Does NOREPINEPHRINE Cause Product preparation error? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product preparation error have been filed in association with NOREPINEPHRINE (NOREPINEPHRINE BITARTRATE). This represents 0.2% of all adverse event reports for NOREPINEPHRINE.
8
Reports of Product preparation error with NOREPINEPHRINE
0.2%
of all NOREPINEPHRINE reports
1
Deaths
2
Hospitalizations
How Dangerous Is Product preparation error From NOREPINEPHRINE?
Of the 8 reports, 1 (12.5%) resulted in death, 2 (25.0%) required hospitalization, and 3 (37.5%) were considered life-threatening.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NOREPINEPHRINE. However, 8 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 preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which NOREPINEPHRINE Alternatives Have Lower Product preparation error Risk?
NOREPINEPHRINE vs NOREPINEPHRINE\NOREPINEPHRINE
NOREPINEPHRINE vs NORETHINDRONE
NOREPINEPHRINE vs NORFLOXACIN
NOREPINEPHRINE vs NORGESTREL
NOREPINEPHRINE vs NORTRIPTYLINE