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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 Discomfort? 141 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 141 reports of Discomfort have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.5% of all adverse event reports for UNSPECIFIED INGREDIENT.

141
Reports of Discomfort with UNSPECIFIED INGREDIENT
0.5%
of all UNSPECIFIED INGREDIENT reports
67
Deaths
77
Hospitalizations

How Dangerous Is Discomfort From UNSPECIFIED INGREDIENT?

Of the 141 reports, 67 (47.5%) resulted in death, 77 (54.6%) required hospitalization, and 58 (41.1%) were considered life-threatening.

Is Discomfort Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 141 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 Discomfort?

ADALIMUMAB (6,569) METHOTREXATE (5,760) PREDNISONE (5,288) INFLIXIMAB (5,209) ETANERCEPT (5,185) ABATACEPT (5,180) RITUXIMAB (5,143) DICLOFENAC (5,111) TOCILIZUMAB (5,111) LEFLUNOMIDE (5,037)

Which UNSPECIFIED INGREDIENT Alternatives Have Lower Discomfort 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 Discomfort Reports All Drugs Causing Discomfort UNSPECIFIED INGREDIENT Demographics