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Prezolon Side Effects

Report Prezolon Side Effects

If you experienced any harmful or unwanted effects of Prezolon, please share your experience. This could help to raise awareness about Prezolon side effects, identify uknown risks and inform health professionals and patients taking Prezolon.

Examples: headache, dizziness


The most commonly reported Prezolon side effects are:
Gained 6kg In 7 Days (3 reports)
Migrain Hedache (2 reports)
Delusions-hallucinations (1 reports)
Gained Weight (1 reports)
Hyperactivity (1 reports)
Lower Libs Paralysis (1 reports)
Nausea (1 reports)
Viagra Simultaneously (1 reports)

If you have experienced a side effect listed above, you can check a box to report it.


To view a complete list of submitted side effects, please follow the link Prezolon side effects . You can also compare Prezolon side effects or view FDA reports.

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).
The 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 identified 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: 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


Record and Track Your Side Effects

It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.

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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.

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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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