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Meloxicam: Pediatric drug information

Meloxicam: Pediatric drug information
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For additional information see "Meloxicam: Drug information" and "Meloxicam: Patient drug information"

For abbreviations, symbols, and age group definitions show table
ALERT: US Boxed Warning
Serious cardiovascular thrombotic events:

Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction (MI) and stroke, which can be fatal. This risk may occur early in treatment and may increase with duration of use.

Meloxicam is contraindicated during the perioperative setting of coronary artery bypass graft (CABG) surgery.

Serious gastrointestinal bleeding, ulcerations, and perforation:

NSAIDs cause an increased risk of serious GI 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 and patients with a prior history of peptic ulcer disease and/or GI bleeding are at greater risk for serious GI events.

Brand Names: US
  • Anjeso [DSC];
  • Mobic [DSC];
  • Qmiiz ODT [DSC];
  • Vivlodex [DSC]
Brand Names: Canada
  • ACT Meloxicam [DSC];
  • APO-Meloxicam;
  • Auro-Meloxicam;
  • PMS-Meloxicam;
  • TEVA-Meloxicam
Therapeutic Category
  • Analgesic, Nonopioid;
  • Anti-inflammatory Agent;
  • Nonsteroidal Anti-inflammatory Drug (NSAID), Oral
Dosing: Pediatric

Dosage guidance:

Dosage form information: Orally disintegrating tablets, capsules, tablets, and oral suspension do not have equivalent systemic exposure and are not interchangeable, even if the total milligram strength is the same; do not substitute similar dose strengths of other meloxicam products. Qmiiz ODT and Anjeso have been discontinued in the United States for >1 year.

Juvenile idiopathic arthritis

Juvenile idiopathic arthritis (JIA): Note: To reduce the risk of adverse cardiovascular and GI effects, use the lowest effective dose for the shortest period of time; adjust dose to patient's clinical needs; higher doses have not demonstrated additional benefit in clinical trials.

Oral suspension:

Children ≥2 years and Adolescents: Oral: 0.125 mg/kg once daily; maximum dose: 7.5 mg/dose.

Orally disintegrating tablets (Qmiiz ODT): Note: Qmiiz ODT has been discontinued in the United States for >1 year.

Children and Adolescents weighing ≥60 kg: Oral: 7.5 mg once daily.

Tablets:

Children and Adolescents weighing ≥60 kg: Oral: 7.5 mg once daily.

Dosage adjustment for concomitant therapy: Significant drug interactions exist, requiring dose/frequency adjustment or avoidance. Consult drug interactions database for more information.

Dosing: Kidney Impairment: Pediatric

Children ≥2 years and Adolescents: Oral:

Mild to moderate impairment: No dosage adjustment necessary.

Severe renal impairment: Use is not recommended (has not been studied).

Hemodialysis: Not dialyzable; additional doses are not required after hemodialysis; maximum dose: 7.5 mg/dose.

KDIGO guidelines provide the following recommendations for NSAIDs (Ref):

eGFR 30 to <60 mL/minute/1.73 m2: Temporarily discontinue in patients with intercurrent disease that increases risk of acute kidney injury.

eGFR <30 mL/minute/1.73 m2: Avoid use.

Dosing: Liver Impairment: Pediatric

Children ≥2 years and Adolescents: Oral:

Mild to moderate impairment: No dosage adjustments are recommended.

Severe impairment: There are no dosage adjustments provided in the manufacturer's labeling (has not been studied); use with caution; meloxicam is significantly metabolized in the liver.

Dosing: Adult

(For additional information see "Meloxicam: Drug information")

Dosage guidance:

Safety: Avoid or use with caution in patients at risk for or with existing cardiovascular disease, GI disease, kidney impairment, chronic liver disease, or a bleeding diathesis due to greater risk for adverse events. Consider proton pump inhibitor coadministration in patients at risk for GI bleeding (eg, taking dual antiplatelet therapy or an anticoagulant, ≥60 years of age, high meloxicam doses) (Ref).

Dosing: Use the lowest effective dose for the shortest duration of time. Lower doses (eg, ≤7.5 mg/day) may be relatively COX-2 selective, but this relative selectivity is lost at higher doses (eg, 15 mg/day) (Ref).

Dosage form information: Capsules, orally disintegrating tablets, oral suspension, and tablets do not have equivalent systemic exposure and are not interchangeable, even if the total milligram strength is the same. Qmiiz ODT and Anjeso have been discontinued in the United States for >1 year.

Acute pain

Acute pain:

Note: Due to slow onset, other oral nonsteroidal anti-inflammatory drugs (NSAIDs) are generally preferred; however, some experts use for postoperative pain management (Ref).

IV: 30 mg once daily.

Capsule: Oral (off-label route): 5 mg to 10 mg once daily; maximum dose: 10 mg/day (Ref).

Orally disintegrating tablet (Omiiz ODT): Oral (off-label route): 7.5 mg to 15 mg once daily; maximum dose: 15 mg/day (Ref).

Suspension: Oral (off-label route): 7.5 mg to 15 mg once daily; maximum dose: 15 mg/day (Ref).

Tablet: Oral (off-label route): 7.5 mg to 15 mg once daily; maximum dose: 15 mg/day (Ref).

Gout, treatment, acute flares

Gout, treatment, acute flares (off-label use):

Tablet: Oral: 15 mg once daily (Ref); initiate within 24 to 48 hours of flare onset; reduce dose as symptoms improve. Discontinue a few days after resolution of clinical signs (usual total duration: 5 to 7 days); longer duration may be required if therapy is delayed (Ref).

