Prescription medication · Calcium Channel Blocker

diltiazem

Also sold as Cardizem, Tiazac. Diltiazem is used to treat high blood pressure.

Data updated 2026-05-15

33,620
FDA reportsModerately reported
46
InteractionsMany interactions
In shortage
FDA status

What the data shows

diltiazem (Cardizem) is a prescription Calcium Channel Blocker, reported at a middle-of-the-pack volume (33,620 FDA reports), with 46 documented drug interactions.

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.

diltiazem (Cardizem) is a prescription Calcium Channel Blocker. Diltiazem is used to treat high blood pressure.

Diltiazem is a medicine that helps lower high blood pressure and prevent chest pain. It belongs to a class of drugs called calcium channel blockers.

Drug Shortage Alert

diltiazem is currently listed as to be discontinued by the FDA. Affected manufacturer: Hospira, Inc., a Pfizer Company.

View all drug shortages →

Drug Pricing (NADAC)

Generic Price

$0.23/unit

Generic Available

Yes (32 manufacturers)

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

View Alternatives → Compare with Another Drug → Full Side Effects Report →

What it does

Diltiazem is used to treat high blood pressure.

Common side effects

Swelling in your ankles or feet, Headache, Dizziness

Key warnings

Diltiazem can interact with other heart medications.

The sections below are summarized in plain English from diltiazem's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.

How It Works

Diltiazem works by relaxing blood vessels, which lowers blood pressure. It also reduces the heart's workload, which can prevent chest pain. This medicine blocks calcium from entering heart and blood vessel cells.

Side Effects (from patient reports)

Based on 33,620 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for diltiazem, by number of reports

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.

Source FDA Adverse Event Reporting System (FAERS) As of 2025

Reports over time

Adverse-event reports filed for diltiazem each year to the FDA Adverse Event Reporting System (FAERS).

05001,0001,5002,0002,500 200320062009201220152018202120242025 1,638

Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.

Where diltiazem sits

diltiazem has more FDA adverse-event reports than 66% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.

fewest reports most reports

Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is diltiazem; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 33,620 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2003–2025.

Total Reports

33,620

Reports Mentioning Death

4,917

14.6% of reports — not proof of cause

Hospitalization Reports

14,360

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 20,122 (64%)
Male 11,326 (36%)

Age Distribution

0–17 101
18–44 1,642
45–64 6,878
65–74 6,680
75+ 7,764

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 DYSPNOEA 3,202
2 FATIGUE 2,638
3 NAUSEA 2,372
4 PAIN 2,365
5 DIZZINESS 2,091
6 DIARRHOEA 2,045
8 FALL 1,954
9 HEADACHE 1,929
10 ATRIAL FIBRILLATION 1,754
11 ASTHENIA 1,705
12 PNEUMONIA 1,605
13 ARTHRALGIA 1,548
14 HYPOTENSION 1,494
15 PAIN IN EXTREMITY 1,449
16 MALAISE 1,411

Reactions in Death Reports

DEATH 1,209
DYSPNOEA 679
FATIGUE 555
DIARRHOEA 526
DIZZINESS 506
NAUSEA 482
PNEUMONIA 462
HEADACHE 458
COMPLETED SUICIDE 451
DECREASED APPETITE 449

Reactions in Hospitalization Reports

DYSPNOEA 1,868
PAIN 1,451
ATRIAL FIBRILLATION 1,358
FALL 1,333
PNEUMONIA 1,268
FATIGUE 1,183
HYPOTENSION 1,162
NAUSEA 993
ASTHENIA 953
DIARRHOEA 928

Source: FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Serious Warnings

Diltiazem can interact with other heart medications. Tell your doctor if you take beta-blockers or digoxin. Using diltiazem with these drugs can cause heart problems. Your doctor may need to adjust your dosages.

Known Drug Interactions

Intervention: For patients taking verapamil, diltiazem, or dronedarone, do not exceed ezetimibe and simvastatin 10 mg/10 mg daily.

Mechanism: Diltiazem can increase the levels of the cholesterol medicine in your blood, which may lead to muscle problems.

Intervention: For patients taking verapamil, diltiazem, or dronedarone, do not exceed VYTORIN 10/10 mg daily.

Mechanism: Diltiazem slows down the breakdown of simvastatin in your body, which can lead to higher levels of the drug in your blood. This increases the risk of serious muscle damage.

