Does NOREPINEPHRINE Cause Product administration error? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Product administration error have been filed in association with NOREPINEPHRINE (NOREPINEPHRINE BITARTRATE). This represents 0.5% of all adverse event reports for NOREPINEPHRINE.
24
Reports of Product administration error with NOREPINEPHRINE
0.5%
of all NOREPINEPHRINE reports
3
Deaths
12
Hospitalizations
How Dangerous Is Product administration error From NOREPINEPHRINE?
Of the 24 reports, 3 (12.5%) resulted in death, 12 (50.0%) required hospitalization, and 13 (54.2%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NOREPINEPHRINE. However, 24 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which NOREPINEPHRINE Alternatives Have Lower Product administration error Risk?
NOREPINEPHRINE vs NOREPINEPHRINE\NOREPINEPHRINE
NOREPINEPHRINE vs NORETHINDRONE
NOREPINEPHRINE vs NORFLOXACIN
NOREPINEPHRINE vs NORGESTREL
NOREPINEPHRINE vs NORTRIPTYLINE