Osteoarthritis

Osteoarthritis:

Capsule: Oral: Initial: 5 mg once daily; may increase to a maximum of 10 mg once daily.

Orally disintegrating tablet: Oral: Initial: 7.5 mg once daily; may increase to a maximum of 15 mg once daily. Note: Qmiiz ODT has been discontinued in the United States for >1 year.

Suspension: Oral: Initial: 7.5 mg once daily; may increase to a maximum of 15 mg once daily.

Tablet: Oral: Initial: 7.5 mg once daily; may increase to a maximum of 15 mg once daily.

Rheumatoid arthritis

Rheumatoid arthritis:

Orally disintegrating tablet: Oral: Initial: 7.5 mg once daily; may increase to a maximum of 15 mg once daily. Note: Qmiiz ODT has been discontinued in the United States for >1 year.

Suspension: Oral: Initial: 7.5 mg once daily; may increase to a maximum of 15 mg once daily.

Tablet: Oral: Initial: 7.5 mg once daily; may increase to a maximum of 15 mg once daily.

Dosage adjustment for concomitant therapy: Significant drug interactions exist, requiring dose/frequency adjustment or avoidance. Consult drug interactions database for more information.

Dosing: Kidney Impairment: Adult

The renal dosing recommendations are based upon the best available evidence and clinical expertise. Senior Editorial Team: Bruce Mueller, PharmD, FCCP, FASN, FNKF; Jason A. Roberts, PhD, BPharm (Hons), B App Sc, FSHP, FISAC; Michael Heung, MD, MS.

IV:

eGFR ≥60 mL/minute/1.73 m2: No dosage adjustment necessary.

eGFR <60 mL/minute/1.73 m2: Use is not recommended; contraindicated in patients who are at risk for renal failure due to volume depletion.

Oral:

Altered kidney function:

CrCl ≥60 mL/minute: No dosage adjustment necessary (Ref).

CrCl >30 to <60 mL/minute: No dosage adjustment necessary (Ref). Use of analgesics other than nonsteroidal anti-inflammatory drugs may be preferred. If necessary, use the lowest effective dose for the shortest duration possible; avoid in patients at high risk for acute kidney injury (ie, volume depleted, hypotensive, elderly, or taking concurrent nephrotoxic medications) (Ref).

CrCl ≤30 mL/minute: Avoid use due to increased risk of acute kidney injury (Ref).

Hemodialysis, intermittent (thrice weekly): Not significantly dialyzable (Ref): Avoid use, as patients with end-stage kidney disease may be at increased risk for bleeding (eg, GI), cardiovascular adverse effects, and loss of residual kidney function (Ref).

Peritoneal dialysis: Avoid use, as patients with end-stage kidney disease may be at increased risk for bleeding (eg, GI), cardiovascular adverse effects, and loss of residual kidney function (Ref).

CRRT: Avoid use (Ref).

PIRRT (eg, sustained, low-efficiency diafiltration): Avoid use (Ref).

Dosing: Liver Impairment: Adult

IV: Mild to severe impairment: There are no dosage adjustments provided in the manufacturer's labeling (has not been studied); use with caution to avoid adverse effects and discontinue if hepatic function worsens.

Oral:

Mild to moderate impairment (Child-Pugh class A or B): No dosage adjustment necessary.

Severe impairment (Child-Pugh class C): There are no dosage adjustments provided in the manufacturer's labeling (has not been studied); use with caution to avoid adverse effects and discontinue if hepatic function worsens.

Adverse Reactions (Significant): Considerations
Cardiovascular events

Use of nonsteroidal anti-inflammatory drugs (NSAIDs) is associated with an increased risk of serious adverse cardiovascular (CV) events, including acute myocardial infarction (MI), cerebrovascular accident, and CV death. New-onset hypertension or exacerbation of hypertension may occur with NSAID use which may also contribute to an increased risk of CV events (Ref). New-onset or exacerbation of heart failure may also occur with nonselective NSAIDs (eg, naproxen), cyclooxygenase (COX)-2 selective NSAIDs (ie, coxibs), and relatively selective COX-2 inhibitors (eg, meloxicam), resulting in an increased risk of hospitalizations for heart failure and death in patients with heart failure (Ref).

Data collected by the Coxib and traditional NSAID Trialists’ (CNT) Collaborative has shown that use of COX-2 selective NSAIDs, including celecoxib, may increase the risk of major vascular events as compared to nonselective NSAIDs (Ref); however, data from the PRECISION trial showed no difference with regards to risk between celecoxib, naproxen, or ibuprofen after a treatment duration of therapy of ~3 years (Ref). A nested matched case-control trial found that use of meloxicam resulted in a 38% increase in the risk of MI (Ref). Additional trial and registry data are also conflicted with regards to the comparative risk of CV events among the COX-2 selective and nonselective NSAIDs (Ref). However, data in those with established heart disease consistently reveals an increased risk of harm with NSAID use (Ref). The FDA states that there is insufficient data to determine if risk of MI or stroke is definitely higher or lower for any particular NSAID as compared to another (Ref).

Mechanism: Dose- and time-related; inhibition of COX-2 by NSAIDs results in a reduction in the production of prostaglandin I2 (prostacyclin) in the vascular endothelium (Ref); animal studies have shown that reduced prostacyclin activity may result in a predisposition to vascular injury (Ref). In addition, prostaglandins inhibit sodium resorption in the thick ascending loop of Henle and collecting tubule; therefore, a reduction in prostaglandin synthesis by NSAIDs may cause sodium and fluid retention and result in hypertension and decreased efficacy of diuretics (Ref).

Onset: Varied; increased risk may be apparent within the first weeks following initiation of treatment (Ref); longer duration of therapy may further increase risk (Ref).

Risk factors:

• ≥65 years of age

• Higher doses (especially with regards to CV thrombotic risk) (Ref)

• Longer duration of use and frequent use (eg, ≥22 days per month) (Ref)

• Preexisting cardiovascular disease (CVD) or presence of risk factors for CVD, including use following coronary artery bypass graft surgery (Ref)

- Note: Relative risk appears to be similar in those with and without known CVD or risk factors for CVD; however, absolute incidence of serious CV thrombotic events appears to be higher in patients with known CVD or risk factors for CVD due to an increased baseline risk (Ref)

Gastrointestinal events

Use of nonsteroidal anti-inflammatory drugs (NSAIDs) is associated with an increased risk of serious gastrointestinal (GI) adverse events, including GI inflammation, gastrointestinal hemorrhage, gastrointestinal ulcer, and gastrointestinal perforation; severity may range from asymptomatic to fatal (Ref). Selective cyclooxygenase (COX)-2 NSAIDs, including relatively selective COX-2 inhibitors (eg, meloxicam), appear to be associated with a lower risk of significant GI adverse events as compared to nonselective NSAIDs; the concomitant use of low-dose aspirin therapy may diminish the safety advantage of COX-2 selective NSAIDs over nonselective NSAIDs (Ref).

Mechanism: Dose- and time-related; inhibition of COX-1 by NSAIDs results in a reduction in the production of mucosal-protective prostaglandin E2. COX-2 selective NSAIDs may block COX-1 in the GI tract, albeit to a lesser degree as compared to nonselective NSAIDs, and therefore have the ability to cause damage (Ref).

Onset: Varied; GI events can occur at any time during use and without warning symptoms.

Risk factors:

• ≥65 years of age (Ref)

• Longer duration of use

• Higher doses (eg, meloxicam 15 mg daily (Ref))

• Prior history of peptic ulcer disease and/or GI bleeding

• Concomitant use of agents known to increase the risk of GI bleeding (eg, aspirin (Ref); anticoagulants, corticosteroids (Ref); selective serotonin reuptake inhibitors (Ref))

• Comorbid Helicobacter pylori infection (Ref)

• Advanced liver disease/cirrhosis

• Coagulopathy

• Smoking

• Consumption of alcohol

• People with poor general health status

• Small intestine damage: Small intestine bacterial overgrowth (SIBO), including SIBO induced by proton pump inhibitor therapy, may be associated with an increased risk of small intestine damage (Ref)

Hematologic effects

Use of nonsteroidal anti-inflammatory drugs (NSAIDs) may result in anemia; drug-induced hemolytic anemia has been reported with use of other NSAIDs, including both non-selective and cyclooxygenase (COX)-2 selective agents (Ref). Use of meloxicam may result in a prolonged bleeding time and an increased risk for hemorrhage (Ref); however, nonselective NSAIDs (eg, ibuprofen) may be more likely to impact platelet function and cause prolonged bleeding time compared to selective and relatively selective COX-2 inhibitors (coxibs and meloxicam respectively) (Ref). Rarely, NSAID use, including meloxicam, has been associated with potentially severe blood dyscrasias (eg, agranulocytosis, thrombocytopenia (Ref), aplastic anemia).

Mechanism:

Anemia: Not clearly established; anemia may be due to occult or gross blood loss, fluid retention, or an incompletely described effect on erythropoiesis.

Prolonged bleeding time: Inhibition of COX-1 causes a decrease in the production of prostaglandins, prostacyclins, and thromboxanes, including thromboxane A2 (TxA2) (Ref). Therefore, patients exposed to NSAIDs, especially nonselective NSAIDs (eg, naproxen), may exhibit a decrease in platelet adhesion and aggregation and subsequent prolonged bleeding time (Ref).

Onset: Prolonged bleeding time: Rapid; suppression of platelet COX-1 activity occurs within hours of administration (Ref). In patients receiving antithrombotic therapy after myocardial infarction, the use of NSAIDs, including COX-2 selective NSAIDs, has been associated with an increased risk of bleeding and excess thrombotic events even after short-term treatment (eg, <3 days) (Ref).

Risk factors:

• Bleeding events:

- Preexisting coagulation disorders

- Concomitant use of agents known to increase the risk of bleeding (eg, anticoagulants, antithrombotics (Ref); antiplatelet agents [eg, aspirin], selective serotonin reuptake inhibitors (Ref); or serotonin norepinephrine reuptake inhibitors).

Hepatic effects

Nonsteroidal anti-inflammatory drugs (NSAIDs) may cause mild transaminase elevations (Ref); meloxicam has been associated with both cholestatic and hepatocellular patterns of transaminase elevations (Ref). The incidence of hepatic adverse events appears similar between cyclooxygenase (COX)-2 selective NSAIDs (ie, coxibs) and nonselective NSAIDs (eg, naproxen, ibuprofen) (Ref); diclofenac exhibits a higher rate of hepatotoxic events compared to other NSAIDs (Ref). Rarely, serious liver injury may occur, such as fulminant hepatitis, hepatic necrosis, and/or hepatic failure; meloxicam-induced autoimmune hepatitis, cholestatic hepatitis, hepatotoxicity, and jaundice have been reported (Ref).

Mechanism: Not clearly established; possible mechanisms include a toxic metabolite or a hypersensitivity reaction (Ref).

