Does NITRIC Cause Product use in unapproved indication? 190 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 190 reports of Product use in unapproved indication have been filed in association with NITRIC (Ulspira). This represents 6.2% of all adverse event reports for NITRIC.
190
Reports of Product use in unapproved indication with NITRIC
6.2%
of all NITRIC reports
119
Deaths
12
Hospitalizations
How Dangerous Is Product use in unapproved indication From NITRIC?
Of the 190 reports, 119 (62.6%) resulted in death, 12 (6.3%) required hospitalization, and 14 (7.4%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NITRIC. However, 190 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)
Oxygen saturation decreased (169)
Off label use (166)
Condition aggravated (122)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which NITRIC Alternatives Have Lower Product use in unapproved indication Risk?
NITRIC vs NITROFURANTOIN
NITRIC vs NITROFURANTOIN\NITROFURANTOIN
NITRIC vs NITROFURAZONE
NITRIC vs NITROGLYCERIN
NITRIC vs NITROUS