Does ALGLUCOSIDASE ALFA Cause Hypersensitivity? 37 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Hypersensitivity have been filed in association with ALGLUCOSIDASE ALFA (Lumizyme). This represents 1.2% of all adverse event reports for ALGLUCOSIDASE ALFA.
37
Reports of Hypersensitivity with ALGLUCOSIDASE ALFA
1.2%
of all ALGLUCOSIDASE ALFA reports
3
Deaths
6
Hospitalizations
How Dangerous Is Hypersensitivity From ALGLUCOSIDASE ALFA?
Of the 37 reports, 3 (8.1%) resulted in death, 6 (16.2%) required hospitalization, and 1 (2.7%) were considered life-threatening.
Is Hypersensitivity Listed in the Official Label?
Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for ALGLUCOSIDASE ALFA.
What Other Side Effects Does ALGLUCOSIDASE ALFA Cause?
Pyrexia (266)
Off label use (210)
Dyspnoea (203)
Inappropriate schedule of product administration (190)
Pneumonia (185)
Malaise (130)
Respiratory failure (128)
Fatigue (122)
Death (120)
Disease progression (111)
What Other Drugs Cause Hypersensitivity?
ETANERCEPT (10,846)
ADALIMUMAB (10,641)
METHOTREXATE (9,799)
TOCILIZUMAB (9,076)
ABATACEPT (8,945)
INFLIXIMAB (8,519)
RITUXIMAB (8,408)
ADAPALENE (8,356)
LEFLUNOMIDE (7,926)
CERTOLIZUMAB PEGOL (7,353)
Which ALGLUCOSIDASE ALFA Alternatives Have Lower Hypersensitivity Risk?
ALGLUCOSIDASE ALFA vs ALIMTA
ALGLUCOSIDASE ALFA vs ALIROCUMAB
ALGLUCOSIDASE ALFA vs ALISKIREN
ALGLUCOSIDASE ALFA vs ALISKIREN HEMIFUMARATE
ALGLUCOSIDASE ALFA vs ALISKIREN\HYDROCHLOROTHIAZIDE