Does NITRIC Cause Device power source issue? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Device power source issue have been filed in association with NITRIC (Ulspira). This represents 0.3% of all adverse event reports for NITRIC.
8
Reports of Device power source issue with NITRIC
0.3%
of all NITRIC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device power source issue From NITRIC?
Of the 8 reports.
Is Device power source issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NITRIC. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does NITRIC Cause?
No adverse event (771)
Device malfunction (553)
Device issue (424)
Underdose (398)
Product use issue (332)
Death (314)
Drug ineffective (192)
Product use in unapproved indication (190)
Oxygen saturation decreased (169)
Off label use (166)
What Other Drugs Cause Device power source issue?
SOMATROPIN (1,219)
PEGFILGRASTIM (486)
TREPROSTINIL (299)
CARBIDOPA\LEVODOPA (62)
ETANERCEPT (54)
BACLOFEN (50)
GLYCOPYRROLATE (39)
DEVICE (20)
FOSCARBIDOPA\FOSLEVODOPA (14)
INTERFERON BETA-1B (13)
Which NITRIC Alternatives Have Lower Device power source issue Risk?
NITRIC vs NITROFURANTOIN
NITRIC vs NITROFURANTOIN\NITROFURANTOIN
NITRIC vs NITROFURAZONE
NITRIC vs NITROGLYCERIN
NITRIC vs NITROUS