Prescription medication · Centrally Acting Muscle Relaxant

carisoprodol

Also sold as Soma. Carisoprodol treats the pain and discomfort caused by acute muscle and bone conditions.

Data updated 2026-05-15

18,851
FDA reportsModerately reported
4
InteractionsFew interactions
94% less
Generic vs brandHuge savings
$10.33
Brand price (NADAC)

What the data shows

carisoprodol (Soma) is a prescription Centrally Acting Muscle Relaxant, reported at a middle-of-the-pack volume (18,851 FDA reports), whose generic costs a fraction of the brand (about 94% less).

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.

carisoprodol (Soma) is a prescription Centrally Acting Muscle Relaxant. Carisoprodol treats the pain and discomfort caused by acute muscle and bone conditions.

Carisoprodol is a muscle relaxant. It helps relieve discomfort from painful muscle and bone problems.

Drug Pricing (NADAC)

Brand Price

$10.33/unit

Generic Price

$0.61/unit

Generic Savings

94%

Generic Available

Yes (8 manufacturers)

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

Compare with Another Drug → Full Side Effects Report →

What it does

Carisoprodol treats the pain and discomfort caused by acute muscle and bone conditions.

Common side effects

Drowsiness (13-17% of users), Dizziness (7-8% of users), Headache (3-5% of users)

Key warnings

Carisoprodol can be habit-forming.

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

How It Works

Carisoprodol works in the brain and spinal cord to relax muscles. It blocks pain signals between your nerves and brain. This helps to reduce muscle spasms and pain.

Side Effects (from patient reports)

Based on 18,851 FDA adverse event reports.

Most-reported reactions

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

05001,0001,5002,000 200120062009201220152018202120242025 197

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

Where carisoprodol sits

carisoprodol has more FDA adverse-event reports than 54% 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 carisoprodol; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 18,851 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2001–2025.

Total Reports

18,851

Reports Mentioning Death

3,997

21.2% of reports — not proof of cause

Hospitalization Reports

4,623

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 12,565 (71%)
Male 5,188 (29%)

Age Distribution

0–17 96
18–44 3,667
45–64 6,347
65–74 1,331
75+ 383

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 PAIN 1,615
2 COMPLETED SUICIDE 1,459
4 NAUSEA 1,280
5 HEADACHE 1,093
6 ANXIETY 989
7 DEPRESSION 985
8 FATIGUE 976
9 TOXICITY TO VARIOUS AGENTS 904
10 INSOMNIA 830
11 VOMITING 806
12 DRUG DEPENDENCE 795
13 FALL 789
14 DYSPNOEA 736
15 OVERDOSE 736
16 BACK PAIN 711

Reactions in Death Reports

COMPLETED SUICIDE 1,457
TOXICITY TO VARIOUS AGENTS 796
CARDIAC ARREST 575
DEATH 570
RESPIRATORY ARREST 546
DRUG ABUSE 413
CARDIO-RESPIRATORY ARREST 402
OVERDOSE 310
DRUG TOXICITY 202
DRUG DEPENDENCE 197

Reactions in Hospitalization Reports

PAIN 580
ANXIETY 431
FALL 421
DEPRESSION 398
NAUSEA 389
DYSPNOEA 349
VOMITING 342
PNEUMONIA 335
HEADACHE 312
CHEST PAIN 299

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

Serious Warnings

Carisoprodol can be habit-forming. Do not take it if you have a history of drug abuse. Stopping it suddenly after long-term use can cause withdrawal symptoms like insomnia, vomiting, and hallucinations. Carisoprodol can also cause seizures, especially if you take too much or mix it with other drugs or alcohol. This medicine can make you sleepy and impair your ability to drive or operate machinery.

Known Drug Interactions

Co-administration of CYP2C19 inhibitors, such as omeprazole or fluvoxamine, with carisoprodol could result in increased exposure of carisoprodol and decreased exposure of meprobamate.

