ANTADYS
Flurbiprofen 100 mg capsules
What it does
Flurbiprofen is a non-steroidal anti-inflammatory drug (NSAID) used to relieve pain and reduce inflammation.
Commonly used for: pain relief, swelling (inflammation), arthritis, muscle pain
Read more in plain English ↓Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.
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Sourcing - Kenya onlyRegistration & product details
Source: Rwanda Food and Drugs Authority · fetched 2026-03-11 22:07:05 · updated 2026-09-17 02:30:43
Drug Interactions
14Pharmacodynamic Warnings
Flurbiprofen appears in TABLE 2: Drugs that cause nephrotoxicity
Flurbiprofen appears in TABLE 4: Drugs with antiplatelet effects
Flurbiprofen appears in TABLE 16: Drugs that increase serum potassium
Flurbiprofen appears in TABLE 18: Drugs that cause hyponatraemia
Severe (1)
Mifamurtide - decreases efficacy
NSAIDs(high-dose)arepredictedtodecreasetheefficacyof mifamurtide.Avoid.rTheoretical
Moderate (5)
Antiarrhythmics - increases exposure
NSAIDs (celecoxib) are predicted to increase the exposure to antiarrhythmics (flecainide, propafenone). Monitor and adjust dose.
Cladribine - increases exposure
NSAIDs(sulindac)mightincreasetheexposuretocladribine. Avoidoradjustdose.oTheoretical
Flecainide - increases exposure
NSAIDs (celecoxib) are predicted to increase the exposure to antiarrhythmics (flecainide, propafenone). Monitor and adjust dose.
Pemetrexed - increases exposure
NSAIDs are predicted to increase the exposure to pemetrexed. Use with caution or avoid. Also see TABLE 2 p. 1517
Propafenone - increases exposure
NSAIDs (celecoxib) are predicted to increase the exposure to antiarrhythmics (flecainide, propafenone). Monitor and adjust dose.
Unknown (8)
Alendronate - increases risk of gastrointestinal irritation
NSAIDs are predicted to increase the risk of gastrointestinal irritation when given with bisphosphonates (alendronate, ibandronate).
Bisphosphonates - increases risk of gastrointestinal irritation
NSAIDs are predicted to increase the risk of gastrointestinal irritation when given with bisphosphonates (alendronate, ibandronate).
Bisphosphonates - increases risk of renal impairment
NSAIDs are predicted to increase the risk of renal impairment when given with bisphosphonates (clodronate).
Clodronate - increases risk of renal impairment
NSAIDs are predicted to increase the risk of renal impairment when given with clodronate.
Deferasirox - increases risk of gastrointestinal bleeding
NSAIDs are predicted to increase the risk of gastrointestinal bleeding when given with deferasirox.
Deferiprone - increases exposure
NSAIDs(diclofenac)arepredictedtoincreasetheexposureto deferiprone.oTheoretical
Ibandronate - increases risk of gastrointestinal irritation
NSAIDs are predicted to increase the risk of gastrointestinal irritation when given with bisphosphonates (alendronate, ibandronate).
Ironchelators - increases risk of gastrointestinal bleeding
NSAIDs are predicted to increase the risk of gastrointestinal bleeding when given with iron chelators (deferasirox).
Data from BNF 85 (British National Formulary). This is not a substitute for professional medical advice. Matched via: class
About this medicine
Flurbiprofen is a non-steroidal anti-inflammatory drug (NSAID) used to relieve pain and reduce inflammation.
What it treats
- pain relief
- swelling (inflammation)
- arthritis
- muscle pain
How it works
Flurbiprofen works by blocking substances in the body that cause pain and inflammation.
Who it's for
Flurbiprofen is suitable for adults and children over a certain age for treating pain and inflammation.
Drug class
NSAIDs
Cautions
- • Be careful if you are taking medications that can harm the kidneys.
- • Use with caution if you are on drugs that affect blood clotting.
- • Avoid if you are taking medications that can raise potassium levels in the blood.
- • Take care if you have medications that can lower sodium levels.
AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.
Clinical monograph: Flurbiprofen
BNF-referencedFlurbiprofen is a nonsteroidal anti-inflammatory drug (NSAID) belonging to the propionic acid class. It is primarily used for its analgesic, anti-inflammatory, and antipyretic properties. Flurbiprofen is indicated for the treatment of pain and inflammation associated with various musculoskeletal disorders, including rheumatic diseases, dysmenorrhoea, and postoperative pain. It is recognized for its potency in inhibiting the synthesis of prostaglandins, which are mediators of pain and inflammation.
