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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 Dyspepsia? 221 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 221 reports of Dyspepsia have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.8% of all adverse event reports for UNSPECIFIED INGREDIENT.

221
Reports of Dyspepsia with UNSPECIFIED INGREDIENT
0.8%
of all UNSPECIFIED INGREDIENT reports
66
Deaths
115
Hospitalizations

How Dangerous Is Dyspepsia From UNSPECIFIED INGREDIENT?

Of the 221 reports, 66 (29.9%) resulted in death, 115 (52.0%) required hospitalization, and 69 (31.2%) were considered life-threatening.

Is Dyspepsia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 221 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 Dyspepsia?

ADALIMUMAB (3,586) METHOTREXATE (2,690) RITUXIMAB (2,289) TOFACITINIB (2,264) PREDNISONE (2,224) APREMILAST (2,207) ETANERCEPT (2,100) ESOMEPRAZOLE (2,064) TOCILIZUMAB (2,046) LEFLUNOMIDE (1,981)

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