Prescription medication · Beta-Blocker
metoprolol
Also sold as Lopressor, Toprol-XL. Metoprolol treats high blood pressure (hypertension).
Data updated 2026-05-15
- 246,252
- FDA reportsHeavily reported
- 18
- InteractionsSeveral interactions
- 96% less
- Generic vs brandHuge savings
- In shortage
- FDA status
What the data shows
metoprolol (Lopressor) is a prescription Beta-Blocker, in the top 5% of tracked drugs by FAERS report volume (246,252 FDA reports), whose generic costs a fraction of the brand (about 96% less).
Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.
metoprolol (Lopressor) is a prescription Beta-Blocker. Metoprolol treats high blood pressure (hypertension).
Metoprolol is a beta-blocker medicine. It can lower blood pressure, reduce chest pain, and improve survival after a heart attack.
Verify with FDA → · CMS NADAC pricing →
Drug Shortage Alert
metoprolol is currently listed as to be discontinued by the FDA. Affected manufacturer: Aurobindo Pharma USA.
View all drug shortages →Drug Pricing (NADAC)
Brand Price
$2.42/unit
Generic Price
$0.10/unit
Generic Savings
96%
Generic Available
Yes (30 manufacturers)
Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →
What it does
Metoprolol treats high blood pressure (hypertension).
Common side effects
Tiredness, Dizziness, Depression
Key warnings
Stopping metoprolol suddenly can make chest pain worse or cause a heart attack.
The sections below are summarized in plain English from metoprolol's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.
How It Works
Metoprolol blocks the effects of adrenaline on the heart. This makes the heart beat slower and with less force. As a result, blood pressure is lowered and the heart does not need as much oxygen.
How to Take It
Take metoprolol once or twice a day with food or right after eating. Your doctor may adjust your dose every week until your blood pressure is under control. The usual starting dose for high blood pressure or angina is 100 mg per day. Do not stop taking this medicine suddenly.
This is a plain-language summary of metoprolol's FDA labeling, not individualized dosing advice. Ask a pharmacist or prescriber before changing how you take this medication.
Pregnancy & Breastfeeding
Tell your doctor if you are pregnant or plan to become pregnant. Metoprolol can cross the placenta, and may cause low blood pressure, low blood sugar, and a slow heart rate in the newborn. Talk to your doctor about the risks and benefits.
This is a plain-language summary of metoprolol'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 metoprolol's FDA labeling, not individualized advice. Ask a pharmacist or prescriber what to do about your specific missed dose.
Storage
Store metoprolol at room temperature, away from moisture and heat.
Side Effects (from patient reports)
Based on 246,252 FDA adverse event reports.
Most-reported reactions
Adverse reactions in FAERS for metoprolol, by number of reports
- Tiredness
Tiredness
15,963 reports
- Shortness of breath
Shortness of breath
14,131 reports
- Diarrhea
Diarrhea
13,634 reports
- Feeling sick to your stomach
Feeling sick to your stomach
13,392 reports
- Feeling lightheaded
Feeling lightheaded
11,697 reports
- Death
Death
9,738 reports
- Weakness
Weakness
9,411 reports
- Pain
Pain
9,113 reports
- Fall
Fall
9,082 reports
- Headache
Headache
8,836 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 metoprolol 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 metoprolol sits
metoprolol has more FDA adverse-event reports than 96% 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 metoprolol; the line is the median (50th percentile).
FDA Adverse Event Report Analysis
Detailed analysis of 246,252 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2001–2025.
Total Reports
246,252
Reports Mentioning Death
27,931
11.3% of reports — not proof of cause
Hospitalization Reports
96,962
Top Indication
Product Used For Unknown Indication
Gender Distribution
Age Distribution
Most Reported Adverse Reactions (FAERS)
| # | Reaction | Reports |
|---|---|---|
| 1 | FATIGUE | 15,966 |
| 2 | DYSPNOEA | 14,128 |
| 3 | DIARRHOEA | 13,635 |
| 4 | NAUSEA | 13,398 |
| 6 | DIZZINESS | 11,699 |
| 8 | DEATH | 9,738 |
| 9 | ASTHENIA | 9,410 |
| 10 | PAIN | 9,111 |
| 11 | FALL | 9,084 |
| 12 | HEADACHE | 8,835 |
| 13 | HYPOTENSION | 7,535 |
| 14 | VOMITING | 7,128 |
| 15 | PNEUMONIA | 7,103 |
| 16 | ARTHRALGIA | 6,782 |
| 17 | ATRIAL FIBRILLATION | 6,687 |
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
Stopping metoprolol suddenly can make chest pain worse or cause a heart attack. If you have heart failure, it could get worse. If you have asthma or other lung problems, avoid beta-blockers if possible.
Known Drug Interactions
albuterol, systemic and inhaled mebendazole amoxicillin medroxyprogesterone ampicillin, with or without sulbactam methylprednisolone atenolol metronidazole azithromycin metoprolol caffeine, dietary ingestion nadolol cefaclor nifedipine co-trimoxazole (trimethoprim and sulfamethoxazole) nizatidine diltiazem norfloxacin dirithromycin ofloxacin enflurane omeprazole famotidine prednisone, prednisolone felodipine ranitidine finasteride rifabutin hydrocortisone roxithromycin isoflurane Sorbitol (purgative doses do not inhibit theophylline absorption) isoniazid sucralfate isradipine terbutaline,...
Mechanism: Metoprolol is a beta-blocker that can block the airway-opening effects of theophylline. This combination can make it harder for you to breathe and may change the amount of medicine in your blood.
What to do: Your doctor may need to adjust your dosages or monitor your blood levels closely. Report any new breathing difficulties to your healthcare provider immediately.
