Does VITAMIN D NOS Cause Incorrect product administration duration? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Incorrect product administration duration have been filed in association with VITAMIN D NOS. This represents 0.4% of all adverse event reports for VITAMIN D NOS.
9
Reports of Incorrect product administration duration with VITAMIN D NOS
0.4%
of all VITAMIN D NOS reports
2
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product administration duration From VITAMIN D NOS?
Of the 9 reports, 2 (22.2%) resulted in death, 2 (22.2%) required hospitalization, and 2 (22.2%) 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 D NOS. However, 9 reports have been filed with the FAERS database.
What Other Side Effects Does VITAMIN D NOS Cause?
Asthma (646)
Dyspnoea (617)
Wheezing (600)
Therapeutic product effect incomplete (495)
Drug ineffective (483)
Pain (377)
Sleep disorder due to a general medical condition (347)
Obstructive airways disorder (309)
Fatigue (304)
Cough (299)
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 D NOS Alternatives Have Lower Incorrect product administration duration Risk?
VITAMIN D NOS vs VITAMINS
VITAMIN D NOS vs VOCLOSPORIN
VITAMIN D NOS vs VOGLIBOSE
VITAMIN D NOS vs VOLTAREN
VITAMIN D NOS vs VON WILLEBRAND FACTOR