Does UNSPECIFIED INGREDIENT Cause Hyperprolactinaemia? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Hyperprolactinaemia have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.1% of all adverse event reports for UNSPECIFIED INGREDIENT.
12
Reports of Hyperprolactinaemia with UNSPECIFIED INGREDIENT
0.1%
of all UNSPECIFIED INGREDIENT reports
0
Deaths
0
Hospitalizations
How Dangerous Is Hyperprolactinaemia From UNSPECIFIED INGREDIENT?
Of the 12 reports.
Is Hyperprolactinaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 12 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 Hyperprolactinaemia?
RISPERIDONE (4,124)
PALIPERIDONE (1,427)
OLANZAPINE (520)
ARIPIPRAZOLE (459)
QUETIAPINE (331)
HALOPERIDOL (214)
CLOZAPINE (157)
AMISULPRIDE (135)
SERTRALINE (120)
LITHIUM (76)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Hyperprolactinaemia Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN