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Fludara (Fludarabine) - Febrile Neutropenia - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Febrile Neutropenia (23)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Fludara (Fludarabine) where reactions include febrile neutropenia. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Fludara side effects in female

Reported by a physician from Japan on 2012-08-13

Patient: female, weighing 48.0 kg (105.6 pounds)

Reactions: Stomatitis, Supraventricular Tachycardia, Shock Haemorrhagic, Disseminated Intravascular Coagulation, Endotoxaemia, Febrile Neutropenia, Pyrexia, Hypokalaemia, Venoocclusive Disease, Hypoalbuminaemia, Oedema, Neutropenia, Engraft Failure, Antithrombin III Decreased, Renal Failure Acute

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Thymoglobulin
    Dosage: 60 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2011-09-18
    End date: 2011-09-19

Fludara
    Dosage: 20 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2011-09-13
    End date: 2011-09-17

Other drugs received by patient: Azasetron Hydrochloride; Antibiotics-Resistant Lactic Acid Bacteriae; Dexchlorpheniramine Maleate; Rebamipide; Aprepitant; Itraconazole; Lansoprazole; Allopurinol; Acyclovir; Methylprednisolone Sodium Succinate; Polymyxin B Sulfate; Sulfamethoprim; Acetaminophen; Clostridium Butyricum; Acetaminophen; Lansoprazole; Cyclosporine; Dalteparin Sodium; Itraconazole; Melphalan Hydrochloride; Methotrexate



Possible Fludara side effects in female

Reported by a physician from Japan on 2012-07-06

Patient: female, weighing 41.0 kg (90.2 pounds)

Reactions: Histiocytosis Haematophagic, Viral Infection, Graft Versus Host Disease, Staphylococcal Infection, Febrile Neutropenia, Engraftment Syndrome

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Thymoglobulin
    Dosage: 50 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2011-01-10
    End date: 2011-01-10

Fludara
    Dosage: 40 mg, qd
    Indication: Adult T-Cell Lymphoma / Leukaemia
    Start date: 2011-01-04
    End date: 2011-01-09

Methylprednisolone Sodium Succinate
    Dosage: unk
    Indication: Pyrexia

Other drugs received by patient: Methotrexate; Fluconazole; Cefepime Hydrochloride; Acyclovir; Methotrexate; Methotrexate; Methotrexate; Sulfamethoprim; Busulfan; Filgrastim; Ciprofloxacin; Tacrolimus



Possible Fludara side effects in female

Reported by a physician from Japan on 2012-06-18

Patient: female, weighing 50.0 kg (110.0 pounds)

Reactions: Bronchopulmonary Aspergillosis, Acute Graft Versus Host Disease, Febrile Neutropenia, Neutropenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fludara
    Dosage: 50 mg, qd, 5 times
    Indication: Acute Myeloid Leukaemia
    Start date: 2010-12-07
    End date: 2010-12-12

Thymoglobulin
    Dosage: 60 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-12-11
    End date: 2010-12-12

Other drugs received by patient: Lansoprazole; Platelets; Sulfamethoprim; Tacrolimus; Methotrexate; Sulfamethoprim; Acyclovir; Levofloxacin; Itraconazole; Busulfan; RED Blood Cells, Concentrated



Possible Fludara side effects in male

Reported by a physician from Japan on 2012-06-15

Patient: male, weighing 60.0 kg (132.0 pounds)

Reactions: Pneumonia, Anaemia, Febrile Neutropenia, Pyrexia, Liver Disorder, Toxoplasmosis, Cytomegalovirus Infection, Platelet Count Decreased, Neutrophil Count Decreased, Acute Respiratory Failure

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Fludara
    Dosage: 50 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-03-08
    End date: 2010-03-13

Thymoglobulin
    Dosage: 150 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-03-12
    End date: 2010-03-13

Other drugs received by patient: Lansoprazole; Sulpiride; Acyclovir; Fluconazole; Busulfan; Tacrolimus; Methotrexate; Sulfamethoxazole W



