Pralatrexate
Active Ingredients
- Pralatrexate
Brands and Other Names
Manufacturers
- Allos Therapeutics Inc
This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Folotyn.
Explanation
The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (FAERS) 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.
Pralatrexate 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.
Tell us about your Experience with Pralatrexate
Druginformer Identified Side Effects: None
Posted By Neurotic8 in healingwell.com on July 19, 2014 @ 12:00 am
“I've had a long standing history with migraines, and I was taking Sibelium/Flunarizine for a while. Over year and a half ago, I noticed changes in my mood and I concluded that I'd become depressed. I...”
Druginformer Identified Side Effects: None
Posted By FDAnewsPharma in twitter.com on July 19, 2014 @ 12:00 am
“Allos Therapeutics Sues Dr. Reddys Over Proposed Folotyn Generic ”
Druginformer Identified Side Effects: None
Posted By TorreyaInsights in twitter.com on July 19, 2014 @ 12:00 am
“Allos Therapeutics Sues Dr. Reddys Over Proposed Folotyn Generic ”
Druginformer Identified Side Effects: None
Posted By gottarun1000 in twitter.com on July 19, 2014 @ 12:00 am
“Allos Therapeutics Sues Dr. Reddys Over Proposed Folotyn Generic CancerNews ”
Druginformer Identified Side Effects: None
Posted By lostinthewoods in healingwell.com on July 18, 2014 @ 12:00 am
“I think I should add an update. I just read my reply and should add something. I was okay with the topiramate until I wasn't. about a year or so into treatment I started having a strange experience. A...”
Druginformer Identified Side Effects: None
Posted By lockett11 in healingwell.com on July 17, 2014 @ 12:00 am
“I have epilepsy and anxiety, which I have been treating with Tegretol and Zoloft with no problems. However, I also have had migraines for years, and just recently went to a neurologist who suggested ...”
Druginformer Identified Side Effects: None
Posted By TNWoCOM in twitter.com on July 12, 2014 @ 12:00 am
“US Pat 6,028,071,Infringed by Dr. Reddy's Generic Folotyn; Analytics via @sharethis ”
Druginformer Identified Side Effects: None
Posted By AMINNpatent in twitter.com on July 12, 2014 @ 12:00 am
“US Pat 6,028,071,Infringed by Dr. Reddy's Generic Folotyn; Analytics via @sharethis ”
Druginformer Identified Side Effects: None
Posted By patentbuddy in twitter.com on July 12, 2014 @ 12:00 am
“US Pat 6,028,071,Infringed by Dr. Reddy's Generic Folotyn; Analytics via @sharethis ”
Druginformer Identified Side Effects: None
Posted By MidNorl in twitter.com on July 9, 2014 @ 12:00 am
“$SPPI: Spectrum confirms FDA approves Beleodaq, updates on PMRs for Beleodaq, Folotyn ”
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.
User Voices
The following are comments from users that experienced side effects while taking Pralatrexate
We do not have any user comments on this drug. Please try again with another drug.