Does ZILUCOPLAN Cause Intentional dose omission? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Intentional dose omission have been filed in association with ZILUCOPLAN (ZILBRYSQ). This represents 3.0% of all adverse event reports for ZILUCOPLAN.
13
Reports of Intentional dose omission with ZILUCOPLAN
3.0%
of all ZILUCOPLAN reports
0
Deaths
10
Hospitalizations
How Dangerous Is Intentional dose omission From ZILUCOPLAN?
Of the 13 reports, 10 (76.9%) required hospitalization, and 3 (23.1%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZILUCOPLAN. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does ZILUCOPLAN Cause?
Myasthenia gravis (184)
Drug ineffective (94)
Injection site pain (56)
Product dose omission issue (55)
Fatigue (36)
Hospitalisation (23)
Weight increased (22)
Dyspnoea (21)
Diarrhoea (20)
Pneumonia (20)
What Other Drugs Cause Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which ZILUCOPLAN Alternatives Have Lower Intentional dose omission Risk?
ZILUCOPLAN vs ZIMBERELIMAB
ZILUCOPLAN vs ZINC
ZILUCOPLAN vs ZINC\ZINC
ZILUCOPLAN vs ZIPRASIDONE
ZILUCOPLAN vs ZIPRASIDONE\ZIPRASIDONE