Does ADALIMUMAB-RYVK Cause Condition aggravated? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Condition aggravated have been filed in association with ADALIMUMAB-RYVK (Simlandi). This represents 2.2% of all adverse event reports for ADALIMUMAB-RYVK.
10
Reports of Condition aggravated with ADALIMUMAB-RYVK
2.2%
of all ADALIMUMAB-RYVK reports
0
Deaths
3
Hospitalizations
How Dangerous Is Condition aggravated From ADALIMUMAB-RYVK?
Of the 10 reports, 3 (30.0%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ADALIMUMAB-RYVK. However, 10 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which ADALIMUMAB-RYVK Alternatives Have Lower Condition aggravated 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