Does ADALIMUMAB-RYVK Cause Inappropriate schedule of product administration? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Inappropriate schedule of product administration have been filed in association with ADALIMUMAB-RYVK (Simlandi). This represents 12.3% of all adverse event reports for ADALIMUMAB-RYVK.
57
Reports of Inappropriate schedule of product administration with ADALIMUMAB-RYVK
12.3%
of all ADALIMUMAB-RYVK reports
8
Deaths
19
Hospitalizations
How Dangerous Is Inappropriate schedule of product administration From ADALIMUMAB-RYVK?
Of the 57 reports, 8 (14.0%) resulted in death, 19 (33.3%) 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 ADALIMUMAB-RYVK. However, 57 reports have been filed with the FAERS database.
What Other Side Effects Does ADALIMUMAB-RYVK Cause?
Off label use (70)
Product dose omission issue (67)
Crohn's disease (65)
Rheumatoid arthritis (47)
Death (45)
Diarrhoea (43)
Arthralgia (42)
Pain (42)
Fatigue (39)
Drug ineffective (38)
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 ADALIMUMAB-RYVK Alternatives Have Lower Inappropriate schedule of product administration Risk?
ADALIMUMAB-RYVK vs ADALIMUMAB\ISOPROPYL ALCOHOL
ADALIMUMAB-RYVK vs ADAPALENE
ADALIMUMAB-RYVK vs ADAPALENE\BENZOYL PEROXIDE
ADALIMUMAB-RYVK vs ADCETRIS
ADALIMUMAB-RYVK vs ADDERALL