Does DORNASE ALFA Cause Product storage error? 242 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 242 reports of Product storage error have been filed in association with DORNASE ALFA (Pulmozyme). This represents 4.5% of all adverse event reports for DORNASE ALFA.
242
Reports of Product storage error with DORNASE ALFA
4.5%
of all DORNASE ALFA reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product storage error From DORNASE ALFA?
Of the 242 reports, 1 (0.4%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DORNASE ALFA. However, 242 reports have been filed with the FAERS database.
What Other Side Effects Does DORNASE ALFA Cause?
No adverse event (889)
Cystic fibrosis (565)
Off label use (522)
Hospitalisation (512)
Pneumonia (377)
Condition aggravated (304)
Dyspnoea (246)
Infective pulmonary exacerbation of cystic fibrosis (245)
Death (225)
Cough (195)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which DORNASE ALFA Alternatives Have Lower Product storage error Risk?
DORNASE ALFA vs DORZOLAMIDE
DORNASE ALFA vs DORZOLAMIDE\TIMOLOL
DORNASE ALFA vs DOSTARLIMAB
DORNASE ALFA vs DOSTARLIMAB-GXLY
DORNASE ALFA vs DOTATATE GALLIUM GA-68