Does TOLNAFTATE Cause Recalled product administered? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Recalled product administered have been filed in association with TOLNAFTATE (NATUREPLEX TOLNAFTATE ANTIFUNGAL). This represents 8.4% of all adverse event reports for TOLNAFTATE.
20
Reports of Recalled product administered with TOLNAFTATE
8.4%
of all TOLNAFTATE reports
1
Deaths
5
Hospitalizations
How Dangerous Is Recalled product administered From TOLNAFTATE?
Of the 20 reports, 1 (5.0%) resulted in death, 5 (25.0%) required hospitalization, and 2 (10.0%) 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 TOLNAFTATE. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does TOLNAFTATE Cause?
Drug ineffective (37)
Pain (22)
Mesothelioma (16)
Anxiety (13)
Exposure to chemical pollution (12)
Off label use (12)
Burning sensation (11)
Pruritus (11)
Drug administered at inappropriate site (10)
Erythema (10)
What Other Drugs Cause Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which TOLNAFTATE Alternatives Have Lower Recalled product administered Risk?
TOLNAFTATE vs TOLODODEKIN ALFA
TOLNAFTATE vs TOLTERODINE
TOLNAFTATE vs TOLVAPTAN
TOLNAFTATE vs TOPAMAX
TOLNAFTATE vs TOPIRAMATE