Does MOXIFLOXACIN Cause Incorrect product administration duration? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Incorrect product administration duration have been filed in association with MOXIFLOXACIN (Moxifloxacin Hydrochloride Tablets, 400 mg). This represents 0.3% of all adverse event reports for MOXIFLOXACIN.
40
Reports of Incorrect product administration duration with MOXIFLOXACIN
0.3%
of all MOXIFLOXACIN reports
7
Deaths
6
Hospitalizations
How Dangerous Is Incorrect product administration duration From MOXIFLOXACIN?
Of the 40 reports, 7 (17.5%) resulted in death, 6 (15.0%) 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 MOXIFLOXACIN. However, 40 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 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 MOXIFLOXACIN Alternatives Have Lower Incorrect product administration duration Risk?
MOXIFLOXACIN vs MOXIFLOXACIN\MOXIFLOXACIN
MOXIFLOXACIN vs MOXONIDINE
MOXIFLOXACIN vs MS CONTIN
MOXIFLOXACIN vs MULTAQ
MOXIFLOXACIN vs MULTIHANCE