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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 TILDRAKIZUMAB-ASMN Cause Therapy interrupted? 17 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Therapy interrupted have been filed in association with TILDRAKIZUMAB-ASMN. This represents 1.1% of all adverse event reports for TILDRAKIZUMAB-ASMN.

17
Reports of Therapy interrupted with TILDRAKIZUMAB-ASMN
1.1%
of all TILDRAKIZUMAB-ASMN reports
1
Deaths
0
Hospitalizations

How Dangerous Is Therapy interrupted From TILDRAKIZUMAB-ASMN?

Of the 17 reports, 1 (5.9%) resulted in death.

Is Therapy interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TILDRAKIZUMAB-ASMN. However, 17 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) Condition aggravated (63) Rash (54) Pruritus (52)

What Other Drugs Cause Therapy interrupted?

ADALIMUMAB (5,755) ETANERCEPT (3,397) RELUGOLIX (3,251) CERTOLIZUMAB PEGOL (3,209) LENALIDOMIDE (2,724) UPADACITINIB (1,741) ABATACEPT (1,726) CLOZAPINE (1,722) AMIKACIN (1,283) TOFACITINIB (1,182)

Which TILDRAKIZUMAB-ASMN Alternatives Have Lower Therapy interrupted Risk?

TILDRAKIZUMAB-ASMN vs TILIDINE TILDRAKIZUMAB-ASMN vs TIMOLOL TILDRAKIZUMAB-ASMN vs TIMOLOL\TRAVOPROST TILDRAKIZUMAB-ASMN vs TINIDAZOLE TILDRAKIZUMAB-ASMN vs TINZAPARIN

Related Pages

TILDRAKIZUMAB-ASMN Full Profile All Therapy interrupted Reports All Drugs Causing Therapy interrupted TILDRAKIZUMAB-ASMN Demographics