Prescription medication · Carbapenem Antibiotic

ertapenem

Also sold as Invanz. Ertapenem treats moderate to severe infections caused by certain bacteria.

Data updated 2026-05-15

3,848
FDA reportsLightly reported
2
InteractionsFew interactions
$37.91
Generic price (NADAC)

What the data shows

ertapenem (Invanz) is a prescription Carbapenem Antibiotic, among the least-reported drugs the FDA tracks (3,848 FDA reports), with 2 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.

ertapenem (Invanz) is a prescription Carbapenem Antibiotic. Ertapenem treats moderate to severe infections caused by certain bacteria.

Ertapenem is an antibiotic medicine. It fights bacteria in your body.

Drug Pricing (NADAC)

Generic Price

$37.91/unit

Generic Available

Yes (5 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

Ertapenem treats moderate to severe infections caused by certain bacteria.

Common side effects

Diarrhea, Nausea, Headache

Key warnings

Ertapenem can cause serious allergic reactions.

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

How It Works

Ertapenem 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 3,848 FDA adverse event reports.

Most-reported reactions

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

0200400600800 20042007201020132016201920222025 424

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

Where ertapenem sits

ertapenem has more FDA adverse-event reports than 22% 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 ertapenem; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 3,848 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

3,848

Reports Mentioning Death

339

8.8% of reports — not proof of cause

Hospitalization Reports

1,953

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 1,799 (52%)
Male 1,632 (47%)

Age Distribution

0–17 72
18–44 435
45–64 851
65–74 747
75+ 662

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
2 MACULAR DEGENERATION 768
4 PYREXIA 358
5 NAUSEA 293
6 PAIN 284
7 WEIGHT DECREASED 248
8 MALAISE 231
9 ANAEMIA 223
10 THERAPEUTIC PRODUCT EFFECT INCOMPLETE 221
11 CHRONIC SINUSITIS 213
12 PARAESTHESIA ORAL 212
13 INFUSION RELATED REACTION 208
14 ABDOMINAL PAIN 203
15 DYSPEPSIA 193
16 PROCEDURAL PAIN 192
17 HEADACHE 186

Reactions in Death Reports

DEATH 57
SEPSIS 31
INFECTION 25
SEPTIC SHOCK 24
MULTIPLE ORGAN DYSFUNCTION SYNDROME 22
ANAEMIA 21
CARDIAC ARREST 21
BONE MARROW FAILURE 20
HYPOTENSION 20
PYREXIA 20

Reactions in Hospitalization Reports

PYREXIA 319
NAUSEA 261
PAIN 242
WEIGHT DECREASED 233
MACULAR DEGENERATION 230
MALAISE 217
THERAPEUTIC PRODUCT EFFECT INCOMPLETE 211
CHRONIC SINUSITIS 210
ANAEMIA 209
PARAESTHESIA ORAL 209

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

Serious Warnings

Ertapenem can cause serious allergic reactions. Tell your doctor if you are allergic to any beta-lactam antibiotics like penicillins or cephalosporins. Seizures have happened during treatment with ertapenem, especially in people with brain problems or kidney issues. Ertapenem can also cause severe diarrhea due to Clostridioides difficile.

Known Drug Interactions

moderate probenecid

7 DRUG INTERACTIONS Co-administration with probenecid inhibits the renal excretion of ertapenem and is therefore not recommended. ( 5.2 , 7.2 ) 7.1 Probenecid Probenecid interferes with the active tubular secretion of ertapenem, resulting in increased plasma concentrations of ertapenem [see Clinical Pharmacology ( 12.3 )] . Co-administration of probenecid with ertapenem is not recommended.

Mechanism: Probenecid stops the kidneys from getting rid of ertapenem, which causes the levels of the antibiotic in the blood to stay higher for longer.

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: Ertapenem causes a large drop in valproate levels in the blood. This reduction can cause the medication to fail, increasing the risk of having a seizure.

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

Common Questions

Can I mix ertapenem with other medications?
No, do not mix or infuse ertapenem with other medications.
Can I use solutions containing dextrose to mix ertapenem?
No, do not use solutions containing dextrose to mix ertapenem.
How long does the IV infusion take?
The intravenous infusion should be given over 30 minutes.
What if I have kidney problems?
Your doctor may need to adjust your dose if you have severe kidney problems.
Can ertapenem interact with other medications I'm taking?
Yes, ertapenem can interact with probenecid and valproic acid. Tell your doctor about all the medicines you take.
What should I do if I develop diarrhea while taking ertapenem?
Tell your doctor right away if you develop diarrhea, especially if it is severe or bloody.
Can ertapenem cause seizures?
Yes, ertapenem can increase the risk of seizures, especially in people with a history of seizures or kidney problems.
What if I am allergic to lidocaine?
If you are allergic to lidocaine, you should not receive ertapenem as an intramuscular injection.
How will I receive ertapenem?
Ertapenem will be given to you by a healthcare provider as an IV infusion or an IM injection.
What should I tell my doctor before starting ertapenem?
Tell your doctor if you are allergic to any antibiotics, have kidney problems, have a history of seizures, or are pregnant or breastfeeding.
What are the common side effects of ertapenem?
The registry lists Diarrhea, Nausea, Headache, Problems where the IV was placed among the most-reported FAERS reaction terms for ertapenem. The compiled record contains 3,848 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does ertapenem interact with other medications?
The registry has 2 documented interaction rows for ertapenem. Notable source-record pairings include probenecid, valproate. These rows are not a complete medication review.
What drug class is ertapenem?
ertapenem belongs to the Carbapenem Antibiotic drug class. It requires a prescription (Rx). Ertapenem treats moderate to severe infections caused by certain bacteria.
What pregnancy or breastfeeding source fields are listed for ertapenem?
The FDA label for ertapenem contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.

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

Compare ertapenem vs amikacin side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for ertapenem: 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 ertapenem

The FDA label for ertapenem (sold under brand names such as Invanz) classifies it as a prescription-only medication in the Carbapenem Antibiotic class. Ertapenem treats moderate to severe infections caused by certain bacteria. Official labeling lists 4 commonly reported side effects, including Diarrhea, Nausea, Headache.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 3,848 voluntary reports. The database also lists 2 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 $37.91.

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: January 9, 2026

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