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Cyclophosphamide (Cyclophosphamide) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Cyclophosphamide. Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.

Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.

All cases (1384)
     Febrile Neutropenia (116)Neutropenia (101)Pyrexia (92)more >>

Cases resulting in a serious event (1344)
     Febrile Neutropenia (116)Neutropenia (94)Pyrexia (91)more >>

Cases resulting in death (381)
     Sepsis (42)Glioma (37)Neutropenia (35)more >>

Cases resulting in life threatening events (126)
     Neutropenia (22)Thrombocytopenia (21)Leukopenia (15)more >>

Cases resulting in hospitalization (659)
     Febrile Neutropenia (102)Pyrexia (68)Neutropenia (57)more >>

Cases resulting in disability (43)
     Optic Atrophy (7)Sepsis (6)Spinal Cord Disorder (6)more >>

Cases resulting in other serious reactions (539)
     Pneumocystis Jiroveci Pneumonia (61)Acute Myeloid Leukaemia (39)Pancytopenia (31)more >>

Below is a sample of reports where side effects / adverse reactions may be related to Cyclophosphamide. For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in female receiving Cyclophosphamide

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-31

Patient: female, weighing 72.2 kg (158.8 pounds)

Adverse reactions / side effects: Vomiting, Diarrhoea, Nausea, Chills, Haemolytic Anaemia, Neutrophil Count Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Cyclophosphamide
    Dosage: 250 mg/m2 days 1-3 q 4 wks x 6 months iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-08-12

Cyclophosphamide
    Dosage: 250 mg/m2 days 1-3 q 4 wks x 6 months iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-08-13

Cyclophosphamide
    Dosage: 250 mg/m2 days 1-3 q 4 wks x 6 months iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-08-14

Fludarabine Phosphate
    Dosage: 25 mg/m2 days 1-3 q 4 wks x 6 months iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-08-12

Fludarabine Phosphate
    Dosage: 25 mg/m2 days 1-3 q 4 wks x 6 months iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-08-13

Fludarabine Phosphate
    Dosage: 25 mg/m2 days 1-3 q 4 wks x 6 months iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-08-14



Adverse event in 7 year old female receiving Cyclophosphamide

Reported by a consumer/non-health professional from Greece on 2007-10-31

Patient: 7 year old female, weighing 25.0 kg (55.0 pounds)

Adverse reactions / side effects: Erythema Infectiosum, Histiocytosis Haematophagic

Adverse event resulted in: death

Suspect drug(s):
Azathioprine
    Indication: Diffuse Vasculitis
    Start date: 2001-08-01

Cyclophosphamide
    Indication: Diffuse Vasculitis
    Start date: 2007-04-27
    End date: 2007-04-27

Cyclosporine
    Indication: Diffuse Vasculitis
    Start date: 2007-05-02
    End date: 2007-05-04

Etanercept
    Indication: Diffuse Vasculitis
    Start date: 2001-08-01

Kineret
    Indication: Diffuse Vasculitis
    Start date: 2006-03-22
    End date: 2007-04-20

Methotrexate
    Indication: Diffuse Vasculitis
    Start date: 2001-08-01

Methylprednisolone
    Indication: Diffuse Vasculitis
    Start date: 2007-05-03
    End date: 2007-05-05

Prednisolone
    Administration route: Oral
    Indication: Diffuse Vasculitis
    Start date: 2001-06-20
    End date: 2002-05-15

Other drugs received by patient: Corticosteroid



Adverse event in receiving Cyclophosphamide

Reported by a individual with unspecified qualification from France on 2007-10-31

Patient:

Adverse reactions / side effects: Drug Toxicity

Adverse event resulted in: death

Suspect drug(s):
Alkeran
    Dosage: oral
    Administration route: Oral
    Indication: Multiple Myeloma

Cyclophosphamide
    Indication: Stem Cell Transplant

Dexamethasone
    Dosage: oral
    Administration route: Oral
    Indication: Multiple Myeloma

Disodium Clodronate (Formulation Unknown) (Disodium Clodronate)
    Dosage: oral
    Administration route: Oral

Doxorubicin HCL
    Dosage: intravenous infus
    Indication: Multiple Myeloma

Granulocyte Col.stim.fact (Formulation Unknown) (Granulocyte Col.stim.

