Prescription medication · ACE Inhibitor
moexipril
Also sold as Univasc. Moexipril is used to treat high blood pressure.
Data updated 2026-05-15
- 67
- FDA reportsRarely reported
- $0.88
- Generic price (NADAC)
moexipril (Univasc) is a prescription ACE Inhibitor. Moexipril is used to treat high blood pressure.
Moexipril is a medicine used to treat high blood pressure. It can be used alone or with a water pill.
Verify with FDA → · CMS NADAC pricing →
Drug Pricing (NADAC)
Generic Price
$0.88/unit
Generic Available
Yes (3 manufacturers)
Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →
What it does
Moexipril is used to treat high blood pressure.
Common side effects
Cough, Dizziness, Diarrhea
Key warnings
This medicine can harm your unborn baby.
The sections below are summarized in plain English from moexipril's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.
How It Works
Moexipril belongs to a class of drugs called ACE inhibitors. It works by blocking a substance in your body that tightens blood vessels. This helps your blood vessels relax and widens them, which lowers your blood pressure.
How to Take It
Take moexipril exactly as your doctor tells you. The tablets come in 7.5 mg and 15 mg strengths. You can take this medicine with or without food. Try to take it at the same time each day.
This is a plain-language summary of moexipril's FDA labeling, not individualized dosing advice. Ask a pharmacist or prescriber before changing how you take this medication.
Pregnancy & Breastfeeding
Moexipril can cause injury or death to a developing fetus. If you become pregnant while taking this medicine, stop taking it immediately and tell your doctor. It is not known if moexipril passes into breast milk, so talk to your doctor before breastfeeding.
This is a plain-language summary of moexipril's FDA labeling, not individualized advice. Ask a pharmacist or prescriber about pregnancy or breastfeeding on this medication.
Missed Dose
If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular schedule.
This is a plain-language summary of moexipril's FDA labeling, not individualized advice. Ask a pharmacist or prescriber what to do about your specific missed dose.
Storage
Store moexipril tablets in a tightly closed container at room temperature (68° to 77°F) and protect from moisture.
Side Effects (from patient reports)
Based on 67 FDA adverse event reports.
Most-reported reactions
Adverse reactions in FAERS for moexipril, by number of reports
- Weakness
Weakness
8 reports
- Shortness of breath
Shortness of breath
6 reports
- Feeling sick to your stomach
Feeling sick to your stomach
5 reports
- Low blood pressure
Low blood pressure
4 reports
- Stroke
Stroke
4 reports
- Cough
Cough
4 reports
- Loss of body fluids
Loss of body fluids
4 reports
- Diarrhea
Diarrhea
4 reports
- Redness of face
Redness of face
4 reports
- Headache
Headache
4 reports
What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.
Reports over time
Adverse-event reports filed for moexipril each year to the FDA Adverse Event Reporting System (FAERS).
Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.
Where moexipril sits
moexipril has more FDA adverse-event reports than 0% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.
Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is moexipril; the line is the median (50th percentile).
FDA Adverse Event Report Analysis
Detailed analysis of 67 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.
Total Reports
67
Reports Mentioning Death
6
9.0% of reports — not proof of cause
Hospitalization Reports
21
Top Indication
Hypertension
Gender Distribution
Age Distribution
Most Reported Adverse Reactions (FAERS)
| # | Reaction | Reports |
|---|---|---|
| 1 | ASTHENIA | 8 |
| 2 | DYSPNOEA | 6 |
| 3 | NAUSEA | 5 |
| 4 | BLOOD PRESSURE DECREASED | 4 |
| 5 | CEREBROVASCULAR ACCIDENT | 4 |
| 6 | COUGH | 4 |
| 7 | DEHYDRATION | 4 |
| 8 | DIARRHOEA | 4 |
| 10 | FLUSHING | 4 |
| 11 | HEADACHE | 4 |
| 12 | HYPERTENSION | 4 |
| 13 | MALAISE | 4 |
| 14 | ARTHRALGIA | 3 |
| 15 | BLOOD PRESSURE INCREASED | 3 |
| 16 | DEATH | 3 |
Reactions in Death Reports
Reactions in Hospitalization Reports
Source: FDA FAERS (Adverse Event Reporting System) FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation
Serious Warnings
This medicine can harm your unborn baby. If you are pregnant or plan to become pregnant, tell your doctor right away. Stop taking moexipril as soon as you know you are pregnant.
Common Questions
What should I tell my doctor before taking moexipril?
Can I take moexipril if I am allergic to other medicines?
Does moexipril interact with other medications?
How long will I need to take moexipril?
Can I stop taking moexipril if my blood pressure is under control?
What should I do if I feel dizzy while taking moexipril?
Can moexipril cause kidney problems?
Is it safe to drink alcohol while taking moexipril?
Are there differences in how this medicine works in different races?
What are the signs of angioedema?
What are the common side effects of moexipril?
What drug class is moexipril?
Is moexipril safe during pregnancy?
Related Medications in ACE Inhibitor
Other drugs grouped near moexipril - same-class peers and common alternatives.
acebutolol
Sectral
Acebutolol is a medicine that helps lower blood pressure and control irregular heartbeats.
Compare with moexipril →
aliskiren
Tekturna
Tekturna is a medicine used to treat high blood pressure.
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amiloride
Midamor
Amiloride is a water pill that helps your body hold onto potassium.
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amlodipine
Norvasc
Amlodipine (Norvasc) is a drug that lowers blood pressure and treats chest pain.
Compare with moexipril →
amlodipine/benazepril
Lotrel
Lotrel is a combination medicine that contains amlodipine and benazepril.
Compare with moexipril →
Medication Guides
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Common Drug Interactions
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What the FDA Data Shows for moexipril
The FDA label for moexipril (sold under brand names such as Univasc) classifies it as a prescription-only medication in the ACE Inhibitor class. Moexipril is used to treat high blood pressure. Official labeling lists 9 commonly reported side effects, including Cough, Dizziness, Diarrhea.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 67 voluntary reports. Interaction data is drawn directly from FDA-approved prescribing information. NADAC pricing from CMS shows a generic unit cost of $0.88.
Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice, always consult a licensed healthcare provider before starting, stopping, or changing any medication.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.
Last updated: March 10, 2025
Read our methodology - how this data is sourced, computed, and verified.
Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled and last refreshed May 2026. See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a correction.
All federal data sources used on this page
- FDA Orange Book - approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed - NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) - post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm - standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files - federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database - current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages