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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.

DEXTROSE\POTASSIUM\SODIUM\SODIUM: 26 Adverse Event Reports & Safety Profile

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26
Total FAERS Reports
16 (61.5%)
Deaths Reported
20
Hospitalizations
26
As Primary/Secondary Suspect
13
Life-Threatening
15
Disabilities

Active Ingredient: DEXTROSE\POTASSIUM CHLORIDE\SODIUM CHLORIDE\SODIUM LACTATE ·

First Report: 20110126 · Latest Report: 20250126

What Are the Most Common DEXTROSE\POTASSIUM\SODIUM\SODIUM Side Effects?

#1 Most Reported
Pneumonia
16 reports (61.5%)
#2 Most Reported
Condition aggravated
15 reports (57.7%)
#3 Most Reported
Vomiting
12 reports (46.2%)

All DEXTROSE\POTASSIUM\SODIUM\SODIUM Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Pneumonia 16 61.5% 13 15
Condition aggravated 15 57.7% 12 15
Dyspnoea 12 46.2% 11 12
Vomiting 12 46.2% 11 12
Ascites 11 42.3% 11 11
Diarrhoea 9 34.6% 7 8
Pyrexia 9 34.6% 7 8
Dehydration 8 30.8% 7 8
Disease complication 8 30.8% 7 8
Motor dysfunction 8 30.8% 7 8
Pneumococcal sepsis 8 30.8% 7 8
Respiratory arrest 8 30.8% 7 8
Spinal muscular atrophy 8 30.8% 7 8
Atelectasis 7 26.9% 7 7
Chest x-ray abnormal 7 26.9% 6 7
Circulatory collapse 7 26.9% 7 7
Constipation 7 26.9% 6 6
Dysphagia 7 26.9% 6 7
Hyponatraemia 7 26.9% 7 7
Increased bronchial secretion 7 26.9% 6 7

Who Reports DEXTROSE\POTASSIUM\SODIUM\SODIUM Side Effects? Age & Gender Data

Gender: 52.9% female, 47.1% male. Average age: 61.3 years. Most reports from: CA. View detailed demographics →

Is DEXTROSE\POTASSIUM\SODIUM\SODIUM Getting Safer? Reports by Year

YearReportsDeathsHosp.
2011 2 0 2
2013 2 1 1
2016 9 7 8
2020 4 3 4
2022 1 0 0
2025 1 0 0

View full timeline →

What Is DEXTROSE\POTASSIUM\SODIUM\SODIUM Used For?

IndicationReports
Pneumonia 6
Product used for unknown indication 6
Intentional product misuse 5
Nutritional supplementation 5
Off label use 5

Official FDA Label for DEXTROSE\POTASSIUM\SODIUM\SODIUM

Official prescribing information from the FDA-approved drug label.