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Ketoprofen  (1606)
[ kee-toe-proe'-fen ]
Ingredients: Ketoprofen
Indications: Arthritis, osteoarthritis; Pain, mild to moderate; Arthritis, rheumatoid; Dysmenorrhea
Pregnancy Category: B
FDA Approved: 1986- 01- 01
Classes: Analgesics, non- narcotic; Nonsteroidal anti- inflammatory drugs
Brand Names: Alrheumat - Denmark, England, Ireland ; Alrheumun - Germany ; Aneol - Japan ; Anzema - Indonesia ; Apo-Keto - Canada ; Arcental - Spain ; Bi-Profenid - France ; Bi-Rofenid - Belgium ; Dolofar - Chile ; Dolomax - Colombia ; Efiken - Mexico ; Epatec - Japan ; Fastum - Italy, Spain ; Fetik - Indonesia ; Floramil - Philippines ; Gabrilen - Germany ; Gabrilen Retard - Germany ; Helenil - Argentina ; Kaltrofen - Indonesia ; Kebanon - Korea ; Keduril - Costa-rica, Dominican-republic, El-salvador, Guatemala, Honduras, Mexico, Nicaragua, Panama ; Kefen - New-zealand ; Kehancer - Singapore ; Kenhancer - Malaysia, Singapore ; Kenofen Gel - Korea ; Keotsan - Peru ; Keprofen - Japan ; Ketadom - Hong-kong ; Ketin - Taiwan ; Ketofen - Taiwan, Thailand ; Keto Film - Korea ; Ketoflam - South-africa ; Ketolgin - MIDDLEEAST(Except Israel ) ; Ketolgin Gel - MIDDLEEAST(Except Israel ) ; Ketolgin SR - MIDDLEEAST(Except Israel ) ; Ketomex - Finland ; Ketonal - Israel ; Ketorin - Finland ; Ketosolan - Spain ; Ketum - Colombia ; Kevadon - Argentina ; Knavon - Greece ; Mohrus - Japan ; Naxal - Japan ; Novo-Keto-EC - Canada ; Orucote - South-africa ; Orudis - MIDDLEEAST, US; Canada, Costa-rica, Denmark, El-salvador, England, Finland, Germany, Guatemala, Honduras, Italy, Malaysia, Netherlands, Nicaragua, Norway, Panama, Spain, Sweden, Uruguay ; Orudis E-100 - Malaysia ; Orudis EC - Philippines ; Orudis R-PR - CARIBBEAN ; Orudis SR - AUSTRALIA; Australia, Switzerland ; Oruvail - AFRICA, US; Canada, China, Denmark, England, Greece, Hong-kong, New-zealand ; Oruvail EC - New-zealand ; Oruvail SR - AUSTRALIA ; Ostofen - India ; Ovurila - Indonesia ; Ovurila E - Indonesia ; Profecom - Indonesia ; Profenid - Austria, Bulgaria, China, Colombia, Czech-republic, Ecuador, Indonesia, Israel, Korea, Mexico, Paraguay, Peru, Poland, Portugal, Russia, Switzerland, Taiwan, Turkey, Venezuela ; Profenid 50 - India ; Profenil - Italy ; Profika - Indonesia ; Protofen - Indonesia ; Provail CR - Singapore ; Rematof - Indonesia ; Rhetoflam - Indonesia ; Rheuna PAP - Korea ; Rofenid - Belgium ; Spondylon - Germany ; Toprec - France ; Treosin - Japan ;
DEA schedules: (none)
Cost of therapy: $20.27 ( Mild-Moderate Pain ; Generic Capsules (Mylan) ; 50 mg ; 3 capsules/day ; 7 day supply )
$25.78 ( Mild-Moderate Pain ; Orudis ; 50 mg ; 3 capsules/day ; 7 day supply )
$84.08 ( Osteoarthritis; Rheumatoid Arthritis ; Generic Extended Release Capsules (Mylan) ; 200 mg ; 1 capsule/day ; 30 day supply )
$101.97 ( Osteoarthritis; Rheumatoid Arthritis ; Oruvail Capsules (extended release) ; 200 mg ; 1 capsule/day ; 30 day supply )
$115.80 ( Osteoarthritis; Rheumatoid Arthritis ; Generic Capsules (Mylan) ; 50 mg ; 4 capsule(s)/day ; 30 day supply )
$147.30 ( Osteoarthritis; Rheumatoid Arthritis ; Orudis ; 50 mg ; 4 capsule(s)/day ; 30 day supply )

BOXED WARNING

 

Cardiovascular Risk

  NSAIDs may cause an increased risk of serious cardiovascular thrombotic events, myocardial infarction (MI), and stroke, which can be fatal. This risk may increase with duration of use. Patients with cardiovascular disease or risk factors for cardiovascular disease may be at greater risk (see WARNINGS ).
Orudis and Oruvail are contraindicated for the treatment of peri- operative pain in the setting of coronary artery bypass graft (CABG) surgery (see WARNINGS ).

Gastrointestinal Risk

  NSAIDs cause an increased risk of serious gastrointestinal adverse events including bleeding, ulceration, and perforation of the stomach or intestines, which can be fatal. These events can occur at any time during use and without warning symptoms. Elderly patients are at greater risk for serious gastrointestinal (GI) events (see WARNINGS ).

DESCRIPTION

  Ketoprofen is a nonsteroidal anti- inflammatory drug. The chemical name for ketoprofen is 2- (3- benzoylphenyl)- propionic acid.
Its empirical formula is C16 H14 O3 , with a molecular weight of 254.29. It has a pKa of 5.94 in methanol: water (3:1) and an n- octanol:water partition coefficient of 0.97 (buffer pH 7.4).
Ketoprofen is a white or off- white, odorless, nonhygroscopic, fine to granular powder, melting at about 95°C. It is freely soluble in ethanol, chloroform, acetone, ether and soluble in benzene and strong alkali, but practically insoluble in water at 20°C.

Orudis Capsules

  Orudis capsules contain 25, 50, or 75 mg of ketoprofen for oral administration. The inactive ingredients present are D&C yellow no. 10, FD&C blue no. 1, FD&C yellow no. 6, gelatin, lactose, magnesium stearate, and titanium dioxide. The 25- mg dosage strength also contains D&C red no. 28 and FD&C red no. 40.

Oruvail Extended-Release Capsules

  Each Oruvail 100, 150, or 200 mg capsule contains ketoprofen in the form of hundreds of coated pellets. The dissolution of the pellets is pH dependent, with optimum dissolution occurring at pH 6.5- 7.5. There is no dissolution at pH 1.
In addition to the active ingredient, each 100, 150, or 200 mg capsule of Oruvail contains the following inactive ingredients: D&C red no. 22, D&C red no. 28, FD&C blue no. 1, ethyl cellulose, gelatin, shellac, silicon dioxide, sodium lauryl sulfate, starch, sucrose, talc, titanium dioxide, and other proprietary ingredients. The 100- and 150- mg capsules also contain D&C yellow no. 10 and FD&C green no. 3.

CLINICAL PHARMACOLOGY

  Ketoprofen is a nonsteroidal anti- inflammatory drug with analgesic and antipyretic properties.
The anti- inflammatory, analgesic, and antipyretic properties of ketoprofen have been demonstrated in classical animal and in vitro test systems. In anti- inflammatory models ketoprofen has been shown to have inhibitory effects on prostaglandin and leukotriene synthesis, to have antibradykinin activity, as well as to have lysosomal membrane- stabilizing action. However, its mode of action, like that of other nonsteroidal anti- inflammatory drugs, is not fully understood.

Pharmacodynamics

  Ketoprofen is a racemate with only the S enantiomer possessing pharmacological activity. The enantiomers have similar concentration time curves and do not appear to interact with one another.
An analgesic effect- concentration relationship for ketoprofen was established in an oral surgery pain study with ketoprofen capsules. The effect- site rate constant (ke0 ) was estimated to be 0.9 hour- 1(95% confidence limits: 0- 2.1), and the concentration (Ce50 ) of ketoprofen that produced one- half the maximum PID (pain intensity difference) was 0.3 μg/ ml (95% confidence limits: 0.1- 0.5). Thirty- three (33) to 68% of patients had an onset of action (as measured by reporting some pain relief) within 30 minutes following a single oral dose in post- operative pain and dysmenorrhea studies. Pain relief (as measured by remedication) persisted for up to 6 hours in 26- 72% of patients in these studies.

