valdecoxib
Dosage Form: tablets
Serious Skin Reactions
- Serious skin reactions (e.g., toxic epidermal necrolysis, Stevens-Johnson syndrome, and erythema multiforme) have been reported in patients receiving Bextra. Some of these reactions have resulted in death.
- Patients appear to be at higher risk for these events within the first 2 weeks of treatment, but these may occur at any time during treatment.
- The reported rate of these serious skin events appears to be greater for Bextra as compared to other COX-2 agents.
- Bextra should be discontinued at the first appearance of skin rash, mucosal lesions, or any other sign of hypersensitivity.
(See WARNINGS – Serious Skin Reactions)
Bextra Description
Valdecoxib is chemically designated as 4-(5-methyl-3-phenyl-4-isoxazolyl) benzenesulfonamide and is a diaryl substituted isoxazole. It has the following chemical structure:
The empirical formula for valdecoxib is C16H14N2O3S, and the molecular weight is 314.36. Valdecoxib is a white crystalline powder that is relatively insoluble in water (10 µg/mL) at 25°C and pH 7.0, soluble in methanol and ethanol, and freely soluble in organic solvents and alkaline (pH=12) aqueous solutions.
Bextra Tablets for oral administration contain either 10 mg or 20 mg of valdecoxib. Inactive ingredients include lactose monohydrate, microcrystalline cellulose, pregelatinized starch, croscarmellose sodium, magnesium stearate, hypromellose, polyethylene glycol, polysorbate 80, and titanium dioxide.
Bextra - Clinical Pharmacology
Mechanism of Action
Valdecoxib is a nonsteroidal anti-inflammatory drug (NSAID) that exhibits anti-inflammatory, analgesic and antipyretic properties in animal models. The mechanism of action is believed to be due to inhibition of prostaglandin synthesis primarily through inhibition of cyclooxygenase-2 (COX-2). At therapeutic plasma concentrations in humans valdecoxib does not inhibit cyclooxygenase-1 (COX-1).
Pharmacokinetics
Absorption
Valdecoxib achieves maximal plasma concentrations in approximately 3 hours. The absolute bioavailability of valdecoxib is 83% following oral administration of Bextra compared to intravenous infusion of valdecoxib.
Dose proportionality was demonstrated after single doses (1–400 mg) of valdecoxib. With multiple doses (up to 100 mg/day for 14 days), valdecoxib exposure as measured by the AUC, increases in a more than proportional manner at doses above 10 mg BID. Steady state plasma concentrations of valdecoxib are achieved by day 4.
The steady state pharmacokinetic parameters of valdecoxib in healthy male subjects are shown in Table 1.
| Steady State Pharmacokinetic Parameters after Valdecoxib 10 mg Once Daily for 14 Days | Healthy Male Subjects (n=8, 20 to 42 yr.) |
|---|---|
| AUC(0–24hr) (hr∙ng/mL) | 1479.0 (291.9) |
| Cmax (ng/mL) | 161.1 (48.1) |
| Tmax (hr) | 2.25 (0.71) |
| Cmin (ng/mL) | 21.9 (7.68) |
| Elimination Half-life (hr) | 8.11 (1.32) |
No clinically significant age or gender differences were seen in pharmacokinetic parameters that would require dosage adjustments.
Effect of Food and Antacid
Bextra can be taken with or without food. Food had no significant effect on either the peak plasma concentration (Cmax) or extent of absorption (AUC) of valdecoxib when Bextra was taken with a high fat meal. The time to peak plasma concentration (Tmax), however, was delayed by 1–2 hours. Administration of Bextra with antacid (aluminum/magnesium hydroxide) had no significant effect on either the rate or extent of absorption of valdecoxib.
Distribution
Plasma protein binding for valdecoxib is about 98% over the concentration range (21–2384 ng/mL). Steady state apparent volume of distribution (Vss/F) of valdecoxib is approximately 86 L after oral administration. Valdecoxib and its active metabolite preferentially partition into erythrocytes with a blood to plasma concentration ratio of about 2.5:1. This ratio remains approximately constant with time and therapeutic blood concentrations.
Metabolism
In humans, valdecoxib undergoes extensive hepatic metabolism involving both P450 isoenzymes (3A4 and 2C9) and non-P450 dependent pathways (i.e., glucuronidation). Concomitant administration of Bextra with known CYP 3A4 and 2C9 inhibitors (e.g., fluconazole and ketoconazole) can result in increased plasma exposure of valdecoxib (see PRECAUTIONS — Drug Interactions).