Possible Fludara side effects in female

Reported by a physician from Japan on 2012-06-07

Patient: female, weighing 49.0 kg (107.8 pounds)

Reactions: Anxiety, Febrile Neutropenia, Hypertension, Cytomegalovirus Gastritis

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Fludara
    Dosage: 25 mg, qd
    Indication: Bone Marrow Conditioning Regimen

Thymoglobulin
    Dosage: 125 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2009-11-12
    End date: 2009-11-12

Other drugs received by patient: Tacrolimus; Tosufloxacin Tosilate; Valproate Sodium; Methylprednisolone Sodium Succinate; Busulfan; Haptoglobins; Sulfamethoxazole W; Cimetidine; Methotrexate; Itraconazole; Acyclovir



Possible Fludara side effects in female

Reported by a physician from Japan on 2012-05-25

Patient: female, weighing 49.0 kg (107.8 pounds)

Reactions: Post Transplant Lymphoproliferative Disorder, Insomnia, Acute Graft Versus Host Disease in Skin, Febrile Neutropenia, Neutrophil Count Decreased

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Thymoglobulin
    Dosage: 62.5 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-11-23
    End date: 2010-11-24

Fludara
    Dosage: 36 mg, qd
    Indication: Epstein-Barr Virus Infection
    Start date: 2010-11-18
    End date: 2010-11-22

Other drugs received by patient: Melphalan Hydrochloride; Tacrolimus; Micafungin Sodium; Lansoprazole; Omeprazole; Acyclovir; Ursodiol; Fluconazole; Methotrexate; Levofloxacin; Azasetron Hydrochloride; Acyclovir; Sulfamethoprim; Methylpednisolone Sodium Succinate



Possible Fludara side effects in female

Reported by a physician from Japan on 2012-04-27

Patient: female, weighing 50.0 kg (110.0 pounds)

Reactions: Febrile Neutropenia, Pyrexia, Hepatic Vein Occlusion

Adverse event resulted in: death

Drug(s) suspected as cause:
Cyclophosphamide
    Dosage: unk
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2009-10-16
    End date: 2009-10-18

Fludara
    Dosage: unk
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2009-10-16
    End date: 2009-10-18

Thymoglobulin
    Dosage: 125 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2009-10-13
    End date: 2009-10-13

Other drugs received by patient: Fresh Frozen Plasma; Micafungin Sodium; RED Blood Cells, Concentrated; Cyclosporine; Methylprednisolone Sodium Succinate; Platelets, Concentrated; Human Blood Coagulation Factor; Rituximab



Possible Fludara side effects in male

Reported by a physician from Japan on 2012-04-27

Patient: male, weighing 54.0 kg (118.8 pounds)

Reactions: Systemic Candida, Renal Impairment, Graft Versus Host Disease, Acute Graft Versus Host Disease, Cytomegalovirus Test Positive, Febrile Neutropenia, Staphylococcal Sepsis

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Fludara
    Dosage: 38 mg, qd, dosing frequency 6 times
    Indication: Product Used FOR Unknown Indication

Thymoglobulin
    Dosage: 67 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-05-06
    End date: 2010-05-07

Other drugs received by patient: Cyclosporine; Cytarabine; Human RED Blood Cells; Fludarabine Phosphate; Acyclovir; Acyclovir; Methylprednisolone Sodium Succinate; Doripenem Hydrate; Methotrexate; Busulfan; Platelets; Melphalan Hydrochloride



Possible Fludara side effects in 53 year old female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-04-13

Patient: 53 year old female, weighing 74.4 kg (163.6 pounds)

Reactions: Hypotension, Dizziness, Febrile Neutropenia, Rash

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Cytoxan
    Dosage: 460 mg, day 1-3 per cycle
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2011-05-16
    End date: 2012-01-16

Rituximab
    Dosage: 920 mg, day 1 every cycle
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2010-01-19
    End date: 2012-01-12

