Skip to content
Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does MOXONIDINE Cause Product use issue? 5 Reports in FDA Database

Lower Your Cholesterol — The Natural Way

The Oxidized Cholesterol Strategy: a science-backed plan for heart health.

See the Strategy

According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product use issue have been filed in association with MOXONIDINE. This represents 0.6% of all adverse event reports for MOXONIDINE.

5
Reports of Product use issue with MOXONIDINE
0.6%
of all MOXONIDINE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product use issue From MOXONIDINE?

Of the 5 reports, 5 (100.0%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MOXONIDINE. However, 5 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 use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which MOXONIDINE Alternatives Have Lower Product use issue Risk?

MOXONIDINE vs MS CONTIN MOXONIDINE vs MULTAQ MOXONIDINE vs MULTIHANCE MOXONIDINE vs MUPIROCIN MOXONIDINE vs MUPIROCIN\MUPIROCIN

Related Pages

MOXONIDINE Full Profile All Product use issue Reports All Drugs Causing Product use issue MOXONIDINE Demographics