One active metabolite of valdecoxib has been identified in human plasma at approximately 10% the concentration of valdecoxib. This metabolite, which is a less potent COX-2 specific inhibitor than the parent, also undergoes extensive metabolism and constitutes less than 2% of the valdecoxib dose excreted in the urine and feces. Due to its low concentration in the systemic circulation, it is not likely to contribute significantly to the efficacy profile of Bextra.
Excretion
Valdecoxib is eliminated predominantly via hepatic metabolism with less than 5% of the dose excreted unchanged in the urine and feces. About 70% of the dose is excreted in the urine as metabolites, and about 20% as valdecoxib N-glucuronide. The apparent oral clearance (CL/F) of valdecoxib is about 6 L/hr. The mean elimination half-life (T1/2) ranges from 8–11 hours, and increases with age.
Special Populations
Geriatric
In elderly subjects (> 65 years), weight-adjusted steady state plasma concentrations (AUC(0–12hr)) are about 30% higher than in young subjects. No dose adjustment is needed based on age.
Pediatric
Bextra has not been investigated in pediatric patients below 18 years of age.
Race
Pharmacokinetic differences due to race have not been identified in clinical and pharmacokinetic studies conducted to date.
Hepatic Insufficiency
Valdecoxib plasma concentrations are significantly increased (130%) in patients with moderate (Child-Pugh Class B) hepatic impairment. In clinical trials, doses of Bextra above those recommended have been associated with fluid retention. Hence, treatment with Bextra should be initiated with caution in patients with mild to moderate hepatic impairment and fluid retention. The use of Bextra in patients with severe hepatic impairment (Child-Pugh Class C) is not recommended.
Renal Insufficiency
The pharmacokinetics of valdecoxib have been studied in patients with varying degrees of renal impairment. Because renal elimination of valdecoxib is not important to its disposition, no clinically significant changes in valdecoxib clearance were found even in patients with severe renal impairment or in patients undergoing renal dialysis. In patients undergoing hemodialysis the plasma clearance (CL/F) of valdecoxib was similar to the CL/F found in healthy elderly subjects (CL/F about 6 to 7 L/hr.) with normal renal function (based on creatinine clearance).
NSAIDs have been associated with worsening renal function and use in advanced renal disease is not recommended (see PRECAUTIONS — Renal Effects).
Drug Interactions
For quantitative information on the following drug interaction studies, see PRECAUTIONS — Drug Interactions.
General
Valdecoxib undergoes both P450 (CYP) dependent and non-P450 dependent (glucuronidation) metabolism. In vitro studies indicate that valdecoxib is not a significant inhibitor of CYP 1A2, 3A4, or 2D6 and is a weak inhibitor of CYP 2C9 and a weak to moderate inhibitor of CYP 2C19 at therapeutic concentrations. The P450-mediated metabolic pathway of valdecoxib predominantly involves the 3A4 and 2C9 isozymes. Using prototype inhibitors and substrates of these isozymes, the following results were obtained. Coadministration of a known inhibitor of CYP 2C9/3A4 (fluconazole) and a CYP 3A4 inhibitor (ketoconazole) enhanced the total plasma exposure (AUC) of valdecoxib. Coadministration of valdecoxib with a CYP 3A4 inducer (phenytoin) decreased total plasma exposure (AUC) of valdecoxib. (See PRECAUTIONS — Drug Interactions.)
Coadministration of valdecoxib with warfarin (a CYP 2C9 substrate) caused a small, but statistically significant increase in plasma exposures of R-warfarin and S-warfarin, and also in the pharmacodynamic effects (International Normalized Ratio-INR) of warfarin. (See PRECAUTIONS — Drug Interactions.)
Coadministration of valdecoxib with diazepam (a CYP 2C19/3A4 substrate) resulted in increased exposure of diazepam, but not its major metabolite, desmethyldiazepam. (See PRECAUTIONS — Drug Interactions.)
Coadministration of valdecoxib with glyburide (a CYP 2C9 substrate) (40 mg valdecoxib QD with 10 mg glyburide BID) resulted in increased exposure of glyburide. (See PRECAUTIONS — Drug Interactions.)
Coadministration of valdecoxib with an oral contraceptive, 1 mg norethindrone/0.035 mg ethinyl estradiol (CYP 3A4 substrates), resulted in increased exposure of both norethindrone and ethinyl estradiol. (See PRECAUTIONS — Drug Interactions.)
Coadministration of valdecoxib with omeprazole (a CYP 3A4/2C19 substrate) caused an increase in omeprazole exposure. (See PRECAUTIONS — Drug Interactions.)
Coadministration of valdecoxib with dextromethorphan (a CYP 2D6/3A4 substrate) resulted in an increase in dextromethorphan plasma levels above those seen in subjects with normal levels of CYP 2D6. Even so these levels were almost 5-fold lower than those seen in CYP 2D6 poor metabolizers. (See PRECAUTIONS — Drug Interactions.)
Coadministration of valdecoxib with phenytoin (a CYP 2C9/2C19 substrate) did not affect the pharmacokinetics of phenytoin.
Coadministration of valdecoxib, or its injectable prodrug, with substrates of CYP 2C9 (propofol) and CYP 3A4 (midazolam, alfentanil, fentanyl) did not inhibit the metabolism of these substrates.
Clinical Studies
The efficacy and clinical utility of Bextra Tablets have been demonstrated in osteoarthritis (OA), rheumatoid arthritis (RA) and in the treatment of primary dysmenorrhea.
Osteoarthritis
Bextra was evaluated for treatment of the signs and symptoms of osteoarthritis of the knee or hip, in five double-blind, randomized, controlled trials in which 3918 patients were treated for 3 to 6 months. Bextra was shown to be superior to placebo in improvement in three domains of OA symptoms: (1) the WOMAC (Western Ontario and McMaster Universities) osteoarthritis index, a composite of pain, stiffness and functional measures in OA, (2) the overall patient assessment of pain, and (3) the overall patient global assessment. The two 3-month pivotal trials in OA generally showed changes statistically significantly different from placebo, and comparable to the naproxen control, in measures of these domains for the 10 mg/day dose. No additional benefit was seen with a valdecoxib 20-mg daily dose.
Rheumatoid Arthritis
Bextra demonstrated significant reduction compared to placebo in the signs and symptoms of RA, as measured by the ACR (American College of Rheumatology) 20 improvement, a composite defined as both improvement of 20% in the number of tender and number of swollen joints, and a 20% improvement in three of the following five: patient global, physician global, patient pain, patient function assessment, and C-reactive protein (CRP). Bextra was evaluated for treatment of the signs and symptoms of rheumatoid arthritis in four double-blind, randomized, controlled studies in which 3444 patients were treated for 3 to 6 months. The two 3-month pivotal trials compared valdecoxib to naproxen and placebo. The results for the ACR20 responses in these trials are shown below (Table 2). Trials of Bextra in rheumatoid arthritis allowed concomitant use of corticosteroids and/or disease-modifying anti-rheumatic drugs (DMARDs), such as methotrexate, gold salts, and hydroxychloroquine. No additional benefit was seen with a valdecoxib 20-mg daily dose.
| Study 1 | Study 2 | |
|---|---|---|
| ||
| Bextra 10 mg/day | 49%* (103/209) | 46%* (103/226) |
| Bextra 20 mg/day | 48%* (102/212) | 47%† (103/219) |
| Naproxen 500 mg BID | 44%† (100/225) | 53%* (115/219) |
| Placebo | 32% (70/222) | 32% (71/220) |
Primary Dysmenorrhea
Bextra was compared to naproxen sodium 550 mg in two placebo-controlled studies of women with moderate to severe primary dysmenorrhea. The onset of analgesia was within 60 minutes for Bextra 20 mg. The onset, magnitude, and duration of analgesic effect with Bextra 20 mg were comparable to naproxen sodium 550 mg.
Safety Studies
Studies in post-surgical patients (Investigational use)
Three placebo-controlled studies (two coronary artery bypass graft (CABG) surgery studies largely in patients with medial sternotomy placed on cardiopulmonary bypass and a single general surgery study) were conducted to evaluate the safety of the investigational agent, parecoxib sodium (the parenteral pro-drug of valdecoxib) and valdecoxib. Patients received parecoxib sodium for at least 3 days and then were transitioned to valdecoxib for a total treatment duration of 10–14 days. All patients received standard of care analgesia during treatment and all patients received low-dose aspirin prior to randomization and throughout the two CABG surgery studies.
In addition to routine adverse event reporting, pre-specified adverse events of interest were adjudicated according to pre-specified definitions by an independent committee who were blinded to treatment assignment. In the three studies, the overall routine adverse event profiles were similar between active treatments and placebo.
The first CABG surgery study evaluated patients treated with IV parecoxib sodium 40 mg bid for a minimum of 3 days, followed by treatment with valdecoxib 40 mg bid (parecoxib sodium/valdecoxib group) (n=311) or placebo/placebo (n=151) in a 14-day, double-blind placebo-controlled study. Nine pre-specified adverse event categories were evaluated (cardiovascular thromboembolic events, pericarditis, new onset or exacerbation of congestive heart failure, renal failure/dysfunction, upper GI ulcer complications, major non-GI bleeds, infections, non-infectious pulmonary complications, and death). There was a significantly (p<0.05) greater incidence of cardiovascular/thromboembolic events (myocardial infarction, ischemia, cerebrovascular accident, deep vein thrombosis and pulmonary embolism) detected in the parecoxib/valdecoxib treatment group compared to the placebo/placebo treatment group for the IV dosing period (2.2% and 0.0% respectively) and over the entire study period (4.8% and 1.3% respectively). Surgical wound complications (most involving the sternal wound) were observed at an increased rate with parecoxib/valdecoxib treatment.
In the second larger CABG surgery study, four pre-specified event categories were evaluated (cardiovascular/thromboembolic; renal dysfunction/renal failure; upper GI ulcer/bleeding; surgical wound complication). Patients were randomized within 24-hours post-CABG surgery to: parecoxib initial dose of 40 mg IV, then 20 mg IV Q12H for a minimum of 3 days followed by valdecoxib PO (20 mg Q12H) (n=544) for the remainder of a 10 day treatment period; placebo IV followed by valdecoxib PO (n=544); or placebo IV followed by placebo PO (n=548). A significantly (p=0.033) greater incidence of events in the cardiovascular/thromboembolic category was detected in the parecoxib /valdecoxib treatment group (2.0%) compared to the placebo/placebo treatment group (0.5%). Placebo/valdecoxib treatment was also associated with a higher incidence of CV thromboembolic events versus placebo treatment, but this difference did not reach statistical significance. Three of the cardiovascular thromboembolic events in the placebo/valdecoxib treatment group occurred during the placebo treatment period; these patients did not receive valdecoxib. Pre-specified events that occurred with the highest incidence in all three treatment groups involved the category of surgical wound complications, including deep surgical infections and sternal wound healing events (see table below).
| Placebo/Placebo | Placebo/Valdecoxib | Parecoxib/Valdecoxib | |
|---|---|---|---|
| |||
| Total Number of Patients Treated (Entire Study and IV Dosing Period) | 548 | 544 | 544 |
| (Oral Dosing Period) | 503 | 500 | 511 |
| Any Prespecified Adverse Event (Entire Study) | 22 (4.0) | 40 (7.4)* | 40 (7.4)* |
| IV dosing period | 5 (0.9) | 10 (1.8) | 13 (2.4) |
| Oral dosing period | 17 (3.4) | 31 (6.2)* | 27 (5.3) |
| Cardiovascular Thromboembolic Events (Entire Study) | 3 (0.5) | 6 (1.1) | 11 (2.0)* |
| IV dosing period | 1 (0.2) | 3 (0.6) | 4 (0.7) |
| Oral dosing period | 2 (0.4) | 3 (0.6) | 7 (1.4) |
| Renal Failure/dysfunction Events (Entire Study) | 3 (0.5) | 4 (0.7) | 7 (1.3) |
| IV dosing period | 3 (0.5) | 4 (0.7) | 6 (1.1) |
| Oral dosing period | 0 (0.0) | 0 (0.0) | 1 (0.2) |
| Upper GI Ulcer Events (Entire Study) | 2 (0.4) | 4 (0.7) | 6 (1.1) |
| IV dosing period | 1 (0.2) | 1 (0.2) | 2 (0.4) |
| Oral dosing period | 1 (0.2) | 3 (0.6) | 4 (0.8) |
| Surgical Wound Events (Entire Study) | 16 (2.9) | 27 (5.0) | 20 (3.7) |
| IV dosing period | 2 (0.4) | 2 (0.4) | 2 (0.4) |
| Oral dosing period | 14 (2.8) | 25 (5.0) | 18 (3.5) |
General Surgery: In the third study, a large (N=1050) major orthopedic/general surgery trial, patients received an initial dose of parecoxib 40 mg IV, then 20 mg IV Q12H for a minimum of 3 days followed by valdecoxib PO (20 mg Q12H) (n=525) for the remainder of a 10 day treatment period, or placebo IV followed by placebo PO (n=525). There were no significant differences in the overall safety profile, including the four pre-specified event categories described above for the second CABG surgery study, for parecoxib sodium/valdecoxib compared to placebo treatment in these post-surgical patients (see table below).
| Placebo/Placebo | Parecoxib /Valdecoxib | |
|---|---|---|
| Total Number of Patients Treated | 525 | 525 |
| Any Prespecified Adverse Event (Entire Study) | 17 (3.2) | 14 (2.7) |
| IV/IM dosing period | 6 (1.1) | 3 (0.6) |
| Oral dosing period | 11 (2.1) | 11 (2.1) |
| Cardiovascular Thromboembolic Events (Entire study) | 5 (1.0) | 5 (1.0) |
| IV/IM dosing period | 1 (0.2) | 2 (0.4) |
| Oral dosing period | 4 (0.8) | 3 (0.6) |
| Renal Failure/dysfunction Events (Entire study) | 0 (0.0) | 1 (0.2) |
| IV/IM dosing period | 0 (0.0) | 1 (0.2) |
| Oral dosing period | 0 (0.0) | 0 (0.0) |
| Upper GI Ulcer Events (Entire study) | 1 (0.2) | 1 (0.2) |
| IV/IM dosing period | 1 (0.2) | 0 (0.0) |
| Oral dosing period | 0 (0.0) | 1 (0.2) |
| Surgical Wound Events (Entire study) | 11 (2.1) | 9 (1.7) |
| IV/IM dosing period | 4 (0.8) | 0 (0.0) |
| Oral dosing period | 7 (1.3) | 9 (1.7) |
No significant differences were observed between the treatment groups
Bextra is contraindicated for the treatment of post-operative pain immediately following coronary artery bypass graft surgery and should not be used in this setting (See CONTRAINDICATIONS).
Cardiovascular Safety Analysis from Osteoarthritis and Rheumatoid Arthritis Studies
Randomized controlled clinical trials with Bextra longer than one year have not been conducted, nor have studies powered to detect differences in cardiovascular events in a chronic setting been conducted.
In an analysis of 10 randomized controlled clinical studies in osteoarthritis and rheumatoid arthritis, 4531 patients received Bextra in doses ranging from 10 mg to 80 mg for periods of 6 to 52 weeks. The majority of these patients received Bextra for 12 weeks or less. This analysis compared the incidence of serious cardiovascular events in Bextra-treated patients with the incidence of these events in patients receiving placebo (N=1142) or NSAID therapy (N=2261). In this analysis, no apparent differences were detected in the exposure-adjusted serious cardiovascular thromboembolic event rates between patients receiving Bextra, placebo and NSAIDs.
Bextra has not been studied in clinical trials beyond 12 months duration.
Gastrointestinal (GI) Endoscopy Studies with Therapeutic Doses
Scheduled upper GI endoscopic evaluations were performed with Bextra at doses of 10 and 20 mg daily in over 800 OA patients who were enrolled into two randomized 3-month studies using active comparators and placebo controls (Study 3 and Study 4). These studies enrolled patients free of endoscopic ulcers at baseline and compared rates of endoscopic ulcers, defined as any gastroduodenal ulcer seen endoscopically provided it was of "unequivocal depth" and at least 3 mm in diameter.
In both studies, Bextra 10 mg daily was associated with a statistically significant lower incidence of endoscopic gastroduodenal ulcers over the study period compared to the active comparators. Figure 1 summarizes the incidence of gastroduodenal ulcers in Studies 3 and 4 for the placebo, valdecoxib, and active control arms.
