : User Ratings c...

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

What is this?

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* 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.