Does DEXMEDETOMIDINE Cause Wrong product administered? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Wrong product administered have been filed in association with DEXMEDETOMIDINE (Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride). This represents 0.6% of all adverse event reports for DEXMEDETOMIDINE.
20
Reports of Wrong product administered with DEXMEDETOMIDINE
0.6%
of all DEXMEDETOMIDINE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Wrong product administered From DEXMEDETOMIDINE?
Of the 20 reports, 5 (25.0%) required hospitalization, and 5 (25.0%) 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 DEXMEDETOMIDINE. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does DEXMEDETOMIDINE Cause?
Bradycardia (363)
Off label use (355)
Drug ineffective (272)
Hypotension (229)
Cardiac arrest (191)
Agitation (132)
Product use in unapproved indication (115)
Diabetes insipidus (110)
Delirium (109)
Product use issue (102)
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 DEXMEDETOMIDINE Alternatives Have Lower Wrong product administered Risk?
DEXMEDETOMIDINE vs DEXMETHYLPHENIDATE
DEXMEDETOMIDINE vs DEXMETHYLPHENIDATE\SERDEXMETHYLPHENIDATE
DEXMEDETOMIDINE vs DEXPANTHENOL
DEXMEDETOMIDINE vs DEXRAZOXANE
DEXMEDETOMIDINE vs DEXTRAN 70\HYPROMELLOSE 2910