Intervention: For patients taking verapamil, diltiazem, or dronedarone, do not exceed ezetimibe and simvastatin 10 mg/10 mg daily.

Mechanism: Diltiazem blocks the enzymes that break down simvastatin, causing the drug to stay in your body longer. This can lead to a higher risk of muscle pain or damage.

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: Diltiazem can slow down the liver's ability to break down theophylline. This can cause the medicine to build up in your body and reach toxic levels.

moderate rifampin

Rifampin : Coadministration of rifampin with diltiazem lowered the diltiazem plasma concentrations to undetectable levels. Avoid coadministration of diltiazem with rifampin or any known CYP3A4 inducer.

Mechanism: Rifampin speeds up how quickly your body breaks down diltiazem, which can cause the diltiazem to disappear from your blood and stop working.

Check all your medications →

This is a plain-language summary of FDA-label interaction records and does not provide individual medication-combination directions.

Common Questions

Can I take diltiazem with other medications?
Diltiazem can interact with other medications. Tell your doctor about all the medicines you take.
How long does it take for diltiazem to start working?
It may take up to 2 weeks to see the full effect of diltiazem on your blood pressure.
Can I drink alcohol while taking diltiazem?
Talk to your doctor about drinking alcohol while taking diltiazem.
What should I do if I experience side effects?
Tell your doctor if you experience any bothersome or severe side effects.
Can I stop taking diltiazem suddenly?
Do not stop taking diltiazem without talking to your doctor first.
Does diltiazem affect my ability to drive or operate machinery?
Diltiazem may cause dizziness. Be careful when driving or operating machinery.
How often should I check my blood pressure?
Follow your doctor's instructions on how often to check your blood pressure.
Can diltiazem cure my high blood pressure or angina?
Diltiazem helps manage high blood pressure and angina, but it may not cure these conditions.
What if I have kidney or liver problems?
Tell your doctor if you have kidney or liver problems, as your dosage may need to be adjusted.
Are there any foods I should avoid while taking diltiazem?
Talk to your doctor or pharmacist about any food restrictions while taking diltiazem.
What are the common side effects of diltiazem?
The registry lists Swelling in your ankles or feet, Headache, Dizziness, Slow heart rate, Constipation among the most-reported FAERS reaction terms for diltiazem. The compiled record contains 33,620 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does diltiazem interact with other medications?
The registry has 46 documented interaction rows for diltiazem. Notable source-record pairings include ezetimibe, ezetimibe/simvastatin, simvastatin. These rows are not a complete medication review.
What drug class is diltiazem?
diltiazem belongs to the Calcium Channel Blocker drug class. It requires a prescription (Rx). Diltiazem is used to treat high blood pressure.
What pregnancy or breastfeeding source fields are listed for diltiazem?
The FDA label for diltiazem contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.
Has diltiazem been recalled?
There are 3 recalls associated with diltiazem products. cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit. Check the recalls section below for full details and affected products.
Is diltiazem currently in shortage?
Yes, diltiazem is currently listed as to be discontinued by the FDA. Affected manufacturer: Hospira, Inc., a Pfizer Company. Visit the FDA Drug Shortages database for the latest updates.

Active Recalls

Class II November 1, 2024

cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

Glenmark Pharmaceuticals Inc., USA

Class II November 1, 2024

cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

Glenmark Pharmaceuticals Inc., USA

Class II November 1, 2024

cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.

Glenmark Pharmaceuticals Inc., USA

Other drugs grouped near diltiazem - same-class peers and common alternatives.

Compare diltiazem vs acebutolol side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for diltiazem: nearest FDA FAERS report volume and nearest death-report share among drugs with at least 1,000 logged reports, excluding same-class neighbors listed above. Counts reflect reporting volume, not proven individual harm.

Medication Guides

Save on diltiazem

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 diltiazem

The FDA label for diltiazem (sold under brand names such as Cardizem, Tiazac) classifies it as a prescription-only medication in the Calcium Channel Blocker class. Diltiazem is used to treat high blood pressure. Official labeling lists 5 commonly reported side effects, including Swelling in your ankles or feet, Headache, Dizziness.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 33,620 voluntary reports. The database also lists 46 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 $0.23.

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 3 recall records on file), and patent information are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.

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. This registry does not provide medication decisions.

Last updated: August 20, 2025

PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.

Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.

All federal data sources used on this page