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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 Product administration interrupted? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product administration interrupted have been filed in association with NITRIC (Ulspira). This represents 0.2% of all adverse event reports for NITRIC.

7
Reports of Product administration interrupted with NITRIC
0.2%
of all NITRIC reports
1
Deaths
1
Hospitalizations

How Dangerous Is Product administration interrupted From NITRIC?

Of the 7 reports, 1 (14.3%) resulted in death, 1 (14.3%) required hospitalization, and 1 (14.3%) were considered life-threatening.

Is Product administration interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NITRIC. However, 7 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 Product administration interrupted?

CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446) SODIUM OXYBATE (1,272) CANNABIDIOL (511) ISOTRETINOIN (503) APREMILAST (314) TREPROSTINIL (295) EPOPROSTENOL (205) LENALIDOMIDE (146) ETANERCEPT (142) INTERFERON BETA-1A (115)

Which NITRIC Alternatives Have Lower Product administration interrupted Risk?

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

Related Pages

NITRIC Full Profile All Product administration interrupted Reports All Drugs Causing Product administration interrupted NITRIC Demographics