Does NOREPINEPHRINE Cause Wrong product administered? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Wrong product administered have been filed in association with NOREPINEPHRINE (NOREPINEPHRINE BITARTRATE). This represents 0.8% of all adverse event reports for NOREPINEPHRINE.
43
Reports of Wrong product administered with NOREPINEPHRINE
0.8%
of all NOREPINEPHRINE reports
5
Deaths
15
Hospitalizations
How Dangerous Is Wrong product administered From NOREPINEPHRINE?
Of the 43 reports, 5 (11.6%) resulted in death, 15 (34.9%) required hospitalization, and 21 (48.8%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NOREPINEPHRINE. However, 43 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which NOREPINEPHRINE Alternatives Have Lower Wrong product administered Risk?
NOREPINEPHRINE vs NOREPINEPHRINE\NOREPINEPHRINE
NOREPINEPHRINE vs NORETHINDRONE
NOREPINEPHRINE vs NORFLOXACIN
NOREPINEPHRINE vs NORGESTREL
NOREPINEPHRINE vs NORTRIPTYLINE