Mechanism: Omeprazole slows down the liver enzyme that breaks down carisoprodol, which can cause the drug to stay in your body longer.

minor aspirin

Low dose aspirin also showed an induction effect on CYP2C19.

Mechanism: Aspirin makes your liver work faster to break down carisoprodol. This can cause the carisoprodol to leave your body too quickly and not work as well.

Co-administration of CYP2C19 inducers, such as rifampin or St.

Mechanism: Rifampin speeds up the liver enzymes that process carisoprodol. This can lower the amount of medicine in your system and make it less effective.

Co-administration of CYP2C19 inhibitors, such as omeprazole or fluvoxamine, with carisoprodol could result in increased exposure of carisoprodol and decreased exposure of meprobamate.

Mechanism: Fluvoxamine slows down the liver's ability to process carisoprodol. This can cause the drug to build up in your body, which may increase side effects.

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

Common Questions

Can I drive while taking carisoprodol?
No, carisoprodol can cause drowsiness and impair your ability to drive or operate machinery.
Can I drink alcohol while taking carisoprodol?
No, alcohol can increase the drowsiness caused by carisoprodol.
How long should I take carisoprodol?
You should only take carisoprodol for up to two or three weeks.
What should I do if I think I am having a side effect?
Tell your doctor about any side effects you experience while taking carisoprodol.
Can I take carisoprodol with other medications?
Talk to your doctor before taking carisoprodol with other medications, especially sedatives, tranquilizers, or pain medications.
What happens if I overdose on carisoprodol?
Overdosing on carisoprodol can cause serious problems, including seizures, slowed breathing, and death. Seek medical attention immediately.
Is carisoprodol addictive?
Yes, carisoprodol can be habit-forming. Do not take it if you have a history of drug abuse.
Can I stop taking carisoprodol suddenly?
No, stopping carisoprodol suddenly after long-term use can cause withdrawal symptoms. Talk to your doctor about how to safely stop taking it.
What does carisoprodol look like?
Carisoprodol tablets are round, white, and have "111" on one side and "O" on the other.
What if this medicine doesn't seem to be working?
Talk to your doctor if carisoprodol does not relieve your pain.
What are the common side effects of carisoprodol?
The registry lists Drowsiness (13-17% of users), Dizziness (7-8% of users), Headache (3-5% of users) among the most-reported FAERS reaction terms for carisoprodol. The compiled record contains 18,851 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does carisoprodol interact with other medications?
The registry has 4 documented interaction rows for carisoprodol. Notable source-record pairings include omeprazole, aspirin, rifampin. These rows are not a complete medication review.
What drug class is carisoprodol?
carisoprodol belongs to the Centrally Acting Muscle Relaxant drug class. It requires a prescription (Rx). Carisoprodol treats the pain and discomfort caused by acute muscle and bone conditions.
Is there a generic version of carisoprodol?
Yes, generic carisoprodol is available from 8 manufacturers. The generic costs $0.61 per unit compared to $10.33 for the brand version, saving approximately 94%. Pricing is based on NADAC (National Average Drug Acquisition Cost) data from CMS.
What pregnancy or breastfeeding source fields are listed for carisoprodol?
The FDA label for carisoprodol contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.

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

Compare carisoprodol vs baclofen side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for carisoprodol: 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 carisoprodol

The FDA label for carisoprodol (sold under brand names such as Soma) classifies it as a prescription-only medication in the Centrally Acting Muscle Relaxant class. Carisoprodol treats the pain and discomfort caused by acute muscle and bone conditions. Official labeling lists 3 commonly reported side effects, including Drowsiness (13-17% of users), Dizziness (7-8% of users), Headache (3-5% of users).

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 18,851 voluntary reports. The database also lists 4 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated minor severity. NADAC pricing from CMS shows a generic unit cost of $0.61 versus $10.33 for the brand - a 94% generic savings.

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: December 24, 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