Onset: Varied; onset of NSAID-induced hepatotoxicity is generally classified as moderate (30 to 90 days) to long (>90 days) (Ref). For meloxicam, onset was <1 month in a few cases (Ref).

Risk factors:

• Prior “oxicam” NSAID (eg, piroxicam)-related liver injury (theoretical risk factor) (Ref)

Hypersensitivity reactions (immediate and delayed)

Hypersensitivity reactions to meloxicam may involve the skin (eg, angioedema, urticaria), airways (eg, dyspnea, rhinorrhea), and/or other organs (Ref). Clinical phenotypes of nonsteroidal anti-inflammatory drug (NSAID) hypersensitivity reactions include NSAID-exacerbated respiratory disease (NERD), NSAID-induced urticaria/angioedema (NIUA), NSAID-exacerbated cutaneous disease (NECD), and single NSAID-induced urticaria/angioedema or anaphylaxis (Ref). Delayed hypersensitivity reactions ranging from mild reactions such as fixed drug eruption (Ref) to more serious reactions including Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) (Ref) have been reported with meloxicam.

Mechanism:

Immediate hypersensitivity reactions: Non–dose-related; most reactions (ie, NERD, NECD, NIUA) are non-immunologic related to inhibition of cyclooxygenase (COX)-1 with subsequent activation of mast cells and eosinophils causing release of inflammatory mediators including cysteinyl-leukotrienes (cysLTs) (Ref). Meloxicam preferentially inhibits COX-2 at lower doses, but at higher doses also inhibits the COX-1 enzyme (Ref).

Delayed hypersensitivity reactions: T-cell-mediated (Ref).

Onset:

Immediate hypersensitivity reactions: Rapid; occur within 1 hour of administration but may occur several hours after exposure (Ref).

Delayed hypersensitivity reactions (including SJS/TEN): Varied, generally occurs after 1 to 8 weeks after initiation (Ref), although time to onset with meloxicam may be 2 to 3 days (Ref).

Risk factors:

• Preferential COX-2 inhibitors (eg, meloxicam) are generally tolerated (especially in low to therapeutic doses) in patients with NERD (Ref) and in many patients with cutaneous reactions to NSAIDs (Ref); ~4% to 9% of NECD, NERD, and NIUA patients may develop reactions with meloxicam (Ref)

• Cross-reactions with meloxicam and other enolic acid derivatives (“oxicams”) NSAIDs (eg, piroxicam, tenoxicam) may occur (Ref)

Kidney effects

Use of nonsteroidal anti-inflammatory drugs (NSAIDs) is associated with an increased risk of several kidney-specific effects: hemodynamically-mediated acute kidney injury (AKI), interstitial nephritis (with or without nephrotic syndrome), and renal papillary necrosis.

Hemodynamically-mediated AK): Hemodynamically-mediated AKI may occur following use of either cyclooxygenase (COX)-2 selective NSAIDs (ie, coxibs) or nonselective NSAIDs (Ref); the risk may be greater with nonselective NSAIDs, especially indomethacin (Ref). The risk of developing AKI is decreased upon discontinuation (Ref). In patients who develop AKI, kidney function is likely to return to baseline following prompt discontinuation of the offending NSAID and supportive care (Ref); however, the mechanism of the damage and other concurrent factors can contribute to irreversibility.

Acute interstitial nephritis (AIN) with or without nephrotic syndrome: Patients may develop NSAID-associated proteinuria combined with interstitial nephritis and varying degrees of kidney impairment; the “classic triad” of fever, rash, and eosinophilia is less commonly observed in NSAID-associated AIN than with antibiotic-induced AIN (Ref). In patients with concurrent nephrotic syndrome, kidney histology may reveal minimal change glomerulonephritis or membranous nephropathy (Ref). While use of meloxicam has been associated with this clinical picture (Ref); the risk may be greatest with fenoprofen as compared to other NSAIDS (Ref). Proteinuria generally improves within weeks following discontinuation; full recovery may require treatment and take up to a year (Ref).

Papillary necrosis: Chronic use of NSAIDs has resulted in the development of papillary necrosis which may occur in conjunction with chronic interstitial nephritis and progressive decline in glomerular filtration rate as a clinical syndrome known as analgesic nephropathy (Ref). However, controversy exists on the degree to which NSAID use increases the risk for chronic kidney disease and analgesic nephropathy (Ref). Acute papillary necrosis may occur following NSAID overdose, especially in a setting of severe dehydration or intravascular volume depletion (Ref).

Mechanism:

Hemodynamically-mediated AKI: Dose- and time-related; inhibition of COX-1 and COX-2 by NSAIDs results in a reduced production of nephroprotective prostaglandins and subsequent attenuation of renal vasodilation (Ref). In addition, an increase in vasoconstriction of the afferent arteriole and impaired renal blood flow causes a reduction in the glomerular capillary pressure and filtration (Ref).

AIN with or without nephrotic syndrome: Not clearly established. Following inhibition of COX-1 and COX-2 by NSAIDs, arachidonic acid is formed which may be further metabolized to leukotrienes via the lipoxygenase pathway; leukotrienes may increase vascular permeability within glomerular capillaries and peritubular capillaries and increase lymphocyte recruitment and activation (Ref).

Papillary necrosis: Time-related; exact mechanism is not clearly established; may be due to direct toxicity and/or inhibition of prostaglandin-mediated vasodilation resulting in ischemic necrosis (Ref).

Onset:

AKI: Rapid; may occur within days of treatment initiation (Ref).

AIN with or without nephrotic syndrome: Varied; mean time of onset of ~5 months (range: 2 weeks to 18 months) has been described following use of nonselective NSAIDs (Ref).

Risk factors:

• AKI:

- Preexisting kidney impairment

- Chronic kidney disease; Note: Higher cumulative doses may increase the risk for progression of chronic kidney disease (Ref)

- ≥65 years of age (Ref); Note: NSAID-associated AKI may also occur in pediatric patients, even at therapeutic doses (Ref)

• Hemodynamically-mediated AKI:

- Preexisting conditions which result in decreased effective arterial circulation (ie, conditions where renal blood flow/renal perfusion may be dependent on prostaglandin-mediated vasodilation) (Ref)

Volume depletion (eg, due to concomitant diuretic use, nausea, or vomiting)

Heart failure (Ref)

Cirrhosis and ascites (Ref)

Nephrotic syndrome

- Concomitant use of diuretics, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, or calcineurin inhibitors (Ref)

• AIN with or without nephrotic syndrome: Prior history of NSAID-induced nephrotic syndrome; recurrence has been described with a nonselective NSAID (Ref)

• Papillary necrosis (acute):

- Massive NSAID ingestion (Ref)

- Dehydration (Ref)

- Intravascular volume depletion (Ref)

• Papillary necrosis (chronic)/analgesic nephropathy: Chronic concomitant use of other analgesics (eg, aspirin, acetaminophen) (Ref)

Adverse Reactions

The following adverse drug reactions and incidences are derived from product labeling unless otherwise specified.

1% to 10%:

Cardiovascular: Acute myocardial infarction (<2%), angina pectoris (<2%), cardiac arrhythmia (<2%), edema (≤5%), heart failure (<2%), hypertension (<2%), hypotension (<2%), palpitations (<2%), presyncope (<2%), syncope (<2%), tachycardia (<2%), vasculitis (<2%)

Dermatologic: Alopecia (<2%), bullous rash (<2%), diaphoresis (<2%), ecchymoses (<2%), pruritus (<2%), skin photosensitivity (<2%), skin rash (<2%), urticaria (<2%)

Endocrine & metabolic: Albuminuria (<2%), dehydration (<2%), hot flash (<2%), hypokalemia (<2%), hypomagnesemia (<2%), weight gain (<2%), weight loss (<2%)

Gastrointestinal: Abdominal distention (<2%), abdominal distress (<2%), abdominal pain (≤3%; more common in pediatric patients), aphthous stomatitis (<2%), colitis (<2%), constipation (8%), diarrhea (≤8%; more common in pediatric patients), duodenal ulcer (<2%; duodenal ulcer with hemorrhage: <2%), dysgeusia (<2%), dyspepsia (6%), epigastric discomfort (<2%), eructation (<2%), esophagitis (<2%), flatulence (<2%), gastric ulcer (<2%; gastric ulcer with hemorrhage: <2%), gastritis (<2%), gastroenteritis (<2%), gastroesophageal reflux disease (<2%), gastrointestinal hemorrhage (<2%), gastrointestinal pain (<2%), gastrointestinal perforation (<2%; including duodenal, gastric), hematemesis (<2%), increased appetite (<2%), intestinal perforation (<2%), melena (<2%), nausea (2% to 4%), pancreatitis (<2%), rectal hemorrhage (<2%), xerostomia (<2%)

Genitourinary: Hematuria (<2%), pollakiuria (<2%), urinary retention (<2%)

Hematologic & oncologic: Anemia (2%) (table 1), leukopenia (<2%), neutropenia (<2%), prolonged bleeding time (<2%), purpuric disease (<2%), thrombocytopenia (<2%), thrombocytosis (<2%), wound hematoma (IV only: <2%)

Meloxicam: Adverse Reaction: Anemia

Drug (Meloxicam)

Placebo

Dosage Form

Number of Patients (Meloxicam)

Number of Patients (Placebo)

2%

1%

IV injection

748

393

Hepatic: Abnormal hepatic function tests (<2%), hepatitis (<2%), hyperbilirubinemia (<2%), increased gamma-glutamyl transferase (≤3%), increased serum alanine aminotransferase (<2%), increased serum aspartate aminotransferase (<2%)

Hypersensitivity: Facial edema (<2%), hypersensitivity reaction (<2%; including angioedema)

Local: Incision-site hemorrhage (IV only: <2%), infusion-site reaction (IV only: <2%), localized rash (IV only, infusion site: <2%)

Nervous system: Abnormal dreams (<2%), anxiety (<2%), asthenia (<2%), confusion (<2%), depression (<2%), disturbance in attention (<2%), dizziness (4%), drowsiness (<2%), falling (3%), fatigue (<2%), headache (2%; more common in pediatric patients), insomnia (<2%), malaise (<2%), migraine (<2%), nervousness (<2%), noncardiac chest pain (<2%), paresthesia (<2%), seizure (<2%), tremor (<2%), vertigo (<2%)

Neuromuscular & skeletal: Back pain (<2%), muscle spasm (<2%)

Ophthalmic: Visual disturbance (<2%)

Otic: Tinnitus (<2%)

Renal: Increased blood urea nitrogen (<2%), increased serum creatinine (<2%), kidney failure (<2%)

Respiratory: Asthma (<2%), bronchospasm (<2%), dyspnea (<2%), epistaxis (<2%), flu-like symptoms (3% to 6%), pharyngitis (3%), upper respiratory tract infection (3% to 7%)

Miscellaneous: Accidental injury (3% to 5%), fever (<2%; more common in pediatric patients), wound dehiscence (<2%)

