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DBL Potassium Dihydrogen Phosphate

DBL Potassium Dihydrogen Phosphate Adverse Reactions

potassium phosphate

Manufacturer:

Pfizer

Distributor:

Zuellig Pharma
Full Prescribing Info
Adverse Reactions
Cardiovascular: Uncommon: hypotension.
Rare: myocardial infarction.
Endocrine/Metabolic: Uncommon: fluid retention as indicated by swelling of feet or lower legs or weight gain. hyperkalaemia leading to confusion, tiredness or weakness, irregular or slow heart rate, numbness or tingling around lips, hands or feet, unexplained anxiety, weakness or heaviness of legs, shortness of breath or troubled breathing; hypernatraemia leading to confusion, tiredness or weakness, convulsions, oliguria or decreased frequency of micturition, tachycardia, headache or dizziness, increased thirst; hyperphosphataemia, hypocalcaemia or hypomagnesaemia leading to convulsions, muscle cramps, numbness, tingling, pain or weakness in hands or feet, shortness of breath or troubled breathing, tremor; extraskeletal calcification as nephrocalcinosis has been reported in children with hypophosphataemic rickets treated with phosphate supplements.
Genitourinary: Rare: acute renal failure.
The symptoms and signs of potassium intoxication include paraesthesias of the extremities, flaccid paralysis, listlessness, mental confusion, weakness and heaviness of the legs, fall in blood pressure, cardiac arrhythmias and heart block. Hyperkalaemia may exhibit the following ECG abnormalities: disappearance of the P-wave, widening and slurring of QRS complex, changes of the S-T segment, tall-peaked T-waves. Nausea, vomiting, diarrhoea and abdominal discomfort have been reported.
Treatment of adverse effects involves withdrawal of phosphate, general supportive measures, and correction of serum-electrolyte concentrations, especially calcium (see Overdosage).
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