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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 Injury associated with device? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Injury associated with device have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.0% of all adverse event reports for UNSPECIFIED INGREDIENT.

8
Reports of Injury associated with device with UNSPECIFIED INGREDIENT
0.0%
of all UNSPECIFIED INGREDIENT reports
0
Deaths
4
Hospitalizations

How Dangerous Is Injury associated with device From UNSPECIFIED INGREDIENT?

Of the 8 reports, 4 (50.0%) required hospitalization, and 1 (12.5%) were considered life-threatening.

Is Injury associated with device Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 8 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 Injury associated with device?

COPPER (2,895) ADALIMUMAB (2,003) EVOLOCUMAB (1,326) INSULIN GLARGINE (849) INSULIN LISPRO (840) TIRZEPATIDE (836) ETANERCEPT (743) ERENUMAB-AOOE (528) DULAGLUTIDE (482) ENOXAPARIN (458)

Which UNSPECIFIED INGREDIENT Alternatives Have Lower Injury associated with device 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 Injury associated with device Reports All Drugs Causing Injury associated with device UNSPECIFIED INGREDIENT Demographics