Frequency not defined:

Cardiovascular: Thrombosis

Gastrointestinal: Vomiting (more common in pediatric patients)

Nervous system: Cerebrovascular accident

Postmarketing:

Dermatologic: Erythema multiforme (Ref), exfoliative dermatitis, fixed drug eruption (Ref), Stevens-Johnson syndrome (Ref), toxic epidermal necrolysis (Ref))

Endocrine & metabolic: Pseudoporphyria (Ref)

Hematologic & oncologic: Agranulocytosis, hemorrhage (Ref)

Hepatic: Autoimmune hepatitis (Ref), cholestatic hepatitis (Ref), hepatic failure, hepatotoxicity (idiosyncratic) (Ref), jaundice (Ref)

Hypersensitivity: Anaphylactic shock, anaphylaxis (Ref), drug reaction with eosinophilia and systemic symptoms (Ref), nonimmune anaphylaxis

Nervous system: Mood changes

Renal: Interstitial nephritis, nephrotic syndrome (Ref), renal papillary necrosis, renal tubular necrosis (Ref)

Contraindications

Hypersensitivity to meloxicam or any component of the formulation; history of asthma, urticaria, or other allergic-type reactions after taking aspirin or other nonsteroidal anti-inflammatory drugs; use in the setting of coronary artery bypass graft surgery; phenylketonuria (orally disintegrating tablet only); moderate to severe renal insufficiency patients who are at risk for renal failure due to volume depletion (injection only).

Canadian labeling: Additional contraindications (not in US labeling): Pregnancy (third trimester); breastfeeding; severe uncontrolled heart failure; active or recent GI/gastric/duodenal/peptic ulceration/perforation; active GI bleeding; cerebrovascular bleeding or other bleeding disorders; inflammatory bowel disease (Crohn disease or ulcerative colitis); severe liver impairment or active liver disease; severe renal impairment (creatinine clearance [CrCl] <30 mL/minute or 0.5 mL/second) or deteriorating renal disease; known hyperkalemia; pediatric patients <18 years; rare hereditary conditions that may be incompatible with an excipient of the product.

Warnings/Precautions

Concerns related to adverse effects:

• CNS effects: May cause drowsiness, dizziness, blurred vision, and other neurologic effects that may impair physical or mental abilities; patients must be cautioned about performing tasks that require mental alertness (eg, operating machinery, driving).

• Hyperkalemia: Non-steroidal anti-inflammatory drug (NSAID) use may increase the risk of hyperkalemia, particularly in the elderly, diabetics, renal disease, and with concomitant use of other agents capable of inducing hyperkalemia (eg, ACE inhibitors). Monitor potassium closely.

• Ophthalmic effects: Blurred and/or diminished vision has been reported; discontinue use and refer for ophthalmologic evaluation if such symptoms occur.

Disease-related concerns:

• Asthma: Contraindicated in patients with aspirin-sensitive asthma; severe potentially fatal bronchospasm may occur. Use caution in patients with other forms of asthma.

• Bariatric surgery: Gastric ulceration: Avoid chronic use of oral nonselective NSAIDs after bariatric surgery; development of anastomotic ulcerations/perforations may occur (Bhangu 2014; Mechanick 2020). Short-term use of celecoxib or IV ketorolac are recommended as part of a multimodal pain management strategy for postoperative pain (Chou 2016; Horsley 2019; Thorell 2016).

• Hepatic impairment: Use with caution in patients with hepatic impairment; patients with hepatic impairment may require reduced doses due to extensive hepatic metabolism.

• Renal impairment: Use with caution in patients with renal impairment.

Special populations:

• CYP2C9 poor metabolizers: Poor metabolizers of CYP2C9 may require dose reduction.

Dosage form specific issues:

• Injection: Not indicated for long-term use. Onset of pain relief may be delayed up to several hours after administration; use of a non-NSAID analgesic with a rapid onset may be needed. Also, inadequate analgesia for the entire 24-hour dosing interval may be experienced; use of a short-acting, non-NSAID, IR analgesic may be required.

• Phenylalanine: Orally disintegrating tablet: May contain phenylalanine; use is contraindicated in patients with phenylketonuria.

Other warnings/precautions:

• Surgical/dental procedures: Withhold for at least 4 to 6 half-lives prior to surgical or dental procedures.

Product Availability

Qamzova (meloxicam 30 mg/mL) injection: FDA approved April 2025; anticipated availability currently unknown. Information pertaining to this product within the monograph is pending revision. Qamzova is indicated for use in adults for the management of moderate-to-severe pain, alone or in combination with non-NSAID analgesics. Consult the prescribing information for additional information.

Qmiiz ODT and Anjeso have been discontinued in the United States for >1 year.

Dosage Forms: US

Excipient information presented when available (limited, particularly for generics); consult specific product labeling. [DSC] = Discontinued product

Capsule, Oral:

Vivlodex: 5 mg [DSC] [contains fd&c blue #2 (indigotine,indigo carmine), fd&c red #40 (allura red ac dye), fd&c yellow #6 (sunset yellow)]

Vivlodex: 10 mg [DSC] [contains carmine (cochineal extract), fd&c blue #2 (indigotine,indigo carmine), fd&c red #40 (allura red ac dye), fd&c yellow #6 (sunset yellow)]

Generic: 5 mg, 10 mg

Injectable, Intravenous [preservative free]:

Anjeso: 30 mg/mL (1 mL [DSC])

Suspension, Oral:

Generic: 7.5 mg/5 mL (100 mL)

Tablet, Oral:

Mobic: 7.5 mg [DSC], 15 mg [DSC]

Generic: 7.5 mg, 15 mg, 15 mg

Tablet Disintegrating, Oral:

Qmiiz ODT: 7.5 mg [DSC], 15 mg [DSC] [contains aspartame]

Generic Equivalent Available: US

May be product dependent

Pricing: US

Capsules (Meloxicam Oral)

5 mg (per each): $31.05

10 mg (per each): $31.05

Suspension (Meloxicam Oral)

7.5 mg/5 mL (per mL): $12.43 - $13.83

Tablets (Meloxicam Oral)

7.5 mg (per each): $0.05 - $3.17

15 mg (per each): $0.06 - $4.85

Disclaimer: A representative AWP (Average Wholesale Price) price or price range is provided as reference price only. A range is provided when more than one manufacturer's AWP price is available and uses the low and high price reported by the manufacturers to determine the range. The pricing data should be used for benchmarking purposes only, and as such should not be used alone to set or adjudicate any prices for reimbursement or purchasing functions or considered to be an exact price for a single product and/or manufacturer. Medi-Span expressly disclaims all warranties of any kind or nature, whether express or implied, and assumes no liability with respect to accuracy of price or price range data published in its solutions. In no event shall Medi-Span be liable for special, indirect, incidental, or consequential damages arising from use of price or price range data. Pricing data is updated monthly.

Dosage Forms: Canada

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Tablet, Oral:

Generic: 7.5 mg, 15 mg

Administration: Pediatric

Oral: May be taken with or without meals; administer with food or milk to minimize gastrointestinal irritation.

Orally disintegrating tablet (Qmiiz ODT): Children and Adolescents weighing ≥60 kg: Do not remove from blister until ready to administer. Using dry hands, peel backing off the blister; do not push tablet through foil. Remove tablet and immediately place in mouth or on tongue and allow to disintegrate. Swallow with saliva (with or without drinking liquid).

Suspension: Shake gently prior to use. Administer with an accurate measuring device (calibrated oral syringe or measuring cup); do not use a household teaspoon or tablespoon to measure dose (overdosage may occur). Administer with or without food.

Administration: Adult

IV: Administer undiluted as an IV bolus over 15 seconds.

Oral: Administer with or without meals; administer with food or milk to minimize GI irritation.

Orally disintegrating tablet: Do not remove from blister until ready to administer. Using dry hands, peel backing off the blister; do not push tablet through foil. Remove tablet and immediately place in mouth or on tongue and allow to disintegrate. Swallow with saliva (with or without drinking liquid).

Suspension: Shake oral suspension gently prior to use.

Storage/Stability

Injection: Store at 15°C to 25°C (59°F to 77°F); excursions permitted between 4°C to 30°C (40°F to 86°F). Do not freeze. Protect from light.

Oral: Store at 25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F). Protect tablets and capsules from moisture. Protect orally disintegrating tablets from exposure to excessive heat (40°C [104°F]) and humidity.

Medication Guide and/or Vaccine Information Statement (VIS)

An FDA-approved patient medication guide, which is available with the product information and as follows, must be dispensed with this medication:

Mobic oral suspension: https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/021530s020lbl.pdf#page=16

Mobic tablets: https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/020938s030lbl.pdf#page=16

Qmiiz ODT: https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/211210s002lbl.pdf#page=37

Vivlodex: https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/207233s005lbl.pdf#page=24

Use

Oral:

Tablets, orally disintegrating tablets (Qmiiz ODT), suspension: Relief of signs and symptoms of pauciarticular or polyarticular course juvenile idiopathic arthritis (JIA) (Suspension: FDA approved in ages ≥2 years and adults; Tablets, orally disintegrating tablets [Qmiiz ODT]: FDA approved in pediatric patients weighing ≥60 kg); relief of signs and symptoms of osteoarthritis and rheumatoid arthritis (all dosage forms: FDA approved in adults).

Capsules: Management of osteoarthritis pain (FDA approved in adults).

IV: Management of moderate to severe pain alone or in combination with non–nonsteroidal anti-inflammatory drug analgesics (FDA approved in adults).

Medication Safety Issues
High alert medication:

The Institute for Safe Medication Practices (ISMP) includes this medication among its list of drugs (pediatric liquid medications requiring measurement) which have a heightened risk of causing significant patient harm when used in error (High-Alert Medications in Community/Ambulatory Care Settings).

Older Adult: High-Risk Medication:

Beers Criteria: Meloxicam is identified in the Beers Criteria as a potentially inappropriate medication to be avoided for chronic use in patients 65 years and older (unless alternative agents ineffective and patient can receive concomitant gastroprotective agent) due to increased risk of GI bleeding and peptic ulcer disease in older adults in high risk category (eg, older than 75 years or receiving concomitant oral/parenteral corticosteroids, anticoagulants, or antiplatelet agents). In addition, avoid for short-term scheduled use in combination with oral/parenteral corticosteroids, anticoagulants, or antiplatelet agents unless alternatives are ineffective and patient can receive concomitant gastroprotective agent (Beers Criteria [AGS 2023]).

Metabolism/Transport Effects

Substrate of CYP2C9 (Major with inhibitors), CYP2C9 (Minor with inducers), CYP3A4 (Minor); Note: Assignment of Major/Minor substrate status based on clinically relevant drug interaction potential;

Drug Interactions

Note: Interacting drugs may not be individually listed below if they are part of a group interaction (eg, individual drugs within “CYP3A4 Inducers [Strong]” are NOT listed). For a complete list of drug interactions by individual drug name and detailed management recommendations, use the drug interactions program by clicking on the “Launch drug interactions program” link above.

