PIROXICAM

N/A

Manufactured by Micro Labs Limited

53,232 FDA adverse event reports analyzed

Last updated: 2026-04-15

About PIROXICAM

PIROXICAM is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Micro Labs Limited. The most commonly reported adverse reactions for PIROXICAM include DRUG HYPERSENSITIVITY, RASH, ARTHRALGIA, CONDITION AGGRAVATED, DRUG INEFFECTIVE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PIROXICAM.

Top Adverse Reactions

DRUG HYPERSENSITIVITY940 reports
RASH874 reports
ARTHRALGIA861 reports
CONDITION AGGRAVATED857 reports
DRUG INEFFECTIVE836 reports
RHEUMATOID ARTHRITIS809 reports
DIARRHOEA806 reports
FATIGUE802 reports
PAIN797 reports
NAUSEA788 reports
PSORIATIC ARTHROPATHY781 reports
SINUSITIS775 reports
OFF LABEL USE726 reports
SCIATICA725 reports
HEADACHE716 reports
DRUG INTOLERANCE676 reports
JOINT SWELLING646 reports
VOMITING615 reports
HYPERTENSION604 reports
DYSPNOEA602 reports
ARTHROPATHY596 reports
DECREASED APPETITE595 reports
TREATMENT FAILURE591 reports
ANXIETY590 reports
ABDOMINAL PAIN UPPER581 reports
PRURITUS581 reports
HYPOAESTHESIA575 reports
ASTHENIA567 reports
ALOPECIA566 reports
MOBILITY DECREASED564 reports
DIZZINESS561 reports
MUSCULOSKELETAL STIFFNESS560 reports
MALAISE558 reports
ABDOMINAL DISCOMFORT552 reports
WEIGHT INCREASED537 reports
CONFUSIONAL STATE536 reports
HYPERSENSITIVITY535 reports
GENERAL PHYSICAL HEALTH DETERIORATION532 reports
SWELLING529 reports
BLOOD CHOLESTEROL INCREASED521 reports
DISCOMFORT520 reports
OEDEMA520 reports
WOUND511 reports
DUODENAL ULCER PERFORATION506 reports
BLISTER500 reports
PERIPHERAL SWELLING498 reports
INFECTION495 reports
NASOPHARYNGITIS490 reports
SYNOVITIS489 reports
C REACTIVE PROTEIN ABNORMAL488 reports
TYPE 2 DIABETES MELLITUS488 reports
FIBROMYALGIA486 reports
HEPATIC ENZYME INCREASED485 reports
PYREXIA483 reports
RHEUMATIC FEVER479 reports
CHEST PAIN478 reports
GASTROINTESTINAL DISORDER478 reports
ASTHMA476 reports
ANTI CYCLIC CITRULLINATED PEPTIDE ANTIBODY POSITIVE474 reports
RHEUMATOID FACTOR POSITIVE473 reports
SYSTEMIC LUPUS ERYTHEMATOSUS472 reports
WHEEZING466 reports
HAND DEFORMITY464 reports
INFUSION RELATED REACTION463 reports
INSOMNIA455 reports
PERICARDITIS454 reports
URTICARIA454 reports
CONTUSION453 reports
INJURY453 reports
PEMPHIGUS452 reports
LIVER INJURY450 reports
DEPRESSION449 reports
GLOSSODYNIA449 reports
DRY MOUTH445 reports
STOMATITIS444 reports
MUSCULOSKELETAL PAIN442 reports
HELICOBACTER INFECTION439 reports
OSTEOARTHRITIS433 reports
ROAD TRAFFIC ACCIDENT433 reports
FOLLICULITIS430 reports
PRODUCT USE ISSUE428 reports
IMPAIRED HEALING426 reports
LOWER RESPIRATORY TRACT INFECTION424 reports
SWOLLEN JOINT COUNT INCREASED422 reports
CONTRAINDICATED PRODUCT ADMINISTERED416 reports
DEEP VEIN THROMBOSIS POSTOPERATIVE416 reports
MEMORY IMPAIRMENT414 reports
LOWER LIMB FRACTURE407 reports
MUSCLE INJURY405 reports
LIVER DISORDER402 reports
MATERNAL EXPOSURE DURING PREGNANCY400 reports
WEIGHT DECREASED399 reports
THERAPEUTIC PRODUCT EFFECT DECREASED397 reports
AUTOIMMUNE DISORDER391 reports
IRRITABLE BOWEL SYNDROME391 reports
PAIN IN EXTREMITY380 reports
BURSITIS372 reports
LUNG DISORDER359 reports
NIGHT SWEATS352 reports
SLEEP DISORDER351 reports

Report Outcomes

Out of 6,175 classified reports for PIROXICAM:

Serious 83.3%Non-Serious 16.7%

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

Female3,947 (70.8%)
Male1,608 (28.8%)
Unknown22 (0.4%)

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 PIROXICAM?

This profile reflects 53,232 FDA FAERS reports that mention PIROXICAM. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for PIROXICAM?

Frequently reported terms in FAERS include DRUG HYPERSENSITIVITY, RASH, ARTHRALGIA, CONDITION AGGRAVATED, DRUG INEFFECTIVE, RHEUMATOID ARTHRITIS. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures PIROXICAM?

Labeling and FAERS entries often list Micro Labs Limited in connection with PIROXICAM. 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.