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cimetidine

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Brand names: Tagamet

H2 Receptor Antagonist OTC

Cimetidine (Tagamet) reduces stomach acid. It is used to treat ulcers, heartburn, and other conditions where too much acid is produced.

Drug Pricing (NADAC)

Generic Price

$0.26/unit

Generic Available

Yes (9 manufacturers)

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

What it does

Cimetidine treats active duodenal ulcers for short periods.

Common side effects

Headache, Dizziness, Diarrhea

Key warnings

Reversible confusional states (like mental confusion, agitation, or hallucinations) have been reported, mostly in severely ill patients.

How It Works

Cimetidine is an H2 receptor antagonist. This means it blocks histamine from attaching to certain cells in your stomach. By blocking histamine, cimetidine reduces the amount of acid your stomach makes.

How to Take It

Take cimetidine exactly as your doctor tells you to. For duodenal ulcers, you might take it once a day at bedtime, or several times a day with meals and at bedtime. Do not take antacids at the same time as cimetidine, as they can interfere with absorption. Continue taking cimetidine for as long as your doctor recommends, even if you start feeling better.

Pregnancy & Breastfeeding

Tell your doctor if you are pregnant or plan to become pregnant. The effects of cimetidine during pregnancy are not fully known. Talk to your doctor about the risks and benefits of taking cimetidine while breastfeeding.

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.

Storage

Store cimetidine tablets at room temperature (68° to 77°F) and protect them from light.

Side Effects (from patient reports)

Based on 6,312 FDA adverse event reports.

Long-term kidney disease
1,264
Sudden kidney damage
710
Kidney failure
694
Feeling sick to your stomach
681
Feeling tired
599
The medicine is not working
505
Shortness of breath
505
Throwing up
483
Loose stools
440
Discomfort
431

FDA Adverse Event Report Analysis

Detailed analysis of 9,140 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 1998–2025.

Total Reports

9,140

Death-Related Reports

1,168

Hospitalization Reports

3,377

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 5,379 (65%)
Male 2,855 (35%)

Age Distribution

0–17 165
18–44 1,019
45–64 2,596
65–74 1,328
75+ 872

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 CHRONIC KIDNEY DISEASE 1,264
2 ACUTE KIDNEY INJURY 710
3 RENAL FAILURE 694
4 NAUSEA 681
5 FATIGUE 598
6 DRUG INEFFECTIVE 504
7 DYSPNOEA 504
8 VOMITING 483
9 DIARRHOEA 440
10 PAIN 432
11 DEATH 399
12 DIZZINESS 386
13 OFF LABEL USE 377
14 HEADACHE 371
15 GASTROOESOPHAGEAL REFLUX DISEASE 370

Reactions in Death Reports

DEATH 399
FATIGUE 141
OFF LABEL USE 139
CHRONIC KIDNEY DISEASE 121
NAUSEA 120
RENAL FAILURE 109
DYSPNOEA 102
PNEUMONIA 94
ACUTE KIDNEY INJURY 93
VOMITING 93

Reactions in Hospitalization Reports

DYSPNOEA 250
NAUSEA 249
VOMITING 248
FATIGUE 239
ACUTE KIDNEY INJURY 229
RENAL FAILURE 223
PNEUMONIA 219
CHRONIC KIDNEY DISEASE 212
HYPERTENSION 212
DIARRHOEA 204

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

Serious Warnings

Reversible confusional states (like mental confusion, agitation, or hallucinations) have been reported, mostly in severely ill patients. These usually appear within 2-3 days of starting treatment and clear up within 3-4 days of stopping the drug.

Known Drug Interactions

7.8 Probenecid and Cimetidine No significant effect of probenecid or cimetidine on the Cmax of levofloxacin was observed in a clinical study involving healthy volunteers. The AUC and t 1/2 of levofloxacin were higher while CL/F and CLR were lower during concomitant treatment of levofloxacin with probenecid or cimetidine compared to levofloxacin alone. However, these changes do not warrant dosage adjustment for levofloxacin when probenecid or cimetidine is co-administered.

Mechanism: Cimetidine makes it harder for the kidneys to clear levofloxacin, causing the antibiotic to stay in the body slightly longer.

What to do: No dosage changes are needed, so you can safely take these medications together as prescribed.

Interaction Drug Interaction Rifabutin, phenytoin, efavirenz, cimetidine, esomeprazole* Avoid coadministration unless the benefit outweighs the risks ( 7.6 , 7.7 , 7.8 , 7.9 ) Other drugs metabolized by CYP3A4 Consider dosage adjustment and monitor for adverse effects and toxicity ( 7.1 , 7.10 , 7.11 ) Digoxin Monitor digoxin plasma concentrations ( 7.12 ) Fosamprenavir, metoclopramide* Monitor for breakthrough fungal infections ( 7.6 , 7.13 ) *The drug interactions with esomeprazole and metoclopramide do not apply to posaconazole tablets.

