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 jeffreybdavis in twitter.com on June 9, 2014 @ 12:00 am
“Folotyn and Affinitor patients suffering with oral mucositis side effect ... see for a treatment alternative. ”
Druginformer Identified Side Effects: None
Posted By ECMC_UK in twitter.com on May 29, 2014 @ 12:00 am
“New trial looking at pralatrexate drug after CHOP chemotherapy for peripheral T cell lymphoma ”
Druginformer Identified Side Effects: None
Posted By Neurotic8 in healingwell.com on May 17, 2014 @ 12:00 am
“I'm supposed to take 25 mgs in the morning and 25 mgs before I go to sleep for my migraines. This has been the plan with my neurologist months ago. Me being me, I read a lot and got discouraged becaus...”
Druginformer Identified Side Effects: None
Posted By GerardNorcia in twitter.com on May 8, 2014 @ 12:00 am
“Allos $ALTH used to say Folotyn was a pipeline unto itself ”
Druginformer Identified Side Effects: None
Posted By DionCapital in twitter.com on May 6, 2014 @ 12:00 am
“ Allos $ALTH used to say Folotyn was a pipeline unto itself ”
Druginformer Identified Side Effects: None
Posted By angel1509 in healingwell.com on April 30, 2014 @ 12:00 am
“Topomax I had severe migraines about 15 or more a month when I first went to see a neurologist he put me on several different meds. Nothing helped, then he put me on Topomax, started me out with 25mg ...”
Druginformer Identified Side Effects: None
Posted By Lymphomation in twitter.com on April 29, 2014 @ 12:00 am
“Comparing Pralatrexate to Observation Following CHOP-based Chemo in Previously Undiagnosed Peripheral T-cell Lymphoma ”
Druginformer Identified Side Effects: None
Posted By Science_Alerts in twitter.com on April 26, 2014 @ 12:00 am
“ ”
Druginformer Identified Side Effects: None
Posted By Catalyst_Fun in twitter.com on April 24, 2014 @ 12:00 am
“$SPPI '13 drug sales: FUSILEV $68.4 million, FOLOTYN $44.4 million, ZEVALIN $29.4 million, MARQIBO $1.3 mill. Current mark… ”
Druginformer Identified Side Effects: None
Posted By Belgadriand in twitter.com on April 24, 2014 @ 12:00 am
“$SPPI '13 drug sales: FUSILEV $68.4 million, FOLOTYN $44.4 million, ZEVALIN $29.4 million, MARQIBO $1.3 mill. Current mark… ”
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.