Pharmacokinetics

 

General

  Ketoprofen capsules and ketoprofen extended- release capsules differ only in their release characteristics. Ketoprofen capsules release drug in the stomach whereas the pellets in ketoprofen extended- release capsules are designed to resist dissolution in the low pH of gastric fluid but release drug at a controlled rate in the higher pH environment of the small intestine (see DESCRIPTION ).
Irrespective of the pattern of release, the systemic availability (Fs ) when either oral formulation is compared with IV administration is approximately 90% in humans. For 75- to 200- mg single doses, the area under the curve has been shown to be dose proportional.
Ketoprofen is >99% bound to plasma proteins, mainly to albumin.
Separate sections follow which delineate differences between ketoprofen capsules and ketoprofen extended- release capsules.

Absorption

 

Capsules

  Ketoprofen is rapidly and well- absorbed, with peak plasma levels occurring within 0.5- 2 hours.
Food intake reduces Cmax by approximately one- half and increases the mean time to peak concentration (Tmax ) from 1.2 hours for fasting subjects (range, 0.5- 3 hours) to 2.0 hours for fed subjects (range, 0.75- 3 hours). The fluctuation of plasma peaks may also be influenced by circadian changes in the absorption process.
Concomitant administration of magnesium hydroxide and aluminum hydroxide does not interfere with absorption of ketoprofen from ketoprofen capsules.

Extended-Release Capsules

  Ketoprofen is also well- absorbed from this dosage form, although an observable increase in plasma levels does not occur until approximately 2- 3 hours after taking the formulation. Peak plasma levels are usually reached 6- 7 hours after dosing. (See TABLE 1 .)
When ketoprofen is administered with food, its total bioavailability (AUC) is not altered; however, the rate of absorption from either dosage form is slowed.
Administration of ketoprofen extended- release capsules with a high- fat meal causes a delay of about 2 hours in reaching the Cmax ; neither the total bioavailability (AUC) nor the Cmax is affected. Circadian changes in the absorption process have not been studied.
The administration of antacids or other drugs which may raise stomach pH would not be expected to change the rate or extent of absorption of ketoprofen from ketoprofen extended- release capsules.

Multiple Dosing

  Steady- state concentrations of ketoprofen are attained within 24 hours after commencing treatment with either formulation. In studies with healthy male volunteers, trough levels at 24 hours following administration of ketoprofen extended- release capsules were 0.4 mg/ L compared with 0.07 mg/ ml at 24 hours following administration of ketoprofen 50 mg capsules qid (12 hours) or 0.13 mg/ L following administration of ketoprofen 75 mg capsules tid for 12 hours. Thus, relative to the peak plasma concentration, the accumulation of ketoprofen after multiple doses of either formulation is minimal.
TABLE 1    Comparison of Pharmacokinetic Parameters* for Ketoprofen Capsules and Ketoprofen Extended- Release Capsules
    Capsules Extended- Release Capsules
Kinetic Parameters (4 × 50 mg) (1 × 200 mg)
Extent of Oral Absorption (bioavailability) Fs (%) ~90 ~90
Peak Plasma Levels Cmax (mg/ L)
  Fasted 3.9 ± 1.3 3.1 ± 1.2
  Fed 2.4 ± 1.0 3.4 ± 1.3
Time to Peak Concentration Tmax (h)
  Fasted 1.2 ± 0.6 6.8 ± 2.1
  Fed 2.0 ± 0.8 9.2 ± 2.6
Area Under Plasma Concentration- Time Curve AUC(0- 24h) (mg·h/ L)
  Fasted 32.1 ± 7.2 30.1 ± 7.9
  Fed 36.6 ± 8.1 31.3 ± 8.1
Oral- Dose Clearance
  CL/ F (L/ h) 6.9 ± 0.8 6.8 ± 1.8
  Half- life T½ (h)† 2.1 ± 1.2 5.4 ± 2.2
* Values expressed are mean ± standard deviation.
In the case of ketoprofen extended- release capsules, absorption is slowed, intrinsic clearance is unchanged, but because the rate of elimination is dependent on absorption, the half- life is prolonged.

Metabolism

  The metabolism fate of ketoprofen is glucuronide conjugation to form an unstable acyl- glucuronide. The glucuronic acid moiety can be converted back to the parent compound. Thus, the metabolite serves as a potential reservoir for parent drug, and this may be important in persons with renal insufficiency, whereby the conjugate may accumulate in the serum and undergo deconjugation back to the parent drug (see Special Populations, Renally Impaired ). The conjugates are reported to appear only in trace amounts in plasma in healthy adults, but are higher in elderly subjects — presumably because of reduced renal clearance. It has been demonstrated that in elderly subjects following multiple doses (50 mg every 6 h), the ratio of conjugated to parent ketoprofen AUC was 30% and 3%, respectively, for the S & R enantiomers.
There are no known active metabolites of ketoprofen. Ketoprofen has been shown not to induce drug- metabolizing enzymes.

Elimination

  The plasma clearance of ketoprofen is approximately 0.08 L/ kg/ h with a Vd of 0.1 L/ kg after IV administration. The elimination half- life of ketoprofen has been reported to be 2.05 ± 0.58 h (Mean ± SD) following IV administration, from 2- 4 hours following administration of ketoprofen capsules, and 5.4 ± 2.2 hours after administration of ketoprofen 200- mg extended- release capsules. In cases of slow drug absorption, the elimination rate is dependent on the absorption rate and thus T½ relative to an IV dose appears prolonged.
After a single 200- mg dose of ketoprofen extended- release capsules, the plasma levels decline slowly, the average 0.4 mg/ L after 24 hours.
In a 24- hour period, approximately 80% of an administered dose of ketoprofen is excreted in the urine, primarily as the glucuronide metabolite.
Enterohepatic recirculation of the drug has been postulated, although biliary levels have never measured to confirm this.

Special Populations

 

Elderly — Clearance and Unbound Fraction

  The plasma and renal clearance of ketoprofen is reduced in the elderly (mean age, 73 years) compared to a younger normal population (mean age, 27 years). Hence, ketoprofen peak concentration and AUC increase with increasing age. In addition, there is a corresponding increase in unbound fraction with increasing age. Data from one trial suggest that the increase is greater in women than in men. It has not been determined whether age- related changes in absorption among the elderly contribute to the changes in bioavailability of ketoprofen (see PRECAUTIONS, Geriatric Use .

Capsules

  In a study conducted with young and elderly men and women, results for subjects older than 75 years of age showed that free drug AUC increased by 40% and Cmax increased by 60% as compared with estimates of the same parameters in young subjects (those younger than 35 years of age; see DOSAGE AND ADMINISTRATION ).
Also in the elderly, the ratio of intrinsic clearance/ availability decreased by 35% and plasma half- life was prolonged by 26%. This reduction is thought to be due to a decrease in hepatic extraction associated with aging.

Extended-Release Capsules

  The effects of age and gender on ketoprofen disposition were investigated in 2 small studies in which elderly male and female subjects received ketoprofen 200- mg extended- release capsules. The results were compared with those from another study conducted in healthy young men.
Compared to the younger subject group, the elimination half- life in the elderly was prolonged by 54% and total drug Cmax and AUC were 40% and 70% higher, respectively. Plasma concentrations in the elderly after single doses and at steady- state were essentially the same. Thus, no drug accumulation occurs.
In comparison to younger subjects taking the immediate- release formulation, there was a decrease of 16% and 25% in the total drug Cmax and AUC, respectively, among the elderly. Free drug data are not available for ketoprofen extended- release capsules.

Renally Impaired

  Studies of the effects of renal- function impairment have been small. They indicate a decrease in clearance in patients with impaired renal function. In 23 patients with renal impairment, free ketoprofen peak concentration was not significantly elevated, but free ketoprofen clearance was reduced from 15 L/ kg/ h for normal subjects to 7 L/ kg/ h in patients with mildly impaired renal function, and to 4 L/ kg/ h in patients with moderately to severely impaired renal function. The elimination T½ was prolonged from 1.6 hours in normal subjects to approximately 3 hours in patients with mild renal impairment, and to approximately 5- 9 hours in patients with moderately to severely impaired renal function.
No studies have been conducted in patients with renal impairment taking ketoprofen extended- release capsules (see DOSAGE AND ADMINISTRATION ).

