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Prezolon adverse events reported to FDA.

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Summary

FDA Adverse Reports: 4. View All

Prezolon FDA safety alerts: No

Reported deaths: 4

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Often additional risks of using a medication, such as Prezolon, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Prezolon users, Learn more about unwanted side effects & find ways to reduce them. Browse Prezolon Adverse Reports reported to FDA and participate in Prezolon discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Prezolon. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Prezolon Adverse Effect Reports (FDA)

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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
on Feb 08, 2008 Female patient from GREECE , child 7 years of age, was diagnosed with vasculitis (What is vasculitis?) and 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: . During the same period patient was treated with 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 ).

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
Patient was taking 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 on Oct 09, 2007 from GREECE Additional patient health information: Female patient , child 7 years of age, was diagnosed with vasculitis (What is vasculitis?) and. Prezolon dosage: . During the same period patient was treated with 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 ).

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
Adverse event was reported on Oct 09, 2007 by a Female patient taking Prezolon (View Usage) (Dosage: ) was diagnosed with vasculitis (What is vasculitis?) and. 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. During the same period patient was treated with 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 ).

5387329-8 | Histiocytosis Haematophagic, Immunosuppression, Parvovirus Infection
on Jul 12, 2007 Female patient from GREECE , child 7 years of age, was diagnosed with vasculitis (What is vasculitis?) and was treated with Prezolon (View Usage). Patient experienced the following unwanted or unexpected effects: histiocytosis haematophagic, immunosuppression, parvovirus infection. Prezolon dosage: . During the same period patient was treated with 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 ).


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Prezolon Questions, Answers, Feedback and Comments

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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Prezolon risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Prezolon quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Prezolon use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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During the same period patient was treated with SINGULAIR (5 Mg 1/d Po) (View Singulair Review and Singulair Label ), PREZOLON (5 Mg /d Po) (View Prezolon Review and Prezolon ...

During the same period patient was treated with PREZOLON (7.5 Mg, Daily (1/d)), ADALAT (30 Mg, Daily (1/d)), KARVEA (150 Mg, Daily (1/d)), CALCIUM W/COLECALCIFEROL (500 Mg ...

... Methotrexate Label ), FILICINE (View Filicine Review and Filicine Label ), DIAREN (View Diaren Review and Diaren Label ), PREZOLON (View Prezolon Review and Prezolon Label ), ...

During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PREZOLON (View Prezolon Review and Prezolon Label ), NORVASC ...

During the same period patient was treated with SERETIDE, PREZOLON, ZANTAC, SEROXAT ^SMITH KLINE BEECHAM^, XANAX, COAPROVEL (Text:150mg/12.5mg-freq:0.5 Df Every 12 Hours ...

During the same period patient was treated with NEXIUM (One Tablet Daily) (View Nexium Review and Nexium Label ), GLOPIR (View Glopir Review and Glopir Label ), PREZOLON (View ...

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Prezolon Reactions
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 Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Prezolon adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!