Does SACUBITRIL\VALSARTAN Cause Type v hyperlipidaemia? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Type v hyperlipidaemia have been filed in association with SACUBITRIL\VALSARTAN. This represents 0.0% of all adverse event reports for SACUBITRIL\VALSARTAN.
25
Reports of Type v hyperlipidaemia with SACUBITRIL\VALSARTAN
0.0%
of all SACUBITRIL\VALSARTAN reports
0
Deaths
4
Hospitalizations
How Dangerous Is Type v hyperlipidaemia From SACUBITRIL\VALSARTAN?
Of the 25 reports, 4 (16.0%) required hospitalization.
Is Type v hyperlipidaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SACUBITRIL\VALSARTAN. However, 25 reports have been filed with the FAERS database.
What Other Side Effects Does SACUBITRIL\VALSARTAN Cause?
Hypotension (11,718)
Death (9,605)
Dyspnoea (8,952)
Dizziness (8,548)
Fatigue (8,172)
Wrong technique in product usage process (8,022)
Cough (7,743)
Weight decreased (5,030)
Cardiac failure (4,504)
Malaise (4,299)
What Other Drugs Cause Type v hyperlipidaemia?
ASPIRIN (24)
CARVEDILOL (23)
ATORVASTATIN (22)
RAMIPRIL (22)
ALENDRONATE (21)
DAPAGLIFLOZIN (21)
ALLOPURINOL (19)
EPLERENONE (19)
EZETIMIBE (19)
METFORMIN (19)
Which SACUBITRIL\VALSARTAN Alternatives Have Lower Type v hyperlipidaemia Risk?
SACUBITRIL\VALSARTAN vs SAFINAMIDE
SACUBITRIL\VALSARTAN vs SAIZEN
SACUBITRIL\VALSARTAN vs SALICYLATE
SACUBITRIL\VALSARTAN vs SALICYLIC ACID
SACUBITRIL\VALSARTAN vs SALMETEROL