Hepatically Impaired

  For patients with alcoholic cirrhosis, no significant changes in the kinetic disposition of ketoprofen capsules were observed relative to age- matched normal subjects: the plasma clearance of drug was 0.07 L/ kg/ h in 26 hepatically impaired patients. The elimination half- life was comparable to that observed for normal subjects. However, the unbound (biologically active) fraction was approximately doubled, probably due to hypoalbuminemia and high variability which was observed in the pharmacokinetics for cirrhotic patients. Therefore, these patients should be carefully monitored and daily doses of ketoprofen kept at the minimum providing the desired therapeutic effect.
No studies have been conducted in patients with hepatic impairment taking ketoprofen extended- release capsules (see DOSAGE AND ADMINISTRATION ).

CLINICAL STUDIES

 

Rheumatoid Arthritis and Osteoarthritis

  The efficacy of ketoprofen has been demonstrated in patients with rheumatoid arthritis and osteoarthritis. Using standard assessments of therapeutic response, there were no detectable differences in effectiveness or in the incidence of adverse events in crossover comparison of ketoprofen capsules and ketoprofen extended- release capsules. In other trials, ketoprofen demonstrated effectiveness comparable to aspirin, ibuprofen, naproxen, piroxicam, diclofenac, and indomethacin. In some of these studies there were more dropouts due to gastrointestinal side effects among patients on ketoprofen than among patients on other NSAIDs.
In studies with patients with rheumatoid arthritis, ketoprofen was administered in combination with gold salts, antimalarials, low- dose methotrexate, d- penicillamine, and/ or corticosteroids with results comparable to those seen with control nonsteroidal drugs.

Management of Pain

  The effectiveness of ketoprofen capsules as a general- purpose analgesic has been studied in standard pain models which have shown the effectiveness of doses of 25- 150 mg. Doses of 25 mg were superior to placebo. Doses larger than 25 mg generally could not be shown to be significantly more effective, but there was a tendency toward faster onset and greater duration of action with 50 mg, and, in the case of dysmenorrhea, a significantly greater effect overall with 75 mg. Doses greater than 50- 75 mg did not have increased analgesic effect. Studies in postoperative pain have shown that ketoprofen capsules in doses of 25- 100 mg were comparable to 650 mg of acetaminophen with 60 mg of codeine, or 650 mg of acetaminophen with 10 mg of oxycodone. Ketoprofen tended to be somewhat slower in onset; peak pain relief was about the same and the duration of the effect tended to be 1- 2 hours longer, particularly with the higher doses of ketoprofen.
The use of ketoprofen extended- release capsules in patients with acute pain is not recommended, since, in comparison to the immediate- release formulation, ketoprofen extended- release capsules would be expected to have a delayed analgesic response due to their extended- release characteristics.

INDICATIONS AND USAGE

  Carefully consider the potential benefits and risks of ketoprofen capsules and extended- release capsules and other treatment options before deciding to use ketoprofen capsules and extended- release capsules. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ).
Ketoprofen capsules and extended- release capsules are indicated for the management of the signs and symptoms of rheumatoid arthritis and osteoarthritis.
Ketoprofen extended- release capsules are not recommended for treatment of acute pain because of its extended- release characteristics (see CLINICAL PHARMACOLOGY, Pharmacokinetics ).
Ketoprofen capsules are indicated for the management of pain. Ketoprofen capsules are also indicated for treatment of primary dysmenorrhea.

CONTRAINDICATIONS

  Orudis and oruvail are contraindicated in patients who have shown hypersensitivity to ketoprofen.
Keroprofen should not be given to patients who have experienced asthma, urticaria, or allergic- typereactions after taking aspirin or other NSAIDs. Severe, rarely fatal, anaphylactic reactions to ketoprofen have been reported in such patients (see WARNINGS, Anaphylactoid Reactions and PRECAUTIONS, Preexisting Asthma) .
Ketoprofen is contraindicated for the treatment of peri- operative pain in the setting of coronary artery bypass graft (CABG) surgery (see WARNINGS ).

WARNINGS

 

Cardiovascular Effects

 

Cardiovascular Thrombotic Events

  Clinical trials of several COX- 2 selective and nonselective NSAIDs of up to 3 years duration have shown an increased risk of serious cardiovascular (CV) thrombotic events, myocardial infarction, and stroke, which can be fatal. All NSAIDs, both COX- 2 selective and nonselective, may have a similar risk. Patients with known CV disease or risk factors for CV disease may be at greater risk. To minimize the potential risk for an adverse CV event in patients treated with an NSAID, the lowest effective dose should be used for the shortest duration possible. Physicians and patients should remain alert for the development of such events, even in the absence of previous CV symptoms. Patients should be informed about the signs and/ or symptoms of serious CV events and the steps to take if they occur.
There is no consistent evidence that concurrent use of aspirin mitigates the increased risk of serious CV thrombotic events associated with NSAID use. The concurrent use of aspirin and an NSAID does increase the risk of serious GI events (see, Gastrointestinal Effects: Risk of Ulceration, Bleeding, and Perforation ).
Two large, controlled, clinical trials of a COX- 2 selective NSAID for the treatment of pain in the first 10- 14 days following CABG surgery found an increased incidence of myocardial infarction and stroke(see CONTRAINDICATIONS ).

Hypertension

  NSAIDs, including ketoprofen, can lead to onset of new hypertension or worsening of preexisting hypertension, either of which may contribute to the increased incidence of CV events. Patients taking thiazides or loop diuretics may have impaired response to these therapies when taking NSAIDs. NSAIDs, including ketoprofen, should be used with caution in patients with hypertension. Blood pressure (BP) should be monitored closely during the initiation of NSAID treatment and throughout the course of therapy.

Congestive Heart Failure and Edema

  Fluid retention and edema have been observed in some patients taking NSAIDs. Peripheral edema has been observed in approximately 2% of patients taking ketoprofen. Ketoprofen should be used with caution in patients with fluid retention or heart failure.

Gastrointestinal Effects: Risk of Ulceration, Bleeding and Perforation

  NSAIDs, including ketoprofen, can cause serious gastrointestinal (GI) adverse events including inflammation, bleeding, ulceration, and perforation, of the stomach, small intestine, or large intestine, which can be fatal. These serious adverse events can occur at any time, with or without warning symptoms, in patients treated with NSAIDs. Only 1 in 5 patients, who develop a serious upper GI adverse event on NSAID therapy, is symptomatic. Upper GI ulcers, gross bleeding, or perforation caused by NSAIDs occur in approximately 1% of patients treated for 3- 6months, and in about 2- 4% of patients treated for 1 year. These trends continue with longer duration of use, increasing the likelihood of developing a serious GI event at some time during the course of therapy. However, even short- term therapy is not without risk.
NSAIDs should be prescribed with extreme caution in those with a prior history of ulcer disease or gastrointestinal bleeding. Patients with a prior history of peptic ulcer disease and/ or gastrointestinal bleeding who use NSAIDs have a greater than 10- fold increased risk for developing a GI bleed compared to patients with neither of these risk factors. Other factors that increase the risk for GI bleeding in patients treated with NSAIDs include concomitant use of oral corticosteroids or anticoagulants, longer duration of NSAID therapy, smoking, use of alcohol, older age, and poor general health status. Most spontaneous reports of fatal GI events are in elderly or debilitated patients and therefore, special care should be taken in treating this population.
To minimize the potential risk for an adverse GI event in patients treated with an NSAID, the lowest effective dose should be used for the shortest possible duration. Patients and physicians should remain alert for signs and symptoms of GI ulceration and bleeding during NSAID therapy and promptly initiate additional evaluation and treatment if a serious GI adverse event is suspected. This should include discontinuation of the NSAID until a serious GI adverse event is ruled out. For high risk patients, alternate therapies that do not involve NSAIDs should be considered.

Renal Effects

  Long- term administration of NSAIDs has resulted in renal papillary necrosis and other renal injury. Renal toxicity has also been seen in patients in whom renal prostaglandins have a compensatory role in the maintenance of renal perfusion. In these patients, administration of a nonsteroidal anti- inflammatory drug may cause a dose- dependent reduction in prostaglandin formation and, secondarily, in renal blood flow, which may precipitate overt renal decompensation. Patients at greater risk of this reaction are those with impaired renal function, heart failure, liver dysfunction, those taking diuretics and ACE inhibitors, and the elderly. Discontinuation of NSAID therapy is usually followed by recovery to the pretreatment state.

