Felden

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Medically reviewed

Marina Burgos

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Felden

Property Description
Active ingredient Piroxicam (or Piroxicam betadex)
Form Capsule, Tablet, Dispersible tablet, Gel
Pharmacological class Nonsteroidal Anti-inflammatory Drug (NSAID)
Common use Relief of inflammation and discomfort
Origin Synthetic compound (oxicam group)

What Type of Medicine is Felden?

Felden is a widely recognized brand of medicine whose active component is Piroxicam, which is officially classified as a Nonsteroidal Anti-inflammatory Drug (NSAID). This substance is a synthetic compound belonging to the oxicam chemical group and is prepared as a single active ingredient product. Piroxicam is administered via two principal routes of administration: systemically through oral forms, which include capsules and various tablets, or locally as a topical gel for application directly to the skin. It is clinically recognized for its efficacy in managing persistent inflammatory conditions.


Piroxicam: Composition and Fundamental Purpose

The core composition utilizes the INN (International Nonproprietary Name) substance, Piroxicam (or its derivative, Piroxicam betadex), combined with appropriate pharmaceutical excipients depending on the form, such as an aqueous or hydroalcoholic base for the topical preparation. The fundamental purpose of this medicine is to provide relief from general discomfort and inflammation by utilizing its anti-inflammatory, analgesic (pain-relieving), and antipyretic (fever-reducing) properties. It achieves this by acting as a non-selective inhibitor, broadly blocking the enzymes responsible for generating prostaglandins, which are the chemical signals mediating pain and swelling. Piroxicam's extended elimination half-life, which is approximately 50 hours, is a key feature of the oxicam class, allowing its therapeutic effects to be sustained over a longer period.

What side effects are possible with Felden?

Felden: Possible side effects and safety information

Felden (piroxicam) is a Nonsteroidal Anti-inflammatory Drug (NSAID) whose safety profile includes warnings for serious adverse reactions. Official regulatory documents include a Boxed Warning concerning major risks.


Serious and Clinically Significant Risks

  • Cardiovascular (CV) Thrombotic Events: NSAIDs may increase the risk of serious CV thrombotic events, such as myocardial infarction (MI) and stroke, which can be fatal. This risk may increase with the duration of use and in patients with pre-existing CV disease. The drug is contraindicated for the treatment of peri-operative pain in the setting of Coronary Artery Bypass Graft (CABG) surgery.
  • Gastrointestinal (GI) Adverse Events: NSAIDs carry an increased risk of serious GI events, including bleeding, ulceration, and perforation of the stomach or intestines, which can be fatal. These events can occur without warning, and elderly patients are at greater risk.
  • Other Serious Reactions: This class of drug is associated with other serious adverse reactions, including Hepatotoxicity (liver damage/failure), Renal Toxicity (kidney damage/failure, hyperkalemia), Anaphylactic Reactions, and Serious Skin Reactions (e.g., Stevens-Johnson Syndrome, Toxic Epidermal Necrolysis).

Common Side Effects and Safety Considerations

The most common adverse reactions reported in clinical trials (incidence greater than 2%) often involve the gastrointestinal and nervous systems. These include nausea, constipation, diarrhea, abdominal pain, headache, dizziness, edema (fluid retention), and rash.

Safety is restricted for certain populations: the drug is contraindicated in patients who have previously experienced asthma, hives, or allergic-type reactions after taking aspirin or other NSAIDs. Use should be avoided in late pregnancy (starting at 30 weeks gestation) due to risks of premature closure of the fetal ductus arteriosus and fetal renal dysfunction.

Overdose and Emergency Response

The official regulatory profile for Piroxicam (Felden) overdose describes a spectrum of clinical manifestations, primarily affecting the gastrointestinal, central nervous, and renal systems. Documented overdose presentations often include gastrointestinal disturbances such as nausea, vomiting, abdominal pain, and diarrhea. Central nervous system effects may manifest as drowsiness, confusion, agitation, or severe headache. The potential for acute organ system toxicity is also noted through signs like oliguria (little urine output) and the development of acute renal failure.

