Does UNSPECIFIED INGREDIENT Cause Hypercholesterolaemia? 97 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 97 reports of Hypercholesterolaemia have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.4% of all adverse event reports for UNSPECIFIED INGREDIENT.
97
Reports of Hypercholesterolaemia with UNSPECIFIED INGREDIENT
0.4%
of all UNSPECIFIED INGREDIENT reports
76
Deaths
75
Hospitalizations
How Dangerous Is Hypercholesterolaemia From UNSPECIFIED INGREDIENT?
Of the 97 reports, 76 (78.4%) resulted in death, 75 (77.3%) required hospitalization, and 66 (68.0%) were considered life-threatening.
Is Hypercholesterolaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 97 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 Hypercholesterolaemia?
ALENDRONATE (1,607)
METHOTREXATE (1,547)
TOCILIZUMAB (1,483)
ADALIMUMAB (1,479)
ABATACEPT (1,410)
RITUXIMAB (1,389)
PREDNISONE (1,377)
INFLIXIMAB (1,338)
DICLOFENAC (1,331)
LEFLUNOMIDE (1,322)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Hypercholesterolaemia Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN