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.

Haldol Janssen Side Effects Reported to FDA

Haldol Janssen Side Effect Report#7802245-7
Menorrhagia, Intraocular Pressure Increased
This is a report of a 50-year-old female patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: NA, who was treated with Haldol Janssen Decanoat (dosage: NA, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Menorrhagia, Intraocular Pressure Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Haldol Janssen Decanoat treatment in female patients, resulting in Menorrhagia side effect.
Haldol Janssen Side Effect Report#7110584-0
Alcohol Poisoning, Suicide Attempt
This report suggests a potential Haldol Janssen Forte Alcohol Poisoning side effect(s) that can have serious consequences. A male patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: ill-defined disorder and used Haldol Janssen Forte (dosage: NA) starting
Nov 09, 2010. After starting Haldol Janssen Forte the patient began experiencing various side effects, including: Alcohol Poisoning, Suicide AttemptAdditional drugs used concurrently:
  • Alcohol
Although Haldol Janssen Forte demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Alcohol Poisoning, may still occur.
Haldol Janssen Side Effect Report#6894132-6
Coma, Miosis
This Coma problem was reported by a physician from Germany. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Haldol Janssen Tropfen (dosage: NA). The following drugs were being taken at the same time:
  • Risperdal
  • Eunerpan
When using Haldol Janssen Tropfen, the patient experienced the following unwanted symptoms/side effects: Coma, MiosisAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Coma, may become evident only after a product is in use by the general population.

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.

What are common Haldol Janssen Side Effects for Women?

Women Side EffectsReports
Intraocular Pressure Increased 1
Menorrhagia 1

What are common Haldol Janssen Side Effects for Men?

Men Side EffectsReports
Alcohol Poisoning 1
Coma 1
Miosis 1
Suicide Attempt 1

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health 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

    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.

    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.

    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.

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    Haldol Janssen Safety Alerts, Active Ingredients, Usage Information

    More About Haldol janssen

    Side Effects reported to FDA: 3

    Haldol Janssen safety alerts: No

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