Does EFGARTIGIMOD ALFA Cause Intentional dose omission? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Intentional dose omission have been filed in association with EFGARTIGIMOD ALFA (VYVGART). This represents 2.4% of all adverse event reports for EFGARTIGIMOD ALFA.
6
Reports of Intentional dose omission with EFGARTIGIMOD ALFA
2.4%
of all EFGARTIGIMOD ALFA reports
1
Deaths
2
Hospitalizations
How Dangerous Is Intentional dose omission From EFGARTIGIMOD ALFA?
Of the 6 reports, 1 (16.7%) resulted in death, 2 (33.3%) required hospitalization.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EFGARTIGIMOD ALFA. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does EFGARTIGIMOD ALFA Cause?
Myasthenia gravis (46)
Off label use (39)
Drug ineffective (25)
Myasthenia gravis crisis (25)
Fatigue (22)
Pneumonia (20)
Muscular weakness (17)
Urinary tract infection (17)
Malaise (14)
Covid-19 (13)
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 EFGARTIGIMOD ALFA Alternatives Have Lower Intentional dose omission Risk?
EFGARTIGIMOD ALFA vs EFGARTIGIMOD ALFA-FCAB
EFGARTIGIMOD ALFA vs EFGARTIGIMOD ALFA\HYALURONIDASE-QVFC
EFGARTIGIMOD ALFA vs EFINACONAZOLE
EFGARTIGIMOD ALFA vs EFLORNITHINE
EFGARTIGIMOD ALFA vs EFMOROCTOCOG ALFA