Does ALGLUCOSIDASE ALFA Cause Device issue? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Device issue have been filed in association with ALGLUCOSIDASE ALFA (Lumizyme). This represents 0.6% of all adverse event reports for ALGLUCOSIDASE ALFA.
18
Reports of Device issue with ALGLUCOSIDASE ALFA
0.6%
of all ALGLUCOSIDASE ALFA reports
1
Deaths
7
Hospitalizations
How Dangerous Is Device issue From ALGLUCOSIDASE ALFA?
Of the 18 reports, 1 (5.6%) resulted in death, 7 (38.9%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALGLUCOSIDASE ALFA. However, 18 reports have been filed with the FAERS database.
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 Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which ALGLUCOSIDASE ALFA Alternatives Have Lower Device issue Risk?
ALGLUCOSIDASE ALFA vs ALIMTA
ALGLUCOSIDASE ALFA vs ALIROCUMAB
ALGLUCOSIDASE ALFA vs ALISKIREN
ALGLUCOSIDASE ALFA vs ALISKIREN HEMIFUMARATE
ALGLUCOSIDASE ALFA vs ALISKIREN\HYDROCHLOROTHIAZIDE