Does UNSPECIFIED INGREDIENT Cause Hyperlipidaemia? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Hyperlipidaemia have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.2% of all adverse event reports for UNSPECIFIED INGREDIENT.
45
Reports of Hyperlipidaemia with UNSPECIFIED INGREDIENT
0.2%
of all UNSPECIFIED INGREDIENT reports
35
Deaths
34
Hospitalizations
How Dangerous Is Hyperlipidaemia From UNSPECIFIED INGREDIENT?
Of the 45 reports, 35 (77.8%) resulted in death, 34 (75.6%) required hospitalization, and 28 (62.2%) were considered life-threatening.
Is Hyperlipidaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 45 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 Hyperlipidaemia?
ALENDRONATE (511)
AMLODIPINE (226)
DENOSUMAB (204)
SITAGLIPTIN (186)
METHOTREXATE (184)
ROSUVASTATIN (179)
PREDNISONE (169)
FINASTERIDE (145)
MYCOPHENOLATE MOFETIL (141)
ASPIRIN (138)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Hyperlipidaemia Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN