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Arcalion Side Effects

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Common Arcalion Side Effects


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

Dermatitis Bullous (3)
Injury (2)
Loss Of Consciousness (2)
Fall (2)
Rash Erythematous (2)
Pruritus (2)
Lupus-like Syndrome (2)
C-reactive Protein Increased (1)
Antinuclear Antibody Positive (1)
Blood Uric Acid Increased (1)
Anti-ss-a Antibody Positive (1)
Conjunctivitis (1)
Stevens-johnson Syndrome (1)
Proteinuria (1)
Sjogren's Syndrome (1)
Renal Failure Acute (1)
Erythema Multiforme (1)
Epidermolysis (1)
Dehydration (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.

Arcalion Side Effects Reported to FDA


Arcalion Side Effect Report#5336784-8
Anti-ss-a Antibody Positive, Antinuclear Antibody Positive, Blood Uric Acid Increased, C-reactive Protein Increased, Conjunctivitis, Dehydration, Dermatitis Bullous, Epidermolysis, Erythema Multiforme
This is a report of a 79-year-old female patient (weight: NA) from France, suffering from the following health symptoms/conditions: depressive symptom, who was treated with Arcalion (dosage: Unk, Unk, start time:
Jun 15, 2006), combined with:
  • Primperan Inj
  • Triflucan
  • Desloratadine (1 Df, Qd)
  • Esidrix (Unk, Unk)
and developed a serious reaction and side effect(s): Anti-ss-a Antibody Positive, Antinuclear Antibody Positive, Blood Uric Acid Increased, C-reactive Protein Increased, Conjunctivitis, Dehydration, Dermatitis Bullous, Epidermolysis, Erythema Multiforme after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Arcalion treatment in female patients, resulting in Anti-ss-a Antibody Positive side effect. The patient was hospitalized.
Arcalion Side Effect Report#5293079-9
Dermatitis Bullous, Fall, Injury, Loss Of Consciousness, Lupus-like Syndrome, Proteinuria, Pruritus, Rash Erythematous, Renal Failure Acute
This report suggests a potential Arcalion Dermatitis Bullous side effect(s) that can have serious consequences. A 79-year-old female patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Arcalion (dosage: Unk, Unk) starting
May 01, 2006. After starting Arcalion the patient began experiencing various side effects, including: Dermatitis Bullous, Fall, Injury, Loss Of Consciousness, Lupus-like Syndrome, Proteinuria, Pruritus, Rash Erythematous, Renal Failure AcuteAdditional drugs used concurrently:
  • Primperan Inj
  • Triflucan
  • Desloratadine
  • Esidrix
The patient was hospitalized. Although Arcalion demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Dermatitis Bullous, may still occur.
Arcalion Side Effect Report#5259647-5
Dermatitis Bullous, Fall, Injury, Loss Of Consciousness, Lupus-like Syndrome, Pruritus, Rash Erythematous, Sjogren's Syndrome, Stevens-johnson Syndrome
This Dermatitis Bullous problem was reported by a consumer or non-health professional from France. A 79-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
May 01, 2006 this consumer started treatment with Arcalion (dosage: Unk, Unk). The following drugs were being taken at the same time:
  • Primperan Inj
  • Triflucan
  • Desloratadine
  • Esidrix
When using Arcalion, the patient experienced the following unwanted symptoms/side effects: Dermatitis Bullous, Fall, Injury, Loss Of Consciousness, Lupus-like Syndrome, Pruritus, Rash Erythematous, Sjogren's Syndrome, Stevens-johnson SyndromeThe 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 Dermatitis Bullous, may become evident only after a product is in use by the general population.



The appearance of Arcalion 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 Arcalion Side Effects for Men?

Men 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.

    Arcalion 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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