Does AMIKACIN Cause Incorrect product administration duration? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Incorrect product administration duration have been filed in association with AMIKACIN (ARIKAYCE). This represents 0.5% of all adverse event reports for AMIKACIN.
52
Reports of Incorrect product administration duration with AMIKACIN
0.5%
of all AMIKACIN reports
8
Deaths
31
Hospitalizations
How Dangerous Is Incorrect product administration duration From AMIKACIN?
Of the 52 reports, 8 (15.4%) resulted in death, 31 (59.6%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMIKACIN. However, 52 reports have been filed with the FAERS database.
What Other Side Effects Does AMIKACIN Cause?
Cough (1,472)
Off label use (1,447)
Dyspnoea (1,367)
Hospitalisation (1,325)
Therapy interrupted (1,283)
Drug ineffective (1,275)
Death (1,005)
Dysphonia (914)
Product dose omission issue (677)
Fatigue (602)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which AMIKACIN Alternatives Have Lower Incorrect product administration duration Risk?
AMIKACIN vs AMILORIDE
AMIKACIN vs AMILORIDE\HYDROCHLOROTHIAZIDE
AMIKACIN vs AMINO ACIDS
AMIKACIN vs AMINO ACIDS, SOURCE UNSPECIFIED
AMIKACIN vs AMINO ACIDS\ANHYDROUS DEXTROSE\CALCIUM\MAGNESIUM HEPTAHYDRATE\POTASSIUM\SODIUM\SODIUM GLYCEROPHOSPHATE ANHYDROUS\SOYBEAN OIL