TROLAMINE SALICYLATE

N/A

Manufactured by Chattem, Inc.

443 FDA adverse event reports analyzed

Last updated: 2026-04-15

About TROLAMINE SALICYLATE

TROLAMINE SALICYLATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Chattem, Inc.. The most commonly reported adverse reactions for TROLAMINE SALICYLATE include DRUG INEFFECTIVE, FATIGUE, NAUSEA, PAIN, DIZZINESS. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for TROLAMINE SALICYLATE.

Top Adverse Reactions

DRUG INEFFECTIVE35 reports
FATIGUE17 reports
NAUSEA15 reports
PAIN15 reports
DIZZINESS14 reports
DEATH13 reports
DIARRHOEA11 reports
OFF LABEL USE11 reports
ARTHRALGIA8 reports
BACK PAIN6 reports
DYSPNOEA6 reports
HEADACHE6 reports
NO ADVERSE EVENT6 reports
PYREXIA6 reports
ABDOMINAL DISTENSION5 reports
ABDOMINAL PAIN UPPER5 reports
ATRIAL FIBRILLATION5 reports
CONDITION AGGRAVATED5 reports
CONSTIPATION5 reports
COUGH5 reports
FALL5 reports
INTENTIONAL PRODUCT USE ISSUE5 reports
PAIN IN EXTREMITY5 reports
PRODUCT DOSE OMISSION ISSUE5 reports
PRODUCT USE IN UNAPPROVED INDICATION5 reports
RASH5 reports
ABDOMINAL DISCOMFORT4 reports
ANAEMIA4 reports
ANXIETY4 reports
ARTHRITIS4 reports
ASTHENIA4 reports
COVID 194 reports
DECREASED APPETITE4 reports
FLATULENCE4 reports
GAIT DISTURBANCE4 reports
HYPERSENSITIVITY4 reports
INSOMNIA4 reports
MALAISE4 reports
NASOPHARYNGITIS4 reports
NECK PAIN4 reports
OEDEMA PERIPHERAL4 reports
PERIPHERAL SWELLING4 reports
RHEUMATOID ARTHRITIS4 reports
ROTATOR CUFF SYNDROME4 reports
URINARY TRACT INFECTION4 reports
WEIGHT INCREASED4 reports
BLOOD PRESSURE INCREASED3 reports
CATARACT3 reports
CHILLS3 reports
CONTUSION3 reports
DEHYDRATION3 reports
FEELING ABNORMAL3 reports
GASTRITIS3 reports
HYPERTENSION3 reports
HYPOAESTHESIA3 reports
HYPOTHYROIDISM3 reports
INFECTION3 reports
MEMORY IMPAIRMENT3 reports
MIGRAINE3 reports
MUSCLE SPASMS3 reports
MUSCULOSKELETAL STIFFNESS3 reports
NEUROPATHY PERIPHERAL3 reports
OROPHARYNGEAL PAIN3 reports
PARKINSON^S DISEASE3 reports
PRODUCT ODOUR ABNORMAL3 reports
PRODUCT USE ISSUE3 reports
STOMATITIS3 reports
THERAPEUTIC RESPONSE DECREASED3 reports
URTICARIA3 reports
VERTIGO3 reports
VISION BLURRED3 reports
WEIGHT DECREASED3 reports
ACUTE KIDNEY INJURY2 reports
ADRENAL INSUFFICIENCY2 reports
APPLICATION SITE BURN2 reports
ASTHMA2 reports
BLOOD CALCIUM DECREASED2 reports
BLOOD CHOLESTEROL INCREASED2 reports
BREATH ODOUR2 reports
CARDIAC DISORDER2 reports
CHRONIC KIDNEY DISEASE2 reports
DEPRESSED MOOD2 reports
DEPRESSION2 reports
DISORIENTATION2 reports
DRUG ADMINISTRATION ERROR2 reports
DRUG HYPERSENSITIVITY2 reports
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION2 reports
DRUG INTOLERANCE2 reports
DRY MOUTH2 reports
DYSGEUSIA2 reports
DYSPHAGIA2 reports
DYSURIA2 reports
ERYTHEMA2 reports
EYE PRURITUS2 reports
FOOT DEFORMITY2 reports
GASTROOESOPHAGEAL REFLUX DISEASE2 reports
HERPES ZOSTER2 reports
HOT FLUSH2 reports
HYPOKALAEMIA2 reports
HYPOTENSION2 reports

Report Outcomes

Out of 189 classified reports for TROLAMINE SALICYLATE:

Serious 50.3%Non-Serious 49.7%

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

Female118 (69.8%)
Male51 (30.2%)

Reports by Age

Age 827 reports
Age 605 reports
Age 615 reports
Age 705 reports
Age 674 reports
Age 744 reports
Age 754 reports
Age 774 reports
Age 804 reports
Age 814 reports
Age 623 reports
Age 633 reports
Age 643 reports
Age 663 reports
Age 693 reports
Age 713 reports
Age 793 reports
Age 833 reports
Age 432 reports
Age 472 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 TROLAMINE SALICYLATE?

This profile reflects 443 FDA FAERS reports that mention TROLAMINE SALICYLATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for TROLAMINE SALICYLATE?

Frequently reported terms in FAERS include DRUG INEFFECTIVE, FATIGUE, NAUSEA, PAIN, DIZZINESS, DEATH. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures TROLAMINE SALICYLATE?

Labeling and FAERS entries often list Chattem, Inc. in connection with TROLAMINE SALICYLATE. 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.