Indications
- Pain and inflammation in musculoskeletal disorders
- Rheumatic diseases
- Dysmenorrhoea
- Postoperative pain
- Mild to moderate pain
Dosage
Children: Refer to the BNF for Children for specific paediatric dosing information
Adults: Refer to the BNF for specific dosing information. Generally, flurbiprofen is administered orally or topically depending on the formulation and condition being treated.
Mechanism of action
Flurbiprofen exerts its anti-inflammatory effects through reversible inhibition of cyclooxygenase (COX) enzymes, which are crucial for the conversion of arachidonic acid to prostaglandins. By inhibiting both COX-1 and COX-2, flurbiprofen decreases the synthesis of prostaglandins involved in the inflammatory response, thereby alleviating pain, swelling, and fever.
Pharmacodynamics
As a nonsteroidal anti-inflammatory agent, flurbiprofen shares structural and pharmacological similarities with other NSAIDs such as ibuprofen and ketoprofen. The drug exhibits significant anti-inflammatory, analgesic, and antipyretic activities. Its therapeutic efficacy is attributed primarily to the S-enantiomer, which demonstrates predominant anti-inflammatory effects, while both enantiomers contribute to its analgesic properties.
Pharmacokinetics
Flurbiprofen is absorbed well from the gastrointestinal tract, with peak plasma concentrations occurring within 1 to 2 hours after oral administration. It is extensively metabolized in the liver, primarily through glucuronidation, and is excreted mainly in the urine. The drug has a half-life of approximately 3 to 6 hours. The pharmacokinetics may vary in individuals with renal impairment, necessitating caution in dosing for this population.
Contra-indications
- Hypersensitivity to flurbiprofen or any of its excipients
- History of gastrointestinal bleeding or ulceration
- Severe renal impairment
- Active peptic ulcer disease
- History of allergic reactions to NSAIDs
Adverse effects
- Gastrointestinal disturbances (nausea, vomiting, diarrhea, constipation)
- Headache
- Dizziness
- Drowsiness
- Rash or allergic reactions
- Renal impairment
- Increased risk of cardiovascular events
- Photosensitivity
Interactions
- Increased risk of gastrointestinal bleeding with anticoagulants
- May reduce the efficacy of antihypertensive medications
- Increased risk of nephrotoxicity with other nephrotoxic agents
- Potentially increased effects of other NSAIDs
Precautions
- Caution in patients with renal impairment, heart failure, or gastrointestinal disorders
- Use with caution in elderly patients due to increased risk of adverse effects
- Monitor for signs of gastrointestinal bleeding
- Consider alternative analgesics in patients with a history of cardiovascular disease
Pregnancy
Flurbiprofen should be avoided, especially in the third trimester due to the risk of fetal cardiovascular effects. Consult healthcare providers for alternatives.
Breast-feeding
Use with caution; flurbiprofen is excreted in breast milk. Monitor infant for any adverse effects.
Storage
Store in a cool, dry place, away from direct sunlight. Keep out of reach of children.
Formulations
- Tablets
- Topical gel
- Eye drops
AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.
Molecular reference: Flurbiprofen
PubChem CID 3394Molecular formula: C15H13FO2
Mechanism of action
Similar to other NSAIAs, the anti-inflammatory effect of flurbiprofen occurs via reversible inhibition of cyclooxygenase (COX), the enzyme responsible for the conversion of arachidonic acid to prostaglandin G2 (PGG2) and PGG2 to prostaglandin H2 (PGH2) in the prostaglandin synthesis pathway. This effectively decreases the concentration of prostaglandins involved in inflammation, pain, swelling and fever. Flurbiprofen is a non-selective COX inhibitor and inhibits the activity of both COX-1 and -2. It is also one of the most potent NSAIAs in terms of prostaglandin inhibitory activity.
Pharmacodynamics
Flurbiprofen, a nonsteroidal anti-inflammatory agent (NSAIA) of the propionic acid class, is structually and pharmacologically related to fenoprofen, ibuprofen, and ketoprofen, and has similar pharmacological actions to other prototypica NSAIAs. Flurbiprofen exhibits antiinflammatory, analgesic, and antipyretic activities. The commercially available flurbiprofen is a racemic mixture of (+)S- and (-) R-enantiomers. The S-enantiomer appears to possess most of the anti-inflammatory, while both enantiomers may possess analgesic activity.
Biological pathways
Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.
This drug in other countries
The same active ingredient registered across other registries we cover - including different brands.