Mesna
    Indication: Stem Cell Transplant

Stem Cell Transplant (Formulation Unknown) (Stem Cell Transplant)

Vincristine
    Dosage: intravenous infus
    Indication: Multiple Myeloma



Adverse event in 70 year old female receiving Cyclophosphamide

Reported by a physician from Germany on 2007-10-31

Patient: 70 year old female

Adverse reactions / side effects: Epstein-Barr Virus Infection, Multi-Organ Failure, Fatigue, Necrosis, Lymphoproliferative Disorder, Lung Infiltration, Disease Progression

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Cyclophosphamide

Everolimus

Fludarabine



Adverse event in receiving Cyclophosphamide

Reported by a individual with unspecified qualification from France on 2007-10-31

Patient:

Adverse reactions / side effects: Drug Toxicity, Cardiac Failure

Adverse event resulted in: death

Suspect drug(s):
Alkeran
    Dosage: oral
    Administration route: Oral
    Indication: Multiple Myeloma

Cyclophosphamide
    Indication: Stem Cell Transplant

Dexamethasone
    Dosage: oral
    Administration route: Oral
    Indication: Multiple Myeloma

Disodium Clodronate (Formulation Unknown) (Disodium Clodronate)
    Dosage: oral
    Administration route: Oral

Doxorubicin Hydrochloride
    Dosage: intravenous infus
    Indication: Multiple Myeloma

Granulocyte Col.stim.fact (Formulation Unknown) (Granulocyte Col.stim.

Mesna
    Indication: Stem Cell Transplant

Stem Cell Transplant (Formulation Unknown) (Stem Cell Transplant)
    Indication: Multiple Myeloma

Vincristine
    Dosage: intravenous infus
    Indication: Multiple Myeloma



Adverse event in 53 year old male receiving Cyclophosphamide

Reported by a physician from Germany on 2007-10-31

Patient: 53 year old male, weighing 100.0 kg (220.0 pounds)

Adverse reactions / side effects: Disseminated Intravascular Coagulation, Hepatic Failure, Continuous Haemodiafiltration, Pulmonary Embolism, Pupils Unequal, Left Ventricular Failure, Erythema, Multi-Organ Failure, Acute Respiratory Distress Syndrome, Thrombocytopenia, Sinusitis, Acute Respiratory Failure, Renal Failure Acute, Tachyarrhythmia, Hypotension, Skin Disorder, Mastoiditis, Haemodialysis, Cardiac Failure, Staphylococcal Infection, Septic Shock, Purulent Discharge

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cyclophosphamide
    Dosage: 1800.00 mg, intravenous
    Indication: Plasmacytoma
    Start date: 2007-07-02
    End date: 2007-07-02

Dexamethasone
    Dosage: 40.00 mg, oral
    Administration route: Oral
    Indication: Plasmacytoma
    Start date: 2007-06-02

Velcade
    Dosage: 2.60 mg, intravenous
    Indication: Plasmacytoma
    Start date: 2007-07-02
    End date: 2007-07-02

Other drugs received by patient: Dipyrone TAB; Buprenorphine Hydrochloride; Pantoprazole Sodium



Adverse event in 54 year old male receiving Cyclophosphamide

Reported by a individual with unspecified qualification on 2007-10-31

Patient: 54 year old male

Adverse reactions / side effects: Jaundice, Graft Versus Host Disease, Lymphopenia, Anaemia, Pyrexia, Generalised Erythema, Diarrhoea, Circulatory Collapse, Neutropenia, Thrombocytopenia, Septic Shock, Leukopenia

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Cyclophosphamide



Adverse event in receiving Cyclophosphamide

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-31

Patient: , weighing 93.8 kg (206.4 pounds)

Adverse reactions / side effects: Pneumonia

Adverse event resulted in: hospitalization

Suspect drug(s):
Cyclophosphamide
    Dosage: 250mg/m2 days 1-3 q4wks x 6 mos iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-07-04

Cyclophosphamide
    Dosage: 250mg/m2 days 1-3 q4wks x 6 mos iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-07-05

Cyclophosphamide
    Dosage: 250mg/m2 days 1-3 q4wks x 6 mos iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-07-06

Fludarabine Phosphate
    Dosage: 25mg/m2 days 1-3 q4wks x 6 mos iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-07-04

Fludarabine Phosphate
    Dosage: 25mg/m2 days 1-3 q4wks x 6 mos iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-07-05

Fludarabine Phosphate
    Dosage: 25mg/m2 days 1-3 q4wks x 6 mos iv
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-07-06



