pharmacopeia

Boxed warning

FETAL TOXICITY See full prescribing information for complete boxed warning. When pregnancy is detected, discontinue moexipril hydrochloride tablets as soon as possible. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. See WARNINGS: Fetal Toxicity

Mechanism of action

Sourced from openFDA

Mechanism-of-action class: Angiotensin-converting Enzyme Inhibitors.

Angiotensin-converting Enzyme

Indications

Sourced from openFDA
  • Moexipril hydrochloride tablets are indicated for treatment of patients with hypertension. It may be used alone or in combination with thiazide diuretics.ICD-10: I10

Contraindications

Sourced from openFDA
  • Moexipril hydrochloride tablets are contraindicated in patients who are hypersensitive to this product and in patients with a history of angioedema related to previous treatment with an ACE inhibitor. Do not co-administer aliskiren with moexipril hydrochloride tablets in patients with diabetes (see PRECAUTIONS, Drug Interactions ).contraindicated

Dosage & administration

Sourced from openFDA

DOSAGE AND ADMINISTRATION

Warnings & precautions

Sourced from openFDA

WARNINGS

Adverse reactions

Sourced from openFDA

Moexipril hydrochloride tablets have been evaluated for safety in more than 2500 patients with hypertension; more than 250 of these patients were treated for approximately one year. The overall incidence of reported adverse events was only slightly greater in patients treated with moexipril hydrochloride tablets than patients treated with placebo. Reported adverse experiences were usually mild and transient, and there were no differences in adverse reaction rates related to gender, race, age, duration of therapy, or total daily dosage within the range of 3.75 mg to 60 mg. Discontinuation of therapy because of adverse experiences was required in 3.4% of patients treated with moexipril hydrochloride tablets and in 1.8% of patients treated with placebo. The most common reasons for discontinuation in patients treated with moexipril hydrochloride tablets were cough (0.7%) and dizziness (0.4%).

Overdosage

Sourced from openFDA

Human overdoses of moexipril have not been reported. In case reports of overdoses with other ACE inhibitors, hypotension has been the principal adverse effect noted. Single oral doses of 2 g/kg moexipril were associated with significant lethality in mice. Rats, however, tolerated single oral doses of up to 3 g/kg. No data are available to suggest that physiological maneuvers (e.g., maneuvers to change the pH of the urine) would accelerate elimination of moexipril and its metabolites. The dialyzability of moexipril is not known. Angiotensin II could presumably serve as a specific antagonist-antidote in the setting of moexipril overdose, but angiotensin II is essentially unavailable outside of research facilities. Because the hypotensive effect of moexipril is achieved through vasodilation and effective hypovolemia, it is reasonable to treat moexipril overdose by infusion of normal saline solution. In addition, renal function and serum potassium should be monitored.

Approval history

Sourced from openFDA
  • May 8, 2003ANDAANDA076204Teva
  • Nov 30, 2006ANDAANDA077536Chartwell Rx
  • Mar 30, 2010ANDAANDA090416Glenmark Pharms Ltd

FAERS reports

View JSON
Reference statistics only. FAERS reports are voluntarily submitted and are not incidence rates, safety signals, or causal evidence. Counts reflect reporting volume — how often a reaction was reported, not how often it occurs. For decision-grade use, consult openFDA and the FAERS Public Dashboard directly.
67 total reports matchedLatest report Share = reports listing the reaction ÷ total matched reports. Rows can sum to >100% because a single report often lists multiple reactions.
  1. 1Asthenia812%
  2. 2Dyspnoea69.0%
  3. 3Nausea57.5%
  4. 4Blood Pressure Decreased46.0%
  5. 5Cerebrovascular Accident46.0%
  6. 6Cough46.0%
  7. 7Dehydration46.0%
  8. 8Diarrhoea46.0%
  9. 9Drug Ineffective46.0%
  10. 10Flushing46.0%
  11. 11Headache46.0%
  12. 12Hypertension46.0%
  13. 13Malaise46.0%
  14. 14Arthralgia34.5%
  15. 15Blood Pressure Increased34.5%

Clinical trials

View JSON

The 10 most recently updated of 12 ClinicalTrials.gov registrations naming Moexipril as an intervention. Registration is not evidence of efficacy or safety — reference crosswalk only.

Frequently asked questions

How does Moexipril work?
Mechanism-of-action class: Angiotensin-converting Enzyme Inhibitors.
What is Moexipril used for?
According to FDA labeling, Moexipril carries indications including: Moexipril hydrochloride tablets are indicated for treatment of patients with hypertension. It may be used alone or in combination with thiazide diuretics.. This is a reference summary of labeled uses, not medical advice or a treatment recommendation.
What class of drug is Moexipril?
Moexipril is classified as ACE inhibitors, plain, Angiotensin-converting Enzyme Inhibitors, Decreased Blood Pressure, Decreased Bradykinin Degradation, Decreased Intravascular Volume, Decreased Mineralocorticoid Secretion, Decreased Renal K+ Excretion, Increased Renal Na+ Excretion, Renal Arterial Vasodilation.
What are the contraindications for Moexipril?
Moexipril labeling lists contraindications including: Moexipril hydrochloride tablets are contraindicated in patients who are hypersensitive to this product and in patients with a history of angioedema related to previous treatment with an ACE inhibitor. Do not co-administer aliskiren with moexipril hydrochloride tablets in patients with diabetes (see PRECAUTIONS, Drug Interactions ).. Always consult the full prescribing information and a clinician.
Note. Data for moexipril is illustrative MVP content compiled from public sources. pharmacopeia is for educational and informational use only and is not a substitute for professional medical advice.

Search pharmacopeia

Search drugs, classes, and ingredients