Fludara
    Dosage: 46 mg, day 1-3 per cycle
    Indication: Chronic Lymphocytic Leukaemia Recurrent
    Start date: 2011-12-14
    End date: 2012-01-16



Possible Fludara side effects in male

Reported by a physician from Japan on 2012-03-20

Patient: male, weighing 53.0 kg (116.6 pounds)

Reactions: Hepatic Function Abnormal, Chest Wall Mass, Enterococcal Infection, Pain, Ewing's Sarcoma, Encephalitis Herpes, Graft Versus Host Disease in Skin, Acute Graft Versus Host Disease in Skin, Bone Marrow Failure, Depression, Urinary Retention, Melaena, Candidiasis, Acute Graft Versus Host Disease in Intestine, Decreased Appetite, Pneumonia, Nausea, Pseudomonas Infection, Lung Neoplasm, Febrile Neutropenia, Hyponatraemia, Lobar Pneumonia, Renal Impairment, Diarrhoea, Insomnia, Pancreatitis, Graft Versus Host Disease in Intestine, Memory Impairment, Radiation Pneumonitis, Infection, Infectious Peritonitis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Thymoglobulin
    Dosage: 66 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-02-10
    End date: 2010-02-11

Fludara
    Dosage: unk
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-02-04
    End date: 2010-02-08

Other drugs received by patient: Etoposide; Cyclophosphamide Monohydrate; Hydrocortisone Sodium Succinate; Ceftriaxone; Ursodiol; Prednisolone; Prednisolone; Ifosfamide; Granisetron HCL; Hydrocortisone Sodium Succinate; Micafungin Sodium; Methotrexate; Methotrexate; Platelets, Concentrated; Etoposide; Melphalan Hydrochloride; Prednisolone Acetate; Vancomycin Hydrochloride; Polymyxin B Sulfate; Itraconazol A; Itraconazol A; Platelets, Concentrated; Platelets, Concentrated; Platelets, Concentrated; Ifosfamide; Dalteparin Sodium; Tacrolimus; Tacrolimus; Zovirax; Ethyl Icosapentate; Pirarubicin Hydrochloride; Carboplatin; Glycyrrhizin Glycine Cyteine Combined; Methylprednisolone Sodium Succinate; Filgrastim; Fluconal; Prednisolone; Platelets, Concentrated; Pirarubicin Hydrochloride; Vincristine Sulfate; Famotidine; Piperacillin Sodium; Sulfamethoprim; Ifosfamide; Pirarubicin Hydrochloride; Carboplatin; Imipem; Ceftriaxone; Carboplatin; Vincristine Sulfate; Cyclophosphamide Monohydrate; Glutathione; Micafungin Sodium; Hydroxyzine Hydrochloride; Platelets, Concentrated; Platelets, Concentrated



Possible Fludara side effects in 3 year old male

Reported by a physician from Japan on 2012-03-20

Patient: 3 year old male, weighing 11.0 kg (24.2 pounds)

Reactions: Acute Graft Versus Host Disease in Skin, Sepsis, Coagulopathy, Febrile Neutropenia, Pyrexia, Convulsion

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Thymoglobulin
    Dosage: 14 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-02-20
    End date: 2010-02-23

Fludara
    Dosage: unk
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-02-20
    End date: 2010-02-23

Other drugs received by patient: Methotrexate; Oseltamivir Phosphate; Acyclovir; Freeze-Dried Sulfonated Human; Platelets; Cyclophosphamide; Tacrolimus; Busulfan; Prednisolone Sodium Succinate INJ; Mycophenolate Mofetil; Meropenem; Human RED Blood Cells



Possible Fludara side effects in male

Reported by a physician from Japan on 2012-03-20

Patient: male, weighing 53.0 kg (116.6 pounds)

