Does NOREPINEPHRINE Cause Product administration interrupted? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product administration interrupted have been filed in association with NOREPINEPHRINE (NOREPINEPHRINE BITARTRATE). This represents 0.2% of all adverse event reports for NOREPINEPHRINE.
11
Reports of Product administration interrupted with NOREPINEPHRINE
0.2%
of all NOREPINEPHRINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration interrupted From NOREPINEPHRINE?
Of the 11 reports, 1 (9.1%) required hospitalization, and 2 (18.2%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NOREPINEPHRINE. However, 11 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 interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which NOREPINEPHRINE Alternatives Have Lower Product administration interrupted Risk?
NOREPINEPHRINE vs NOREPINEPHRINE\NOREPINEPHRINE
NOREPINEPHRINE vs NORETHINDRONE
NOREPINEPHRINE vs NORFLOXACIN
NOREPINEPHRINE vs NORGESTREL
NOREPINEPHRINE vs NORTRIPTYLINE