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Haldol Janssen Side Effects

Common Haldol Janssen Side Effects


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If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

Haldol Janssen Side Effects Reported to FDA

The following Haldol Janssen reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.


The appearance of Haldol Janssen on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.
Menorrhagia, Intraocular Pressure Increased
on Sep 28, 2011 Female from GERMANY , 50 years of age, was treated with Haldol Janssen Decanoat. Directly after, patient experienced the unwanted or unexpected Haldol Janssen side effects: menorrhagia, intraocular pressure increased. Haldol Janssen Decanoat dosage: N/A.

Alcohol Poisoning, Suicide Attempt
Patient was taking Haldol Janssen Forte. Patient felt the following Haldol Janssen side effects: alcohol poisoning, suicide attempt on Nov 09, 2010 from GERMANY Additional patient health information: Male , weighting 132.3 lb, was diagnosed with and. Haldol Janssen Forte dosage: N/A.
Multiple prescriptions taken:
  • Alcohol


Coma, Miosis
Adverse event was reported on Jul 25, 2010 by a Male taking Haldol Janssen Tropfen (Dosage: N/A) . Location: GERMANY , weighting 154.3 lb, After Haldol Janssen was administered, patient encountered several Haldol Janssen side effects: coma, miosis.
Multiple concurrent drugs taken:
  • Risperdal
  • Eunerpan


Keep Track of Side Effects

Note Your Observations

It is really important to keep of your symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:

     

    Side Effects

    Scale

    Date & Time

    Other Medicine(s) or Treatment(s)

     

     

     

     

    Scale: 1 = very mild to 10 = very bad


    Track Online

  • User Sign In
  • Register to track your side effects

  • You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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    Safety Alerts, Active Ingredients, Usage Information

    More About Haldol janssen

    Side Effects reported to FDA: 3

    Haldol Janssen safety alerts: No

    Latest Haldol Janssen clinical trials

    Haldol Janssen Reviews

    No reviews, be a first to report a side effect via side effect reporting form