Reactions: Hepatic Function Abnormal, Pain, Chest Wall Mass, Enterococcal Infection, Ewing's Sarcoma, Encephalitis Herpes, Graft Versus Host Disease in Skin, Acute Graft Versus Host Disease in Skin, Bone Marrow Failure, Urinary Retention, Depression, Melaena, Candidiasis, Decreased Appetite, Acute Graft Versus Host Disease in Intestine, Pneumonia, Nausea, Lung Neoplasm, Pseudomonas Infection, Febrile Neutropenia, Hyponatraemia, Lobar Pneumonia, Renal Impairment, Diarrhoea, Insomnia, Graft Versus Host Disease in Intestine, Pancreatitis, Radiation Pneumonitis, Memory Impairment, Infection, Infectious Peritonitis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Thymoglobulin
    Dosage: 66 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-02-10
    End date: 2010-02-11

Fludara
    Dosage: unk
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-02-04
    End date: 2010-02-08

Other drugs received by patient: Carboplatin; Hydrocortisone Sodium Succinate; Imipem; Ceftriaxone; Itraconazol A; Pirarubicin Hydrochloride; Platelets, Concentrated; Platelets, Concentrated; Vincristine Sulfate; Micafungin Sodium; Prednisolone Acetate; Ethyl Icosapentate; Platelets, Concentrated; Platelets, Concentrated; Ifosfamide; Etoposide; Famotidine; Methylprednisolone Sodium Succinate; Vancomycin Hydrochloride; Ursodiol; Sulfamethoprim; Platelets, Concentrated; Platelets, Concentrated; Pirarubicin Hydrochloride; Pirarubicin Hydrochloride; Glycyrrhizin Glycine Cyteine Combined; Tacrolimus; Filgrastim; Polymyxin B Sulfate; Prednisolone; Platelets, Concentrated; Ifosfamide; Carboplatin; Vincristine Sulfate; Cyclophosphamide Monohydrate; Micafungin Sodium; Methotrexate; Ceftriaxone; Zovirax; Prednisolone; Ifosfamide; Etoposide; Carboplatin; Cyclophosphamide Monohydrate; Glutathione; Hydrocortisone Sodium Succinate; Dalteparin Sodium; Hydroxyzine Hydrochloride; Tacrolimus; Prednisolone; Itraconazol A; Granisetron HCL; Piperacillin Sodium; Melphalan Hydrochloride; Methotrexate; Fluconal



Possible Fludara side effects in female

Reported by a physician from Japan on 2012-03-19

Patient: female, weighing 49.0 kg (107.8 pounds)

Reactions: Post Transplant Lymphoproliferative Disorder, Acute Graft Versus Host Disease in Skin, Insomnia, Febrile Neutropenia, Neutrophil Count Decreased

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Fludara
    Dosage: 36 mg, qd
    Indication: Epstein-Barr Virus Infection
    Start date: 2010-11-18
    End date: 2010-11-22

Thymoglobulin
    Dosage: 62.5 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-11-23
    End date: 2010-11-24

Other drugs received by patient: Acyclovir; Lansoprazole; Levofloxacin; Sulfamethoprim; Azasetron Hydrochloride; Methylprednisolone Sodium Succinate; Methotrexate; Fluconazole; Melphalan Hydrochloride; Omeprazole; Tacrolimus; Micafungin Sodium; Ursodiol; Acyclovir



Possible Fludara side effects in female

Reported by a physician from Japan on 2012-03-19

Patient: female, weighing 50.0 kg (110.0 pounds)

Reactions: Diarrhoea, Febrile Neutropenia

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Fludara
    Dosage: unk
    Indication: Acute Myeloid Leukaemia
    Start date: 2010-07-01
    End date: 2010-07-05

Thymoglobulin
    Dosage: 62.5 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-07-06
    End date: 2010-07-07

