Brexin Side Effects


Common Brexin Side Effects

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

Porphyrins Urine Increased (1)
Stevens-johnson Syndrome (1)
Swelling Face (1)
Laryngeal Oedema (1)
Haemochromatosis (1)
Blister (1)
Blood Iron Increased (1)
Cytolytic Hepatitis (1)
Arthralgia (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.

Brexin Side Effects Reported to FDA

Brexin Side Effect Report#7271481-3
Arthralgia, Cytolytic Hepatitis
This is a report of a 50-year-old male patient (weight: NA) from France, suffering from the following health symptoms/conditions: NA, who was treated with Brexin /00500404/ (dosage: Unk, start time:
Jan 01, 2008), combined with:
  • Arava (Unk)
  • Enbrel (50 Mg, Weekly)
  • Di-antalvic /00016701/ (Unk)
  • Nexium (Unk)
  • Brexin /00500404/ (Unk)
and developed a serious reaction and side effect(s): Arthralgia, Cytolytic Hepatitis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Brexin /00500404/ treatment in male patients, resulting in Arthralgia side effect.
Brexin Side Effect Report#5179364-X
Blister, Blood Iron Increased, Haemochromatosis, Porphyrins Urine Increased
This report suggests a potential Brexin Blister side effect(s) that can have serious consequences. A 59-year-old male patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Brexin (dosage: Unk) starting
Jun 01, 2006. After starting Brexin the patient began experiencing various side effects, including: Blister, Blood Iron Increased, Haemochromatosis, Porphyrins Urine IncreasedAdditional drugs used concurrently:
  • Piascledine (Unk)
  • Hysaar (Unk)
  • Levothyroxine Sodium (Unk)
  • Plavix
The patient was hospitalized. Although Brexin demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blister, may still occur.
Brexin Side Effect Report#4713046-0
Laryngeal Oedema, Stevens-johnson Syndrome, Swelling Face
This Laryngeal Oedema problem was reported by a health professional from . A 36-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: inflammation,erysipelas. On
Mar 25, 2005 this consumer started treatment with Brexin (piroxicam Betadex) (dosage: 20 Mg (1 In 1 D), Oral). The following drugs were being taken at the same time:
  • Clindamycin Hydrochloride (1800 Mg (daily), Oral)
  • Acetaminophen
When using Brexin (piroxicam Betadex), the patient experienced the following unwanted symptoms/side effects: Laryngeal Oedema, Stevens-johnson Syndrome, Swelling FaceAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Laryngeal Oedema, may become evident only after a product is in use by the general population.

The appearance of Brexin 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 Brexin Side Effects for Women?

Women Side EffectsReports

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.

    Brexin 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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