SULFUR

N/A

Manufactured by Alchemee, LLC

20,945 FDA adverse event reports analyzed

Last updated: 2026-04-14

About SULFUR

SULFUR is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Alchemee, LLC. The most commonly reported adverse reactions for SULFUR include DRY SKIN, ACNE, ERYTHEMA, SKIN BURNING SENSATION, DRUG INEFFECTIVE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for SULFUR.

Top Adverse Reactions

DRY SKIN2,549 reports
ACNE2,256 reports
ERYTHEMA2,047 reports
SKIN BURNING SENSATION2,016 reports
DRUG INEFFECTIVE1,426 reports
SKIN IRRITATION1,265 reports
SKIN EXFOLIATION1,152 reports
RASH821 reports
PRURITUS650 reports
PAIN OF SKIN633 reports
OVERDOSE516 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION455 reports
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION331 reports
HYPERSENSITIVITY315 reports
RASH PAPULAR283 reports
UNDERDOSE267 reports
CONDITION AGGRAVATED234 reports
PRODUCT USE IN UNAPPROVED INDICATION223 reports
RASH MACULAR201 reports
DRUG HYPERSENSITIVITY185 reports
URTICARIA180 reports
SKIN HYPERPIGMENTATION163 reports
SKIN FRAGILITY162 reports
SKIN DISCOLOURATION129 reports
SWELLING FACE120 reports
RASH ERYTHEMATOUS115 reports
DERMATITIS114 reports
SKIN FISSURES107 reports
ACNE CYSTIC104 reports
SEBORRHOEA98 reports
SKIN SWELLING95 reports
SCAR93 reports
SENSITIVE SKIN85 reports
BLISTER72 reports
EYE SWELLING67 reports
PRODUCT USE ISSUE67 reports
SKIN REACTION67 reports
SCAB61 reports
CHEMICAL BURN OF SKIN54 reports
SKIN TIGHTNESS50 reports
SKIN HAEMORRHAGE49 reports
PARAESTHESIA47 reports
SKIN DISCOMFORT44 reports
PAIN35 reports
EYE IRRITATION33 reports
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE29 reports
ECZEMA29 reports
RASH PRURITIC29 reports
SKIN HYPOPIGMENTATION29 reports
SKIN WARM28 reports
CHEMICAL BURN27 reports
DIZZINESS27 reports
HEADACHE27 reports
MALAISE26 reports
FATIGUE24 reports
SUNBURN23 reports
SWELLING21 reports
DYSPNOEA20 reports
OCULAR HYPERAEMIA20 reports
ROSACEA19 reports
SKIN INJURY18 reports
ACNE PUSTULAR17 reports
ARTHRALGIA17 reports
ABDOMINAL DISTENSION16 reports
FURUNCLE16 reports
LIP SWELLING16 reports
SKIN EROSION16 reports
THERAPEUTIC PRODUCT EFFECT DECREASED16 reports
ABDOMINAL PAIN UPPER15 reports
OFF LABEL USE15 reports
PNEUMONIA15 reports
PYREXIA15 reports
ALOPECIA14 reports
ASTHENIA14 reports
INSOMNIA14 reports
LACRIMATION INCREASED14 reports
VOMITING14 reports
BURNING SENSATION13 reports
FEELING ABNORMAL13 reports
FEELING HOT13 reports
NAUSEA13 reports
RHEUMATOID ARTHRITIS13 reports
SKIN INFECTION13 reports
ADVERSE REACTION12 reports
BLOOD GLUCOSE INCREASED12 reports
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION12 reports
GAIT DISTURBANCE12 reports
PANCREATITIS12 reports
ADVERSE DRUG REACTION11 reports
DIABETES MELLITUS11 reports
DRY MOUTH11 reports
EYE PRURITUS11 reports
GENERAL PHYSICAL HEALTH DETERIORATION11 reports
HYPOAESTHESIA11 reports
LOWER RESPIRATORY TRACT INFECTION VIRAL11 reports
MUSCULOSKELETAL STIFFNESS11 reports
MYALGIA11 reports
OVARIAN CYST11 reports
SKIN ULCER11 reports
DIARRHOEA10 reports

Report Outcomes

Out of 8,372 classified reports for SULFUR:

Serious 2.3%Non-Serious 97.7%

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

Female6,600 (82.3%)
Male1,407 (17.5%)
Unknown16 (0.2%)

Reports by Age

Age 15409 reports
Age 14375 reports
Age 16308 reports
Age 13279 reports
Age 17232 reports
Age 18218 reports
Age 19180 reports
Age 21155 reports
Age 24144 reports
Age 12138 reports
Age 23137 reports
Age 26129 reports
Age 27129 reports
Age 28129 reports
Age 29129 reports
Age 20128 reports
Age 22127 reports
Age 30126 reports
Age 25114 reports
Age 33105 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 SULFUR?

This profile reflects 20,945 FDA FAERS reports that mention SULFUR. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for SULFUR?

Frequently reported terms in FAERS include DRY SKIN, ACNE, ERYTHEMA, SKIN BURNING SENSATION, DRUG INEFFECTIVE, SKIN IRRITATION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures SULFUR?

Labeling and FAERS entries often list Alchemee, LLC in connection with SULFUR. 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.