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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 ETHYLENEDIAMINE Cause Off label use? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Off label use have been filed in association with ETHYLENEDIAMINE. This represents 46.7% of all adverse event reports for ETHYLENEDIAMINE.

21
Reports of Off label use with ETHYLENEDIAMINE
46.7%
of all ETHYLENEDIAMINE reports
12
Deaths
20
Hospitalizations

How Dangerous Is Off label use From ETHYLENEDIAMINE?

Of the 21 reports, 12 (57.1%) resulted in death, 20 (95.2%) required hospitalization, and 12 (57.1%) were considered life-threatening.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ETHYLENEDIAMINE. However, 21 reports have been filed with the FAERS database.

What Other Side Effects Does ETHYLENEDIAMINE Cause?

Drug hypersensitivity (37) Drug ineffective (32) Drug intolerance (32) Condition aggravated (31) Hepatotoxicity (31) Musculoskeletal stiffness (31) Pain in extremity (31) Arthralgia (30) Infection (30) Joint swelling (30)

What Other Drugs Cause Off label use?

RITUXIMAB (39,751) INFLIXIMAB (34,801) DENOSUMAB (34,612) METHOTREXATE (24,020) VEDOLIZUMAB (21,017) ETANERCEPT (20,178) TOCILIZUMAB (18,256) PREDNISONE (17,867) LENALIDOMIDE (17,017) ADALIMUMAB (16,417)

Related Pages

ETHYLENEDIAMINE Full Profile All Off label use Reports All Drugs Causing Off label use ETHYLENEDIAMINE Demographics