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Prezolon Side Effects

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.

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.

Prezolon Side Effects Reported to FDA

The following 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.


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.
Abortion
on Jan 26, 2011 Female from GREECE , 31 years of age, was diagnosed with and was treated with Prezolon. Directly after, patient experienced the unwanted or unexpected Prezolon side effects: abortion. Prezolon dosage: N/A.

Hepatitis B
Patient was taking Prezolon. Patient felt the following Prezolon side effects: hepatitis b on Mar 04, 2011 from GREECE Additional patient health information: Female , 72 years of age, . Prezolon dosage: Corticosteroids.
Multiple prescriptions taken:
  • Arava
  • Orencia
Patient was hospitalized.

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
Adverse event was reported on Feb 08, 2008 by a Female taking Prezolon (Dosage: N/A) . Location: GREECE , child 7 years of age, After Prezolon was administered, patient encountered several Prezolon 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 infection.
Multiple concurrent drugs taken:
  • Methylprednisolone
  • Kineret (1-2.5 Mg/kg/d)
  • Corticosteroids
  • Methotrexate
  • Cyclophosphamide
  • Enbrel
  • Azathioprine
  • Sandimmune (Unk, Unk)


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
on Oct 09, 2007 Female from GREECE , child 7 years of age, was treated with Prezolon. Directly after, patient experienced the unwanted or unexpected Prezolon 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 infection. Prezolon dosage: N/A.
Associated medications used:
  • Methylprednisolone
  • Kineret
  • Corticosteroids
  • Methotrexate
  • Cyclophosphamide
  • Enbrel
  • Azathioprine
  • Sandimmune



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
on Oct 09, 2007 Female from GREECE , child 7 years of age, was treated with Prezolon. Patient felt the following Prezolon 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 infection. Prezolon dosage: N/A.
Multiple prescriptions taken:
  • Methylprednisolone
  • Kineret
  • Corticosteroids
  • Methotrexate
  • Cyclophosphamide
  • Enbrel
  • Azathioprine
  • Sandimmune


Histiocytosis Haematophagic, Immunosuppression, Parvovirus Infection
Patient was taking Prezolon. After Prezolon was administered, patient encountered several Prezolon side effects: histiocytosis haematophagic, immunosuppression, parvovirus infection on Jul 12, 2007 from GREECE Additional patient health information: Female , child 7 years of age, . Prezolon dosage: N/A.
Multiple concurrent drugs taken:
  • Methylprednisolone
  • Kineret
  • Corticosteroids
  • Methotrexate
  • Cyclophosphamide
  • Etanercept
  • Azathioprine
  • Sandimmune


Keep Track of Side Effects

Note Your Observations

It is really important to keep of your 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


    Track Online

  • User Sign In
  • Register to track your side effects

  • 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.

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    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

    Latest Prezolon clinical trials

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