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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DEXTROSE\NIKETHAMIDE Cause Product administration error? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with DEXTROSE\NIKETHAMIDE. This represents 16.7% of all adverse event reports for DEXTROSE\NIKETHAMIDE.

5
Reports of Product administration error with DEXTROSE\NIKETHAMIDE
16.7%
of all DEXTROSE\NIKETHAMIDE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product administration error From DEXTROSE\NIKETHAMIDE?

Of the 5 reports, 5 (100.0%) required hospitalization.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEXTROSE\NIKETHAMIDE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does DEXTROSE\NIKETHAMIDE Cause?

Fall (27) Osteoporosis (27) Hypotension (25) Hypoglycaemia (22) Hyponatraemia (22) Dementia (21) Mobility decreased (21) Cognitive disorder (20) Abdominal pain upper (19) Dizziness (19)

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)

Related Pages

DEXTROSE\NIKETHAMIDE Full Profile All Product administration error Reports All Drugs Causing Product administration error DEXTROSE\NIKETHAMIDE Demographics