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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 issue? 424 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 424 reports of Device issue have been filed in association with NITRIC (Ulspira). This represents 13.8% of all adverse event reports for NITRIC.

424
Reports of Device issue with NITRIC
13.8%
of all NITRIC reports
21
Deaths
0
Hospitalizations

How Dangerous Is Device issue From NITRIC?

Of the 424 reports, 21 (5.0%) resulted in death, and 11 (2.6%) were considered life-threatening.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NITRIC. However, 424 reports have been filed with the FAERS database.

What Other Side Effects Does NITRIC Cause?

No adverse event (771) Device malfunction (553) 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) Condition aggravated (122)

What Other Drugs Cause Device issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Which NITRIC Alternatives Have Lower Device issue Risk?

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

Related Pages

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