Other drugs received by patient: Fentanyl; Micafungin Sodium; Ursodiol; Atenolol; Diltiazem HCL; Omeprazole; Melphalan Hydrochloride; Acyclovir; Acyclovir; Methotrexate; Fentanyl; Losartan Potassium; Granisetron HCL; Methylprednisolone Sodium Succinate; Fluconazole; Cefepime Hydrochloride; Tacrolimus



Possible Fludara side effects in male

Reported by a physician from Japan on 2012-03-15

Patient: male, weighing 60.0 kg (132.0 pounds)

Reactions: Pneumonia, Anaemia, Febrile Neutropenia, Pyrexia, Liver Disorder, Toxoplasmosis, Cytomegalovirus Infection, Platelet Count Decreased, Neutrophil Count Decreased, Acute Respiratory Failure

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Fludara
    Dosage: 50 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-03-08
    End date: 2010-03-13

Thymoglobulin
    Dosage: 150 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-03-12
    End date: 2010-03-13

Other drugs received by patient: Fluconazole; Acyclovir; Busulfan; Methotrexate; Sulfamethoxazole W; Sulpiride; Lansoprazole; Tacrolimus



Possible Fludara side effects in male

Reported by a physician from Japan on 2012-03-09

Patient: male, weighing 60.0 kg (132.0 pounds)

Reactions: Pneumonia, Anaemia, Febrile Neutropenia, Pyrexia, Liver Disorder, Platelet Count Decreased, Cytomegalovirus Infection, Acute Respiratory Failure, Neutrophil Count Decreased

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Thymoglobulin
    Dosage: 150 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-03-12
    End date: 2010-03-13

Fludara
    Dosage: 50 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-03-08
    End date: 2010-03-13

Other drugs received by patient: Busulfan; Acyclovir; Methotrexate; Tacrolimus; Sulpiride; Lansoprazole; Sulfamethoxazole W; Fluconazole



Possible Fludara side effects in male

Reported by a health professional (non-physician/pharmacist) from Japan on 2012-03-07

Patient: male, weighing 76.0 kg (167.2 pounds)

Reactions: Weight Increased, Stomatitis, Hypomagnesaemia, Febrile Neutropenia, Neutropenia, Pyrexia, Engraft Failure, Decreased Appetite

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fludara
    Dosage: unk
    Indication: Premedication
    Start date: 2010-01-11
    End date: 2010-01-16

Thymoglobulin
    Dosage: 83 mg, qd, injection
    Indication: Acute Myeloid Leukaemia
    Start date: 2010-01-07

Fludara
    Indication: Acute Myeloid Leukaemia

Thymoglobulin
    Dosage: unk
    Indication: Premedication
    Start date: 2010-12-03
    End date: 2010-12-04

Other drugs received by patient: Busulfan; Methotrexate; Ciprofloxacin Hydrochloride; Urso 250; Lansoprazole; Methylprednisolone Sodium Succinate; Busulfan; Methylprednisolone Sodium Succinate; Methylprednisolone Sodium Succinate; Leucovorin Calcium; Granisetron Hydrochloride; Tacrolimus; Hydroxyzine Pamoate; Acyclovir; Levofloxacin; Valproate Sodium; Rabeprazole Sodium; Itraconazol A



Possible Fludara side effects in 51 year old male

Reported by a physician from Japan on 2011-12-19

Patient: 51 year old male, weighing 60.0 kg (132.0 pounds)

Reactions: White Blood Cell Count Decreased, Neoplasm Progression, Cytomegalovirus Viraemia, Febrile Neutropenia, Gamma-Glutamyltransferase Increased, Neoplasm Malignant, Sepsis, Bone Marrow Failure, Meningitis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Alkeran
    Dosage: 100 mg, daily
    Start date: 2011-04-03
    End date: 2011-04-04

Fludara
    Dosage: 39 mg, daily
    Start date: 2011-03-30
    End date: 2011-04-03

Prednisolone
    Dosage: 30 mg, daily
    Start date: 2011-02-15
    End date: 2011-07-12