Advanced Renal Disease

  No information is available from controlled clinical studies regarding the use of ketoprofen in patients with advanced renal disease. Therefore, treatment with ketoprofen is not recommended in these patients with advanced renal disease. If ketoprofen therapy must be initiated, close monitoring of the patient’s renal function is advisable.

Anaphylactoid Reactions

  As with other NSAIDs, anaphylactoid reactions may occur in patients without known prior exposure to ketoprofen. Ketoprofen should not be given to patients with the aspirin triad. This symptom complex typically occurs in asthmatic patients who experience rhinitis with or without nasal polyps, or who exhibit severe, potentially fatal bronchospasm after taking aspirin or other NSAIDs (see CONTRAINDICATIONS and PRECAUTIONS, Preexisting Asthma ). Emergency help should besought in cases where an anaphylactoid reaction occurs.

Skin Reactions

  NSAIDs, including ketoprofen, can cause serious skin adverse events such as exfoliative dermatitis, Stevens- Johnson Syndrome (SJS), and toxic epidermal necrolysis (TEN), which can be fatal. These serious events may occur without warning. Patients should be informed about the signs and symptoms of serious skin manifestations and use of the drug should be discontinued at the first appearance of skin rash or any other sign of hypersensitivity.

Pregnancy

  In late pregnancy, as with other NSAIDs, ketoprofen should be avoided because they may cause premature closure of the ductus arteriosus.

PRECAUTIONS

 

General

  Ketoprofen cannot be expected to substitute for corticosteroids or to treat corticosteroid insufficiency. Abrupt discontinuation of corticosteroids may lead to disease exacerbation. Patients on prolonged corticosteroid therapy should have their therapy tapered slowly if a decision is made to discontinue corticosteroids.
If steroid dosage is reduced or eliminated during therapy, it should be reduced slowly and the patients observed closely for any evidence of adverse effects, including adrenal insufficiency and exacerbation of symptoms of arthritis.
The pharmacological activity of ketoprofen in reducing [fever and] inflammation may diminish the utility of these diagnostic signs in detecting complications of presumed noninfectious, painful conditions.
Ketoprofen and other nonsteroidal anti- inflammatory drugs cause nephritis in mice and rats associated with chronic administration. Rare cases of interstitial nephritis or nephrotic syndrome have been reported in humans with ketoprofen since it has been marketed.
A second form of renal toxicity has been seen in patients with conditions leading to a reduction in renal blood flow or blood volume, where renal prostaglandins have a supportive role in the maintenance of renal blood flow. In these patients, administration of a nonsteroidal anti- inflammatory drug results in a dose- dependent decrease in prostaglandin synthesis and, secondarily, in renal blood flow which may precipitate overt renal failure. Patients at greatest risk of this reaction are those with impaired renal function, heart failure, liver dysfunction, those taking diuretics, and the elderly. Discontinuation of nonsteroidal anti- inflammatory drug therapy is typically followed by recovery to the pretreatment state.
Since ketoprofen is primarily eliminated by the kidneys and its pharmacokinetics are altered by renal failure (see CLINICAL PHARMACOLOGY ), patients with significantly impaired renal function should be closely monitored, and a reduction of dosage should be anticipated to avoid accumulation of ketoprofen and/ or its metabolites (see DOSAGE AND ADMINISTRATION ).

Hepatic Effects

  Borderline elevations of one or more liver tests may occur in up to 15% of patients taking NSAIDs including ketoprofen. These laboratory abnormalities may progress, may remain unchanged, or may be transient with continuing therapy. Notable elevations of ALT or AST (approximately three or more times the upper limit of normal) have been reported in approximately 1% of patients in clinical trials with NSAIDs. In addition, rare cases of severe hepatic reactions, including jaundice, and fatal fulminant hepatitis, liver necrosis and hepatic failure, some of them with fatal outcomes have been reported.
A patient with symptoms and/ or signs suggesting liver dysfunction, or in whom an abnormal liver test has occurred, should be evaluated for evidence of the development of a more severe hepatic reaction while on therapy with ketoprofen. If clinical signs and symptoms consistent with liver disease develop, or if systemic manifestations occur ( e.g., eosinophilia, rash, etc.), ketoprofen should be discontinued.
In patients with chronic liver disease with reduced serum albumin levels, ketoprofen's pharmacokinetics are altered (see CLINICAL PHARMACOLOGY ). Such patients should be closely monitored, and a reduction of dosage should be anticipated to avoid high blood levels of ketoprofen and/ or its metabolites (see DOSAGE AND ADMINISTRATION, ).

Hematological Effects

  Anemia is sometimes seen in patients receiving NSAIDs, including ketoprofen. This may be due to fluid retention, occult or gross GI blood loss, or an incompletely described effect upon erythropoiesis. Patients on long- term treatment with NSAIDs, including ketoprofen, should have their hemoglobin or hematocrit checked if they exhibit any signs or symptoms of anemia.
NSAIDs inhibit platelet aggregation and have been shown to prolong bleeding time in some patients.Unlike aspirin, their effect on platelet function is quantitatively less, of shorter duration, and reversible. Patients receiving ketoprofen who may be adversely affected by alterations in platelet function, such as those with coagulation disorders or patients receiving anticoagulants, should be carefully monitored.

Preexisting Asthma

  Patients with asthma may have aspirin- sensitive asthma. The use of aspirin in patients with aspirin- sensitive asthma has been associated with severe bronchospasm which can be fatal. Since cross reactivity, including bronchospasm, between aspirin and other nonsteroidal anti- inflammatory drugs has been reported in such aspirin- sensitive patients, ketoprofen should not be administered to patients with this form of aspirin sensitivity and should be used with caution in patients with preexisting asthma.

Information for the Patient

  Patients should be informed of the following information before initiating therapy with an NSAID and periodically during the course of ongoing therapy. Patients should also be encouraged to read the NSAID Medication Guide that accompanies each prescription dispensed.
Ketoprofen, like other NSAIDs, may cause serious CV side effects, such as MI or stroke, which may result in hospitalization and even death. Although serious CV events can occur without warning symptoms, patients should be alert for the signs and symptoms of chest pain, shortness of breath, weakness, slurring of speech, and should ask for medical advice when observing any indicative sign or symptoms. Patients should be apprised of the importance ofthis follow- up (see WARNINGS, Cardiovascular Effects ).
Ketoprofen, like other NSAIDs, can cause GI discomfort and, rarely, serious GI side effects, such as ulcers and bleeding, which may result in hospitalization and even death.Although serious GI tract ulcerations and bleeding can occur without warning symptoms, patients should be alert for the signs and symptoms of ulcerations and bleeding, and should ask for medical advice when observing any indicative sign or symptoms including epigastric pain, dyspepsia, melena, and hematemesis. Patients should be apprised of the importance of this follow- up (see WARNINGS, Gastrointestinal Effects: Risk of Ulceration, Bleeding, andPerforation ).
Ketoprofen, like other NSAIDs, can cause serious skin side effects such as exfoliative dermatitis, SJS, and TEN, which may result in hospitalizations and even death. Although serious skin reactions may occur without warning, patients should be alert for the signs and symptoms of skin rash and blisters, fever, or other signs of hypersensitivity such as itching, and should ask for medical advice when observing any indicative signs or symptoms. Patients should be advised to stop the drug immediately if they develop any type of rash and contact their physicians as soon as possible.
Patients should promptly report signs or symptoms of unexplained weight gain or edema to their physicians.
Patients should be informed of the warning signs and symptoms of hepatotoxicity ( e.g., nausea, fatigue, lethargy, pruritus, jaundice, right upper quadrant tenderness, and “flu- like” symptoms).If these occur, patients should be instructed to stop therapy and seek immediate medical therapy.
Patients should be informed of the signs of an anaphylactoid reaction ( e.g., difficulty breathing, swelling of the face or throat). If these occur, patients should be instructed to seek immediate emergency help (see WARNINGS ).
In late pregnancy, as with other NSAIDs, ketoprofen should be avoided because it may cause premature closure of the ductus arteriosus.

