Aurorix Side Effects


Common Aurorix Side Effects

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

Syncope (1)
Heart Rate Increased (1)
Convulsion (1)
Blood Pressure Increased (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.

Aurorix Side Effects Reported to FDA

Aurorix Side Effect Report#8351242-4
This is a report of a 44-year-old male patient (weight: NA) from Denmark, suffering from the following health symptoms/conditions: NA, who was treated with Aurorix (dosage: NA, start time: NS), combined with:
  • Escitalopram
and developed a serious reaction and side effect(s): Syncope after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Aurorix treatment in male patients, resulting in Syncope side effect. The patient was hospitalized.
Aurorix Side Effect Report#8133960-6
Blood Pressure Increased, Heart Rate Increased
This report suggests a potential Aurorix Blood Pressure Increased side effect(s) that can have serious consequences. A 87-year-old male patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: NA and used Aurorix (dosage: NA) starting
Jan 20, 2012. After starting Aurorix the patient began experiencing various side effects, including: Blood Pressure Increased, Heart Rate IncreasedAdditional drugs used concurrently:
  • Delix Plus
  • Metoprolol Succinate
The patient was hospitalized. Although Aurorix demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blood Pressure Increased, may still occur.
Aurorix Side Effect Report#5318012-2
This Convulsion problem was reported by a physician from Russian Federation. A 37-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: depression. On
Apr 01, 2007 this consumer started treatment with Aurorix (dosage: Indication Reported As Depression, Sociophobia.). The following drugs were being taken at the same time: NA. When using Aurorix, the patient experienced the following unwanted symptoms/side effects: ConvulsionAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Convulsion, may become evident only after a product is in use by the general population.

The appearance of Aurorix 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 Aurorix Side Effects for Women?

Women Side EffectsReports
Convulsion 1

What are common Aurorix Side Effects for Men?

Men Side EffectsReports
Blood Pressure Increased 1
Heart Rate Increased 1
Syncope 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.

    Aurorix 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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    Aurorix Safety Alerts, Active Ingredients, Usage Information

    More About Aurorix

    Side Effects reported to FDA: 3

    Aurorix safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 2

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