Common Prevagen Side Effects

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

Dizziness (2)
Hip Fracture (2)
Fall (2)
Unevaluable Event (1)
Grand Mal Convulsion (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.

Prevagen Side Effects Reported to FDA

Prevagen Side Effect Report#9225222
Grand Mal Convulsion
This is a report of a 70-year-old male patient (weight: NA) from US, suffering from the following health symptoms/conditions: amnesia, who was treated with Prevagen (dosage: NA, start time:
Dec 07, 2012), combined with: NA. and developed a serious reaction and side effect(s): Grand Mal Convulsion after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Prevagen treatment in male patients, resulting in Grand Mal Convulsion side effect.
Prevagen Side Effect Report#6994657-9
Dizziness, Fall, Hip Fracture
This report suggests a potential Prevagen (apoaequorin) 10 Mg, Quincy Bioscience Inc. Dizziness side effect(s) that can have serious consequences. A 80-year-old female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: supportive care and used Prevagen (apoaequorin) 10 Mg, Quincy Bioscience Inc. (dosage: One Capsule, Qd, Oral) starting
May 22, 2010. After starting Prevagen (apoaequorin) 10 Mg, Quincy Bioscience Inc. the patient began experiencing various side effects, including: Dizziness, Fall, Hip FractureAdditional drugs used concurrently: NA.The patient was hospitalized. Although Prevagen (apoaequorin) 10 Mg, Quincy Bioscience Inc. demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Dizziness, may still occur.
Prevagen Side Effect Report#6945012-9
Dizziness, Fall, Hip Fracture, Unevaluable Event
This Dizziness problem was reported by a consumer or non-health professional from United States. A 80-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
May 22, 2010 this consumer started treatment with Prevagen (apoaequorin) 10 Mg, Quincy Bioscience Inc. (dosage: One Capsule, Qd, Oral). The following drugs were being taken at the same time: NA. When using Prevagen (apoaequorin) 10 Mg, Quincy Bioscience Inc., the patient experienced the following unwanted symptoms/side effects: Dizziness, Fall, Hip Fracture, Unevaluable EventThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Dizziness, may become evident only after a product is in use by the general population.

The appearance of Prevagen 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 Prevagen Side Effects for Women?

Women Side Effects Reports
Dizziness 2
Fall 2
Hip Fracture 2
Unevaluable Event 1

What are common Prevagen Side Effects for Men?

Men Side Effects Reports
Grand Mal Convulsion 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.

    Prevagen 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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    More About Prevagen

    Side Effects reported to FDA: 3

    Prevagen safety alerts: No

    Reported hospitalizations: 2

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