( 7.3 ) Concomitant use of glycosides, clonidine, and diltiazem and verapamil with beta-blockers can increase the risk of bradycardia. ( 7.4 ) Beta-blockers including metoprolol, may exacerbate the rebound hypertension that can follow the withdrawal of clonidine. 7.4 Negative Chronotropes Digitalis glycosides, clonidine, diltiazem and verapamil slow atrioventricular conduction and decrease heart rate.
Mechanism: Both drugs work to slow down your heart rate, which can cause your heart to beat too slowly when taken together. Additionally, stopping one of these drugs suddenly can cause a dangerous rise in blood pressure.
What to do: Your doctor should monitor your heart rate and blood pressure regularly. Do not stop taking either medication without first consulting your healthcare provider.
( 7.3 ) Concomitant use of glycosides, clonidine, and diltiazem and verapamil with beta-blockers can increase the risk of bradycardia. 7.4 Negative Chronotropes Digitalis glycosides, clonidine, diltiazem and verapamil slow atrioventricular conduction and decrease heart rate.
Mechanism: Both of these medicines slow down your heart rate and the electrical signals that tell your heart when to beat. Taking them together can make your heart beat much slower than it should.
What to do: Your doctor should monitor your heart rate and pulse closely while you are taking both medications. Tell your healthcare provider if you feel dizzy, weak, or faint.
( 7.3 ) Concomitant use of glycosides, clonidine, and diltiazem and verapamil with beta-blockers can increase the risk of bradycardia. 7.4 Negative Chronotropes Digitalis glycosides, clonidine, diltiazem and verapamil slow atrioventricular conduction and decrease heart rate.
Mechanism: These drugs both work to lower your heart rate and slow down the electrical conduction in your heart. Using them at the same time increases the risk of your heart rate becoming dangerously slow.
What to do: Your healthcare provider should check your heart rhythm regularly. Your doctor may need to adjust your dosages to ensure your heart rate stays in a safe range.
7.3 CYP2D6 Inhibitors Drugs that are strong inhibitors of CYP2D6 such as quinidine, fluoxetine, paroxetine, and propafenone were shown to double metoprolol concentrations.
Mechanism: Fluoxetine blocks the liver from breaking down metoprolol, which can cause the amount of metoprolol in your blood to double.
What to do: Your doctor may need to lower your metoprolol dose and monitor your heart rate closely.
This is a plain-language summary of interactions documented in FDA labeling, not individualized advice. Ask a pharmacist or prescriber before combining medications.
Common Questions
Can I drink alcohol while taking metoprolol?
Will metoprolol make me gain weight?
Can I exercise while taking metoprolol?
Does metoprolol interact with other medications?
Can I take metoprolol if I have diabetes?
What should I do if I feel dizzy while taking metoprolol?
How long does it take for metoprolol to start working?
Can I stop taking metoprolol if I feel better?
Does metoprolol cause erectile dysfunction?
Can metoprolol affect my cholesterol?
What are the common side effects of metoprolol?
Does metoprolol interact with other medications?
What drug class is metoprolol?
Is there a generic version of metoprolol?
Is metoprolol safe during pregnancy?
Has metoprolol been recalled?
Is metoprolol currently in shortage?
Active Recalls
Failed Dissolution Specifications
Ascend Laboratories, LLC
Failed Dissolution Specifications
Teva Pharmaceuticals USA, Inc
Failed Dissolution Specifications
Teva Pharmaceuticals USA, Inc
Failed Dissolution Specifications
Teva Pharmaceuticals USA, Inc
Failed Dissolution Specifications
Teva Pharmaceuticals USA, Inc
Presence of Foreign Substance: metal in tablet
Rubicon Research Private Limited
Related Medications in Beta-Blocker
Other drugs grouped near metoprolol - same-class peers and common alternatives.
acebutolol
Sectral
Acebutolol is a medicine that helps lower blood pressure and control irregular heartbeats.
Compare with metoprolol →
aliskiren
Tekturna
Tekturna is a medicine used to treat high blood pressure.
Compare with metoprolol →
amiloride
Midamor
Amiloride is a water pill that helps your body hold onto potassium.
Compare with metoprolol →
amlodipine
Norvasc
Amlodipine (Norvasc) is a drug that lowers blood pressure and treats chest pain.
Compare with metoprolol →
amlodipine/benazepril
Lotrel
Lotrel is a combination medicine that contains amlodipine and benazepril.
Compare with metoprolol →
Medication Guides
Understanding Drug Interactions
How CYP450 enzymes, inhibitors, and inducers affect your medications
Generic vs Brand Name Drugs
FDA requirements, cost savings, and when the difference matters
Narrow Therapeutic Index Drugs
Why some drugs demand precise dosing and monitoring
Common Drug Interactions
Dangerous medication combinations and how to protect yourself
Save on metoprolol
Compare prices and find discounts at pharmacies near you. Free coupons can save up to 80% on prescriptions.
Disclosure: This link may earn us a commission at no extra cost to you. See our terms.
What the FDA Data Shows for metoprolol
The FDA label for metoprolol (sold under brand names such as Lopressor, Toprol-XL) classifies it as a prescription-only medication in the Beta-Blocker class. Metoprolol treats high blood pressure (hypertension). Official labeling lists 9 commonly reported side effects, including Tiredness, Dizziness, Depression.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 246,252 voluntary reports. The database also lists 18 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated major severity. NADAC pricing from CMS shows a generic unit cost of $0.10 versus $2.42 for the brand - a 96% generic savings.
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 (currently 6 recall records on file), 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). Shortage status: FDA Drug Shortages Database.
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: June 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