Does MOXONIDINE Cause Off label use? 36 Reports in FDA Database
Lower Your Cholesterol — The Natural Way
The Oxidized Cholesterol Strategy: a science-backed plan for heart health.
According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Off label use have been filed in association with MOXONIDINE. This represents 4.6% of all adverse event reports for MOXONIDINE.
36
Reports of Off label use with MOXONIDINE
4.6%
of all MOXONIDINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Off label use From MOXONIDINE?
Of the 36 reports, 3 (8.3%) required hospitalization, and 1 (2.8%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MOXONIDINE. However, 36 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 Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which MOXONIDINE Alternatives Have Lower Off label use Risk?
MOXONIDINE vs MS CONTIN
MOXONIDINE vs MULTAQ
MOXONIDINE vs MULTIHANCE
MOXONIDINE vs MUPIROCIN
MOXONIDINE vs MUPIROCIN\MUPIROCIN