NSAIDs are often essential agents in the management of arthritis and have a major role in the treatment of pain, but they also may be commonly employed for conditions which are less serious. Physicians may wish to discuss with their patients the potential risks (see WARNINGS ; PRECAUTIONS, General ; and ADVERSE REACTIONS ) and likely benefits of NSAID treatment, particularly when the drugs are used for less serious conditions where treatment without NSAIDs might represent an acceptable alternative to both the patient and physician.
Because aspirin causes an increase in the level of unbound ketoprofen, patients should be advised not to take aspirin while taking ketoprofen (see DRUG INTERACTIONS ). It is possible that minor adverse symptoms of gastric intolerance may be prevented by administering ketoprofen capsules with antacids, food, or milk. Ketoprofen extended- release capsules have not been studied with antacids. Because food and milk do affect the rate but not the extent of absorption (see CLINICAL PHARMACOLOGY ), physicians may want to make specific recommendations to patients about when they should take ketoprofen in relation to food and/ or what patients should do if they experience minor GI symptoms associated with ketoprofen therapy.

Laboratory Tests

  Because serious GI- tract ulceration and bleeding can occur without warning symptoms, physicians should monitor for signs or symptoms of GI bleeding. Patients on long- term treatment with NSAIDs, should have their CBC and a chemistry profile checked periodically. If clinical signs and symptoms consistent with liver or renal disease develop, systemic manifestations occur ( e.g., eosinophilia, rash, etc.) or if abnormal liver tests persist or worsen, ketoprofen should be discontinued.

Drug/Laboratory Test Interactions

 

Effect on Blood Coagulation

  Ketoprofen decreases platelet adhesion and aggregation. Therefore, it can prolong bleeding time by approximately 3- 4 minutes from baseline values. There is no significant change in platelet count, prothrombin time, partial thromboplastin time, or thrombin time.

Carcinogenesis, Mutagenesis, and Impairment of Fertility

  Chronic oral toxicity studies in mice (up to 32 mg/ kg/ day; 96 mg/ m2/ day) did not indicate a carcinogenic potential for ketoprofen. The maximum recommended human therapeutic dose is 300 mg/ day for a 60- kg patient with a body surface area of 1.6 m2, which is 5 mg/ kg/ day or 185 mg/ m2/ day. Thus the mice were treated at 0.5 times the maximum human daily dose based on surface area.
A 2- year carcinogenicity study in rats, using doses up to 6.0 mg/ kg/ day (36 mg/ m2/ day), showed no evidence of tumorigenic potential. All groups were treated for 104 weeks except the females receiving 6.0 mg/ kg/ day (36 mg/ m2/ day) where the drug treatment was terminated in Week 81 because of low survival; the remaining rats were sacrificed after Week 87. Their survival in the groups treated for 104 weeks was within 6% of the control group. An earlier 2- year study with doses up to 12.5 mg/ kg/ day (75 mg/ m2/ day) also showed no evidence of tumorigenicity, but the survival rate was low and the study was therefore judged inconclusive. Ketoprofen did not show mutagenic potential in the Ames Test. Ketoprofen administered to male rats (up to 9 mg/ kg/ day; or 54 mg/ m2/ day) had no significant effect on reproductive performance or fertility. In female rats administered 6 or 9 mg/ kg/ day (36 or 54 mg/ m2/ day), a decrease in the number of implantation sites has been noted. The dosages of 36 mg/ m2/ day in rats represent 0.2 times the maximum recommended human dose of 185 mg/ m2/ day (see above).
Abnormal spermatogenesis or inhibition of spermatogenesis developed in rats and dogs at high doses, and a decrease in the weight of the testes occurred in dogs and baboons at high doses.

Pregnancy Category C

 

Teratogenic Effects

  In teratology studies ketoprofen administered to mice at doses up to 12 mg/ kg/ day (36 mg/ m2/ day) and rats at doses up to 9 mg/ kg/ day (54 mg/ m2/ day), the approximate equivalent of 0.2 times the maximum recommended therapeutic dose of 185 mg/ m2/ day, showed no teratogenic or embryotoxic effects. In separate studies in rabbits, maternally toxic doses were associated with embryotoxicity but not teratogenicity. However, animal reproduction studies are not always predictive of human response.There are no adequate and well- controlled studies in pregnant women. Ketoprofen should beused in pregnancy only if the potential benefit justifies the potential risk to the fetus.

Nonteratogenic Effects

  Because of the known effects of nonsteroidal anti- inflammatory drugs on the fetal cardiovascular system (closure of ductus arteriosus), use during pregnancy (particularly late pregnancy) should be avoided.

Labor and Delivery

  The effects of ketoprofen on labor and delivery in pregnant women are unknown. Studies in rats have shown ketoprofen at doses of 6 mg/ kg (36 mg/ m2/ day, approximately equal to 0.2 times the maximum recommended human dose) prolongs pregnancy when given before the onset of labor. Because of the known effects of prostaglandin- inhibiting drugs on the fetal cardiovascular system (closure of ductus arteriosus), use of ketoprofen during late pregnancy should be avoided.

Nursing Mothers

  It is not known whether this drug is excreted in human milk. Data on secretion in human milk after ingestion of ketoprofen do not exist. In rats, ketoprofen at doses of 9 mg/ kg (54 mg/ m2/ day;approximately 0.3 times the maximum human therapeutic dose) did not affect perinatal development.Upon administration to lactating dogs, the milk concentration of ketoprofen was found to be 4- 5% of the plasma drug level. As with other drugs that are excreted in milk, ketoprofen is not recommended for use in nursing mothers.

Pediatric Use

  Safety and effectiveness in pediatric patients below the age of 18 have not been established.

Geriatric Use

  As with any NSAIDs, caution should be exercised in treating the elderly (65 years and older).In pharmacokinetic studies, ketoprofen clearance was reduced in older patients receiving ketoprofen, compared with younger patients. Peak ketoprofen concentrations and free drug AUC were increased in older patients (see CLINICAL PHAMACOLOGY, Special Populations ). The glucuronide conjugate of ketoprofen, which can serve as a potential reservoir for the parent drug, is known to be substantially excreted by the kidney. Because elderly patients are more likely to have decreased renal function, care should betaken in dose selection. It is recommended that the initial dosage of ketoprofen should be reduced for patients over 75 years of age and it may be useful to monitor renal function (see DOSAGE AND ADMINISTRATION ). In addition, the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Elderly patients may be more sensitive to the antiprostaglandin effects of NSAIDS (on the gastrointestinal tract and kidneys) than younger patients (see WARNINGS and PRECAUTIONS ). In particular, elderly or debilitated patients who receive NSAID therapy seem to tolerate gastrointestinal ulceration or bleeding less well than other individuals, and most spontaneous reports of fatal GI events are in this population. Therefore, caution should be exercised in treating the elderly, and when individualizing their dosage, extra care should be taken when increasing the dose (see DOSAGE AND ADMINISTRATION ).
In ketoprofen clinical studies involving a total of 1540 osteoarthritis or rheumatoid arthritis patients, 369 (24%) were ≥65 years of age, and 92 (6%) were ≥75 years of age. For ketoprofen acute pain studies, 23 (5%) of 484 patients were ≥60 years of age. In ketoprofen extended- release capsule clinical studies, 356 (42%) of 840 osteoarthritis or rheumatoid arthritis patients were ≥65 years of age, and less than 100 of these were ≥75 years of age. No overall differences in effectiveness were observed between these patients and younger patients.

DRUG INTERACTIONS

  The following drug interactions were studied with ketoprofen doses of 200 mg/ day. The possibility of increased interaction should be kept in mind when ketoprofen doses greater than 50 mg as a single dose or 200 mg of ketoprofen per day are used concomitantly with highly bound drugs.

ACE-inhibitors

  Reports suggest that NSAIDs may diminish the antihypertensive effect of ACE- inhibitors. This interaction should be given consideration in patients taking NSAIDs concomitantly with ACE- inhibitors.

Antacids

  Concomitant administration of magnesium hydroxide and aluminum hydroxide does not interfere with the rate or extent of the absorption of ketoprofen administered as capsules.

Aspirin

  Ketoprofen does not alter aspirin absorption; however, in a study of 12 normal subjects, concurrent administration of aspirin decreased ketoprofen protein binding and increased ketoprofen plasma clearance from 0.07 L/ kg/ h without aspirin to 0.11 L/ kg/ h with aspirin. The clinical significance of these changes is not known; however, as with other NSAIDs, concomitant administration of ketoprofen and aspirin is not generally recommended because of the potential of increased adverse effects.

Diuretics

  NSAIDs can reduce the natriuetic effect of furosemide and thiazides in some patients. Hydrochlorothiazide, given concomitantly with ketoprofen, produces a reduction in urinary potassium and chloride excretion compared to hydrochlorothiazide alone. Patients taking diuretics are at a greater risk of developing renal failure secondary to a decrease in renal blood flow caused by prostaglandin inhibition (see PRECAUTIONS ). During concomitant therapy with NSAIDs, the patient should be observed closely for signs of renal failure (see WARNINGS, Renal Effects ), as well as to assure diuretic efficacy.

