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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ZINC Cause Product administration error? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product administration error have been filed in association with ZINC (LAURA GELLER X BLISS SHINE - N - SHIELD LIP BALM SPF 15 Sunset Sands). This represents 0.3% of all adverse event reports for ZINC.

7
Reports of Product administration error with ZINC
0.3%
of all ZINC reports
0
Deaths
3
Hospitalizations

How Dangerous Is Product administration error From ZINC?

Of the 7 reports, 3 (42.9%) required hospitalization.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ZINC. However, 7 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 Product administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which ZINC Alternatives Have Lower Product administration error Risk?

ZINC vs ZINC\ZINC ZINC vs ZIPRASIDONE ZINC vs ZIPRASIDONE\ZIPRASIDONE ZINC vs ZITHROMAX ZINC vs ZIV-AFLIBERCEPT

Related Pages

ZINC Full Profile All Product administration error Reports All Drugs Causing Product administration error ZINC Demographics