Does ADALIMUMAB-RYVK Cause Product administration error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product administration error have been filed in association with ADALIMUMAB-RYVK (Simlandi). This represents 1.5% of all adverse event reports for ADALIMUMAB-RYVK.
7
Reports of Product administration error with ADALIMUMAB-RYVK
1.5%
of all ADALIMUMAB-RYVK reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From ADALIMUMAB-RYVK?
Of the 7 reports, 2 (28.6%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ADALIMUMAB-RYVK. However, 7 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)
Inappropriate schedule of product administration (57)
Rheumatoid arthritis (47)
Death (45)
Diarrhoea (43)
Arthralgia (42)
Pain (42)
Fatigue (39)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which ADALIMUMAB-RYVK Alternatives Have Lower Product administration error 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