Prescription medication · Carbapenem Antibiotic

meropenem

Also sold as Merrem. Meropenem treats complicated skin infections in adults and kids 3 months and older.

Data updated 2026-05-15

30,400
FDA reportsModerately reported
3
InteractionsFew interactions
$6.84
Generic price (NADAC)

What the data shows

meropenem (Merrem) is a prescription Carbapenem Antibiotic, reported at a middle-of-the-pack volume (30,400 FDA reports), with 3 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.

meropenem (Merrem) is a prescription Carbapenem Antibiotic. Meropenem treats complicated skin infections in adults and kids 3 months and older.

Meropenem is an antibiotic medicine. It fights bacteria in your body to treat different kinds of infections.

Drug Pricing (NADAC)

Generic Price

$6.84/unit

Generic Available

Yes (9 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

Meropenem treats complicated skin infections in adults and kids 3 months and older.

Common side effects

Headache, Nausea, Constipation

Key warnings

You should not take this medicine if you are allergic to meropenem or similar antibiotics.

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

How It Works

Meropenem belongs to a class of drugs called carbapenem antibiotics. It works by stopping the growth of bacteria. This helps your body fight off the infection.

Side Effects (from patient reports)

Based on 30,400 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for meropenem, 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 meropenem each year to the FDA Adverse Event Reporting System (FAERS).

01,0002,0003,0004,000 199920062009201220152018202120242025 3,010

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

Where meropenem sits

meropenem has more FDA adverse-event reports than 64% 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 meropenem; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 30,400 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 1999–2025.

Total Reports

30,400

Reports Mentioning Death

9,111

30.0% of reports — not proof of cause

Hospitalization Reports

16,201

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 12,088 (43%)
Male 15,759 (56%)

Age Distribution

0–17 3,399
18–44 5,539
45–64 8,170
65–74 5,097
75+ 3,735

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
3 PYREXIA 2,089
4 PNEUMONIA 1,433
5 SEPSIS 1,363
6 SEPTIC SHOCK 1,353
7 MULTIPLE ORGAN DYSFUNCTION SYNDROME 1,220
8 ACUTE KIDNEY INJURY 1,212
9 CONDITION AGGRAVATED 1,145
10 RESPIRATORY FAILURE 1,084
11 THROMBOCYTOPENIA 1,075
12 FEBRILE NEUTROPENIA 1,072
13 DIARRHOEA 1,067
14 DRUG INTERACTION 915
15 NEUTROPENIA 883
16 ANAEMIA 849
17 HYPOTENSION 820

Reactions in Death Reports

MULTIPLE ORGAN DYSFUNCTION SYNDROME 1,027
SEPTIC SHOCK 941
PNEUMONIA 768
SEPSIS 755
RESPIRATORY FAILURE 653
DEATH 625
PYREXIA 599
CONDITION AGGRAVATED 468
CARDIAC ARREST 383
THROMBOCYTOPENIA 353

Reactions in Hospitalization Reports

PYREXIA 1,469
PNEUMONIA 1,015
ACUTE KIDNEY INJURY 857
SEPTIC SHOCK 856
SEPSIS 855
FEBRILE NEUTROPENIA 810
DIARRHOEA 794
RESPIRATORY FAILURE 764
MULTIPLE ORGAN DYSFUNCTION SYNDROME 758
CONDITION AGGRAVATED 692

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

Serious Warnings

You should not take this medicine if you are allergic to meropenem or similar antibiotics. This drug may cause serious allergic reactions, including trouble breathing. Meropenem can also cause seizures, especially if you have kidney problems or a history of seizures. Diarrhea can occur, and could be a sign of a serious infection in your colon.

Known Drug Interactions

moderate probenecid

7 DRUG INTERACTIONS Co-administration of Meropenem for Injection, USP with probenecid inhibits renal excretion of meropenem and is therefore not recommended. ( 5.4 , 7.2 ) 7.1 Probenecid Probenecid competes with meropenem for active tubular secretion, resulting in increased plasma concentrations of meropenem. Co-administration of probenecid with meropenem is not recommended.

