Does MOXONIDINE Cause Product prescribing error? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Product prescribing error have been filed in association with MOXONIDINE. This represents 3.1% of all adverse event reports for MOXONIDINE.
24
Reports of Product prescribing error with MOXONIDINE
3.1%
of all MOXONIDINE reports
0
Deaths
24
Hospitalizations
How Dangerous Is Product prescribing error From MOXONIDINE?
Of the 24 reports, 24 (100.0%) required hospitalization, and 5 (20.8%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOXONIDINE. However, 24 reports have been filed with the FAERS database.
What Other Side Effects Does MOXONIDINE Cause?
Hypotension (97)
Renal impairment (86)
Dizziness (85)
Hyperkalaemia (76)
Abdominal pain (69)
Acute kidney injury (67)
Bradycardia (58)
Drug ineffective (55)
Hypertension (55)
Nausea (50)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which MOXONIDINE Alternatives Have Lower Product prescribing error Risk?
MOXONIDINE vs MS CONTIN
MOXONIDINE vs MULTAQ
MOXONIDINE vs MULTIHANCE
MOXONIDINE vs MUPIROCIN
MOXONIDINE vs MUPIROCIN\MUPIROCIN