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Befizal Side Effects

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Common Befizal Side Effects


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

Ischaemic Stroke (1)
Hemiplegia (1)
Neutropenia (1)
Respiratory Disorder (1)
Deep Vein Thrombosis (1)
Vomiting (1)
Asthenia (1)
Anaemia (1)
Diarrhoea (1)
Dehydration (1)
Dyspepsia (1)
Facial Palsy (1)
Abdominal Pain (1)
Weight Decreased (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.

Befizal Side Effects Reported to FDA


Befizal Side Effect Report#7236053-5
Deep Vein Thrombosis
This is a report of a female patient (weight: NA) from , suffering from the following health symptoms/conditions: NA, who was treated with Befizal (dosage: 200 Mg, start time:
Dec 16, 2010), combined with:
  • Pradaxa (150 Mg)
  • Naropin (2 Mg/ml: 4ml/hour)
  • Acupan (60 Mg)
  • Enalapril Maleate (20 Mg)
  • Imovane
  • Doliprane (4000 Mg)
and developed a serious reaction and side effect(s): Deep Vein Thrombosis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Befizal treatment in female patients, resulting in Deep Vein Thrombosis side effect. The patient was hospitalized.
Befizal Side Effect Report#7213019-2
Diarrhoea, Neutropenia, Dehydration, Abdominal Pain, Asthenia, Dyspepsia, Vomiting, Respiratory Disorder, Weight Decreased
This report suggests a potential Befizal Diarrhoea side effect(s) that can have serious consequences. A female patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Befizal (dosage: 400mg Per Day) starting
Jun 02, 2009. After starting Befizal the patient began experiencing various side effects, including: Diarrhoea, Neutropenia, Dehydration, Abdominal Pain, Asthenia, Dyspepsia, Vomiting, Respiratory Disorder, Weight DecreasedAdditional drugs used concurrently:
  • Dafalgan (4g Per Day)
  • Aerius (5mg Per Day)
  • Thalidomide (200mg Per Day)
The patient was hospitalized. Although Befizal demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Diarrhoea, may still occur.
Befizal Side Effect Report#5689082-7
Anaemia, Facial Palsy, Hemiplegia, Ischaemic Stroke
This Anaemia problem was reported by a physician from France. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: blood cholesterol,arteritis. On
Jan 17, 2008 this consumer started treatment with Befizal (dosage: 1 Unk). The following drugs were being taken at the same time:
  • Buflomedil (3 Unk)
  • Plavix
When using Befizal, the patient experienced the following unwanted symptoms/side effects: Anaemia, Facial Palsy, Hemiplegia, Ischaemic StrokeThe 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 Anaemia, may become evident only after a product is in use by the general population.



The appearance of Befizal 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 Befizal Side Effects for Women?

Women Side EffectsReports
Abdominal Pain 1
Asthenia 1
Deep Vein Thrombosis 1
Dehydration 1
Diarrhoea 1
Dyspepsia 1
Neutropenia 1
Respiratory Disorder 1
Vomiting 1
Weight Decreased 1

What are common Befizal Side Effects for Men?

Men Side EffectsReports
Anaemia 1
Facial Palsy 1
Hemiplegia 1
Ischaemic Stroke 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.

    Befizal 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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    Discuss Befizal Side Effects

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    Befizal Safety Alerts, Active Ingredients, Usage Information

    More About Befizal

    Side Effects reported to FDA: 3

    Befizal safety alerts: No

    Reported deaths: 1

    Reported hospitalizations: 3

    Latest Befizal clinical trials

    Befizal Reviews

    No reviews, be a first to report a side effect via side effect reporting form