Does SACUBITRIL\VALSARTAN Cause Device malfunction? 226 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 226 reports of Device malfunction have been filed in association with SACUBITRIL\VALSARTAN. This represents 0.2% of all adverse event reports for SACUBITRIL\VALSARTAN.
226
Reports of Device malfunction with SACUBITRIL\VALSARTAN
0.2%
of all SACUBITRIL\VALSARTAN reports
13
Deaths
114
Hospitalizations
How Dangerous Is Device malfunction From SACUBITRIL\VALSARTAN?
Of the 226 reports, 13 (5.8%) resulted in death, 114 (50.4%) required hospitalization, and 12 (5.3%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SACUBITRIL\VALSARTAN. However, 226 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 Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which SACUBITRIL\VALSARTAN Alternatives Have Lower Device malfunction Risk?
SACUBITRIL\VALSARTAN vs SAFINAMIDE
SACUBITRIL\VALSARTAN vs SAIZEN
SACUBITRIL\VALSARTAN vs SALICYLATE
SACUBITRIL\VALSARTAN vs SALICYLIC ACID
SACUBITRIL\VALSARTAN vs SALMETEROL