MINOCYCLINE

N/A

Manufactured by Journey Medical Corporation

54,303 FDA adverse event reports analyzed

Last updated: 2026-04-14

About MINOCYCLINE

MINOCYCLINE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Journey Medical Corporation. The most commonly reported adverse reactions for MINOCYCLINE include DRUG INEFFECTIVE, OFF LABEL USE, NAUSEA, PAIN, ARTHRALGIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for MINOCYCLINE.

Top Adverse Reactions

DRUG INEFFECTIVE1,908 reports
OFF LABEL USE1,394 reports
NAUSEA1,028 reports
PAIN987 reports
ARTHRALGIA959 reports
FATIGUE913 reports
DRUG INTOLERANCE874 reports
DRUG HYPERSENSITIVITY867 reports
RASH867 reports
RHEUMATOID ARTHRITIS834 reports
JOINT SWELLING833 reports
HEADACHE767 reports
CONDITION AGGRAVATED719 reports
PNEUMONIA718 reports
DIARRHOEA702 reports
GENERAL PHYSICAL HEALTH DETERIORATION647 reports
DIZZINESS641 reports
HYPERTENSION632 reports
ABDOMINAL DISCOMFORT593 reports
C REACTIVE PROTEIN INCREASED589 reports
URTICARIA588 reports
PAIN IN EXTREMITY581 reports
MALAISE578 reports
TREATMENT FAILURE577 reports
HEPATIC ENZYME INCREASED557 reports
OSTEOARTHRITIS555 reports
PRODUCT USE IN UNAPPROVED INDICATION554 reports
ALOPECIA552 reports
INFLAMMATION550 reports
DEPRESSION548 reports
VOMITING548 reports
HYPOAESTHESIA545 reports
SYSTEMIC LUPUS ERYTHEMATOSUS543 reports
DYSPNOEA540 reports
INFUSION RELATED REACTION539 reports
CONTRAINDICATED PRODUCT ADMINISTERED537 reports
MATERNAL EXPOSURE DURING PREGNANCY536 reports
MOBILITY DECREASED533 reports
SYNOVITIS531 reports
ARTHROPATHY521 reports
INTENTIONAL PRODUCT USE ISSUE516 reports
PEMPHIGUS509 reports
GLOSSODYNIA506 reports
CONFUSIONAL STATE504 reports
STOMATITIS504 reports
INSOMNIA503 reports
ASTHENIA496 reports
PSORIATIC ARTHROPATHY491 reports
PERIPHERAL SWELLING489 reports
PERICARDITIS486 reports
GASTROOESOPHAGEAL REFLUX DISEASE482 reports
BLOOD CHOLESTEROL INCREASED481 reports
DRUG INDUCED LIVER INJURY480 reports
ANTI CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE472 reports
HYPERSENSITIVITY471 reports
FOLLICULITIS470 reports
SLEEP DISORDER469 reports
SWELLING464 reports
INJURY461 reports
HAND DEFORMITY458 reports
NASOPHARYNGITIS458 reports
ABDOMINAL PAIN UPPER457 reports
MUSCULOSKELETAL STIFFNESS447 reports
NECK PAIN447 reports
TYPE 2 DIABETES MELLITUS447 reports
FALL445 reports
HELICOBACTER INFECTION445 reports
MUSCULAR WEAKNESS445 reports
DYSPEPSIA444 reports
PARAESTHESIA442 reports
MUSCLE SPASMS434 reports
ONYCHOMADESIS430 reports
BLISTER428 reports
WOUND428 reports
LIVER FUNCTION TEST INCREASED425 reports
FIBROMYALGIA418 reports
BURSITIS414 reports
GAIT INABILITY408 reports
DUODENAL ULCER PERFORATION399 reports
IRRITABLE BOWEL SYNDROME399 reports
THERAPEUTIC PRODUCT EFFECT DECREASED399 reports
IMPAIRED HEALING397 reports
ABDOMINAL DISTENSION395 reports
BACK INJURY390 reports
PRODUCT USE ISSUE387 reports
WEIGHT INCREASED385 reports
GASTROINTESTINAL DISORDER384 reports
PYREXIA382 reports
NAIL DISORDER380 reports
DRY MOUTH379 reports
RHEUMATIC FEVER378 reports
MEMORY IMPAIRMENT369 reports
C REACTIVE PROTEIN ABNORMAL368 reports
HYPERCHOLESTEROLAEMIA367 reports
LUNG DISORDER364 reports
FACET JOINT SYNDROME351 reports
OBESITY346 reports
LOWER RESPIRATORY TRACT INFECTION345 reports
NIGHT SWEATS345 reports
HEPATITIS335 reports

Report Outcomes

Out of 11,256 classified reports for MINOCYCLINE:

Serious 76.3%Non-Serious 23.7%

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

Female6,488 (64.3%)
Male3,574 (35.4%)
Unknown35 (0.3%)

Reports by Age

Age 40632 reports
Age 43294 reports
Age 17247 reports
Age 16220 reports
Age 59193 reports
Age 65184 reports
Age 55178 reports
Age 15170 reports
Age 57161 reports
Age 75159 reports
Age 18150 reports
Age 58146 reports
Age 66139 reports
Age 19137 reports
Age 54133 reports
Age 62124 reports
Age 14119 reports
Age 70116 reports
Age 60114 reports
Age 61114 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 MINOCYCLINE?

This profile reflects 54,303 FDA FAERS reports that mention MINOCYCLINE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for MINOCYCLINE?

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

Who manufactures MINOCYCLINE?

Labeling and FAERS entries often list Journey Medical Corporation in connection with MINOCYCLINE. 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.