Mechanism: Cimetidine changes the environment in the stomach, which can prevent the body from absorbing enough posaconazole into the bloodstream.

What to do: Avoid taking these two medicines together unless your doctor determines that the benefits are greater than the risks.

Dose adjustment is not recommended for risperidone tablets when co-administered with ranitidine, cimetidine, amitriptyline, or erythromycin [see Table 18 ] . Do not exceed twice the patient’s usual dose Enzyme (CYP3A) inhibitors Ranitidine 150 mg twice daily 1 mg single dose 1.2 1.4 Dose adjustment not needed Cimetidine 400 mg twice daily 1 mg single dose 1.1 1.3 Dose adjustment not needed Erythromycin 500 mg four times daily 1 mg single dose 1.1 0.94 Dose adjustment not needed Other Drugs Amitriptyline 50 mg twice daily 3 mg twice daily 1.2 1.1 Dose adjustment not Needed *Change relative t...

Mechanism: Cimetidine can slightly slow down the enzymes that break down risperidone, but the effect is very small.

What to do: No dose changes are needed when taking these two medicines together.

Cimetidine and Ranitidine Cimetidine and ranitidine do not affect the clearance of valproate.

Mechanism: Cimetidine does not interfere with how the body breaks down or clears valproate. This means the amount of valproate in your blood should remain stable.

What to do: You can take these medications together without needing to change your dose. Your doctor will continue to monitor you as usual.

Drugs that Reduce Metformin Clearance Clinical Impact Concomitant use of drugs that interfere with common renal tubular transport systems involved in the renal elimination of metformin (e.g., organic cationic transporter-2 [OCT2] / multidrug and toxin extrusion [MATE] inhibitors such as ranolazine, vandetanib, dolutegravir, and cimetidine) could increase systemic exposure to metformin and may increase the risk for lactic acidosis [see Clinical Pharmacology (12.3) ] .

Mechanism: Cimetidine stops the kidneys from getting rid of metformin as quickly as they should. This can cause metformin to build up in your blood and increase the risk of a serious acid problem.

What to do: Your doctor may need to monitor you more frequently or adjust your medication levels.

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Common Questions

Can I take antacids with cimetidine?
It is not recommended to take antacids at the same time as cimetidine.
How long does it take for cimetidine to heal an ulcer?
Healing often occurs within the first week or two, but treatment should continue for 4 to 6 weeks.
What should I do if I experience confusion while taking cimetidine?
Contact your doctor immediately if you experience confusion, agitation, or hallucinations.
Can cimetidine cause any changes in my hormone levels?
Gynecomastia (breast enlargement in men) has been reported, but endocrine dysfunction is rare.
What if I am a heavy smoker with a large ulcer?
Your doctor may prescribe a higher dose of cimetidine (1600 mg at bedtime) to ensure healing within 4 weeks.
How often should I take Cimetidine?
Take this medicine exactly as directed by your doctor. Do not take more or less of it, and do not take it more often than your doctor ordered.
What do I do if I think I am having a side effect?
Tell your doctor right away if you have any side effects.
Can Cimetidine cause issues with my blood?
Decreased white blood cell counts have been reported rarely.
Does Cimetidine interact with other medications?
Yes, Cimetidine can interact with other medications. Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
Can Cimetidine cause liver problems?
Dose-related increases in liver enzymes have been reported. In most cases they did not progress with continued therapy and returned to normal at the end of therapy.
What are the common side effects of cimetidine?
The most commonly reported side effects of cimetidine include Headache, Dizziness, Diarrhea. Based on 6,312 FDA adverse event reports. Always consult your healthcare provider about potential side effects.
Does cimetidine interact with other medications?
Yes, cimetidine has 77 known drug interactions. Notable interactions include levofloxacin, posaconazole, risperidone. Always inform your doctor about all medications you are taking.
What drug class is cimetidine?
cimetidine belongs to the H2 Receptor Antagonist drug class. It is available over the counter (OTC). Cimetidine treats active duodenal ulcers for short periods.
Is cimetidine safe during pregnancy?
Tell your doctor if you are pregnant or plan to become pregnant. The effects of cimetidine during pregnancy are not fully known. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.

Related Medications in H2 Receptor Antagonist

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

Compare cimetidine vs alosetron side-by-side →

Medication Guides

Related Health & Safety Data

What the FDA Data Shows for cimetidine

The FDA label for cimetidine (sold under brand names such as Tagamet) classifies it as an over-the-counter product in the H2 Receptor Antagonist class. Cimetidine treats active duodenal ulcers for short periods. Official labeling lists 3 commonly reported side effects, including Headache, Dizziness, Diarrhea.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 6,312 voluntary reports. The database also lists 77 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 $0.26.

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: August 18, 2023

All federal data sources used on this page