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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 Dyskinesia? 62 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 62 reports of Dyskinesia have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.2% of all adverse event reports for UNSPECIFIED INGREDIENT.

62
Reports of Dyskinesia with UNSPECIFIED INGREDIENT
0.2%
of all UNSPECIFIED INGREDIENT reports
7
Deaths
24
Hospitalizations

How Dangerous Is Dyskinesia From UNSPECIFIED INGREDIENT?

Of the 62 reports, 7 (11.3%) resulted in death, 24 (38.7%) required hospitalization.

Is Dyskinesia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 62 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 Dyskinesia?

CARBIDOPA\LEVODOPA (5,368) QUETIAPINE (1,529) ARIPIPRAZOLE (1,496) RISPERIDONE (1,363) OLANZAPINE (1,060) CLOZAPINE (890) PALIPERIDONE (794) LURASIDONE (791) VALBENAZINE (772) SERTRALINE (597)

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