Adverse event in 52 year old female receiving Cyclophosphamide

Reported by a individual with unspecified qualification from United Kingdom on 2007-10-31

Patient: 52 year old female, weighing 54.0 kg (118.8 pounds)

Adverse reactions / side effects: Malaise, Nausea, Drug Interaction

Suspect drug(s):
Cyclizine

Cyclophosphamide
    Indication: Lymphoma

Doxorubicin HCL
    Indication: Lymphoma

Fludarabine Phosphate
    Indication: Chronic Lymphocytic Leukaemia

Granisetron HCL
    Dosage: 3 mg qd iv
    Indication: Lymphoma
    Start date: 2007-08-28

Prednisone TAB
    Indication: Lymphoma

Tegretol
    Dosage: 400 mg tid po
    Administration route: Oral
    Indication: Epilepsy

Vincristine
    Indication: Lymphoma

Zofran
    Dosage: 8 mg tid po
    Administration route: Oral



Adverse event in 68 year old male receiving Cyclophosphamide

Reported by a individual with unspecified qualification on 2007-10-31

Patient: 68 year old male

Adverse reactions / side effects: Erythema Infectiosum, Disease Recurrence, Hepatitis Acute, Epstein-Barr Virus Test Positive, Aplasia Pure RED Cell, Lymphoproliferative Disorder

Suspect drug(s):
Campath
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-04-01
    End date: 2006-06-01

Cyclophosphamide
    Administration route: Oral
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2003-09-01
    End date: 2004-02-01

Fludarabine Phosphate
    Administration route: Oral
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2003-09-01
    End date: 2004-02-01

Other drugs received by patient: Immunoglobulins



Adverse event in 4 year old male receiving Cyclophosphamide

Reported by a physician from United States on 2007-10-30

Patient: 4 year old male

Adverse reactions / side effects: Acute Myeloid Leukaemia

Suspect drug(s):
Carboplatin
    Indication: Retinoblastoma Unilateral

Cyclophosphamide
    Indication: Retinoblastoma Unilateral

Etoposide
    Indication: Retinoblastoma Unilateral

Vincristine
    Indication: Retinoblastoma Unilateral



Adverse event in male receiving Cyclophosphamide

Reported by a individual with unspecified qualification from United States on 2007-10-30

Patient: male, weighing 76.0 kg (167.2 pounds)

Adverse reactions / side effects: Klebsiella Infection, Culture Urine Positive

Adverse event resulted in: hospitalization

Suspect drug(s):
Cyclophosphamide
    Dosage: 1965 mg

Doxorubicin Hydrochloride
    Dosage: 104 mg

Etoposide
    Dosage: 520 mg

Prednisone TAB
    Dosage: 990 mg

Rituximab (Moab C2b8 Anti Cd20, Chimeric)
    Dosage: 680 mg

Vincristine Sulfate
    Dosage: 2.8 mg



Adverse event in 6 year old female receiving Cyclophosphamide

Reported by a physician from United States on 2007-10-30

Patient: 6 year old female

Adverse reactions / side effects: Acute Myeloid Leukaemia, Sepsis, Acute Respiratory Distress Syndrome

Suspect drug(s):
Carboplatin
    Indication: Retinoblastoma Bilateral

Cyclophosphamide
    Indication: Retinoblastoma Bilateral

Etoposide
    Indication: Retinoblastoma Bilateral

Vincristine
    Indication: Retinoblastoma Bilateral



Adverse event in male receiving Cyclophosphamide

Reported by a individual with unspecified qualification from United States on 2007-10-30

Patient: male, weighing 97.0 kg (213.4 pounds)

Adverse reactions / side effects: White Blood Cell Count Decreased, Neutropenia

Adverse event resulted in: hospitalization

Suspect drug(s):
Cyclophosphamide
    Dosage: 1650 mg

Doxorubicin Hydrochloride
    Dosage: 110 mg

Prednisone TAB
    Dosage: 1000 mg

Rituximab (Moab C2b8 Anti Cd20, Chimeric)
    Dosage: 800 mg

Vincristine Sulfate
    Dosage: 2 mg



Adverse event in 62 year old female receiving Cyclophosphamide

Reported by a individual with unspecified qualification from United Kingdom on 2007-10-30

Patient: 62 year old female

Adverse reactions / side effects: Viral Infection, JC Virus Infection, Muscle Twitching, Progressive Multifocal Leukoencephalopathy