Exjade
    Dosage: 500 mg, daily
    Administration route: Oral
    Indication: Iron Overload
    Start date: 2011-01-07
    End date: 2011-01-11

Exjade
    Dosage: 1000 mg, daily
    Start date: 2011-01-12
    End date: 2011-03-29

Prograf
    Dosage: 1 mg, daily
    Start date: 2011-04-05
    End date: 2011-07-14

Other drugs received by patient: Neoral; Magmitt Kenei; Levofloxacin; Omeprazole; BIO Three; Sulfamethoxazole and Trimethoprim; Clarithromycin; Itraconazole; Urso 250; Zolpidem



Possible Fludara side effects in male

Reported by a physician from Japan on 2011-12-08

Patient: male, weighing 53.0 kg (116.6 pounds)

Reactions: Hepatic Function Abnormal, Chest Wall Mass, Pain, Enterococcal Infection, Ewing's Sarcoma, Encephalitis Herpes, Graft Versus Host Disease in Skin, Acute Graft Versus Host Disease in Skin, Bone Marrow Failure, Urinary Retention, Depression, Melaena, Decreased Appetite, Acute Graft Versus Host Disease in Intestine, Candidiasis, Pneumonia, Nausea, Pseudomonas Infection, Lung Neoplasm, Febrile Neutropenia, Hyponatraemia, Lobar Pneumonia, Renal Impairment, Diarrhoea, Insomnia, Graft Versus Host Disease in Intestine, Pancreatitis, Radiation Pneumonitis, Memory Impairment, Infection, Infectious Peritonitis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Fludara
    Dosage: unk
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-02-04
    End date: 2010-02-08

Thymoglobulin
    Dosage: 66 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-02-10
    End date: 2010-02-11

Other drugs received by patient: Etoposide; Carboplatin; Carboplatin; Melphalan Hydrochloride; Hydroxyzine Hydrochloride; Tacrolimus; Ceftriaxone; Vancomycin HCL; Fluconal; Prednisolone; Platelets, Concentrated; Platelets, Concentrated; Pirarubicin Hydrochloride; Vincristine Sulfate; Cyclophosphamide Monohydrate; Hydrocortisone Sodium Succinate; Ceftriaxone; Polymyxin B Sulfate; Ifosfamide; Ifosfamide; Ifosfamide; Glycyrrhizin Glycine Cyteine Combined; Glutathione; Dalteparin Sodium; Piperacillin Sodium; Prednisolone Acetate; Imipem; Methotrexate; Platelets, Concentrated; Famotidine; Filgrastim; Platelets, Concentrated; Platelets, Concentrated; Vincristine Sulfate; Granisetron HCL; Micafungin Sodium; Ethyl Icosapentate; Prednisolone; Itraconazol A; Platelets, Concentrated; Etoposide; Pirarubicin Hydrochloride; Pirarubicin Hydrochloride; Micafungin Sodium; Methylprednisolone Sodium Succinate; Tacrolimus; Methotrexate; Sulfamethoprim; Platelets, Concentrated; Carboplatin; Cyclophosphamide Monohydrate; Hydrocortisone Sodium Succinate; Zovirax; Ursodiol



Possible Fludara side effects in 51 year old male

Reported by a physician from Japan on 2011-11-01

Patient: 51 year old male, weighing 60.0 kg (132.0 pounds)

Reactions: White Blood Cell Count Decreased, Febrile Neutropenia, Cytomegalovirus Viraemia, Neoplasm Progression, Neoplasm Malignant, Gamma-Glutamyltransferase Increased, Sepsis, Bone Marrow Failure, Meningitis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Prograf

Exjade
    Dosage: 500 mg, daily
    Administration route: Oral
    Indication: Iron Overload
    Start date: 2011-01-07
    End date: 2011-01-11

Exjade
    Dosage: 1000 mg, daily
    Start date: 2011-01-12
    End date: 2011-03-29

