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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 AMILORIDE\FUROSEMIDE Cause Product use in unapproved indication? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product use in unapproved indication have been filed in association with AMILORIDE\FUROSEMIDE. This represents 7.9% of all adverse event reports for AMILORIDE\FUROSEMIDE.

6
Reports of Product use in unapproved indication with AMILORIDE\FUROSEMIDE
7.9%
of all AMILORIDE\FUROSEMIDE reports
0
Deaths
6
Hospitalizations

How Dangerous Is Product use in unapproved indication From AMILORIDE\FUROSEMIDE?

Of the 6 reports, 6 (100.0%) required hospitalization.

Is Product use in unapproved indication Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AMILORIDE\FUROSEMIDE. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does AMILORIDE\FUROSEMIDE Cause?

Hyperkalaemia (22) Hyponatraemia (19) Muscular weakness (15) Orthostatic hypotension (12) Diabetic ketoacidosis (11) Renal impairment (9) Wernicke's encephalopathy (7) Blood creatinine increased (6) Blood sodium increased (6) Blood urea increased (6)

What Other Drugs Cause Product use in unapproved indication?

DUPILUMAB (33,452) DICLOFENAC (12,197) METHOTREXATE (8,930) PREDNISONE (7,625) RITUXIMAB (7,519) MYCOPHENOLATE MOFETIL (5,910) ACETAMINOPHEN (5,819) CYCLOPHOSPHAMIDE (5,750) RISPERIDONE (5,551) TACROLIMUS (5,057)

Related Pages

AMILORIDE\FUROSEMIDE Full Profile All Product use in unapproved indication Reports All Drugs Causing Product use in unapproved indication AMILORIDE\FUROSEMIDE Demographics