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Gemtuzumab Ozogamicin

Popular Brands: : Mylotarg, Gemtuzumab Ozogamicin, Gemtuzumab, Gemtuzumab-ozogamicin
Official FDA Reports12,236
Social Media Events0
Total Posts13
Avg. Review Score0.00/ 5
Active Ingredients
  • Gemtuzumab Ozogamicin
Approved Uses *
  • No other uses available

* Extracted from Drug Label

Manufacturers
  • Wyeth Pharmaceuticals Inc

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

* Extracted from FDA Adverse Event Report

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.


Gemtuzumab Ozogamicin 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.


User Voices

The following are comments from users that experienced side effects while taking Gemtuzumab Ozogamicin

We do not have any user comments on this drug. Please try again with another drug.


Tell us about your Experience with Gemtuzumab Ozogamicin

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Share Your Experience

Druginformer Identified Side Effects: None

Posted By problemOfHeart in facebook.com on March 28, 2015 @ 12:00 am

March 27 at 6:49pm · Background Video Gallery Projects Top Pro & Con Quotes Comments Studies Related to Our Core Question "Should Prescription Drugs Be Advertised Directly to Consumers?" DTC Pre...

Druginformer Identified Side Effects: None

Posted By kysoguxu in twitter.com on July 31, 2014 @ 12:00 am

Pfizer's 10-year-old leukemia drug Mylotarg increases the chance of the patient dying by 47%.

Druginformer Identified Side Effects: None

Posted By mnewtonPharmD in twitter.com on July 31, 2014 @ 12:00 am

More support for the return of Mylotarg? leukemia

Druginformer Identified Side Effects: None

Posted By mmansur92 in twitter.com on July 31, 2014 @ 12:00 am

Pfizer's 10-year-old leukemia drug Mylotarg increases the chance of the patient dying by 47%.

Druginformer Identified Side Effects: None

Posted By bepuqijujev in twitter.com on July 31, 2014 @ 12:00 am

Pfizer's 10-year-old leukemia drug Mylotarg increases the chance of the patient dying by 47%.

Druginformer Identified Side Effects: None

Posted By buhifogucow in twitter.com on July 31, 2014 @ 12:00 am

Pfizer's 10-year-old leukemia drug Mylotarg increases the chance of the patient dying by 47%.

Druginformer Identified Side Effects: None

Posted By watogulukeda in twitter.com on July 31, 2014 @ 12:00 am

Pfizer's 10-year-old leukemia drug Mylotarg increases the chance of the patient dying by 47%.

Druginformer Identified Side Effects: None

Posted By duduxosaxor in twitter.com on July 31, 2014 @ 12:00 am

Pfizer's 10-year-old leukemia drug Mylotarg increases the chance of the patient dying by 47%.

Druginformer Identified Side Effects: None

Posted By owusugag in twitter.com on July 31, 2014 @ 12:00 am

Pfizer's 10-year-old leukemia drug Mylotarg increases the chance of the patient dying by 47%.

Druginformer Identified Side Effects: None

Posted By ArabNewsRt11 in twitter.com on July 31, 2014 @ 12:00 am

Pfizer's 10-year-old leukemia drug Mylotarg increases the chance of the patient dying by 47%.


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.