Safety Study with Supratherapeutic Doses
Scheduled upper GI endoscopic evaluations were performed in a randomized 6-month study of 1217 patients with OA and RA comparing valdecoxib 20 mg BID (40 mg daily) and 40 mg BID (80 mg daily) (4 to 8 times the recommended therapeutic dose) to naproxen 500 mg BID (Study 5). This study also formally assessed renal events as a primary outcome with supratherapeutic doses of Bextra. The renal endpoint was defined as any of the following: new/increase in edema, new/increase in congestive heart failure, increase in blood pressure (BP; >20 mm Hg systolic, >10 mm Hg diastolic), new/increase in BP treatment, new/increase in diuretic therapy, creatinine increase over 30% (or >1.2 mg/dL if baseline <0.9 mg/dL), BUN increase over 200% or >50 mg/dL, 24-hr urinary protein increase to >500 mg (if baseline 0–150 mg or >750 if baseline 151–300 or >1000 if baseline 301–500), serum potassium increase to >6 mEq/L, or serum sodium decrease to <130 mEq/L.
Figure 2 summarizes the incidence rates of gastroduodenal ulcers and renal events that were seen in Study 5. Bextra 40 mg daily and 80 mg daily were associated with a statistically significant lower incidence of endoscopic gastroduodenal ulcers over the study period compared to naproxen. The incidence of renal events was significantly different between the Bextra 80 mg daily group and naproxen. The clinical relevance of renal events observed with supratherapeutic doses (4 to 8 times the recommended therapeutic dose) of Bextra is not known (see PRECAUTIONS — Renal Effects).
Figure 2 Incidence of Endoscopic Gastroduodenal Ulcers and Renal Events in the High-dose Safety Study
Renal Safety at the Therapeutic Chronic Dose
The renal effects of valdecoxib compared with placebo and conventional NSAIDs were also assessed by prospectively designed pooled analyses of renal events data (see definition above —Supratherapeutic Doses) from five placebo- and active-controlled 12-week arthritis trials that included 995 OA or RA patients given valdecoxib 10 mg daily. The incidence of renal events observed in this analysis with valdecoxib 10 mg daily (3%), ibuprofen 800 mg TID (7%), naproxen 500 mg BID (2%) and diclofenac 75 mg BID (4%) were significantly higher than placebo-treated patients (1%). In all treatment groups, the majority of renal events were either due to the occurrence of edema or worsening BP.
Gastrointestinal Ulcers in High-Risk Patients
Subset analyses were performed of patients with risk factors (age, concomitant low-dose aspirin use, history of prior ulcer disease) enrolled in four upper GI endoscopic studies. Table 3 summarizes the trends seen.
| Placebo-controlled Studies | Active-controlled Studies | |||||
|---|---|---|---|---|---|---|
| Risk Factor | Placebo | Valdecoxib (10–20 mg daily) | Valdecoxib (10–80 mg daily) | Ibuprofen 800 mg TID | Naproxen 500 mg BID | Diclofenac 75 mg BID |
| No statistical conclusions can be drawn from these comparisons. | ||||||
| Age | ||||||
| <65 yrs | 3.7% (8/219) | 3.5% (17/484) | 3.7% (48/1306) | 8.2% (9/110) | 12.8% (51/397) | 13.2% (34/258) |
| ≥65 yrs | 5.8% (8/137) | 4.6% (12/262) | 7.6% (43/568) | 21.6% (16/74) | 22.0% (33/150) | 18.2% (25/137) |
| Concomitant Low Dose Aspirin Use | ||||||
| no | 4.4% (13/298) | 3.2% (21/650) | 3.8% (64/1671) | 9.8% (15/153) | 16.0% (75/468) | 12.8% (45/351) |
| yes | 5.2% (3/58) | 8.3% (8/96) | 13.3%(27/203) | 32.3% (10/31) | 11.4% (9/79) | 31.8% (14/44) |
| History of Ulcer Disease | ||||||
| no | 4.4% (14/317) | 3.4% (22/647) | 4.1% (68/1666) | 13.8% (22/160) | 13.3% (63/475) | 14.7% (52/354) |
| yes | 5.1% (2/39) | 7.1% (7/99) | 11.1% (23/208) | 12.5% (3/24) | 29.2% (21/72) | 17.1% (7/41) |
The correlation between findings of endoscopic studies, and the incidence of clinically significant serious upper GI events has not been established.
