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Prezolon Side Effects

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Common Prezolon Side Effects


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

Histiocytosis Haematophagic (4)
Parvovirus Infection (4)
Immunosuppression (4)
Blood Urea Increased (3)
Activated Partial Thromboplastin Time Prolonged (3)
Fibrin D Dimer Increased (3)
Haematocrit Decreased (3)
Haemoglobin Decreased (3)
Parvovirus B19 Serology Positive (3)
Hepatitis B (1)
Abortion (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.

Prezolon Side Effects Reported to FDA



Prezolon Side Effect Report#7342869-7
Abortion
This is a report of a 31-year-old female patient (weight: NA) from Greece, suffering from the following health symptoms/conditions: rheumatoid arthritis, who was treated with Prezolon (dosage: NA, start time:
Jul 01, 2010), combined with: NA. and developed a serious reaction and side effect(s): Abortion after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Prezolon treatment in female patients, resulting in Abortion side effect.
Prezolon Side Effect Report#7342757-6
Hepatitis B
This report suggests a potential Prezolon Hepatitis B side effect(s) that can have serious consequences. A 72-year-old female patient (weight: NA) from Greece was diagnosed with the following symptoms/conditions: NA and used Prezolon (dosage: Corticosteroids) starting
Jan 01, 2009. After starting Prezolon the patient began experiencing various side effects, including: Hepatitis BAdditional drugs used concurrently:
  • Arava
  • Orencia
The patient was hospitalized. Although Prezolon demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hepatitis B, may still occur.
Prezolon Side Effect Report#5624216-1
Activated Partial Thromboplastin Time Prolonged, Blood Urea Increased, Fibrin D Dimer Increased, Haematocrit Decreased, Haemoglobin Decreased, Histiocytosis Haematophagic, Immunosuppression, Parvovirus B19 Serology Positive, Parvovirus Infection
This Activated Partial Thromboplastin Time Prolonged problem was reported by a consumer or non-health professional from Greece. A 7-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
May 02, 2007 this consumer started treatment with Prezolon (dosage: NA). The following drugs were being taken at the same time:
  • Methylprednisolone
  • Kineret (1-2.5 Mg/kg/d)
  • Corticosteroids
  • Methotrexate
  • Cyclophosphamide
  • Enbrel
  • Azathioprine
  • Sandimmune (Unk, Unk)
When using Prezolon, the patient experienced the following unwanted symptoms/side effects: Activated Partial Thromboplastin Time Prolonged, Blood Urea Increased, Fibrin D Dimer Increased, Haematocrit Decreased, Haemoglobin Decreased, Histiocytosis Haematophagic, Immunosuppression, Parvovirus B19 Serology Positive, Parvovirus InfectionAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Activated Partial Thromboplastin Time Prolonged, may become evident only after a product is in use by the general population.
Prezolon Side Effect Report#5485252-1
Activated Partial Thromboplastin Time Prolonged, Blood Urea Increased, Fibrin D Dimer Increased, Haematocrit Decreased, Haemoglobin Decreased, Histiocytosis Haematophagic, Immunosuppression, Parvovirus B19 Serology Positive, Parvovirus Infection
This Activated Partial Thromboplastin Time Prolonged side effect was reported by a consumer or non-health professional from Greece. A 7-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Prezolon (drug dosage: NA), which was initiated on
Apr 14, 2007. Concurrently used drugs:
  • Methylprednisolone
  • Kineret
  • Corticosteroids
  • Methotrexate
  • Cyclophosphamide
  • Enbrel
  • Azathioprine
  • Sandimmune
.After starting to take Prezolon the consumer reported adverse symptoms, such as: Activated Partial Thromboplastin Time Prolonged, Blood Urea Increased, Fibrin D Dimer Increased, Haematocrit Decreased, Haemoglobin Decreased, Histiocytosis Haematophagic, Immunosuppression, Parvovirus B19 Serology Positive, Parvovirus InfectionThese side effects may potentially be related to Prezolon.
Prezolon Side Effect Report#5485173-4
Activated Partial Thromboplastin Time Prolonged, Blood Urea Increased, Fibrin D Dimer Increased, Haematocrit Decreased, Haemoglobin Decreased, Histiocytosis Haematophagic, Immunosuppression, Parvovirus B19 Serology Positive, Parvovirus Infection
This is a report of a 7-year-old female patient (weight: NA) from Greece, suffering from the following health symptoms/conditions: NA, who was treated with Prezolon (dosage: NA, start time:
Apr 14, 2007), combined with:
  • Methylprednisolone
  • Kineret
  • Corticosteroids
  • Methotrexate
  • Cyclophosphamide
  • Enbrel
  • Azathioprine
  • Sandimmune
and developed a serious reaction and side effect(s): Activated Partial Thromboplastin Time Prolonged, Blood Urea Increased, Fibrin D Dimer Increased, Haematocrit Decreased, Haemoglobin Decreased, Histiocytosis Haematophagic, Immunosuppression, Parvovirus B19 Serology Positive, Parvovirus Infection after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Prezolon treatment in female patients, resulting in Activated Partial Thromboplastin Time Prolonged side effect.
Prezolon Side Effect Report#5387329-8
Histiocytosis Haematophagic, Immunosuppression, Parvovirus Infection
This report suggests a potential Prezolon Histiocytosis Haematophagic side effect(s) that can have serious consequences. A 7-year-old female patient (weight: NA) from Greece was diagnosed with the following symptoms/conditions: NA and used Prezolon (dosage: NA) starting
Apr 14, 2007. After starting Prezolon the patient began experiencing various side effects, including: Histiocytosis Haematophagic, Immunosuppression, Parvovirus InfectionAdditional drugs used concurrently:
  • Methylprednisolone
  • Kineret
  • Corticosteroids
  • Methotrexate
  • Cyclophosphamide
  • Etanercept
  • Azathioprine
  • Sandimmune
Although Prezolon demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Histiocytosis Haematophagic, may still occur.



The appearance of Prezolon 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 Prezolon 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.

    Prezolon 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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    Prezolon Safety Alerts, Active Ingredients, Usage Information

    More About Prezolon

    Side Effects reported to FDA: 6

    Prezolon safety alerts: No

    Reported deaths: 4

    Reported hospitalizations: 1

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