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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 Incorrect product administration duration? 5 Reports in FDA Database

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

5
Reports of Incorrect product administration duration with DEXTROSE\NIKETHAMIDE
16.7%
of all DEXTROSE\NIKETHAMIDE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Incorrect product administration duration From DEXTROSE\NIKETHAMIDE?

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

Is Incorrect product administration duration 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 Incorrect product administration duration?

ETONOGESTREL (3,974) POLYETHYLENE GLYCOL 3350 (2,129) NIRMATRELVIR\RITONAVIR (744) DOCOSANOL (634) LANSOPRAZOLE (564) LOPERAMIDE (543) NAPROXEN (499) INSULIN LISPRO (479) DICLOFENAC (362) OMEPRAZOLE (302)

Related Pages

DEXTROSE\NIKETHAMIDE Full Profile All Incorrect product administration duration Reports All Drugs Causing Incorrect product administration duration DEXTROSE\NIKETHAMIDE Demographics