Does NOREPINEPHRINE Cause Intentional product use issue? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Intentional product use issue have been filed in association with NOREPINEPHRINE (NOREPINEPHRINE BITARTRATE). This represents 0.1% of all adverse event reports for NOREPINEPHRINE.
6
Reports of Intentional product use issue with NOREPINEPHRINE
0.1%
of all NOREPINEPHRINE reports
2
Deaths
3
Hospitalizations
How Dangerous Is Intentional product use issue From NOREPINEPHRINE?
Of the 6 reports, 2 (33.3%) resulted in death, 3 (50.0%) required hospitalization, and 5 (83.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NOREPINEPHRINE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does NOREPINEPHRINE Cause?
Drug ineffective (1,915)
Hypotension (595)
Off label use (577)
Condition aggravated (439)
Multiple organ dysfunction syndrome (417)
Cardiogenic shock (381)
Toxicity to various agents (381)
Sepsis (280)
Acute kidney injury (273)
General physical health deterioration (266)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which NOREPINEPHRINE Alternatives Have Lower Intentional product use issue Risk?
NOREPINEPHRINE vs NOREPINEPHRINE\NOREPINEPHRINE
NOREPINEPHRINE vs NORETHINDRONE
NOREPINEPHRINE vs NORFLOXACIN
NOREPINEPHRINE vs NORGESTREL
NOREPINEPHRINE vs NORTRIPTYLINE