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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 NITRIC Cause Device failure? 112 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 112 reports of Device failure have been filed in association with NITRIC (Ulspira). This represents 3.7% of all adverse event reports for NITRIC.

112
Reports of Device failure with NITRIC
3.7%
of all NITRIC reports
8
Deaths
0
Hospitalizations

How Dangerous Is Device failure From NITRIC?

Of the 112 reports, 8 (7.1%) resulted in death, and 3 (2.7%) were considered life-threatening.

Is Device failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NITRIC. However, 112 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 failure?

EPINEPHRINE (1,344) SOMATROPIN (1,141) PEGFILGRASTIM (829) TREPROSTINIL (713) BACLOFEN (691) BUDESONIDE\FORMOTEROL (686) ETANERCEPT (576) GOLIMUMAB (487) LEVONORGESTREL (332) ACLIDINIUM (304)

Which NITRIC Alternatives Have Lower Device failure Risk?

NITRIC vs NITROFURANTOIN NITRIC vs NITROFURANTOIN\NITROFURANTOIN NITRIC vs NITROFURAZONE NITRIC vs NITROGLYCERIN NITRIC vs NITROUS

Related Pages

NITRIC Full Profile All Device failure Reports All Drugs Causing Device failure NITRIC Demographics