Does ZINC Cause Incorrect product administration duration? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Incorrect product administration duration have been filed in association with ZINC (LAURA GELLER X BLISS SHINE - N - SHIELD LIP BALM SPF 15 Sunset Sands). This represents 0.7% of all adverse event reports for ZINC.
16
Reports of Incorrect product administration duration with ZINC
0.7%
of all ZINC reports
16
Deaths
16
Hospitalizations
How Dangerous Is Incorrect product administration duration From ZINC?
Of the 16 reports, 16 (100.0%) resulted in death, 16 (100.0%) required hospitalization, and 16 (100.0%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZINC. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does ZINC Cause?
Drug ineffective (605)
Off label use (578)
Macular degeneration (452)
Pain (335)
Malaise (297)
Nausea (296)
Dyspepsia (255)
Infusion related reaction (247)
Therapeutic product effect incomplete (230)
Headache (226)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ZINC Alternatives Have Lower Incorrect product administration duration Risk?
ZINC vs ZINC\ZINC
ZINC vs ZIPRASIDONE
ZINC vs ZIPRASIDONE\ZIPRASIDONE
ZINC vs ZITHROMAX
ZINC vs ZIV-AFLIBERCEPT