Does ADALIMUMAB-BWWD 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-BWWD. This represents 1.4% of all adverse event reports for ADALIMUMAB-BWWD.
10
Reports of Condition aggravated with ADALIMUMAB-BWWD
1.4%
of all ADALIMUMAB-BWWD reports
0
Deaths
3
Hospitalizations
How Dangerous Is Condition aggravated From ADALIMUMAB-BWWD?
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-BWWD. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does ADALIMUMAB-BWWD Cause?
Injection site pain (95)
Off label use (64)
Drug ineffective (60)
Fatigue (48)
Arthralgia (46)
Device issue (42)
Rheumatoid arthritis (42)
Product substitution issue (40)
Accidental exposure to product (37)
Exposure via skin contact (34)
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-BWWD Alternatives Have Lower Condition aggravated Risk?
ADALIMUMAB-BWWD vs ADALIMUMAB-FKJP
ADALIMUMAB-BWWD vs ADALIMUMAB-RYVK
ADALIMUMAB-BWWD vs ADALIMUMAB\ISOPROPYL ALCOHOL
ADALIMUMAB-BWWD vs ADAPALENE
ADALIMUMAB-BWWD vs ADAPALENE\BENZOYL PEROXIDE