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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 UNSPECIFIED INGREDIENT Cause Hypersensitivity? 324 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 324 reports of Hypersensitivity have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.2% of all adverse event reports for UNSPECIFIED INGREDIENT.

324
Reports of Hypersensitivity with UNSPECIFIED INGREDIENT
1.2%
of all UNSPECIFIED INGREDIENT reports
78
Deaths
132
Hospitalizations

How Dangerous Is Hypersensitivity From UNSPECIFIED INGREDIENT?

Of the 324 reports, 78 (24.1%) resulted in death, 132 (40.7%) required hospitalization, and 72 (22.2%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 324 reports have been filed with the FAERS database.

What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?

Death (2,090) Off label use (1,306) Drug ineffective (1,227) Completed suicide (1,190) Nausea (1,041) Fatigue (1,020) Dyspnoea (934) Pneumonia (903) Asthenia (894) Vomiting (877)

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 UNSPECIFIED INGREDIENT Alternatives Have Lower Hypersensitivity Risk?

UNSPECIFIED INGREDIENT vs UPADACITINIB UNSPECIFIED INGREDIENT vs URAPIDIL UNSPECIFIED INGREDIENT vs UREA UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE UNSPECIFIED INGREDIENT vs UROFOLLITROPIN

Related Pages

UNSPECIFIED INGREDIENT Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity UNSPECIFIED INGREDIENT Demographics