Digoxin

  In a study in 12 patients with congestive heart failure where ketoprofen and digoxin were concomitantly administered, ketoprofen did not alter the serum levels of digoxin.

Lithium

  NSAIDs have produced an elevation of plasma lithium levels and a reduction in renal lithium clearance. The mean minimum lithium concentration increased 15% and the renal clearance was decreased by approximately 20%. These effects have been attributed to inhibition of renal prostaglandin synthesis by the NSAID. Thus, when NSAIDs and lithium are administered concurrently, subjects should be observed carefully for signs of lithium toxicity.

Methotrexate

  Ketoprofen, like other NSAIDs, may cause changes in the elimination of methotrexate leading to elevated serum levels of the drug and increased toxicity. NSAIDs have been reported to competitively inhibit methotrexate accumulation in rabbit kidney slices. This may indicate that they could enhance the toxicity of methotrexate. Caution should be used when NSAIDs are administered concomitantly with methotrexate.

Probenecid

  Probenecid increases both free and bound ketoprofen by reducing the plasma clearance of ketoprofen to about one- third, as well as decreasing its protein binding. Therefore, the combination of ketoprofen and probenecid is not recommended.

Warfarin

  The effects of warfarin and NSAIDs on GI bleeding are synergistic, such that users of both drugs together have a risk of serious GI bleeding higher than users of either drug alone. In a short- term controlled study in 14 normal volunteers, ketoprofen did not significantly interfere with the effect of warfarin on prothrombin time. Bleeding from a number of sites may be a complication of warfarin treatment and GI bleeding a complication of ketoprofen treatment. Because prostaglandins play an important role in hemostasis and ketoprofen has an effect on platelet function as well (see PRECAUTIONS, Drug/ Laboratory Test Interactions, Effect on Blood Coagulation ), concurrent therapy with ketoprofen and warfarin requires close monitoring of patients on both drugs.

ADVERSE REACTIONS

  The incidence of common adverse reactions (above 1%) was obtained from a population of 835 patients treated with ketoprofen capsules in double- blind trials lasting from 4- 54 weeks and in 622 ketoprofen extended- release capsules (200 mg/ day) patients in trials lasting from 4- 16 weeks.
Minor gastrointestinal side effects predominated; upper gastrointestinal symptoms were more common than lower gastrointestinal symptoms. In crossover trials in 321 patients with rheumatoid arthritis or osteoarthritis, there was no difference in either upper or lower gastrointestinal symptoms between patients treated with 200 mg of ketoprofen extended- release capsules once a day or 75 mg of ketoprofen capsules tid (225 mg/ day). Peptic ulcer or GI bleeding occurred in controlled clinical trials in less than 1% of 1076 patients; however, in open label continuation studies in 1292 patients the rate was greater than 2%.
The incidence of peptic ulceration in patients on NSAIDs is dependent on many risk factors including age, sex, smoking, alcohol use, diet, stress, concomitant drugs such as aspirin and corticosteroids, as well as the dose and duration of treatment with NSAIDs (see WARNINGS ).
Gastrointestinal reactions were followed in frequency by central nervous system side effects, such as headache, dizziness, or drowsiness. The incidence of some adverse reactions appears to be dose- related (see DOSAGE AND ADMINISTRATION ). Rare adverse reactions (incidence less than 1%) were collected from one or more of the following sources: foreign reports to manufacturers and regulatory agencies, publications, and US clinical trials, and/ or US postmarketing spontaneous reports.
Reactions are listed below under body system, then by incidence or number of cases in decreasing incidence.
Incidence Greater Than 1% (probable causal relationship):
Digestive: Dyspepsia (11%), nausea, * abdominal pain, * diarrhea, * constipation, * flatulence, * anorexia, vomiting, stomatitis.
Nervous System: Headache, * dizziness, CNS inhibition ( i.e., pooled reports of somnolence, malaise, depression, etc.) or excitation ( i.e., insomnia, nervousness, dreams, etc.).*
Special Senses: Tinnitus, visual disturbance.
Skin and Appendages: Rash.
Urogenital: Impairment of renal function (edema, increased BUN), * signs or symptoms of urinary- tract irritation.
*Adverse events occurring in 3- 9% of patients.

Incidence Less Than 1% (probable causal relationship):
Body as a Whole: Chills, facial edema, infection, pain, allergic reaction, anaphylaxis.
Cardiovascular: Hypertension, palpitation, tachycardia, congestive heart failure, peripheral vascular disease, vasodilation.
Digestive: Appetite increased, dry mouth, eructation, gastritis, rectal hemorrhage, melena, fecal occult blood, salivation, peptic ulcer, gastrointestinal perforation, hematemesis, intestinal ulceration, hepatic dysfunction, hepatitis, cholestatic hepatitis, jaundice.
Hemic: Hypocoagulability, agranulocytosis, anemia, hemolysis, purpura, thrombocytopenia.
Metabolic and Nutritional: Thirst, weight gain, weight loss, hyponatremia.
Musculoskeletal: Myalgia.
Nervous System: Amnesia, confusion, impotence, migraine, paresthesia, vertigo.
Respiratory: Dyspnea, hemoptysis, epistaxis, pharyngitis, rhinitis, bronchospasm, laryngeal edema.
Skin and Appendages: Alopecia, eczema, pruritus, purpuric rash, sweating, urticaria, bullous rash, exfoliative dermatitis, photosensitivity, skin discoloration, onycholysis, toxic epidermal necrolysis, erythema multiforme, Stevens- Johnson syndrome.
Special Senses: Conjunctivitis, conjunctivitis sicca, eye pain, hearing impairment, retinal hemorrhage and pigmentation change, taste perversion.
Urogenital: Menometrorrhagia, hematuria, renal failure, interstitial nephritis, nephrotic syndrome.


Incidence Less Than 1% (causal relationship unknown): The following rare adverse reactions, whose causal relationship to ketoprofen is uncertain, are being listed to serve as alerting information to the physician.
Body as a Whole: Septicemia, shock.
Cardiovascular: Arrhythmias, myocardial infarction.
Digestive: Buccal necrosis, ulcerative colitis, microvesicular steatosis, jaundice, pancreatitis.
Endocrine: Diabetes mellitus (aggravated).
Nervous System: Dysphoria, hallucination, libido disturbance, nightmares, personality disorder, aseptic meningitis.
Urogenital: Acute tubulopathy, gynecomastia.

OVERDOSAGE

  Signs and symptoms following acute NSAID overdose are usually limited to lethargy, drowsiness, nausea, vomiting, and epigastric pain, which are generally reversible with supportive care. Respiratory depression, coma, or convulsions have occurred following large ketoprofen overdoses. Gastrointestinal bleeding, hypotension, hypertension, or acute renal failure may occur, but are rare.
Patients should be managed by symptomatic and supportive care following an NSAID overdose. There are no specific antidotes. Gut decontamination may be indicated in patients with symptoms seen within 4 hours (longer for sustained- release products) or following a large overdose (5- 10 times the usual dose). This should be accomplished via emesis and/ or activated charcoal (60- 100 g in adults, 1- 2 g/ kg in children) with a saline cathartic or sorbitol added to the first dose. Forced diuresis, alkalinization of the urine, hemodialysis or hemoperfusion would probably not be useful due to ketoprofen's high protein binding.
Case reports include 26 overdoses: 6 were in children, 16 in adolescents, and 4 in adults. Five (5) of these patients had minor symptoms (vomiting in 4, drowsiness in 1 child). A 12- year- old girl had tonic- clonic convulsions 1- 2 hours after ingesting an unknown quantity of ketoprofen and 1 or 2 tablets of acetaminophen with hydrocodone. Her ketoprofen level was 1128 mg/ L (56 times the upper therapeutic level of 20 mg/ L) 3- 4 hours post ingestion. Full recovery ensued 18 hours after ingestion following management with intubation, diazepam, and activated charcoal. A 45- year- old woman ingested twelve 200- mg ketoprofen extended- release capsules and 375 ml vodka, was treated with emesis and supportive measures 2 hours after ingestion, and recovered completely with her only complaint being mild epigastric pain.

