Does VITAMIN D NOS Cause Recalled product? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Recalled product have been filed in association with VITAMIN D NOS. This represents 0.3% of all adverse event reports for VITAMIN D NOS.
7
Reports of Recalled product with VITAMIN D NOS
0.3%
of all VITAMIN D NOS reports
0
Deaths
3
Hospitalizations
How Dangerous Is Recalled product From VITAMIN D NOS?
Of the 7 reports, 3 (42.9%) required hospitalization.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VITAMIN D NOS. However, 7 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 Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which VITAMIN D NOS Alternatives Have Lower Recalled product 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