Overdose with very large doses can lead to severe and life-threatening outcomes. The most serious documented complications include extensive gastrointestinal bleeding, ulceration, and perforation, as well as CNS depression progressing to seizures or coma. Systemic events such as shock (severe low blood pressure) are also associated with severe toxicity.

Immediate Medical Attention Required: Regulatory guidance mandates that immediate medical attention must be sought for any suspected overdose. Emergency services should be contacted if the affected individual exhibits severe signs such as collapse, respiratory difficulty, unresponsiveness, or seizure activity. As no specific antidote is known, the management strategy is strictly symptomatic and supportive. This includes monitoring of vital signs and ECG, along with procedural steps like the potential use of activated charcoal to reduce drug absorption, as described in regulatory documents.

Therapeutic Uses of Felden

What Felden Treats: Main Uses and Benefits

Felden (Piroxicam) is commonly used to provide symptomatic relief for chronic, long-term inflammatory joint diseases, including the signs and symptoms of Osteoarthritis and Rheumatoid Arthritis. It addresses symptoms related to inflammatory or irritative states, such as joint pain, swelling, and morning stiffness. This supportive symptomatic management helps maintain a sense of stability when symptoms are more noticeable, contributing to improved day-to-day functional stability for patients with these chronic conditions.

The medicine is also relevant when supportive symptom management is appropriate for episodes of heightened physiological activity. Relevant indications include providing symptomatic support for Acute Gout and various musculoskeletal disorders. It is often used during phases when symptoms become more noticeable, providing support that helps ease the overall symptom burden when symptoms interfere with daily comfort.

“Felden is used in situations involving certain distressing symptoms that cluster together, helping patients cope more steadily with symptom fluctuations.”

Quick Fact: Symptomatic support for Inflammatory Joint Pain

Felden assists with managing pronounced pain, swelling, and physical stiffness, contributing to maintaining functional stability and providing supportive relief when symptoms interfere with routine activities.

Regulatory References

  1. U.S. Food and Drug Administration (FDA) drug label

Eligibility and Restrictions for Use

Felden (piroxicam) is a nonsteroidal anti-inflammatory drug (NSAID) and is generally used for the relief of pain and inflammation associated with osteoarthritis and rheumatoid arthritis.


Contraindications (Who Cannot Use Felden)

Felden should not be used by patients with certain medical conditions or circumstances due to the risk of serious side effects. Absolute contraindications include:

  • A known allergy or hypersensitivity to piroxicam, or a history of asthma, hives (urticaria), or allergic-type reactions after taking aspirin or other NSAIDs.
  • Treatment of peri-operative pain in the setting of coronary artery bypass graft (CABG) surgery.
  • Active peptic ulceration, inflammatory gastrointestinal disease, or a history of gastrointestinal bleeding, ulceration, or perforation.
  • Severe heart failure (NYHA Class II-IV).

Patient Warnings (Use with Caution)

Caution is advised and a healthcare provider should be consulted before use if a patient has pre-existing conditions that may increase the risk of adverse cardiovascular, gastrointestinal, or renal events. These include a history of:

  • Cardiovascular disease (e.g., heart attack, stroke, blood clots, uncontrolled hypertension, or fluid retention).
  • Kidney or liver disease.
  • Advanced pregnancy (after 20 weeks gestation, and especially after 30 weeks).

The concomitant use of Felden with other medications, such as anticoagulants, aspirin, other NSAIDs, or oral corticosteroids, may increase the risk of bleeding and other serious adverse events.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Felden (Piroxicam) interactions are officially documented in regulatory information and primarily concern combined risks and alterations to drug exposure.

Documented Pharmacodynamic and Safety Risks

Official labeling identifies several combinations that pose an increased risk:

  • Anticoagulants and Antiplatelet Agents (e.g., Warfarin, Aspirin): Co-administration with these, alongside SSRIs or oral corticosteroids, carries a synergistic risk of serious gastrointestinal bleeding.
  • ACE Inhibitors / ARBs and Diuretics: Felden may diminish the antihypertensive or natriuretic effect of these medications and increase the risk of renal function deterioration, especially in elderly or volume-depleted patients.
  • Lithium and Methotrexate: Co-use can elevate the plasma levels of both substances, requiring clinical attention.

