DrugInformer Search

Chlorpheniramine Maleate Related Nausea

Official FDA Reports164
Social Media Events3
Active Ingredients
  • Chlorpheniramine Maleate
Additional Terms for Nausea
  • Nauseated
  • Nausa
  • Nausia
  • Naseau
  • Nausaus
Show more

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Chlorpheniramine Maleate.


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

Chlorpheniramine Maleate

It took years to find the right combination of medications for me. Without it, I am a leaky faucet, with morning nausea and vomiting, constant runny nose, sore throat. They keep recalling this. I coul...


Source:" comments/chlorpheniramine-methscopolam...

View full report on drug related nausea

Did the author experience nausea while taking chlorpheniramine maleate?

What is this?

Chlorpheniramine Maleate

Holy pain I have been suffering from serious back pain for over a week... It's hard to explain but it is not my spine I've gone to the chiropractor and that did nothing... The pain is middle to...


Source:" Back Pain Forum

View full report on drug related nausea

Did the author experience nausea while taking chlorpheniramine maleate?

What is this?

Chlorpheniramine Maleate

... the same as the name brands. Under the laws of the U.S. FDA, they are allowed to differ, in the active ingredients, by as much as plus or minus 20%. Since the dizziness, nausea and light headed f...


Source:" Hydrocodone-Chlorpheniram Susp

View full report on drug related nausea

Did the author experience nausea while taking chlorpheniramine maleate?

What is this?

Tell us about your Experience with Chlorpheniramine Maleate Related Nausea

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Nausea, Rhinorrhoea, Oropharyngeal pain

Posted By Anonymous in drugs.com on May 6, 2010 @ 12:00 am

It took years to find the right combination of medications for me. Without it, I am a leaky faucet, with morning nausea and vomiting, constant runny nose, sore throat. They keep recalling this. I coul...

Druginformer Identified Side Effects: Nausea

Posted By Jamielm in ehealthforum.com on June 2, 2012 @ 12:00 am

Holy pain I have been suffering from serious back pain for over a week... It's hard to explain but it is not my spine I've gone to the chiropractor and that did nothing... The pain is middle to...

Druginformer Identified Side Effects: Nausea, Euphoric mood

Posted By Verwon in prescriptiondrug-info.com on April 21, 2011 @ 12:00 am

... the same as the name brands. Under the laws of the U.S. FDA, they are allowed to differ, in the active ingredients, by as much as plus or minus 20%. Since the dizziness, nausea and light headed f...



* 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.