Fludara

Alkeran

Prednisolone

Other drugs received by patient: BIO Three; Magmitt Kenei; Omeprazole; Levofloxacin; Zolpidem; Clarithromycin; Neoral; Urso 250; Sulfamethoxazole; Itraconazole



Possible Fludara side effects in male

Reported by a physician from Japan on 2011-10-17

Patient: male, weighing 60.0 kg (132.0 pounds)

Reactions: Pneumonia, Anaemia, Febrile Neutropenia, Pyrexia, Liver Disorder, Platelet Count Decreased, Cytomegalovirus Infection, Acute Respiratory Failure, Neutrophil Count Decreased

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Thymoglobulin
    Dosage: 150 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-03-12
    End date: 2010-03-13

Fludara
    Dosage: 50 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-03-08
    End date: 2010-03-13

Other drugs received by patient: Fluconazole; Busulfan; Lansoprazole; Acyclovir; Sulpiride; Tacrolimus; Methotrexate; Sulfamethoxazole W



Possible Fludara side effects in 65 year old

Reported by a health professional (non-physician/pharmacist) from Italy on 2011-10-11

Patient: 65 year old

Reactions: Mucosal Inflammation, Opportunistic Infection, Febrile Neutropenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Cyclophosphamide
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2011-08-30
    End date: 2011-08-30

Fludara
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2011-08-30
    End date: 2011-08-30

Other drugs received by patient: Rabeprazole Sodium; Zovirax; Neulasta; Atorvastatin Calcium



Possible Fludara side effects in male

Reported by a physician from Japan on 2011-10-03

Patient: male, weighing 53.0 kg (116.6 pounds)

Reactions: Hepatic Function Abnormal, Chest Wall Mass, Pain, Enterococcal Infection, Encephalitis Herpes, Acute Graft Versus Host Disease in Skin, Bone Marrow Failure, Depression, Urinary Retention, Melaena, Decreased Appetite, Acute Graft Versus Host Disease in Intestine, Candidiasis, Pneumonia, Nausea, Pseudomonas Infection, Lung Neoplasm, Hyponatraemia, Febrile Neutropenia, Lobar Pneumonia, Renal Impairment, Diarrhoea, Insomnia, Pancreatitis, Memory Impairment, Radiation Pneumonitis, Infection, Infectious Peritonitis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Thymoglobulin
    Dosage: 66 mg, qd
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-02-10
    End date: 2010-02-11

Fludara
    Dosage: unk
    Indication: Bone Marrow Conditioning Regimen
    Start date: 2010-02-04
    End date: 2010-02-08

Other drugs received by patient: Glutathione; Granisetron Hydrochloride; Hydrocortisone Sodium Succinate; Dalteparin Sodium; Piperacillin Sodium; Platelets, Concentrated; Platelets, Concentrated; Ifosfamide; Pirarubicin Hydrochloride; Melphalan Hydrochloride; Tacrolimus; Methotrexate; Zovirax; Ethyl Icosapentate; Carboplatin; Prednisolone; Itraconazol A; Platelets, Concentrated; Platelets, Concentrated; Etoposide; Pirarubicin Hydrochloride; Carboplatin; Cyclophosphamide Monohydrate; Glycyrrhizin Glycine Cyteine Combined; Prednisolone Acetate; Filgrastim; Imipem; Prednisolone; Platelets, Concentrated; Platelets, Concentrated; Ifosfamide; Micafungin Sodium; Methylprednisolone Sodium Succinate; Hydroxyzine Hydrochloride; Tacrolimus; Methotrexate; Ceftriaxone; Vancomycin Hychloride; Carboplatin; Ceftriaxone; Polymyxin B Sulfate; Fluconal; Sulfamethoprim; Ifosfamide; Vincristine Sulfate; Vincristine Sulfate; Cyclophosphamide Monohydrate; Famotidine; Hydrocortisone Sodium Succinate; Ursodiol; Platelets, Concentrated; Etoposide; Pirarubicin Hydrochloride; Micafungin Sodium

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