Pharmacokinetic and Exposure Constraints

Interaction Type Affected Substance/Pattern Official Regulatory Statement
Metabolic Pathway CYP2C9 Inhibitors/Poor Metabolizers Risk of abnormally high plasma levels due to reduced clearance; dose adjustment may be necessary.
Protein Binding Highly Protein Bound Drugs Piroxicam may displace other highly protein-bound drugs, potentially changing their dosage requirements.

Formal Restrictions and Lifestyle Factors

Felden is contraindicated for treating peri-operative pain in the setting of Coronary Artery Bypass Graft (CABG) surgery. The use of other systemic NSAIDs and analgesic doses of aspirin is generally advised against due to documented increased GI risk. Official sources also note that consumption of alcohol is a factor that increases the risk of serious GI complications.

Mechanism of Action

Inhibiting the Cyclooxygenase Enzyme System

Felden (Piroxicam) operates as a non-selective inhibitor within the Arachidonic Acid Cascade. Its action targets both Cyclooxygenase-1 (COX-1) and Cyclooxygenase-2 (COX-2) enzymes. By binding to the active sites of these enzymes, Felden blocks the enzymatic conversion of arachidonic acid into prostaglandin and thromboxane precursors, which are essential pro-inflammatory mediators.

Modulating the Prostaglandin Synthesis Cascade

The primary result of this mechanism is the reduction in the local synthesis of pro-inflammatory prostaglandins (e.g., PGE2) at the tissue level. By limiting the concentration of these lipid mediators, the drug modifies the signal transduction that drives the inflammatory process, contributing to a decrease in localized vasodilation, tissue fluid accumulation (edema), and nociceptor sensitization.

️ Dampening Peripheral Pain and Fever Pathways

The resulting physiological effect of the mechanistic cascade is the modulation of processes related to analgesia and antipyresis. This is achieved through the peripheral reduction of nociceptor sensitization and the central reduction of PGE2-mediated signaling in the hypothalamus, contributing to an adjustment in the body's pain and temperature regulation systems.

Dosage and Administration Information

Felden (Piroxicam) is administered via two primary routes: the oral route, available as capsules and tablets, and the topical route, used as a gel. The specific method and duration of use depend on the condition being addressed.


Standard Dosing and Frequency

For the long-term management of chronic conditions such as Osteoarthritis and Rheumatoid Arthritis, the standard dose is 20 mg administered once daily. The maximum recommended daily dose for chronic use is generally restricted to 20 mg. Dosing is typically scheduled as a single daily intake, although a divided daily dose is sometimes permitted.

For short-term treatment of acute musculoskeletal disorders, the regimen involves taking 40 mg daily for the first two days, which is then reduced to 20 mg daily for the remainder of the treatment course.


Administration Conditions

To ensure proper intake, oral forms of Piroxicam should be taken with or immediately after food or with a full glass of water. Capsules must be swallowed whole and are not intended to be crushed. Dispersible tablets can be swallowed whole or dispersed in water or saliva before intake. Treatment is structured by duration, ranging from short-term, defined courses for acute episodes to long-term therapy for chronic conditions. The benefit and tolerability of chronic use must be reviewed within 14 days of treatment initiation. For older adults, initiating treatment with a lower starting dose should be considered.

Recent Clinical Evidence

Overview of Studies and Research Evidence for Felden (Piroxicam)

This section summarizes the published research and clinical trials that have investigated Felden, focusing only on the type of evidence available, the patient populations studied, and what the research observed or is still exploring. This information provides context but is not clinical advice.

Evidence for Use in Rheumatoid Arthritis

Research on Felden was evaluated in various study designs, including randomized controlled trials (RCTs) and comparative clinical trials, involving adult patients diagnosed with chronic polyarthritis. These studies explored patient-reported outcomes describing perceived discomfort (such as pain scores) and measurements of systemic or functional changes. Studies monitored the measured outcomes related to joint symptoms over defined time intervals. Long-term effects are not fully established regarding sustained patterns of response beyond the immediate study durations.

