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Aloperidin Side Effects

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Common Aloperidin Side Effects


The most commonly reported Aloperidin side effects (click to view or check a box to report):

Pyrexia (1)
Tremor (1)
Musculoskeletal Stiffness (1)
Lethargy (1)
Dysphagia (1)
Fatigue (1)
Communication Disorder (1)


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.

Aloperidin Side Effects Reported to FDA


Aloperidin Side Effect Report#6681469-9
Dysphagia, Musculoskeletal Stiffness, Pyrexia
This is a report of a 82-year-old female patient (weight: NA) from Greece, suffering from the following health symptoms/conditions: dementia, who was treated with Aloperidin (dosage: Drops, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Dysphagia, Musculoskeletal Stiffness, Pyrexia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Aloperidin treatment in female patients, resulting in Dysphagia side effect. The patient was hospitalized.
Aloperidin Side Effect Report#5971623-3
Communication Disorder, Fatigue, Lethargy, Tremor
This report suggests a potential Aloperidin Communication Disorder side effect(s) that can have serious consequences. A male patient (weight: NA) from Greece was diagnosed with the following symptoms/conditions: hypermobility syndrome,anxiety and used Aloperidin (dosage: NA) starting NS. After starting Aloperidin the patient began experiencing various side effects, including: Communication Disorder, Fatigue, Lethargy, TremorAdditional drugs used concurrently: NA. Although Aloperidin demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Communication Disorder, may still occur.



The appearance of Aloperidin 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.

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What are common Aloperidin Side Effects for Women?

Women Side EffectsReports
Dysphagia 1
Musculoskeletal Stiffness 1
Pyrexia 1

What are common Aloperidin Side Effects for Men?

Men Side EffectsReports
Communication Disorder 1
Fatigue 1
Lethargy 1
Tremor 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.

    Aloperidin 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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    Aloperidin Safety Alerts, Active Ingredients, Usage Information

    More About Aloperidin

    Side Effects reported to FDA: 2

    Aloperidin safety alerts: No

    Reported hospitalizations: 1

    Latest Aloperidin clinical trials

    Aloperidin Reviews

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