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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

CYCLOPHOSPHAMIDE for Factor viii deficiency: Side Effects & Safety Data

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There are 22 adverse event reports in the FDA FAERS database where CYCLOPHOSPHAMIDE was used for Factor viii deficiency.

Most Reported Side Effects for CYCLOPHOSPHAMIDE

Side Effect Reports % Deaths Hosp.
Off label use 12,578 9.8% 2,788 3,928
Febrile neutropenia 11,318 8.8% 1,348 7,223
Drug ineffective 8,142 6.3% 2,157 2,184
Neutropenia 7,352 5.7% 1,287 2,890
Disease progression 7,100 5.5% 1,730 1,008
Pyrexia 6,126 4.8% 832 4,228
Product use in unapproved indication 5,750 4.5% 1,245 1,392
Thrombocytopenia 4,669 3.6% 902 1,799
Pneumonia 4,595 3.6% 1,633 2,604
Nausea 4,561 3.6% 363 2,190
Anaemia 4,486 3.5% 664 2,040
Death 4,270 3.3% 4,260 453
Sepsis 4,041 3.1% 2,077 1,841
Myelosuppression 3,603 2.8% 209 1,796
Diarrhoea 3,602 2.8% 566 1,861

Other Indications for CYCLOPHOSPHAMIDE

Diffuse large b-cell lymphoma (16,598) Plasma cell myeloma (9,148) Breast cancer (8,826) Product used for unknown indication (8,261) Acute lymphocytic leukaemia (5,495) B-cell lymphoma (4,766) Bone marrow conditioning regimen (4,485) Non-hodgkin's lymphoma (3,805) Chemotherapy (3,372) Chronic lymphocytic leukaemia (3,085)

Other Drugs Used for Factor viii deficiency

EMICIZUMAB-KXWH (6,532) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (4,268) EFMOROCTOCOG ALFA (832) --BLOOD-COAGULATION FACTOR VIII FUSION PROTEIN WITH IMMUNOGLOBULIN G1 , ,-BIS WITH IMMUNOGLOBULIN G1 (722) ANTIHEMOPHILIC FACTOR, PEGYLATED HUMAN SEQUENCE RECOMBINANT (352) ANTI-INHIBITOR COAGULANT COMPLEX (317) EMICIZUMAB (315) DAMOCTOCOG ALFA PEGOL (310) EFANESOCTOCOG ALFA (292) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT RESIDUES 743-1636 DELETED (180)

Related Pages

CYCLOPHOSPHAMIDE Full Profile All Factor viii deficiency Drugs CYCLOPHOSPHAMIDE Demographics CYCLOPHOSPHAMIDE Timeline