Evidence for Use in Osteoarthritis

For osteoarthritis, research was studied for Felden using designs such as randomized controlled trials and double-blind crossover studies. These studies primarily focused on patients with conditions marked by functional limitations, typically affecting the hip or knee. Researchers examined outcomes related to physical discomfort, such as weight-bearing pain and night pain, alongside overall disease severity. Data on the sustainability of observed effects are predominantly limited to intermediate follow-up periods.

What Is Still Uncertain About Felden Research

The existing evidence base shows variability in the specific doses, formulations, and assessment instruments used across trials. Limitations include follow-up durations were limited and modest sample sizes in some key comparative trials. Studies explored whether outcomes such as measurements of disease progression or structural joint damage were primary or well-documented outcomes, and generally, existing research had limited focus on these long-term structural outcomes. The research highlights what is known — and what is still uncertain — and indicates where further, comprehensive research is still needed to provide clearer insight.

Key Studies & References

  1. Efficacy and safety of piroxicam revisited: a global meta-analysis of randomised clinical trials
  2. Drugs@FDA: Drug Product Feldene (piroxicam), NDA018147 (CYP2C9 metabolizer information)

Frequently Asked Questions (FAQ)

Common questions about Felden (FAQ)

Q: What is Felden (piroxicam) and how does it work?

A: Felden is a brand name for the non-steroidal anti-inflammatory drug (NSAID) piroxicam. It works by blocking certain substances in the body that cause inflammation, pain, and fever. Piroxicam is primarily used to relieve symptoms of inflammatory or degenerative rheumatic diseases.


Q: What is the maximum recommended dose of Felden (piroxicam) injection?

A: The maximum recommended daily dose for Felden (piroxicam) injection is 20 mg. To minimize the risk of side effects, the lowest effective dose should be used for the shortest possible duration to control symptoms. Treatment benefit and safety should be reassessed within 14 days of starting therapy.


Q: For how long is the injectable form of Felden typically used?

A: The duration of treatment with the injectable form of Felden is typically limited to 2 to 3 days. The injectable route is generally administered only when oral or rectal administration of piroxicam is not possible. If continued treatment is needed, a switch to the oral or rectal form is usually recommended.


Q: What serious side effects are associated with Felden?

A: As with all NSAIDs, Felden is associated with a risk of serious side effects, including:

  • Gastrointestinal (GI) Events: This includes potentially fatal bleeding, ulceration, and perforation of the stomach, small intestine, or large intestine. The risk of these events increases with age, especially in patients over 70, and should generally be avoided in those over 80. Doses greater than 20 mg per day increase this risk.
  • Cardiovascular (CV) Events: NSAIDs may lead to the onset or increase of high blood pressure (hypertension), which can increase the risk of CV effects. Felden should be used with caution in patients with hypertension.
  • Serious Skin Reactions: Studies suggest Felden may be associated with a higher risk of serious skin reactions compared to some other NSAIDs. These reactions are most common during the first month of treatment.

Treatment must be stopped immediately at the first sign of a skin rash, mucosal lesions, or a suspected gastrointestinal complication.


Q: When should I stop taking Felden?

A: You should stop taking Felden immediately if you experience:

  • The first appearance of a skin rash, mucosal lesions, or any other sign of a hypersensitivity (allergic) reaction.
  • Any signs or symptoms of a suspected gastrointestinal complication, such as unusual or new abdominal pain or discomfort, or indications of bleeding.

Your clinical benefit and tolerability should be re-evaluated periodically by your healthcare provider, and treatment should be discontinued if concerns arise.

How should Felden be stored and disposed of?

How to Store and Dispose of Felden (Piroxicam)

Official Storage Requirements

Felden (piroxicam) must be stored at room temperature, generally below 30°C, and must be protected from excess heat and moisture. The medicine must be kept in its original container with the lid tightly closed to maintain product stability.

Child Safety and Handling

It is mandatory to store the medication out of the sight and reach of children in a secure location that is up and away. Always ensure child-resistant caps are properly locked.

Disposal Instructions

Expired or unused Felden must not be disposed of by throwing it into household waste or pouring it down a drain. Consult a pharmacist or follow local official guidance, such as drug take-back programs, for the proper disposal of the unused product.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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