UNDECYLENIC ACID

N/A

Manufactured by Blaine Labs Inc.

121 FDA adverse event reports analyzed

Last updated: 2026-04-15

About UNDECYLENIC ACID

UNDECYLENIC ACID is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Blaine Labs Inc.. The most commonly reported adverse reactions for UNDECYLENIC ACID include NAUSEA, SOMNOLENCE, TREATMENT FAILURE, WRONG TECHNIQUE IN PRODUCT USAGE PROCESS, ASTHENIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for UNDECYLENIC ACID.

Top Adverse Reactions

NAUSEA3 reports
SOMNOLENCE3 reports
TREATMENT FAILURE3 reports
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS3 reports
ASTHENIA2 reports
CONFUSIONAL STATE2 reports
DIARRHOEA2 reports
DIZZINESS2 reports
DRUG HYPERSENSITIVITY2 reports
FATIGUE2 reports
HYPERHIDROSIS2 reports
INTENTIONAL DOSE OMISSION2 reports
INTENTIONAL PRODUCT USE ISSUE2 reports
INTERNATIONAL NORMALISED RATIO INCREASED2 reports
PAIN IN EXTREMITY2 reports
PRODUCT USE IN UNAPPROVED INDICATION2 reports
VISION BLURRED2 reports
ABDOMINAL DISCOMFORT1 reports
ACUTE KIDNEY INJURY1 reports
AGITATION1 reports
ANAPHYLACTIC REACTION1 reports
ANKLE FRACTURE1 reports
APPLICATION SITE BURN1 reports
ARTHRALGIA1 reports
ARTHROPOD BITE1 reports
BLOOD CALCIUM INCREASED1 reports
BLOOD GLUCOSE INCREASED1 reports
BRADYCARDIA1 reports
BRAIN FOG1 reports
CHEMICAL BURN1 reports
CHEST PAIN1 reports
CHILLS1 reports
CONDITION AGGRAVATED1 reports
COUGH1 reports
COVID 191 reports
DEFAECATION URGENCY1 reports
DEPRESSION1 reports
DRUG ABUSE1 reports
DRUG EFFECT LESS THAN EXPECTED1 reports
DRUG ERUPTION1 reports
DRUG INTERACTION1 reports
DRUG INTOLERANCE1 reports
DRY MOUTH1 reports
DYSARTHRIA1 reports
ENCEPHALOPATHY1 reports
EPISTAXIS1 reports
ERYTHEMA MULTIFORME1 reports
FEELING OF DESPAIR1 reports
FOREIGN BODY IN THROAT1 reports
GLYCOSYLATED HAEMOGLOBIN INCREASED1 reports
HEAD BANGING1 reports
HEAD INJURY1 reports
HEADACHE1 reports
HOSPITALISATION1 reports
HYPERSENSITIVITY1 reports
HYPERTENSION1 reports
HYPOPHAGIA1 reports
HYPOTENSION1 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION1 reports
INCORRECT DOSE ADMINISTERED1 reports
INFECTION1 reports
INFUSION RELATED REACTION1 reports
INJECTION SITE REACTION1 reports
INSOMNIA1 reports
IRRITABLE BOWEL SYNDROME1 reports
LIGAMENT SPRAIN1 reports
LUNG DISORDER1 reports
LYME DISEASE1 reports
MIDDLE INSOMNIA1 reports
MIGRAINE1 reports
MOANING1 reports
MORNING SICKNESS1 reports
MOVEMENT DISORDER1 reports
MUSCULOSKELETAL CHEST PAIN1 reports
MUSCULOSKELETAL PAIN1 reports
MYALGIA1 reports
MYOCARDIAL INFARCTION1 reports
NEUROPATHY PERIPHERAL1 reports
NIGHTMARE1 reports
NO ADVERSE EVENT1 reports
NO THERAPEUTIC RESPONSE1 reports
OFF LABEL USE1 reports
PALPITATIONS1 reports
PARANASAL SINUS HYPERSECRETION1 reports
PRE EXISTING CONDITION IMPROVED1 reports
RESPIRATORY DISORDER1 reports
SCHIZOPHRENIA1 reports
SEDATION1 reports
SEIZURE1 reports
SELF DESTRUCTIVE BEHAVIOUR1 reports
SELF INJURIOUS IDEATION1 reports
SUICIDAL IDEATION1 reports
SUPRAVENTRICULAR TACHYCARDIA1 reports
SURGERY1 reports
SYNCOPE1 reports
TACHYCARDIA1 reports
TENDON PAIN1 reports
TENDONITIS1 reports
THERAPEUTIC RESPONSE UNEXPECTED1 reports
THERAPY CESSATION1 reports

Report Outcomes

Out of 37 classified reports for UNDECYLENIC ACID:

Serious 73.0%Non-Serious 27.0%

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

Female22 (61.1%)
Male14 (38.9%)

Reports by Age

Age 583 reports
Age 222 reports
Age 502 reports
Age 572 reports
Age 622 reports
Age 782 reports
Age 291 reports
Age 311 reports
Age 331 reports
Age 361 reports
Age 541 reports
Age 601 reports
Age 681 reports
Age 711 reports
Age 731 reports
Age 751 reports
Age 761 reports
Age 831 reports
Age 871 reports
Age 881 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 UNDECYLENIC ACID?

This profile reflects 121 FDA FAERS reports that mention UNDECYLENIC ACID. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for UNDECYLENIC ACID?

Frequently reported terms in FAERS include NAUSEA, SOMNOLENCE, TREATMENT FAILURE, WRONG TECHNIQUE IN PRODUCT USAGE PROCESS, ASTHENIA, CONFUSIONAL STATE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures UNDECYLENIC ACID?

Labeling and FAERS entries often list Blaine Labs Inc. in connection with UNDECYLENIC ACID. 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.