Does MOXIFLOXACIN Cause Product administration error? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product administration error have been filed in association with MOXIFLOXACIN (Moxifloxacin Hydrochloride Tablets, 400 mg). This represents 0.1% of all adverse event reports for MOXIFLOXACIN.
14
Reports of Product administration error with MOXIFLOXACIN
0.1%
of all MOXIFLOXACIN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From MOXIFLOXACIN?
Of the 14 reports, 2 (14.3%) required hospitalization, and 1 (7.1%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOXIFLOXACIN. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does MOXIFLOXACIN Cause?
Drug hypersensitivity (2,013)
Off label use (1,563)
Dyspnoea (1,543)
Drug ineffective (1,496)
Vomiting (1,377)
Pain (1,368)
Asthma (1,342)
Neuropathy peripheral (1,331)
Rash (1,212)
Pneumonia (1,172)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which MOXIFLOXACIN Alternatives Have Lower Product administration error Risk?
MOXIFLOXACIN vs MOXIFLOXACIN\MOXIFLOXACIN
MOXIFLOXACIN vs MOXONIDINE
MOXIFLOXACIN vs MS CONTIN
MOXIFLOXACIN vs MULTAQ
MOXIFLOXACIN vs MULTIHANCE