Does VALSARTAN Cause Recalled product administered? 267 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 267 reports of Recalled product administered have been filed in association with VALSARTAN (valsartan). This represents 1.2% of all adverse event reports for VALSARTAN.
267
Reports of Recalled product administered with VALSARTAN
1.2%
of all VALSARTAN reports
12
Deaths
35
Hospitalizations
How Dangerous Is Recalled product administered From VALSARTAN?
Of the 267 reports, 12 (4.5%) resulted in death, 35 (13.1%) required hospitalization, and 8 (3.0%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VALSARTAN. However, 267 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 administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
LOSARTAN (141)
Which VALSARTAN Alternatives Have Lower Recalled product administered Risk?
VALSARTAN vs VALTREX
VALSARTAN vs VAMOROLONE
VALSARTAN vs VANCOMYCIN
VALSARTAN vs VANDETANIB
VALSARTAN vs VARDENAFIL