Does ZILUCOPLAN Cause Wrong technique in product usage process? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Wrong technique in product usage process have been filed in association with ZILUCOPLAN (ZILBRYSQ). This represents 3.6% of all adverse event reports for ZILUCOPLAN.
16
Reports of Wrong technique in product usage process with ZILUCOPLAN
3.6%
of all ZILUCOPLAN reports
1
Deaths
6
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ZILUCOPLAN?
Of the 16 reports, 1 (6.3%) resulted in death, 6 (37.5%) required hospitalization, and 1 (6.3%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZILUCOPLAN. However, 16 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ZILUCOPLAN Alternatives Have Lower Wrong technique in product usage process Risk?
ZILUCOPLAN vs ZIMBERELIMAB
ZILUCOPLAN vs ZINC
ZILUCOPLAN vs ZINC\ZINC
ZILUCOPLAN vs ZIPRASIDONE
ZILUCOPLAN vs ZIPRASIDONE\ZIPRASIDONE