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Haloperidol Decanoate

Popular Brands: : Haloperidol Decanoate, Haldol Decanoate
Official FDA Reports2,827
Social Media Events0
Total Posts0
Avg. Review Score0.00/ 5
Active Ingredients
  • Haloperidol Decanoate
Approved Uses *

* Extracted from Drug Label

Brands and Other Names
  • Fresenius Kabi Usa Llc
  • Janssen 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 Haloperidol Decanoate.

* Extracted from FDA Adverse Event Report


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.

Haloperidol Decanoate Side Effects

  Social Media
(Online Comments)
(Reports Submitted to FDA)
Side Effect On Drug
Reports % of
Alarm Reports % of

* 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 Haloperidol Decanoate

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Druginformer Identified Side Effects: Anger, Violence-related symptom, Tremor, Vomiting, Akathisia, Dry throat, Restlessness, Memory impairment, Speech disorder, Disturbance in attention, Injection site erythema, Weight abnormal, Appetite disorder, Thought withdrawal, Thought blocking, Somnolence, Abnormal sleep-related event, Insomnia

Effectiveness Rating:     Overall Rating:

Posted By Ryan on March 13, 2017 @ 12:20 am

Drugs should not be mixed currently on 300 Haloperidol Decanoate and 40 Latuda this month the Latuda will be history but the anger and everything else remains.

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.