COAL TAR

N/A

Manufactured by Kobayashi Healthcare International, Inc.

11,295 FDA adverse event reports analyzed

Last updated: 2026-04-15

About COAL TAR

COAL TAR is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Kobayashi Healthcare International, Inc.. The most commonly reported adverse reactions for COAL TAR include PSORIASIS, MALAISE, FATIGUE, PAIN, NASOPHARYNGITIS. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for COAL TAR.

Top Adverse Reactions

PSORIASIS401 reports
MALAISE276 reports
FATIGUE244 reports
PAIN229 reports
NASOPHARYNGITIS213 reports
PYREXIA198 reports
SKIN EXFOLIATION198 reports
COUGH197 reports
FALL197 reports
ANXIETY194 reports
NAUSEA194 reports
RHINORRHOEA194 reports
INFLUENZA192 reports
PNEUMONIA190 reports
BLOOD PRESSURE INCREASED189 reports
VOMITING189 reports
HEADACHE188 reports
SKIN HAEMORRHAGE185 reports
SINUS DISORDER182 reports
SNEEZING182 reports
SINUS CONGESTION180 reports
CYSTITIS179 reports
CEREBROVASCULAR ACCIDENT178 reports
DYSPHAGIA176 reports
INFLUENZA LIKE ILLNESS176 reports
RESPIRATORY TRACT CONGESTION176 reports
SENSORY LOSS171 reports
CONFUSIONAL STATE169 reports
AFFECT LABILITY168 reports
APHASIA168 reports
CAROTID ARTERY THROMBOSIS168 reports
COORDINATION ABNORMAL168 reports
DYSARTHRIA168 reports
HEMIPLEGIA166 reports
MOTOR DYSFUNCTION166 reports
MUSCLE SPASTICITY166 reports
NEUROLOGIC NEGLECT SYNDROME166 reports
PERSONALITY DISORDER166 reports
HEMIPARESIS165 reports
MUSCULAR WEAKNESS165 reports
EATING DISORDER164 reports
ADJUSTMENT DISORDER163 reports
ANGINA PECTORIS163 reports
CHEST DISCOMFORT161 reports
SINUSITIS160 reports
RHEUMATOID ARTHRITIS157 reports
ARTHRITIS156 reports
PALPITATIONS153 reports
CATARACT152 reports
ARTERIAL OCCLUSIVE DISEASE151 reports
DRUG INEFFECTIVE151 reports
GANGRENE151 reports
GASTROINTESTINAL DISORDER145 reports
ASTHENIA131 reports
PRURITUS81 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION74 reports
PSORIATIC ARTHROPATHY74 reports
PAIN IN EXTREMITY65 reports
DYSPNOEA62 reports
MOVEMENT DISORDER51 reports
PANIC ATTACK48 reports
ABDOMINAL DISCOMFORT45 reports
ARTHRALGIA45 reports
SKIN PLAQUE44 reports
CHEST PAIN41 reports
FEELING ABNORMAL40 reports
INCORRECT DOSE ADMINISTERED38 reports
SECRETION DISCHARGE36 reports
PULMONARY CONGESTION34 reports
CONTUSION32 reports
PULMONARY MASS32 reports
RASH32 reports
ILLNESS31 reports
OROPHARYNGEAL PAIN31 reports
INJECTION SITE PAIN30 reports
CARDIAC DISORDER29 reports
DEVICE MALFUNCTION28 reports
DIARRHOEA26 reports
DIZZINESS26 reports
DRUG INTOLERANCE26 reports
HYPERTENSION25 reports
ERYTHEMA24 reports
SKIN FISSURES24 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE23 reports
PRODUCT USE ISSUE22 reports
BACK PAIN21 reports
HYPERHIDROSIS21 reports
SKIN BURNING SENSATION20 reports
WEIGHT DECREASED20 reports
DEVICE ISSUE19 reports
DRY SKIN19 reports
INSOMNIA19 reports
DEPRESSED MOOD18 reports
DRUG INTERACTION18 reports
FUNGAL INFECTION18 reports
LIMB DISCOMFORT18 reports
PRODUCT DOSE OMISSION ISSUE18 reports
PRODUCT PRESCRIBING ERROR18 reports
ANAEMIA MACROCYTIC17 reports
DIABETIC NEUROPATHY17 reports

Report Outcomes

Out of 748 classified reports for COAL TAR:

Serious 91.0%Non-Serious 9.0%

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

Female443 (62.3%)
Male268 (37.7%)

Reports by Age

Age 65139 reports
Age 6147 reports
Age 5446 reports
Age 7641 reports
Age 5026 reports
Age 2725 reports
Age 4620 reports
Age 6413 reports
Age 4112 reports
Age 4212 reports
Age 6612 reports
Age 4010 reports
Age 5510 reports
Age 5610 reports
Age 6710 reports
Age 539 reports
Age 779 reports
Age 628 reports
Age 808 reports
Age 387 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 COAL TAR?

This profile reflects 11,295 FDA FAERS reports that mention COAL TAR. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for COAL TAR?

Frequently reported terms in FAERS include PSORIASIS, MALAISE, FATIGUE, PAIN, NASOPHARYNGITIS, PYREXIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures COAL TAR?

Labeling and FAERS entries often list Kobayashi Healthcare International, Inc. in connection with COAL TAR. 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.