This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Alimta.
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.
|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.
Thank you for sharing your experience with us!Share Your Experience
Druginformer Identified Side Effects: Pain, Death, Gastrointestinal disorder, Migraine, Swelling
Posted By Anonymous in fdb.rxlist.com on November 2, 2012 @ 12:00 am
“... and swelling in a knee. I believe it helped but started having frequent and severe migraines, so I discontinued for 3 weeks. Then SUDDENLY I awoke with UNBEARABLE pain in entire body cavity- turned ...”
* 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.
Social Media Comments From Around the Web
The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride
“I took Celebrex for 5 weeks to treat arthritis and swelling in a knee. I believe it helped but started having frequent and severe migraines, so I discontinued for 3 weeks. Then SUDDENLY I awoke with...”
Source:" Celebrex Oral : User Ratings covering ...
View full report on drug related death
Did the author experience death while taking pemetrexed disodium?What is this?