Does SACUBITRIL\VALSARTAN Cause Condition aggravated? 684 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 684 reports of Condition aggravated have been filed in association with SACUBITRIL\VALSARTAN. This represents 0.6% of all adverse event reports for SACUBITRIL\VALSARTAN.
684
Reports of Condition aggravated with SACUBITRIL\VALSARTAN
0.6%
of all SACUBITRIL\VALSARTAN reports
59
Deaths
301
Hospitalizations
How Dangerous Is Condition aggravated From SACUBITRIL\VALSARTAN?
Of the 684 reports, 59 (8.6%) resulted in death, 301 (44.0%) required hospitalization, and 50 (7.3%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SACUBITRIL\VALSARTAN. However, 684 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which SACUBITRIL\VALSARTAN Alternatives Have Lower Condition aggravated Risk?
SACUBITRIL\VALSARTAN vs SAFINAMIDE
SACUBITRIL\VALSARTAN vs SAIZEN
SACUBITRIL\VALSARTAN vs SALICYLATE
SACUBITRIL\VALSARTAN vs SALICYLIC ACID
SACUBITRIL\VALSARTAN vs SALMETEROL