Platelets
In four clinical studies with young and elderly (≥65 years) subjects, single and multiple doses up to 7 days of Bextra 10 to 40 mg BID had no effect on platelet aggregation.
Indications and Usage for Bextra
Bextra Tablets are indicated:
- For relief of the signs and symptoms of osteoarthritis and adult rheumatoid arthritis.
- For the treatment of primary dysmenorrhea.
Contraindications
Bextra should not be given to patients who have demonstrated allergic-type reactions to sulfonamides.
Bextra Tablets are contraindicated in patients with known hypersensitivity to valdecoxib. Bextra should not be given to patients who have experienced asthma, urticaria, or allergic-type reactions after taking aspirin or NSAIDs. Severe, rarely fatal, anaphylactic-like reactions to NSAIDs are possible in such patients (see WARNINGS — Anaphylactoid Reactions, and PRECAUTIONS — Preexisting Asthma).
Bextra is contraindicated for the treatment of post-operative pain immediately following coronary artery bypass graft (CABG) surgery and should not be used in this setting. (See CLINICAL STUDIES — Safety Studies).
Warnings
Gastrointestinal (GI) Effects — Risk of GI Ulceration, Bleeding, and Perforation
Serious gastrointestinal toxicity such as bleeding, ulceration and perforation of the stomach, small intestine or large intestine can occur at any time with or without warning symptoms in patients treated with nonsteroidal anti-inflammatory drugs (NSAIDs). Minor gastrointestinal problems such as dyspepsia are common and may also occur at any time during NSAID therapy. Therefore, physicians and patients should remain alert for ulceration and bleeding even in the absence of previous GI tract symptoms. Patients should be informed about the signs and symptoms of serious GI toxicity and the steps to take if they occur. The utility of periodic laboratory monitoring has not been demonstrated, nor has it been adequately assessed. Only one in five patients who develop a serious upper GI adverse event on NSAID therapy is symptomatic. It has been demonstrated that upper GI ulcers, gross bleeding or perforation caused by NSAIDs appear to occur in approximately 1% of patients treated for 3 to 6 months and 2–4% of patients treated for one year. These trends continue, thus 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 patients with a prior history of ulcer disease or gastrointestinal bleeding. Most spontaneous reports of fatal GI events are in elderly or debilitated patients and therefore special care should be taken in treating this population. For high risk patients, alternate therapies that do not involve NSAIDs should be considered.
Studies have shown that patients with a prior history of peptic ulcer disease and/or gastrointestinal bleeding and who use NSAIDs, have a greater than 10-fold higher risk for developing a GI bleed than patients with neither of these risk factors. In addition to a past history of ulcer disease, pharmacoepidemiological studies have identified several other co-therapies or co-morbid conditions that may increase the risk for GI bleeding such as: treatment with oral corticosteroids, treatment with anticoagulants, longer duration of NSAID therapy, smoking, alcoholism, older age, and poor general health status. (See CLINICAL STUDIES — Safety Studies.)
Serious Skin Reactions
Valdecoxib contains a sulfonamide moiety and patients with a known history of a sulfonamide allergy may be at a greater risk of skin reactions. Patients without a history of sulfonamide allergy may also be at risk for serious skin reactions.
Serious skin reactions, including erythema multiforme, Stevens-Johnson syndrome, and toxic epidermal necrolysis, have been reported through postmarketing surveillance in patients receiving Bextra (see ADVERSE REACTIONS — Postmarketing Experience). Fatalities due to Stevens-Johnson syndrome and toxic epidermal necrolysis have been reported. Patients appear to be at higher risk for these events early in the course of therapy, with the onset of the event occurring in the majority of cases within the first two weeks of treatment. Bextra should be discontinued at the first appearance of skin rash, mucosal lesions or any other sign of hypersensitivity. Serious skin reactions have been reported with other COX-2 inhibitors during postmarketing experience. The reported rate of these events appears to be greater for Bextra as compared to other COX-2 agents (see Boxed Warning — Serious Skin Reactions).
Anaphylactoid Reactions
In postmarketing experience, cases of hypersensitivity reactions (anaphylactic reactions and angioedema) have been reported in patients receiving Bextra (see ADVERSE REACTIONS — Postmarketing Experience). These cases have occurred in patients with and without a history of allergic-type reactions to sulfonamides (see CONTRAINDICATIONS). Bextra 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 be sought in cases where an anaphylactoid reaction occurs.
