Does VALSARTAN Cause Recalled product? 32 Reports in FDA Database
Lower Your Cholesterol — The Natural Way
The Oxidized Cholesterol Strategy: a science-backed plan for heart health.
According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Recalled product have been filed in association with VALSARTAN (valsartan). This represents 0.2% of all adverse event reports for VALSARTAN.
32
Reports of Recalled product with VALSARTAN
0.2%
of all VALSARTAN reports
1
Deaths
7
Hospitalizations
How Dangerous Is Recalled product From VALSARTAN?
Of the 32 reports, 1 (3.1%) resulted in death, 7 (21.9%) required hospitalization, and 5 (15.6%) were considered life-threatening.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VALSARTAN. However, 32 reports have been filed with the FAERS database.
What Other Side Effects Does VALSARTAN Cause?
Drug ineffective (1,845)
Blood pressure increased (1,682)
Dizziness (1,527)
Headache (1,361)
Hypertension (1,341)
Acute kidney injury (1,301)
Dyspnoea (1,239)
Fatigue (1,156)
Malaise (1,139)
Hypotension (1,032)
What Other Drugs Cause Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
LEVOTHYROXINE (24)
Which VALSARTAN Alternatives Have Lower Recalled product Risk?
VALSARTAN vs VALTREX
VALSARTAN vs VAMOROLONE
VALSARTAN vs VANCOMYCIN
VALSARTAN vs VANDETANIB
VALSARTAN vs VARDENAFIL