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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 Somnolence? 428 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 428 reports of Somnolence have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.6% of all adverse event reports for UNSPECIFIED INGREDIENT.

428
Reports of Somnolence with UNSPECIFIED INGREDIENT
1.6%
of all UNSPECIFIED INGREDIENT reports
130
Deaths
179
Hospitalizations

How Dangerous Is Somnolence From UNSPECIFIED INGREDIENT?

Of the 428 reports, 130 (30.4%) resulted in death, 179 (41.8%) required hospitalization, and 86 (20.1%) were considered life-threatening.

Is Somnolence Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 428 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 Somnolence?

PREGABALIN (5,528) QUETIAPINE (4,394) ACETAMINOPHEN (3,923) GABAPENTIN (3,798) SODIUM OXYBATE (3,642) CETIRIZINE (3,058) OLANZAPINE (2,612) DIAZEPAM (2,547) RISPERIDONE (2,496) OXYCODONE (2,494)

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