Mechanism: Probenecid blocks the kidneys from clearing meropenem out of your system. This leads to higher levels of meropenem in your blood than intended.

( 7.4 , 12.3 ) 7.1 Valproic Acid Case reports in the literature have shown that co-administration of carbapenems, including meropenem, to patients receiving valproic acid or divalproex sodium results in a reduction in valproic acid concentrations. 7.2 Probenecid Probenecid competes with meropenem for active tubular secretion, resulting in increased plasma concentrations of meropenem.

Mechanism: Meropenem can significantly lower the amount of seizure medication in your blood, which increases the risk of having a seizure.

Carbapenem Antibiotics A clinically significant reduction in serum valproic acid concentration has been reported in patients receiving carbapenem antibiotics (for example, ertapenem, imipenem, meropenem this is not a complete list) and may result in loss of seizure control.

Mechanism: Meropenem can significantly lower the amount of valproate in your blood. This can make the valproate stop working and may lead to a breakthrough seizure.

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

Common Questions

What should I tell my doctor before taking meropenem?
Tell your doctor if you are allergic to any medicines, especially penicillins or other beta-lactam antibiotics. Also, tell them if you have kidney problems, seizures, or any other medical conditions.
Can meropenem interact with other medications?
Yes, meropenem can interact with certain medications, such as valproic acid (used to treat seizures). Be sure to tell your doctor about all the medicines you are taking.
What are the symptoms of an allergic reaction?
Symptoms of an allergic reaction can include rash, hives, itching, swelling, wheezing, or trouble breathing. If you experience any of these symptoms, get medical help right away.
Can meropenem cause diarrhea?
Yes, meropenem can cause diarrhea. If you develop severe diarrhea, especially with fever or stomach pain, tell your doctor right away.
How will I receive meropenem?
Meropenem is given through a needle into your vein (IV).
What if my symptoms don't improve?
If your symptoms do not improve after a few days of treatment, contact your doctor.
Can I drink alcohol while taking meropenem?
It's best to avoid alcohol while taking meropenem, as it could worsen some side effects.
Will meropenem affect my ability to drive or operate machinery?
Meropenem may cause dizziness or seizures in some people. Be careful driving or operating machinery until you know how this medicine affects you.
How long will I need to take meropenem?
Your doctor will determine how long you need to take meropenem. Take it for the full prescribed time, even if you feel better.
What if I have kidney problems?
If you have kidney problems, your doctor may need to adjust your dose of meropenem.
What are the common side effects of meropenem?
The registry lists Headache, Nausea, Constipation, Diarrhea, Anemia among the most-reported FAERS reaction terms for meropenem. The compiled record contains 30,400 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does meropenem interact with other medications?
The registry has 3 documented interaction rows for meropenem. Notable source-record pairings include probenecid, meropenem/vaborbactam, valproate. These rows are not a complete medication review.
What drug class is meropenem?
meropenem belongs to the Carbapenem Antibiotic drug class. It requires a prescription (Rx). Meropenem treats complicated skin infections in adults and kids 3 months and older.
What pregnancy or breastfeeding source fields are listed for meropenem?
The FDA label for meropenem contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.

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

Compare meropenem vs amikacin side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for meropenem: 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.

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What the FDA Data Shows for meropenem

The FDA label for meropenem (sold under brand names such as Merrem) classifies it as a prescription-only medication in the Carbapenem Antibiotic class. Meropenem treats complicated skin infections in adults and kids 3 months and older. Official labeling lists 8 commonly reported side effects, including Headache, Nausea, Constipation.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 30,400 voluntary reports. The database also lists 3 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated moderate severity. NADAC pricing from CMS shows a generic unit cost of $6.84.

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 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).

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: July 10, 2024

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