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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ABROCITINIB Cause Condition aggravated? 316 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 316 reports of Condition aggravated have been filed in association with ABROCITINIB (CIBINQO). This represents 10.0% of all adverse event reports for ABROCITINIB.

316
Reports of Condition aggravated with ABROCITINIB
10.0%
of all ABROCITINIB reports
0
Deaths
18
Hospitalizations

How Dangerous Is Condition aggravated From ABROCITINIB?

Of the 316 reports, 18 (5.7%) required hospitalization, and 3 (0.9%) 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 ABROCITINIB. However, 316 reports have been filed with the FAERS database.

What Other Side Effects Does ABROCITINIB Cause?

Drug ineffective (398) Off label use (269) Therapeutic product effect incomplete (186) Pruritus (171) Rash (134) Nausea (130) Dermatitis atopic (110) Headache (85) Acne (73) Fatigue (70)

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 ABROCITINIB Alternatives Have Lower Condition aggravated Risk?

ABROCITINIB vs ACALABRUTINIB ABROCITINIB vs ACAMPROSATE ABROCITINIB vs ACARBOSE ABROCITINIB vs ACCUTANE ABROCITINIB vs ACEBUTOLOL

Related Pages

ABROCITINIB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated ABROCITINIB Demographics