DOSAGE AND ADMINISTRATION

  Carefully consider the potential benefits and risks of ketoprofen and other treatment options before deciding to use ketoprofen. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ).
After observing the response to initial therapy with ketoprofen, the dose and frequency shouldbe adjusted to suit an individual patient’s needs.
Concomitant use of ketoprofen is not recommended.
If minor side effects appear, they may disappear at a lower dose which may still have an adequate therapeutic effect. If well tolerated but not optimally effective, the dosage may be increased. Individual patients may show a better response to 300 mg of ketoprofen daily as compared to 200 mg, although in well- controlled clinical trials patients on 300 mg did not show greater mean effectiveness. They did, however, show an increased frequency of upper- and lower- GI distress and headaches. It is of interest that women also had an increased frequency of these adverse effects compared to men. When treating patients with 300 mg/ day, the physician should observe sufficient increased clinical benefit to offset potential increased risk.
In patients with mildly impaired renal function, the maximum recommended total daily dose of ketoprofen is 150 mg. In patients with a more severe renal impairment (GFR less than25 ml/ min/ 1.73 m2or end- stage renal impairment), the maximum total daily dose of ketoprofen should not exceed 100 mg.
In elderly patients, renal function may be reduced with apparently normal serum creatinine and/ orBUN levels. Therefore, it is recommended that the initial dosage of ketoprofen should be reduced for patients over 75 years of age (see PRECAUTIONS, Geriatric Use ).
It is recommended that for patients with impaired liver function and serum albumin concentration lessthan 3.5 g/ dl, the maximum initial total daily dose of ketoprofen should be 100 mg. All patients with metabolic impairment, particularly those with both hypoalbuminemia and reduced renal function, may have increased levels of free (biologically active) ketoprofen and should be closely monitored. The dosage may be increased to the range recommended for the general population, if necessary, only after good individual tolerance has been ascertained.
Because hypoalbuminemia and reduced renal function both increase the fraction of free drug (biologically active form), patients who have both conditions may be at greater risk of adverse effects. Therefore, it is recommended that such patients also be started on lower doses of ketoprofen and closely monitored.

Rheumatoid Arthritis and Osteoarthritis

  The recommended starting dose of ketoprofen in otherwise healthy patients is for ketoprofen capsules 75 mg three times or 50 mg four times a day, or for ketoprofen extended- release capsules 200 mg administered once a day. Smaller doses of ketoprofen capsules and ketoprofen extended- release capsules should be utilized initially in small individuals or in debilitated or elderly patients. The recommended maximum daily dose of ketoprofen is 300 mg/ day for ketoprofen or 200 mg/ day for ketoprofen extended- release capsules.
Dosages higher than 300 mg/ day of ketoprofen capsules or 200 mg/ day of ketoprofen extended- release capsules are not recommended because they have not been studied. Concomitant use of ketoprofen capsules and ketoprofen extended- release capsules is not recommended. Relatively smaller people may need smaller doses.
As with other nonsteroidal anti- inflammatory drugs, the predominant adverse effects of ketoprofen are gastrointestinal. To attempt to minimize these effects, physicians may wish to prescribe that ketoprofen be taken with antacids, food, or milk. Although food delays the absorption of both formulations (see CLINICAL PHARMACOLOGY ), in most of the clinical trials ketoprofen was taken with food or milk.
Physicians may want to make specific recommendations to patients about when they should take ketoprofen in relation to food and/ or what patients should do if they experience minor GI symptoms associated with either formulation.

Management of Pain and Dysmenorrhea

  The usual dose of ketoprofen capsules recommended for mild- to- moderate pain and dysmenorrhea is 25- 50 mg every 6- 8 hours as necessary. A smaller dose should be utilized initially in small individuals, in debilitated or elderly patients, or in patients with renal or liver disease (see PRECAUTIONS ). A larger dose may be tried if the patient's response to a previous dose was less than satisfactory, but doses above 75 mg have not been shown to give added analgesia. Daily doses above 300 mg are not recommended because they have not been adequately studied. Because of its typical nonsteroidal anti- inflammatory drug- side- effect profile, including as its principal adverse effect GI side effects (see WARNINGS and ADVERSE REACTIONS ), higher doses of ketoprofen capsules should be used with caution and patients receiving them observed carefully.
Ketoprofen is not recommended for use in treating acute pain because of its extended- release characteristics.

HOW SUPPLIED

 

Orudis Capsules

  Orudis capsules are available as follows:
25 mg: Dark- green and red capsule marked "WYETH 4186" on one side and "ORUDIS 25" on the reverse side.
50 mg: Dark- green and light- green capsule marked "WYETH 4181" on one side and "ORUDIS 50" on the reverse side.
75 mg: Dark- green and white capsule marked "WYETH 4187" on one side and "ORUDIS 75" on the reverse side.


Storage: Keep tightly closed. Store at room temperature, approximately 25°C (77°F). Dispense in a tight container. Protect from direct light and excessive heat and humidity.

Oruvail Extended-Release Capsules

  Orudis extended- release capsules are available as follows:
100 mg: Opaque pink and dark- green capsule marked with two radial bands and "ORUVAIL 100".
150 mg: Opaque pink and light- green capsule marked with two radial bands and "ORUVAIL 150".
200 mg: Opaque pink and off- white capsule marked with two radial bands and "ORUVAIL 200".


Storage: Keep tightly closed. Store at room temperature, approximately 25°C (77°F). Dispense in a tight container. Oruvail capsules should be protected from direct light and excessive heat and humidity.

PRODUCT IDENTIFICATION

  Ketoprofen , capsule , 50 mg [ Teva Pharmaceuticals USA ]
Ketoprofen , capsule , 75 mg [ Teva Pharmaceuticals USA ]
Ketoprofen , capsule , 50 mg [ ESI Lederle Generics ]
Ketoprofen , capsule , 75 mg [ ESI Lederle Generics ]
Ketoprofen , capsule , 50 mg [ Mylan Pharmaceuticals Inc ]
Ketoprofen , capsule , 75 mg [ Mylan Pharmaceuticals Inc ]
Ketoprofen , capsule, extended release , 100 mg [ Wyeth-Ayerst Laboratories ]
Ketoprofen , capsule, extended release , 150 mg [ Wyeth-Ayerst Laboratories ]

PATIENT DRUG CONSULT HANDOUT

  Ketoprofen (oral)

