DrugInformer Search

Anaprox Related Vomiting

Official Government Database Reports19
Online Conversations3
Share

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


Tell us about your Experience with Anaprox

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Headache, Vomiting, Drug ineffective, Muscle spasms

Posted By Anonymous in askapatient.com on November 16, 2007 @ 12:00 am

Side Effects: The absolute worse Drug I've taken. Didnt work, bad Headache and Vomiting for 2 hours on 500mg. I should have never listen to the Urgent Care Doctor. Tanks for nothing. This D...

Druginformer Identified Side Effects: Vomiting, Nerve injury

Posted By Anonymous in drugratingz.com on February 24, 2007 @ 12:00 am

THe name of this drug makes me want to cry. My rheumotologist said this was safe for me to take, but it led to nerve damage in my stomach and a life long long term illness of vomiting, and a very limi...

Druginformer Identified Side Effects: Vomiting, Muscle spasms

Posted By Anonymous in drugratingz.com on November 30, 2005 @ 12:00 am

Dr. said this drug was safe, but it should not be prescribed from people over 60. I spent nights from hell with cramping and vomiting.


* 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.