Does VITAMIN A Cause Incorrect product administration duration? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Incorrect product administration duration have been filed in association with VITAMIN A (SKINEEZ). This represents 1.6% of all adverse event reports for VITAMIN A.
11
Reports of Incorrect product administration duration with VITAMIN A
1.6%
of all VITAMIN A reports
11
Deaths
11
Hospitalizations
How Dangerous Is Incorrect product administration duration From VITAMIN A?
Of the 11 reports, 11 (100.0%) resulted in death, 11 (100.0%) required hospitalization, and 11 (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 VITAMIN A. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does VITAMIN A Cause?
Off label use (243)
Gastrooesophageal reflux disease (202)
Drug ineffective (181)
Product use in unapproved indication (168)
Swelling (166)
Nausea (161)
Somnolence (156)
Drug hypersensitivity (144)
Pain (143)
Dyspnoea (140)
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 VITAMIN A Alternatives Have Lower Incorrect product administration duration Risk?
VITAMIN A vs VITAMIN B
VITAMIN A vs VITAMIN D NOS
VITAMIN A vs VITAMINS
VITAMIN A vs VOCLOSPORIN
VITAMIN A vs VOGLIBOSE