POTASSIUM CHLORATE: 82 Adverse Event Reports & Safety Profile
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Drug Class: Increased Large Intestinal Motility [PE] · Route: ORAL · Manufacturer: Hahnemann Laboratories, INC. · HUMAN OTC DRUG · FDA Label: Available
First Report: 20140501 · Latest Report: 20240920
What Are the Most Common POTASSIUM CHLORATE Side Effects?
All POTASSIUM CHLORATE Side Effects by Frequency
| Side Effect | Reports | % of Total | Deaths | Hosp. |
|---|---|---|---|---|
| Abdominal distension | 62 | 75.6% | 62 | 35 |
| Abdominal pain | 62 | 75.6% | 62 | 35 |
| Appendicitis | 62 | 75.6% | 62 | 35 |
| Appendicolith | 62 | 75.6% | 62 | 35 |
| Ascites | 62 | 75.6% | 62 | 35 |
| Constipation | 61 | 74.4% | 61 | 34 |
| General physical health deterioration | 61 | 74.4% | 61 | 34 |
| Nausea | 61 | 74.4% | 61 | 34 |
| Vomiting | 61 | 74.4% | 61 | 34 |
| Blood phosphorus increased | 60 | 73.2% | 60 | 33 |
| Hyponatraemia | 60 | 73.2% | 60 | 33 |
| Ventricular fibrillation | 60 | 73.2% | 60 | 33 |
| Cardiogenic shock | 59 | 72.0% | 59 | 32 |
| Condition aggravated | 59 | 72.0% | 59 | 35 |
| Dry mouth | 59 | 72.0% | 59 | 35 |
| Multiple organ dysfunction syndrome | 58 | 70.7% | 58 | 31 |
| Sepsis | 58 | 70.7% | 58 | 31 |
| Somnolence | 58 | 70.7% | 58 | 34 |
| Stress | 58 | 70.7% | 58 | 31 |
| Off label use | 55 | 67.1% | 55 | 33 |
Who Reports POTASSIUM CHLORATE Side Effects? Age & Gender Data
Gender: 10.8% female, 89.2% male. Average age: 79.3 years. Most reports from: CA. View detailed demographics →
Is POTASSIUM CHLORATE Getting Safer? Reports by Year
| Year | Reports | Deaths | Hosp. |
|---|---|---|---|
| 2014 | 1 | 0 | 1 |
| 2020 | 30 | 30 | 25 |
| 2021 | 10 | 9 | 2 |
| 2024 | 1 | 0 | 0 |
What Is POTASSIUM CHLORATE Used For?
| Indication | Reports |
|---|---|
| Product used for unknown indication | 52 |
| Constipation | 28 |
Other Drugs in Same Class: Increased Large Intestinal Motility [PE]
Official FDA Label for POTASSIUM CHLORATE
Official prescribing information from the FDA-approved drug label.
FDA Approved Uses (Indications)
Use For use with 3-pump hemodialysis machines only, using purified water (Standard 13959:2014) and in combination with sodium bicarbonate.
Dosage & Administration
Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
Warnings
Warnings For use with 3-pump hemodialysis machines only.
Active Ingredient
KALI CHLORICUM 200CK HPUS Active ingredient**: See product name on front panel (contains 0.443 mg of the active ingredient per pellet).
Inactive Ingredients
Inactive ingredients Sodium chloride, calcium chloride, magnesium chloride, acetic acid, dextrose, purified water USP