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Cyclophosphamide
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2003-09-01
    End date: 2004-02-01

Doxorubicin Hydrochloride
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2003-09-01
    End date: 2004-02-01

Prednisone
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2003-09-01
    End date: 2004-02-01

Rituximab
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2003-09-01
    End date: 2006-02-01

Vincristine
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2003-09-01
    End date: 2004-02-01

Other drugs received by patient: Chlorambucil; Fludarabine Phosphate



Adverse event in 7 year old female receiving Cyclophosphamide

Reported by a physician from Greece on 2007-10-30

Patient: 7 year old female, weighing 25.0 kg (55.0 pounds)

Adverse reactions / side effects: Parvovirus Infection, Histiocytosis Haematophagic, Drug Interaction, Immunosuppression

Adverse event resulted in: death

Suspect drug(s):
Azathioprine
    Indication: Drug USE FOR Unknown Indication

Cyclophosphamide
    Dosage: 800 mg iv
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-04-27
    End date: 2007-04-27

Cyclosporine
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-05-02
    End date: 2007-05-04

Entanercept
    Indication: Drug USE FOR Unknown Indication

Kineret
    Dosage: 25 mg/kg once sc
    Indication: Vasculitis
    Start date: 2006-03-22
    End date: 2007-04-20

Methotrexate
    Indication: Drug USE FOR Unknown Indication

Methylprednisolone
    Dosage: 300 mg/kg iv
    Indication: Drug USE FOR Unknown Indication
    Start date: 2007-05-03
    End date: 2007-05-05

Prednisolone
    Indication: Drug USE FOR Unknown Indication
    Start date: 2001-06-21
    End date: 2002-05-15



Adverse event in female receiving Cyclophosphamide

Reported by a individual with unspecified qualification from Germany on 2007-10-30

Patient: female

Adverse reactions / side effects: Neck Pain, Headache

Adverse event resulted in: hospitalization

Suspect drug(s):
Cyclophosphamide
    Dosage: daily dose:375mg/m2-freq:once every cycle

Docetaxel
    Dosage: daily dose:60mg/m2-freq:once every cycle

Doxorubicin Hydrochloride
    Dosage: daily dose:37.5mg/m2-freq:once every cycle

Granisetron HCL
    Dosage: daily dose:1mg
    Start date: 2007-03-29
    End date: 2007-03-29

Neulasta
    Dosage: daily dose:6mg-freq:once every cycle
    Indication: Chemotherapy
    Start date: 2007-03-29
    End date: 2007-06-30



Adverse event in female receiving Cyclophosphamide

Reported by a physician from Germany on 2007-10-30

Patient: female, weighing 76.0 kg (167.2 pounds)

Adverse reactions / side effects: Diverticulum Intestinal, Gastritis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Cyclophosphamide
    Dosage: 350 mg, unk
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-08-28
    End date: 2007-02-13

Fludarabine Phosphate
    Dosage: 35 mg, unk
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-08-28
    End date: 2007-02-13

Neulasta
    Dosage: 6 mg, unk
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-10-13
    End date: 2007-02-13

Rituximab
    Dosage: 880 mg, unk
    Indication: Chronic Lymphocytic Leukaemia
    Start date: 2006-08-28
    End date: 2007-02-13

Uromitexan
    Dosage: 100 mg, unk
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-08-28
    End date: 2007-02-13

Other drugs received by patient: Dexamethasone 0.5mg TAB; Kevatril; Tavegil; Acetaminophen; Prednisolut



Adverse event in 65 year old male receiving Cyclophosphamide

Reported by a physician from United States on 2007-10-29

Patient: 65 year old male

Adverse reactions / side effects: Renal Failure, Transient Ischaemic Attack, Hypertension

Adverse event resulted in: hospitalization

Suspect drug(s):
Cyclophosphamide
    Dosage: 600 mg/m2, unk
    Indication: Chronic Lymphocytic Leukaemia

Pentostatin
    Dosage: 4 mg/m2, unk
    Indication: Chronic Lymphocytic Leukaemia

Rituxan
    Dosage: 100 mg, unk
    Indication: Chronic Lymphocytic Leukaemia

Other drugs received by patient: Fluids (Unk Ingredients); IV Hydration (Unk Ingredients); Anti Nausea Medicine Unkown Name; Anti Nausea Medicine Unkown Name; Acetaminophen; Diphenhydramine HCL; Allopurinol; Trimethoprim + Sulfamethoxazole; Neupogen



