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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.

PLERIXAFOR for Combined immunodeficiency: Side Effects & Safety Data

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There are 8 adverse event reports in the FDA FAERS database where PLERIXAFOR was used for Combined immunodeficiency.

Most Reported Side Effects for PLERIXAFOR

Side Effect Reports % Deaths Hosp.
Febrile neutropenia 69 15.4% 13 18
Mucosal inflammation 47 10.5% 6 3
Nausea 29 6.5% 2 11
Off label use 29 6.5% 4 4
Dyspnoea 28 6.3% 1 19
Pyrexia 27 6.0% 6 16
Diarrhoea 24 5.4% 7 6
Thrombocytopenia 23 5.2% 2 6
Acute kidney injury 21 4.7% 2 18
Acute respiratory distress syndrome 20 4.5% 3 17
Escherichia infection 18 4.0% 6 11
Alanine aminotransferase increased 17 3.8% 1 16
Colitis 17 3.8% 0 16
Herpes simplex 17 3.8% 3 0
Stomatitis 17 3.8% 1 2

Other Indications for PLERIXAFOR

Haematopoietic stem cell mobilisation (151) Plasma cell myeloma (30) Bone marrow conditioning regimen (21) Diffuse large b-cell lymphoma (17) Product used for unknown indication (17) Transplant (16) Acute myeloid leukaemia (13) Stem cell transplant (11) Non-hodgkin's lymphoma (9) Peripheral blood stem cell apheresis (9)

Other Drugs Used for Combined immunodeficiency

HUMAN IMMUNOGLOBULIN G (346) ELAPEGADEMASE-LVLR (242) BUSULFAN (83) FLUDARABINE (56) PEGADEMASE BOVINE (34) HUMAN IMMUNOGLOBULIN G\HYALURONIDASE RECOMBINANT HUMAN (29) ETANERCEPT (25) LAPINE T-LYMPHOCYTE IMMUNE GLOBULIN (23) ADALIMUMAB (22) FILGRASTIM (18)

Related Pages

PLERIXAFOR Full Profile All Combined immunodeficiency Drugs PLERIXAFOR Demographics PLERIXAFOR Timeline