Does TILDRAKIZUMAB-ASMN Cause Condition aggravated? 63 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Condition aggravated have been filed in association with TILDRAKIZUMAB-ASMN. This represents 3.9% of all adverse event reports for TILDRAKIZUMAB-ASMN.
63
Reports of Condition aggravated with TILDRAKIZUMAB-ASMN
3.9%
of all TILDRAKIZUMAB-ASMN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Condition aggravated From TILDRAKIZUMAB-ASMN?
Of the 63 reports, 2 (3.2%) required hospitalization, and 1 (1.6%) 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 TILDRAKIZUMAB-ASMN. However, 63 reports have been filed with the FAERS database.
What Other Side Effects Does TILDRAKIZUMAB-ASMN Cause?
Product dose omission issue (363)
Drug ineffective (223)
Psoriasis (86)
Death (84)
Product storage error (74)
Self-medication (74)
Off label use (66)
Rash (54)
Pruritus (52)
Therapy cessation (50)
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 TILDRAKIZUMAB-ASMN Alternatives Have Lower Condition aggravated Risk?
TILDRAKIZUMAB-ASMN vs TILIDINE
TILDRAKIZUMAB-ASMN vs TIMOLOL
TILDRAKIZUMAB-ASMN vs TIMOLOL\TRAVOPROST
TILDRAKIZUMAB-ASMN vs TINIDAZOLE
TILDRAKIZUMAB-ASMN vs TINZAPARIN