TETRACYCLINE HYDROCHLORIDE

N/A

Manufactured by Accuria, LLC

5,771 FDA adverse event reports analyzed

Last updated: 2026-04-15

About TETRACYCLINE HYDROCHLORIDE

TETRACYCLINE HYDROCHLORIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Accuria, LLC. The most commonly reported adverse reactions for TETRACYCLINE HYDROCHLORIDE include OFF LABEL USE, DRUG HYPERSENSITIVITY, HYPERSENSITIVITY, PNEUMONIA, INTENTIONAL PRODUCT USE ISSUE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for TETRACYCLINE HYDROCHLORIDE.

Top Adverse Reactions

OFF LABEL USE213 reports
DRUG HYPERSENSITIVITY150 reports
HYPERSENSITIVITY123 reports
PNEUMONIA103 reports
INTENTIONAL PRODUCT USE ISSUE97 reports
PAIN IN EXTREMITY93 reports
ARTHRALGIA90 reports
MOBILITY DECREASED89 reports
NECK PAIN88 reports
HEPATITIS84 reports
DRUG INEFFECTIVE83 reports
URTICARIA82 reports
VOMITING82 reports
FALL81 reports
MUSCULAR WEAKNESS81 reports
GASTROOESOPHAGEAL REFLUX DISEASE80 reports
INJURY80 reports
NAUSEA80 reports
INFLAMMATION77 reports
FOLLICULITIS75 reports
HYPOAESTHESIA75 reports
JOINT SWELLING75 reports
BURSITIS74 reports
LIVER FUNCTION TEST INCREASED74 reports
FINGER DEFORMITY73 reports
RASH69 reports
WEIGHT INCREASED69 reports
RHEUMATOID ARTHRITIS68 reports
WHEEZING67 reports
DRUG INTOLERANCE65 reports
FATIGUE63 reports
BACK INJURY62 reports
DIARRHOEA62 reports
PERIPHERAL SWELLING62 reports
DIZZINESS61 reports
MALAISE61 reports
OSTEOARTHRITIS61 reports
PRODUCT USE ISSUE60 reports
STOMATITIS60 reports
PAIN59 reports
PARAESTHESIA59 reports
PERIPHERAL VENOUS DISEASE58 reports
TASTE DISORDER57 reports
GAIT INABILITY55 reports
WOUND INFECTION55 reports
OVERDOSE53 reports
BLISTER51 reports
DYSPNOEA51 reports
OBESITY51 reports
CONDITION AGGRAVATED49 reports
INCORRECT PRODUCT ADMINISTRATION DURATION49 reports
PRODUCT QUALITY ISSUE49 reports
ASTHENIA48 reports
HEADACHE48 reports
HELICOBACTER INFECTION48 reports
SYNOVITIS48 reports
DEPRESSION46 reports
GENERAL PHYSICAL HEALTH DETERIORATION46 reports
INSOMNIA46 reports
TREATMENT FAILURE46 reports
ABDOMINAL PAIN UPPER45 reports
DYSPEPSIA45 reports
TYPE 2 DIABETES MELLITUS45 reports
UNDERDOSE45 reports
BREAST CANCER STAGE III43 reports
DRY MOUTH43 reports
SLEEP DISORDER43 reports
SYSTEMIC LUPUS ERYTHEMATOSUS43 reports
ABDOMINAL DISCOMFORT42 reports
FIBROMYALGIA42 reports
HYPERCHOLESTEROLAEMIA42 reports
BLEPHAROSPASM41 reports
HYPERTENSION41 reports
ABDOMINAL DISTENSION40 reports
C REACTIVE PROTEIN ABNORMAL40 reports
FACET JOINT SYNDROME40 reports
GASTROINTESTINAL DISORDER40 reports
WOUND40 reports
ALOPECIA39 reports
BLOOD CHOLESTEROL INCREASED39 reports
DUODENAL ULCER PERFORATION38 reports
EXPOSURE DURING PREGNANCY38 reports
HEPATIC ENZYME INCREASED37 reports
ONYCHOMYCOSIS37 reports
ILL DEFINED DISORDER36 reports
CONFUSIONAL STATE35 reports
EPILEPSY35 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE35 reports
PRODUCT USE IN UNAPPROVED INDICATION33 reports
PSORIATIC ARTHROPATHY33 reports
RHEUMATIC FEVER33 reports
SWELLING33 reports
INJECTION SITE REACTION32 reports
PERICARDITIS32 reports
DRUG INDUCED LIVER INJURY31 reports
MUSCULOSKELETAL STIFFNESS31 reports
ARTHROPATHY30 reports
MUSCLE SPASMS30 reports
NAIL DISORDER30 reports
NON HODGKIN^S LYMPHOMA30 reports

Report Outcomes

Out of 740 classified reports for TETRACYCLINE HYDROCHLORIDE:

Serious 64.3%Non-Serious 35.7%

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

Female464 (80.6%)
Male111 (19.3%)
Unknown1 (0.2%)

Reports by Age

Age 40173 reports
Age 6529 reports
Age 5910 reports
Age 147 reports
Age 627 reports
Age 737 reports
Age 486 reports
Age 546 reports
Age 696 reports
Age 275 reports
Age 445 reports
Age 495 reports
Age 565 reports
Age 765 reports
Age 805 reports
Age 825 reports
Age 344 reports
Age 504 reports
Age 614 reports
Age 634 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 TETRACYCLINE HYDROCHLORIDE?

This profile reflects 5,771 FDA FAERS reports that mention TETRACYCLINE HYDROCHLORIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for TETRACYCLINE HYDROCHLORIDE?

Frequently reported terms in FAERS include OFF LABEL USE, DRUG HYPERSENSITIVITY, HYPERSENSITIVITY, PNEUMONIA, INTENTIONAL PRODUCT USE ISSUE, PAIN IN EXTREMITY. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures TETRACYCLINE HYDROCHLORIDE?

Labeling and FAERS entries often list Accuria, LLC in connection with TETRACYCLINE HYDROCHLORIDE. 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.