Prezolon Side Effects
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Did You Have a Prezolon Side Effect? How Effective is Prezolon for You? |
Abortion (7342869-7)
on Jan 26, 2011 Female patient from GREECE , 31 years of age, was diagnosed with
Hepatitis B (7342757-6)
Patient was taking Prezolon (View Usage). Patient had the following side effects: hepatitis b (hepatitis b Questions) on Mar 04, 2011 from GREECE Additional patient health information: Female patient , 72 years of age, . Prezolon dosage: Corticosteroids.
Patient was taking other medications:
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 patient taking Prezolon (View Usage) (Dosage: N/A) . Location: GREECE , child 7 years of age, After Prezolon was administered, patient had the following 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.
Patient was taking other medications:
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 patient from GREECE , child 7 years of age, was treated with Prezolon (View Usage). Patient experienced the following unwanted or unexpected 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.
Patient was taking other medications:
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 patient from GREECE , child 7 years of age, was treated with Prezolon(View Usage). Patient had the following 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.
Patient was taking other medications:
Histiocytosis Haematophagic, Immunosuppression, Parvovirus Infection (5387329-8)
Patient was taking Prezolon (View Usage). After Prezolon was administered, patient had the following side effects: histiocytosis haematophagic, immunosuppression, parvovirus infection on Jul 12, 2007 from GREECE Additional patient health information: Female patient , child 7 years of age, . Prezolon dosage: N/A.
Patient was taking other medications:
on Jan 26, 2011 Female patient from GREECE , 31 years of age, was diagnosed with
- rheumatoid arthritis (rheumatoid arthritis Questions)
Hepatitis B (7342757-6)
Patient was taking Prezolon (View Usage). Patient had the following side effects: hepatitis b (hepatitis b Questions) on Mar 04, 2011 from GREECE Additional patient health information: Female patient , 72 years of age, . Prezolon dosage: Corticosteroids.
Patient was taking other medications:
- ARAVA (View Arava Review and Arava Label )
- ORENCIA (View Orencia Review and Orencia Label )
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 patient taking Prezolon (View Usage) (Dosage: N/A) . Location: GREECE , child 7 years of age, After Prezolon was administered, patient had the following 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.
Patient was taking other medications:
- METHYLPREDNISOLONE (View Methylprednisolone Review and Methylprednisolone Label )
- KINERET (1-2.5 Mg/kg/d) (View Kineret Review and Kineret Label )
- CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label )
- METHOTREXATE (View Methotrexate Review and Methotrexate Label )
- CYCLOPHOSPHAMIDE (View Cyclophosphamide Review and Cyclophosphamide Label )
- ENBREL (View Enbrel Review and Enbrel Label )
- AZATHIOPRINE (View Azathioprine Review and Azathioprine Label )
- SANDIMMUNE (Unk, Unk) (View Sandimmune Review and Sandimmune Label )
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 patient from GREECE , child 7 years of age, was treated with Prezolon (View Usage). Patient experienced the following unwanted or unexpected 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.
Patient was taking other medications:
- METHYLPREDNISOLONE (View Methylprednisolone Review and Methylprednisolone Label )
- KINERET (View Kineret Review and Kineret Label )
- CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label )
- METHOTREXATE (View Methotrexate Review and Methotrexate Label )
- CYCLOPHOSPHAMIDE (View Cyclophosphamide Review and Cyclophosphamide Label )
- ENBREL (View Enbrel Review and Enbrel Label )
- AZATHIOPRINE (View Azathioprine Review and Azathioprine Label )
- SANDIMMUNE (View Sandimmune Review and Sandimmune Label )
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 patient from GREECE , child 7 years of age, was treated with Prezolon(View Usage). Patient had the following 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.
Patient was taking other medications:
- METHYLPREDNISOLONE (View Methylprednisolone Review and Methylprednisolone Label )
- KINERET (View Kineret Review and Kineret Label )
- CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label )
- METHOTREXATE (View Methotrexate Review and Methotrexate Label )
- CYCLOPHOSPHAMIDE (View Cyclophosphamide Review and Cyclophosphamide Label )
- ENBREL (View Enbrel Review and Enbrel Label )
- AZATHIOPRINE (View Azathioprine Review and Azathioprine Label )
- SANDIMMUNE (View Sandimmune Review and Sandimmune Label )
Histiocytosis Haematophagic, Immunosuppression, Parvovirus Infection (5387329-8)
Patient was taking Prezolon (View Usage). After Prezolon was administered, patient had the following side effects: histiocytosis haematophagic, immunosuppression, parvovirus infection on Jul 12, 2007 from GREECE Additional patient health information: Female patient , child 7 years of age, . Prezolon dosage: N/A.
Patient was taking other medications:
- METHYLPREDNISOLONE (View Methylprednisolone Review and Methylprednisolone Label )
- KINERET (View Kineret Review and Kineret Label )
- CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label )
- METHOTREXATE (View Methotrexate Review and Methotrexate Label )
- CYCLOPHOSPHAMIDE (View Cyclophosphamide Review and Cyclophosphamide Label )
- ETANERCEPT (View Etanercept Review and Etanercept Label )
- AZATHIOPRINE (View Azathioprine Review and Azathioprine Label )
- SANDIMMUNE (View Sandimmune Review and Sandimmune Label )
Prezolon Forum
Prezolon Adverse Effect Reports (FDA)
Prezolon InformationSide Effects reported to FDA: 6. View FDA Adverse Reports Prezolon safety alerts: No Reported deaths: 4 Reported hospitalizations: 1
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