Prescription medication · Muscle Relaxant

methocarbamol

Also sold as Robaxin. This medicine treats the discomfort caused by painful muscle problems.

Data updated 2026-05-15

21,191
FDA reportsModerately reported
1
Recall record

What the data shows

methocarbamol (Robaxin) is a prescription Muscle Relaxant, reported at a middle-of-the-pack volume (21,191 FDA reports).

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.

methocarbamol (Robaxin) is a prescription Muscle Relaxant. This medicine treats the discomfort caused by painful muscle problems.

Methocarbamol is a muscle relaxant. It helps to relieve discomfort from painful muscle problems.

Drug Pricing (NADAC)

Generic Price

$0.03/unit

Generic Available

Yes (16 manufacturers)

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

NADAC price trail: METHOCARBAMOL 500 MG TABLET

Same CMS presentation as the headline generic unit price above (3 effective dates). Adjacent % compares consecutive NADAC releases for this description only, not a patient out-of-pocket quote. Latest step: -2.2% vs prior release.

3.5¢4.5¢ 2024-022024-042024-12 3.2¢
Effective NADAC / unit vs prior NDCs
February 21, 2024 $0.0424/EA - 1
April 17, 2024 $0.0327/EA -22.9% 1
December 18, 2024 $0.0320/EA -2.2% 23
View Alternatives → Compare with Another Drug → Full Side Effects Report →

What it does

This medicine treats the discomfort caused by painful muscle problems.

Common side effects

Drowsiness, Dizziness, Lightheadedness

Key warnings

Methocarbamol can interact with alcohol and other drugs that affect your central nervous system.

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

How It Works

Methocarbamol is a central nervous system depressant. It likely works by making you feel calm and relaxed. This may help to relieve muscle discomfort.

Side Effects (from patient reports)

Based on 21,191 FDA adverse event reports.

Most-reported reactions

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

05001,0001,5002,0002,500 20042007201020132016201920222025 2,132

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

Where methocarbamol sits

methocarbamol has more FDA adverse-event reports than 56% 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 methocarbamol; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 21,191 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

21,191

Reports Mentioning Death

1,643

7.8% of reports — not proof of cause

Hospitalization Reports

6,345

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 13,996 (70%)
Male 5,871 (30%)

Age Distribution

0–17 183
18–44 2,697
45–64 6,430
65–74 2,486
75+ 1,452

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 PAIN 1,639
2 NAUSEA 1,565
3 FATIGUE 1,531
5 HEADACHE 1,201
6 DIARRHOEA 1,078
7 FALL 1,046
8 DYSPNOEA 995
9 ARTHRALGIA 963
10 DIZZINESS 909
11 ANXIETY 884
12 BACK PAIN 884
14 DEPRESSION 797
15 VOMITING 789
16 PAIN IN EXTREMITY 762
17 CHRONIC KIDNEY DISEASE 761

Reactions in Death Reports

DEATH 528
COMPLETED SUICIDE 323
TOXICITY TO VARIOUS AGENTS 169
CARDIAC ARREST 132
CARDIO-RESPIRATORY ARREST 109
PNEUMONIA 83
DYSPNOEA 80
RESPIRATORY ARREST 73
RENAL FAILURE 72
FALL 69

Reactions in Hospitalization Reports

FALL 588
PAIN 534
NAUSEA 509
PNEUMONIA 470
DYSPNOEA 466
FATIGUE 434
DIARRHOEA 378
HEADACHE 365
VOMITING 365
BACK PAIN 361

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

Serious Warnings

Methocarbamol can interact with alcohol and other drugs that affect your central nervous system. Be careful when taking these together.

Common Questions

Can I drink alcohol while taking this medicine?
It is best to avoid alcohol while taking methocarbamol.
Will this medicine make me sleepy?
Yes, drowsiness is a common side effect.
Can I drive while taking this medicine?
Be careful driving or operating machinery until you know how this medicine affects you.
What should I do if I have side effects?
Tell your doctor about any side effects you experience.
Can I take this with other medicines?
Tell your doctor about all the medicines you take, including over-the-counter drugs.
How long does it take for this medicine to work?
It should start working within a few hours.
What if this medicine doesn't relieve my pain?
Talk to your doctor if your pain does not improve.
Can I stop taking this medicine when I feel better?
Talk to your doctor before stopping this medicine.
Is it okay to take this medication if I have kidney problems?
Talk to your doctor if you have kidney problems.
Can children take this medicine?
This medicine is for adults. Talk to your doctor about treatment options for children.
What are the common side effects of methocarbamol?
The registry lists Drowsiness, Dizziness, Lightheadedness, Blurred vision, Nausea among the most-reported FAERS reaction terms for methocarbamol. The compiled record contains 21,191 FDA adverse-event reports. These counts are not an individual symptom assessment.
What drug class is methocarbamol?
methocarbamol belongs to the Muscle Relaxant drug class. It requires a prescription (Rx). This medicine treats the discomfort caused by painful muscle problems.
What pregnancy or breastfeeding source fields are listed for methocarbamol?
The FDA label for methocarbamol contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.
Has methocarbamol been recalled?
There is 1 recall associated with methocarbamol products. Lack of Assurance of Sterility: Media fill with bacterial contamination. Check the recalls section below for full details and affected products.

Active Recalls

Class II March 21, 2025

Lack of Assurance of Sterility: Media fill with bacterial contamination

Somerset Therapeutics Private Limited

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

Compare methocarbamol vs baclofen side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for methocarbamol: 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

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What the FDA Data Shows for methocarbamol

The FDA label for methocarbamol (sold under brand names such as Robaxin) classifies it as a prescription-only medication in the Muscle Relaxant class. This medicine treats the discomfort caused by painful muscle problems. Official labeling lists 5 commonly reported side effects, including Drowsiness, Dizziness, Lightheadedness.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 21,191 voluntary reports. Interaction data is drawn directly from FDA-approved prescribing information. NADAC pricing from CMS shows a generic unit cost of $0.03.

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 1 recall record 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).

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 1, 2020

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