Does ADALIMUMAB-ATTO Cause Condition aggravated? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Condition aggravated have been filed in association with ADALIMUMAB-ATTO. This represents 1.9% of all adverse event reports for ADALIMUMAB-ATTO.
22
Reports of Condition aggravated with ADALIMUMAB-ATTO
1.9%
of all ADALIMUMAB-ATTO reports
2
Deaths
10
Hospitalizations
How Dangerous Is Condition aggravated From ADALIMUMAB-ATTO?
Of the 22 reports, 2 (9.1%) resulted in death, 10 (45.5%) required hospitalization, and 2 (9.1%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ADALIMUMAB-ATTO. However, 22 reports have been filed with the FAERS database.
What Other Side Effects Does ADALIMUMAB-ATTO Cause?
Device difficult to use (328)
Product storage error (279)
Drug dose omission by device (219)
Circumstance or information capable of leading to medication error (194)
Accidental exposure to product (123)
Injection site pain (100)
Intercepted product administration error (75)
Wrong technique in product usage process (69)
Drug ineffective (48)
Off label use (47)
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-ATTO Alternatives Have Lower Condition aggravated Risk?
ADALIMUMAB-ATTO vs ADALIMUMAB-BWWD
ADALIMUMAB-ATTO vs ADALIMUMAB-FKJP
ADALIMUMAB-ATTO vs ADALIMUMAB-RYVK
ADALIMUMAB-ATTO vs ADALIMUMAB\ISOPROPYL ALCOHOL
ADALIMUMAB-ATTO vs ADAPALENE