Does RITLECITINIB Cause Condition aggravated? 85 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 85 reports of Condition aggravated have been filed in association with RITLECITINIB (Litfulo). This represents 5.9% of all adverse event reports for RITLECITINIB.
85
Reports of Condition aggravated with RITLECITINIB
5.9%
of all RITLECITINIB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Condition aggravated From RITLECITINIB?
Of the 85 reports.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITLECITINIB. However, 85 reports have been filed with the FAERS database.
What Other Side Effects Does RITLECITINIB Cause?
Drug ineffective (259)
Therapeutic product effect incomplete (122)
Off label use (82)
Headache (70)
Diarrhoea (49)
Product dose omission issue (45)
Alopecia (44)
Fatigue (36)
Urticaria (36)
Acne (35)
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 RITLECITINIB Alternatives Have Lower Condition aggravated Risk?
RITLECITINIB vs RITODRINE
RITLECITINIB vs RITONAVIR
RITLECITINIB vs RITUXAN
RITLECITINIB vs RITUXIMAB
RITLECITINIB vs RITUXIMAB-ABBS