CARISOPRODOL

N/A

Manufactured by Viatris Specialty LLC

45,997 FDA adverse event reports analyzed

Last updated: 2026-04-14

About CARISOPRODOL

CARISOPRODOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Viatris Specialty LLC. The most commonly reported adverse reactions for CARISOPRODOL include PAIN, COMPLETED SUICIDE, DRUG INEFFECTIVE, NAUSEA, HEADACHE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CARISOPRODOL.

Top Adverse Reactions

PAIN1,612 reports
COMPLETED SUICIDE1,458 reports
DRUG INEFFECTIVE1,318 reports
NAUSEA1,280 reports
HEADACHE1,094 reports
ANXIETY990 reports
DEPRESSION986 reports
FATIGUE977 reports
TOXICITY TO VARIOUS AGENTS904 reports
INSOMNIA830 reports
VOMITING804 reports
DRUG DEPENDENCE795 reports
FALL789 reports
OVERDOSE736 reports
DYSPNOEA733 reports
BACK PAIN712 reports
DIZZINESS707 reports
DIARRHOEA693 reports
CHRONIC KIDNEY DISEASE659 reports
ARTHRALGIA638 reports
PAIN IN EXTREMITY631 reports
MALAISE630 reports
CARDIAC ARREST604 reports
WEIGHT DECREASED594 reports
DRUG ABUSE580 reports
ASTHENIA575 reports
DEATH570 reports
RESPIRATORY ARREST570 reports
FEELING ABNORMAL525 reports
SOMNOLENCE519 reports
RENAL FAILURE506 reports
CHEST PAIN488 reports
MUSCLE SPASMS488 reports
HYPERTENSION476 reports
ACUTE KIDNEY INJURY464 reports
PNEUMONIA448 reports
DRUG WITHDRAWAL SYNDROME446 reports
WEIGHT INCREASED442 reports
OFF LABEL USE436 reports
TREMOR430 reports
CONSTIPATION413 reports
CARDIO RESPIRATORY ARREST404 reports
HYPOAESTHESIA395 reports
PYREXIA386 reports
GAIT DISTURBANCE383 reports
HYPERHIDROSIS381 reports
LOSS OF CONSCIOUSNESS380 reports
RASH372 reports
ABDOMINAL PAIN367 reports
PRURITUS359 reports
EMOTIONAL DISTRESS350 reports
MEMORY IMPAIRMENT348 reports
DRUG HYPERSENSITIVITY337 reports
SUICIDAL IDEATION332 reports
CONDITION AGGRAVATED329 reports
COUGH324 reports
MIGRAINE323 reports
ABDOMINAL PAIN UPPER319 reports
PARAESTHESIA319 reports
DECREASED APPETITE317 reports
MYOCARDIAL INFARCTION314 reports
ROAD TRAFFIC ACCIDENT309 reports
OEDEMA PERIPHERAL307 reports
CONFUSIONAL STATE306 reports
GASTROOESOPHAGEAL REFLUX DISEASE304 reports
URINARY TRACT INFECTION301 reports
DRUG DOSE OMISSION296 reports
MYALGIA288 reports
INJURY287 reports
VISION BLURRED274 reports
AMNESIA259 reports
HYPOTENSION259 reports
CONVULSION258 reports
CEREBROVASCULAR ACCIDENT249 reports
BRONCHITIS245 reports
DEHYDRATION245 reports
ANAEMIA242 reports
BLOOD PRESSURE INCREASED235 reports
DIABETES MELLITUS233 reports
PRODUCT QUALITY ISSUE228 reports
NECK PAIN227 reports
INTENTIONAL DRUG MISUSE226 reports
DRUG TOXICITY224 reports
SINUSITIS223 reports
SUICIDE ATTEMPT223 reports
ALOPECIA222 reports
PALPITATIONS222 reports
CONTUSION221 reports
ABDOMINAL DISCOMFORT217 reports
MULTIPLE DRUG OVERDOSE217 reports
WRONG TECHNIQUE IN DRUG USAGE PROCESS215 reports
INJECTION SITE PAIN213 reports
DEEP VEIN THROMBOSIS208 reports
ACCIDENTAL OVERDOSE207 reports
DRUG INTERACTION207 reports
MUSCULAR WEAKNESS206 reports
ARTHRITIS205 reports
DEPENDENCE202 reports
END STAGE RENAL DISEASE199 reports
INTERVERTEBRAL DISC PROTRUSION199 reports

Report Outcomes

Out of 18,847 classified reports for CARISOPRODOL:

Serious 68.8%Non-Serious 31.2%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female12,565 (70.5%)
Male5,188 (29.1%)
Unknown67 (0.4%)

Reports by Age

Age 53431 reports
Age 51425 reports
Age 54371 reports
Age 52358 reports
Age 57351 reports
Age 55349 reports
Age 50347 reports
Age 46346 reports
Age 56331 reports
Age 58331 reports
Age 59327 reports
Age 49316 reports
Age 45290 reports
Age 48289 reports
Age 47286 reports
Age 60280 reports
Age 61275 reports
Age 44268 reports
Age 41264 reports
Age 43255 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with CARISOPRODOL?

This profile reflects 45,997 FDA FAERS reports that mention CARISOPRODOL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CARISOPRODOL?

Frequently reported terms in FAERS include PAIN, COMPLETED SUICIDE, DRUG INEFFECTIVE, NAUSEA, HEADACHE, ANXIETY. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures CARISOPRODOL?

Labeling and FAERS entries often list Viatris Specialty LLC in connection with CARISOPRODOL. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.