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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 ETONOGESTREL Cause Hypersensitivity? 157 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 157 reports of Hypersensitivity have been filed in association with ETONOGESTREL (Nexplanon). This represents 0.4% of all adverse event reports for ETONOGESTREL.

157
Reports of Hypersensitivity with ETONOGESTREL
0.4%
of all ETONOGESTREL reports
0
Deaths
13
Hospitalizations

How Dangerous Is Hypersensitivity From ETONOGESTREL?

Of the 157 reports, 13 (8.3%) required hospitalization, and 4 (2.5%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for ETONOGESTREL.

What Other Side Effects Does ETONOGESTREL Cause?

No adverse event (8,827) Complication associated with device (6,047) Product quality issue (4,651) Device breakage (4,140) Incorrect product administration duration (3,974) Device difficult to use (3,799) Unintended pregnancy (3,707) Device deployment issue (3,621) Pregnancy with implant contraceptive (3,587) Complication of device removal (3,578)

What Other Drugs Cause Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which ETONOGESTREL Alternatives Have Lower Hypersensitivity Risk?

ETONOGESTREL vs ETOPOSIDE ETONOGESTREL vs ETORICOXIB ETONOGESTREL vs ETRASIMOD ARGININE ETONOGESTREL vs ETRAVIRINE ETONOGESTREL vs EUCALYPTOL\MENTHOL\METHYL SALICYLATE\THYMOL

Related Pages

ETONOGESTREL Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity ETONOGESTREL Demographics