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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 INCOBOTULINUMTOXINA Cause Condition aggravated? 26 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Condition aggravated have been filed in association with INCOBOTULINUMTOXINA. This represents 0.5% of all adverse event reports for INCOBOTULINUMTOXINA.

26
Reports of Condition aggravated with INCOBOTULINUMTOXINA
0.5%
of all INCOBOTULINUMTOXINA reports
2
Deaths
0
Hospitalizations

How Dangerous Is Condition aggravated From INCOBOTULINUMTOXINA?

Of the 26 reports, 2 (7.7%) resulted in death.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for INCOBOTULINUMTOXINA. However, 26 reports have been filed with the FAERS database.

What Other Side Effects Does INCOBOTULINUMTOXINA Cause?

Drug ineffective (1,621) Off label use (1,127) Therapeutic response decreased (598) Injection site pain (300) Product preparation issue (174) Headache (164) Injection site swelling (164) Overdose (152) Pain (145) Eyelid ptosis (122)

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 INCOBOTULINUMTOXINA Alternatives Have Lower Condition aggravated Risk?

INCOBOTULINUMTOXINA vs INDACATEROL INCOBOTULINUMTOXINA vs INDAPAMIDE INCOBOTULINUMTOXINA vs INDAPAMIDE\PERINDOPRIL INCOBOTULINUMTOXINA vs INDAPAMIDE\PERINDOPRIL ARGININE INCOBOTULINUMTOXINA vs INDAPAMIDE\PERINDOPRIL ERBUMINE

Related Pages

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