Microplastics and Misinformation: What Science Really Says
November 12, 2025
Brand Name :
Moxocard, Moxodil
Synonyms :
moxonidine
Class :
Antihypertensives agent
Dosage Forms & StrengthsÂ
Tablet Â
0.2 mg Â
0.3 mg Â
Take an initial dose of 200 mcg orally one time daily in the morning, then it may raise if required; after 3 weeks, up to 400 mcg daily as a single dose
Not determined Â
Refer to adult dosingÂ
moxonidine: it may decrease activities of antihypertensive drugs
moxonidine: it may decrease activities of antihypertensive drugs
moxonidine: it may decrease activities of antihypertensive drugs
moxonidine: it may decrease activities of antihypertensive drugs
moxonidine: it may decrease activities of antihypertensive drugs
Actions and SpectrumÂ
moxonidine stimulates alpha-2 adrenergic receptors in the brainstem. This results in decreased nerve signals to the blood vessels and the heart, leading to relaxation of blood vessels and a decrease in heart rate and cardiac output.
Frequency not defined Â
BradycardiaÂ
TinnitusÂ
headache Â
DizzinessÂ
Somnolence Â
SyncopeÂ
Hypotension Â
Diarrhea Â
Dry mouth Â
NauseaÂ
VomitingÂ
Dyspepsia Â
PruritusÂ
Angioedema Â
Oedema Â
InsomniaÂ
NervousnessÂ
Black Box WarningÂ
None
Contraindication/Caution:Â
Contraindication:Â
Caution:Â
Pregnancy consideration:Â
Pregnancy category: N/AÂ
Lactation: Excretion into human milk is unknown Â
Pregnancy Categories:        Â
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.Â
Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women. Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.Â
Category D: adequate data with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.Â
Category N: There is no data available for the drug under this category.Â
Pharmacology Â
moxonidine’s pharmacological effect is the reduction of blood pressure.Â
By activating central alpha-2 adrenergic receptors, it reduces the release of norepinephrine, which in turn reduces sympathetic outflow from the central nervous system.Â
PharmacodynamicsÂ
moxonidine’s primary therapeutic effect is the reduction of blood pressure.Â
The combined effects of vasodilation, decreased cardiac output, and reduced sympathetic activity led to a decrease in both systolic and diastolic blood pressure.Â
PharmacokineticsÂ
Absorption  Â
moxonidine is well-absorbed when taken orally.Â
The peak plasma concentrations of moxonidine are reached within 2 to 4 hours after oral administration.Â
DistributionÂ
moxonidine is distributed throughout the body.Â
MetabolismÂ
moxonidine undergoes hepatic metabolism to form metabolites.Â
Elimination and excretionÂ
moxonidine is primarily excreted in urine. The elimination half-life of moxonidine is approximately 2 to 3 hours.Â
AdministrationÂ
moxonidine is administered orally and available in the form of a tablet.
Patient information leafletÂ
Generic Name: moxonidineÂ
Why do we use moxonidine?Â
moxonidine is used for the management of hypertension. Â
moxonidine is also used to help manage symptoms of opioid withdrawal.