PRODUCT LISTING - RATED THERAPEUTICALLY EQUIVALENT

 
capsule - oral - 25 mg -
100.0 $65.68 GENERIC
IVAX Corporation
00182195801
100.0 $70.98 GENERIC
Sandoz Inc
00781240901
100.0 $72.15 GENERIC
West Point Pharma
59591000168
100.0 $74.35 GENERIC
ESI Lederle Generics
00005328443
capsule - oral - 50 mg -
30.0 $12.38 GENERIC
PD- RX Pharmaceuticals
55289028730
30.0 $36.83 Orudis
Pharma Pac
54569217800
100.0 $80.62 GENERIC
Qualitest Pharmaceuticals Inc
00603417721
100.0 $89.11 GENERIC
United Research Laboratories/ Mutual Pharmaceutical Company
00677146301
100.0 $89.15 GENERIC
West Point Pharma
59591000268
100.0 $89.25 GENERIC
Major Pharmaceuticals Inc
00904771160
100.0 $90.44 GENERIC
IVAX Corporation
00182195901
100.0 $91.00 GENERIC
Sandoz Inc
00781241001
100.0 $91.91 GENERIC
ESI Lederle Generics
00005328543
100.0 $96.50 GENERIC
Mylan Pharmaceuticals Inc
00378407001
100.0 $96.50 GENERIC
Teva Pharmaceuticals USA
00093319301
100.0 $122.75 Orudis
Wyeth- Ayerst Laboratories
00008418101
capsule - oral - 75 mg -
12.0 $17.93 GENERIC
DHS Inc
55887091212
15.0 $13.96 GENERIC
PD- RX Pharmaceuticals
55289018115
18.0 $27.76 Orudis
Physicians Total Care
54868105204
20.0 $11.96 GENERIC
PD- RX Pharmaceuticals
55289018120
21.0 $12.23 GENERIC
PD- RX Pharmaceuticals
55289018121
21.0 $31.66 GENERIC
DHS Inc
55887091221
30.0 $14.94 GENERIC
PD- RX Pharmaceuticals
55289018130
30.0 $42.11 GENERIC
DHS Inc
55887091230
100.0 $23.11 GENERIC
ESI Lederle Generics
00005328643
100.0 $98.90 GENERIC
Qualitest Pharmaceuticals Inc
00603417821
100.0 $99.15 GENERIC
West Point Pharma
59591000368
100.0 $99.30 GENERIC
Major Pharmaceuticals Inc
00904771260
100.0 $100.30 GENERIC
IVAX Corporation
00182196001
100.0 $102.19 GENERIC
Sandoz Inc
00781241101
100.0 $107.30 GENERIC
Mylan Pharmaceuticals Inc
00378575001
100.0 $107.30 GENERIC
Teva Pharmaceuticals USA
00093319501
500.0 $427.12 GENERIC
Qualitest Pharmaceuticals Inc
00603417828
500.0 $472.14 GENERIC
Sandoz Inc
00781241105
500.0 $472.40 GENERIC
Major Pharmaceuticals Inc
00904771240
500.0 $472.40 GENERIC
IVAX Corporation
00182196005
500.0 $472.40 GENERIC
Teva Pharmaceuticals USA
00093319505
capsule, extended release - oral - 200 mg -
7.0 $22.79 Oruvail
Allscripts Healthcare Solutions
54569379201
10.0 $36.74 Oruvail
Physicians Total Care
54868338003
10.0 $41.18 Oruvail
PD- RX Pharmaceuticals
55289036910
10.0 $42.34 GENERIC
Pharma Pac
52959052010
15.0 $48.84 Oruvail
Allscripts Healthcare Solutions
54569379202
15.0 $54.52 Oruvail
Physicians Total Care
54868338002
15.0 $54.91 Oruvail
Pharma Pac
52959034715
15.0 $63.06 GENERIC
Pharma Pac
52959052015
20.0 $70.58 Oruvail
Pharma Pac
52959034720
20.0 $83.62 GENERIC
Pharma Pac
52959052020
30.0 $94.47 Oruvail
Allscripts Healthcare Solutions
54569379200
30.0 $98.05 Oruvail
Pharma Pac
52959034730
30.0 $107.87 Oruvail
Physicians Total Care
54868338001
30.0 $124.67 GENERIC
Pharma Pac
52959052030
100.0 $280.25 GENERIC
Andrx Pharmaceuticals
62037052001
100.0 $336.47 Oruvail
Physicians Total Care
54868338000
100.0 $339.91 Oruvail
Wyeth- Ayerst Laboratories
00008069001

PRODUCT LISTING - EQUIVALENTS NOT AVAILABLE

 
capsule - oral - 50 mg -
10.0 $11.13 GENERIC
Southwood Pharmaceuticals Inc
58016026210
15.0 $16.69 GENERIC
Southwood Pharmaceuticals Inc
58016026215
20.0 $22.25 GENERIC
Southwood Pharmaceuticals Inc
58016026220
21.0 $23.44 GENERIC
Pharma Pac
52959050321
28.0 $31.15 GENERIC
Southwood Pharmaceuticals Inc
58016026228
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Physicians Total Care
54868241400
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Southwood Pharmaceuticals Inc
58016026230
40.0 $38.58 GENERIC
Pharma Pac
52959050340
60.0 $66.75 GENERIC
Southwood Pharmaceuticals Inc
58016026260
100.0 $111.25 GENERIC
Southwood Pharmaceuticals Inc
58016026200
capsule - oral - 75 mg -
3.0 $4.39 GENERIC
Prescript Pharmaceuticals
00247036603
4.0 $4.73 GENERIC
Prescript Pharmaceuticals
00247036604
10.0 $6.80 GENERIC
Prescript Pharmaceuticals
00247036610
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Southwood Pharmaceuticals Inc
58016038010
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Allscripts Healthcare Solutions
54569368802
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Southwood Pharmaceuticals Inc
58016038012
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Southwood Pharmaceuticals Inc
58016038014
15.0 $8.52 GENERIC
Prescript Pharmaceuticals
00247036615
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Allscripts Healthcare Solutions
54569368803
15.0 $18.60 GENERIC
Southwood Pharmaceuticals Inc
58016038015
20.0 $6.30 GENERIC
Physicians Total Care
54868241500
20.0 $10.24 GENERIC
Prescript Pharmaceuticals
00247036620
20.0 $18.90 GENERIC
Allscripts Healthcare Solutions
54569368801
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Southwood Pharmaceuticals Inc
58016038020
20.0 $25.79 GENERIC
Cardinal Pharmaceuticals
63874041820
20.0 $26.68 GENERIC
Direct Dispensing Inc
57866463902
20.0 $27.44 GENERIC
Pharma Pac
52959024520
21.0 $10.58 GENERIC
Prescript Pharmaceuticals
00247036621
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Allscripts Healthcare Solutions
54569368804
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Southwood Pharmaceuticals Inc
58016038021
21.0 $28.85 GENERIC
Pharma Pac
52959024521
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Southwood Pharmaceuticals Inc
58016038024
28.0 $34.72 GENERIC
Southwood Pharmaceuticals Inc
58016038028
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Physicians Total Care
54868241502
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Prescript Pharmaceuticals
00247036630
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Allscripts Healthcare Solutions
54569368800
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Southwood Pharmaceuticals Inc
58016038030
30.0 $38.44 GENERIC
Direct Dispensing Inc
57866463901
30.0 $38.69 GENERIC
Cardinal Pharmaceuticals
63874041830
30.0 $39.22 GENERIC
Pharma Pac
52959024530
40.0 $49.60 GENERIC
Southwood Pharmaceuticals Inc
58016038040
50.0 $62.00 GENERIC
Southwood Pharmaceuticals Inc
58016038050
60.0 $15.55 GENERIC
Physicians Total Care
54868241501
60.0 $24.00 GENERIC
Prescript Pharmaceuticals
00247036660
60.0 $74.40 GENERIC
Southwood Pharmaceuticals Inc
58016038060
90.0 $111.60 GENERIC
Southwood Pharmaceuticals Inc
58016038090
100.0 $124.00 GENERIC
Southwood Pharmaceuticals Inc
58016038000
capsule, extended release - oral - 100 mg -
15.0 $33.83 GENERIC
Southwood Pharmaceuticals Inc
58016049615
20.0 $45.10 GENERIC
Southwood Pharmaceuticals Inc
58016049620
30.0 $67.65 GENERIC
Southwood Pharmaceuticals Inc
58016049630
40.0 $90.20 GENERIC
Southwood Pharmaceuticals Inc
58016049640
50.0 $112.75 GENERIC
Southwood Pharmaceuticals Inc
58016049650
60.0 $135.30 GENERIC
Southwood Pharmaceuticals Inc
58016049660
100.0 $225.50 GENERIC
Southwood Pharmaceuticals Inc
58016049600
100.0 $247.69 Oruvail
Wyeth- Ayerst Laboratories
00008082101
capsule, extended release - oral - 150 mg -
100.0 $301.05 Oruvail
Wyeth- Ayerst Laboratories
00008082201
capsule, extended release - oral - 200 mg -
15.0 $42.04 GENERIC
Allscripts Healthcare Solutions
54569458100
30.0 $84.07 GENERIC
Southwood Pharmaceuticals Inc
58016075430
30.0 $84.08 GENERIC
Allscripts Healthcare Solutions
54569458101
100.0 $249.00 GENERIC
Watson Pharmaceuticals
00364266701
100.0 $280.25 GENERIC
Mylan Pharmaceuticals Inc
00378820001
powder - compounding - 100% -
5.0 gm $10.90 GENERIC
A- A Spectrum Healthcare Products
49452391602
25.0 gm $16.10 GENERIC
Medisca Inc
38779007804
25.0 gm $18.50 GENERIC
A- A Spectrum Healthcare Products
49452391603
25.0 gm $20.00 GENERIC
Medisca Inc
38779007825
100.0 gm $65.20 GENERIC
A- A Spectrum Healthcare Products
49452391604
100.0 gm $65.22 GENERIC
Medisca Inc
38779007810
100.0 gm $68.10 GENERIC
A- A Spectrum Healthcare Products
49452391704
100.0 gm $132.50 GENERIC
Medisca Inc
38779007805
500.0 gm $295.00 GENERIC
Medisca Inc
38779007850
500.0 gm $525.00 GENERIC
Medisca Inc
38779007808
1000.0 gm $543.80 GENERIC
A- A Spectrum Healthcare Products
49452391606
1000.0 gm $545.00 GENERIC
Medisca Inc
38779007800
1000.0 gm $937.50 GENERIC
Medisca Inc
38779007809

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