Does ANIFROLUMAB Cause Inappropriate schedule of product administration? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Inappropriate schedule of product administration have been filed in association with ANIFROLUMAB (SAPHNELO). This represents 3.8% of all adverse event reports for ANIFROLUMAB.
14
Reports of Inappropriate schedule of product administration with ANIFROLUMAB
3.8%
of all ANIFROLUMAB reports
0
Deaths
4
Hospitalizations
How Dangerous Is Inappropriate schedule of product administration From ANIFROLUMAB?
Of the 14 reports, 4 (28.6%) required hospitalization.
Is Inappropriate schedule of product administration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ANIFROLUMAB. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does ANIFROLUMAB Cause?
Off label use (33)
Systemic lupus erythematosus (31)
Drug ineffective (26)
Fatigue (19)
Arthralgia (18)
Pyrexia (18)
Covid-19 (17)
Cough (16)
Headache (16)
Lupus nephritis (16)
What Other Drugs Cause Inappropriate schedule of product administration?
ADAPALENE (16,473)
DUPILUMAB (14,927)
AVOBENZONE\OCTISALATE\OCTOCRYLENE (12,546)
INSULIN GLARGINE (8,982)
INFLIXIMAB (6,847)
INFLIXIMAB-DYYB (5,977)
SECUKINUMAB (4,817)
DULAGLUTIDE (3,606)
VEDOLIZUMAB (3,259)
SACUBITRIL\VALSARTAN (2,870)
Which ANIFROLUMAB Alternatives Have Lower Inappropriate schedule of product administration Risk?
ANIFROLUMAB vs ANIFROLUMAB-FNIA
ANIFROLUMAB vs ANIFROLUMAB\ANIFROLUMAB-FNIA
ANIFROLUMAB vs ANTHOXANTHUM ODORATUM POLLEN\DACTYLIS GLOMERATA POLLEN\LOLIUM PERENNE POLLEN\PHLEUM PRATENSE POLLEN\POA PRATENSIS POLLEN
ANIFROLUMAB vs ANTI-INHIBITOR COAGULANT COMPLEX
ANIFROLUMAB vs ANTIHEMOPHILIC FACTOR HUMAN