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Gained 6kg In 7 Days (3)
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Prezolon Side Effects and Adverse Effects reported to US Food and Drug Administration (FDA)

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Abortion (7342869-7)
on Jan 26, 2011 Female from GREECE , 31 years of age, was diagnosed with
  • rheumatoid arthritis
and was treated with Prezolon. Directly after, patient experienced the unwanted or unexpected Prezolon side effects: abortion. Prezolon dosage: N/A.

Hepatitis B (7342757-6)
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 (5624216-1)
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 (5485252-1)
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 (5485173-4)
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 (5387329-8)
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


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Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.

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 Information

More About Prezolon

Side Effects reported to FDA: 6. View Prezolon Adverse Reports

Prezolon safety alerts: No

Reported deaths: 4

Reported hospitalizations: 1

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