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Review Amiloride Safety Reports submitted to FDA

Total Amiloride reports: 2.
Amiloride FDA safety alerts: No.
   Reported hospitalizations: 2.
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FDA Reported Amiloride Side Effects: hyponatraemia, hypokalaemia, headache, dizziness, hyperkalaemia.
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Amiloride Side Effects Report #5417711-1
Pharmacist from UNITED STATES reported AMILORIDE problem on Aug 15, 2007. Female patient, weighting 170.0 lb, was diagnosed with hypertension and was treated with AMILORIDE. After drug was administered, patient experienced the following problems/side effects: dizziness, headache, hypokalaemia, hyponatraemia. AMILORIDE dosage: 5/50 MG PO QD PRIOR TO ADMISSION. During the same period patient was treated with VYTORIN, MOBIC, EVISTA, ARICEPT. Patient was hospitalized. Patient recovered.

Amiloride Side Effects Report #5746010-3
AMILORIDE problem was reported by a Health Professional from UNITED KINGDOM on May 15, 2008. Female patient was diagnosed with oedema, cardiac failure congestive, hypertension, atrial fibrillation and was treated with AMILORIDE. After drug was administered, patient experienced the following problems/side effects: atrioventricular block complete, blood potassium increased, blood pressure decreased, renal failure acute, syncope. AMILORIDE dosage: 10 MG, QD. During the same period patient was treated with BISOPROLOL FUMARATE, DIGOXIN, RAMIPRIL, SPIRONOLACTONE, BUMETANIDE, GABAPENTIN, WARFARIN. Patient was hospitalized. Patient recovered.


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dizziness, headache, hypokalaemia, hyponatraemia, atrioventricular block complete, blood potassium increased, blood pressure decreased, renal failure acute, syncope, , was diagnosed with hypertension and was diagnosed with oedema, cardiac failure congestive, hypertension, atrial fibrillation and