Does NOREPINEPHRINE Cause Device use error? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device use error have been filed in association with NOREPINEPHRINE (NOREPINEPHRINE BITARTRATE). This represents 0.1% of all adverse event reports for NOREPINEPHRINE.
5
Reports of Device use error with NOREPINEPHRINE
0.1%
of all NOREPINEPHRINE reports
1
Deaths
0
Hospitalizations
How Dangerous Is Device use error From NOREPINEPHRINE?
Of the 5 reports, 1 (20.0%) resulted in death, and 2 (40.0%) were considered life-threatening.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NOREPINEPHRINE. However, 5 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 Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
Which NOREPINEPHRINE Alternatives Have Lower Device use error Risk?
NOREPINEPHRINE vs NOREPINEPHRINE\NOREPINEPHRINE
NOREPINEPHRINE vs NORETHINDRONE
NOREPINEPHRINE vs NORFLOXACIN
NOREPINEPHRINE vs NORGESTREL
NOREPINEPHRINE vs NORTRIPTYLINE