Adverse event in female receiving Cyclophosphamide

Reported by a consumer/non-health professional from United States on 2007-10-29

Patient: female

Adverse reactions / side effects: Respiratory Failure, Pulmonary Fibrosis

Adverse event resulted in: death

Suspect drug(s):
Cyclophosphamide
    Indication: Chemotherapy

Doxorubicin HCL
    Indication: Chemotherapy

Neulasta
    Indication: Prophylactic Chemotherapy

Rituximab
    Indication: Chemotherapy

Vincristine Sulfate
    Indication: Chemotherapy

Other drugs received by patient: Prednisolone



Adverse event in 72 year old female receiving Cyclophosphamide

Reported by a physician from United States on 2007-10-29

Patient: 72 year old female

Adverse reactions / side effects: Neutropenic Sepsis, Haemolytic Anaemia

Suspect drug(s):
Cyclophosphamide
    Dosage: 600 mg/m2, q3w
    Indication: Chronic Lymphocytic Leukaemia

Pentostatin
    Dosage: 4 mg/m2, q3w
    Indication: Chronic Lymphocytic Leukaemia

Rituxan
    Dosage: 100 mg, unk
    Indication: Chronic Lymphocytic Leukaemia

Rituxan
    Dosage: 375 mg/m2, unk

Other drugs received by patient: Hydration (Unk Ingredients)



Adverse event in female receiving Cyclophosphamide

Reported by a individual with unspecified qualification from United States on 2007-10-29

Patient: female, weighing 56.1 kg (123.4 pounds)

Adverse reactions / side effects: Lymphopenia, Neutropenia, Leukopenia

Suspect drug(s):
Cyclophosphamide
    Dosage: 960 mg

Doxorubicin Hydrochloride
    Dosage: 50 mg



Adverse event in 46 year old female receiving Cyclophosphamide

Reported by a individual with unspecified qualification from Japan on 2007-10-29

Patient: 46 year old female

Adverse reactions / side effects: Cytomegalovirus Antigen Positive, Haptoglobin Decreased, RED Blood Cell Abnormality, Proteinuria, Blood Lactate Dehydrogenase Increased, Thrombotic Microangiopathy, Focal Glomerulosclerosis

Adverse event resulted in: disablity

Suspect drug(s):
Cyclophosphamide

Neoral
    Dosage: unk, unk
    Administration route: Oral
    Indication: Allogenic Bone Marrow Transplantation Therapy
    End date: 2007-03-22

Sandimmune
    Dosage: 3 mg/kg/day
    Indication: Allogenic Bone Marrow Transplantation Therapy
    Start date: 2006-12-12

Other drugs received by patient: Methotrexate; Campath; Fludarabine Phosphate



Adverse event in 75 year old male receiving Cyclophosphamide

Reported by a individual with unspecified qualification from Japan on 2007-10-29

Patient: 75 year old male

Adverse reactions / side effects: Nutritional Condition Abnormal, Pneumonia Aspiration, Rectal Haemorrhage, Clostridium Difficile Colitis, Melaena

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Adriamycin PFS
    Indication: Leukaemia Plasmacytic

Cyclophosphamide
    Indication: Leukaemia Plasmacytic

Dexamethasone 0.5mg TAB
    Indication: Leukaemia Plasmacytic

Melphalan
    Indication: Leukaemia Plasmacytic

Prednisone
    Indication: Leukaemia Plasmacytic

Vincristine
    Indication: Leukaemia Plasmacytic



Adverse event in receiving Cyclophosphamide

Reported by a physician from Italy on 2007-10-29

Patient:

Adverse reactions / side effects: JC Virus Infection, Progressive Multifocal Leukoencephalopathy

Adverse event resulted in: death

Suspect drug(s):
Cyclophosphamide
    Dosage: 7 g/m2, unk
    Indication: Diffuse Large B-Cell Lymphoma

Cytarabine
    Dosage: 2 g/m2, unk
    Indication: Diffuse Large B-Cell Lymphoma

Doxorubicin HCL
    Dosage: 50 mg/m2, unk
    Indication: Diffuse Large B-Cell Lymphoma

Doxorubicin HCL
    Dosage: 75 mg/m2, x2

Rituxan
    Dosage: 375 mg/m2, unk
    Indication: Diffuse Large B-Cell Lymphoma

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