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Oxaliplatin Related Blood Count

Official FDA Reports0
Social Media Events1
Active Ingredients
  • Oxaliplatin
Additional Drug Brands and Names
Additional Terms for Blood Count
  • No additional name found

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


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

Oxaliplatin

... the lesion completely healed and mum had a substantial reduction in the tumour size and progression rate. The problem with the treatment is the severe side effects mainly reduced white blood count ....


Source:" Oxaliplatin User Reviews for Colorecta...

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Druginformer Identified Side Effects: Leukopenia, Blood count

Posted By omaralim in drugs.com on July 21, 2008 @ 12:00 am

... the lesion completely healed and mum had a substantial reduction in the tumour size and progression rate. The problem with the treatment is the severe side effects mainly reduced white blood count....



* 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.