Coronary Artery Bypass Graft Surgery
Patients treated with Bextra for pain following coronary artery bypass graft surgery have a higher risk for cardiovascular/thromboembolic events, deep surgical infections or sternal wound complications. Bextra is therefore contraindicated for the treatment of postoperative pain following CABG surgery. (See CONTRAINDICATIONS and CLINICAL STUDIES-Safety Studies).
Advanced Renal Disease
No information is available regarding the safe use of Bextra Tablets in patients with advanced kidney disease. Therefore, treatment with Bextra is not recommended in these patients. If therapy with Bextra must be initiated, close monitoring of the patient's kidney function is advisable (see PRECAUTIONS — Renal Effects).
Pregnancy
In late pregnancy, Bextra should be avoided because it may cause premature closure of the ductus arteriosus.
Precautions
General
Bextra Tablets cannot be expected to substitute for corticosteroids or to treat corticosteroid insufficiency. Abrupt discontinuation of corticosteroids may lead to exacerbation of corticosteroid-responsive illness. Patients on prolonged corticosteroid therapy should have their therapy tapered slowly if a decision is made to discontinue corticosteroids.
The pharmacological activity of valdecoxib in reducing fever and inflammation may diminish the utility of these diagnostic signs in detecting complications of presumed noninfectious, painful conditions.
Hepatic Effects
Borderline elevations of one or more liver tests may occur in up to 15% of patients taking NSAIDs. 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. These laboratory abnormalities may progress, may remain unchanged, or may remain transient with continuing therapy. Rare cases of severe hepatic reactions, including jaundice and fatal fulminant hepatitis, liver necrosis and hepatic failure (some with fatal outcome) have been reported with NSAIDs. In controlled clinical trials of valdecoxib, the incidence of borderline (defined as 1.2- to 3.0-fold) elevations of liver tests was 8.0% for valdecoxib and 8.4% for placebo, while approximately 0.3% of patients taking valdecoxib, and 0.2% of patients taking placebo, had notable (defined as greater than 3-fold) elevations of ALT or AST.
A patient with symptoms and/or signs suggesting liver dysfunction, or in whom an abnormal liver test has occurred, should be monitored carefully for evidence of the development of a more severe hepatic reaction while on therapy with Bextra. If clinical signs and symptoms consistent with liver disease develop, or if systemic manifestations occur (e.g., eosinophilia, rash), Bextra should be discontinued.
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 greatest risk of this reaction are those with impaired renal function, heart failure, liver dysfunction, those taking diuretics and Angiotensin Converting Enzyme (ACE) inhibitors, and the elderly. Discontinuation of NSAID therapy is usually followed by recovery to the pretreatment state.
Caution should be used when initiating treatment with Bextra in patients with considerable dehydration. It is advisable to rehydrate patients first and then start therapy with Bextra. Caution is also recommended in patients with preexisting kidney disease. (See WARNINGS — Advanced Renal Disease.)
Hematological Effects
Anemia is sometimes seen in patients receiving Bextra. Patients on long-term treatment with Bextra should have their hemoglobin or hematocrit checked if they exhibit any signs or symptoms of anemia.
Bextra does not generally affect platelet counts, prothrombin time (PT), or activated partial thromboplastin time (APTT), and does not appear to inhibit platelet aggregation at indicated dosages (see CLINICAL STUDIES — Safety Studies — Platelets).
Fluid Retention and Edema
Fluid retention and edema have been observed in some patients taking Bextra (see ADVERSE REACTIONS). Therefore, Bextra should be used with caution in patients with fluid retention, hypertension, or heart failure.
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, Bextra 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 Patients
Bextra can cause GI discomfort and, rarely, more serious GI side effects, which may result in hospitalization and even fatal outcomes. 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. Patients should be apprised of the importance of this follow-up (see WARNINGS — Gastrointestinal (GI) Effects — Risk of GI Ulceration, Bleeding, and Perforation).
Patients should report to their physicians, signs or symptoms of gastrointestinal ulceration or bleeding, weight gain, or edema.
Patients should be instructed to discontinue treatment and seek medical attention at the first signs of a skin reaction (pruritus, rash, erythema, or mucosal lesions) (see WARNINGS — Serious Skin Reactions).
Patients should also be instructed to seek immediate emergency help in the case
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