Note: Interacting drugs may not be individually listed below if they are part of a group interaction (eg, individual drugs within “CYP3A4 Inducers [Strong]” are NOT listed). For a complete list of drug interactions by individual drug name and detailed management recommendations, use the drug interactions program

5-Aminosalicylic Acid Derivatives: Nonsteroidal Anti-Inflammatory Agents may increase nephrotoxic effects of 5-Aminosalicylic Acid Derivatives. Risk C: Monitor

Abciximab: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Abrocitinib: Agents with Antiplatelet Effects may increase antiplatelet effects of Abrocitinib. Risk X: Avoid

Acalabrutinib: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Acemetacin: May increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents. Risk X: Avoid

Alcohol (Ethyl): May increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents. Specifically, the risk of GI bleeding may be increased with this combination. Risk C: Monitor

Aliskiren: Nonsteroidal Anti-Inflammatory Agents may increase nephrotoxic effects of Aliskiren. Nonsteroidal Anti-Inflammatory Agents may decrease antihypertensive effects of Aliskiren. Risk C: Monitor

Aminoglycosides: Nonsteroidal Anti-Inflammatory Agents may decrease excretion of Aminoglycosides. Data only in premature infants. Risk C: Monitor

Aminolevulinic Acid (Systemic): Photosensitizing Agents may increase photosensitizing effects of Aminolevulinic Acid (Systemic). Risk X: Avoid

Aminolevulinic Acid (Topical): Photosensitizing Agents may increase photosensitizing effects of Aminolevulinic Acid (Topical). Risk C: Monitor

Amiodarone: May increase serum concentration of Meloxicam. Risk C: Monitor

Anagrelide: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Angiotensin II Receptor Blockers: Nonsteroidal Anti-Inflammatory Agents may decrease therapeutic effects of Angiotensin II Receptor Blockers. The combination of these two agents may also significantly decrease glomerular filtration and renal function. Angiotensin II Receptor Blockers may increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents. Specifically, the combination may result in a significant decrease in renal function. Risk C: Monitor

Angiotensin-Converting Enzyme Inhibitors: Nonsteroidal Anti-Inflammatory Agents may decrease antihypertensive effects of Angiotensin-Converting Enzyme Inhibitors. Angiotensin-Converting Enzyme Inhibitors may increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents. Specifically, the combination may result in a significant decrease in renal function. Risk C: Monitor

Anticoagulants (Miscellaneous Agents): Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase anticoagulant effects of Anticoagulants (Miscellaneous Agents). Risk C: Monitor

Antiplatelet Agents (P2Y12 Inhibitors): Agents with Antiplatelet Effects may increase antiplatelet effects of Antiplatelet Agents (P2Y12 Inhibitors). Risk C: Monitor

Aspirin: Nonsteroidal Anti-Inflammatory Agents (Nonselective) may decrease therapeutic effects of Aspirin. Aspirin may increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents (Nonselective). Specifically, the risk for bleeding may be increased. Aspirin may decrease serum concentration of Nonsteroidal Anti-Inflammatory Agents (Nonselective). Management: In general, avoid regular, frequent use of NSAIDs with aspirin whenever possible. If combined, monitor for increased bleeding and a reduced cardioprotective effect of aspirin. Risk D: Consider Therapy Modification

Bemiparin: Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase anticoagulant effects of Bemiparin. Management: Avoid this combination if possible, due to an increased risk of bleeding. If coadministration cannot be avoided, monitor patients closely for clinical and laboratory evidence of bleeding. Risk D: Consider Therapy Modification

Beta-Blockers: Nonsteroidal Anti-Inflammatory Agents may decrease antihypertensive effects of Beta-Blockers. Risk C: Monitor

Bile Acid Sequestrants: May decrease absorption of Nonsteroidal Anti-Inflammatory Agents. Risk C: Monitor

Bisphosphonate Derivatives: Nonsteroidal Anti-Inflammatory Agents may increase adverse/toxic effects of Bisphosphonate Derivatives. Both an increased risk of gastrointestinal ulceration and an increased risk of nephrotoxicity are of concern. Risk C: Monitor

Calcium Polystyrene Sulfonate: Meloxicam may increase adverse/toxic effects of Calcium Polystyrene Sulfonate. More specifically, concomitant use of meloxicam oral suspension (which contains sorbitol) may increase the risk for intestinal necrosis. Risk X: Avoid

Caplacizumab: Agents with Antiplatelet Effects may increase adverse/toxic effects of Caplacizumab. Specifically, the risk of bleeding may be increased. Risk C: Monitor

Cardiac Glycosides: Nonsteroidal Anti-Inflammatory Agents may increase serum concentration of Cardiac Glycosides. Risk C: Monitor

Collagenase (Systemic): Agents with Antiplatelet Effects may increase adverse/toxic effects of Collagenase (Systemic). Specifically, the risk of injection site bruising and or bleeding may be increased. Risk C: Monitor

Corticosteroids (Systemic): May increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents (Nonselective). Risk C: Monitor

CycloSPORINE (Systemic): Nonsteroidal Anti-Inflammatory Agents may increase nephrotoxic effects of CycloSPORINE (Systemic). Nonsteroidal Anti-Inflammatory Agents may increase serum concentration of CycloSPORINE (Systemic). CycloSPORINE (Systemic) may increase serum concentration of Nonsteroidal Anti-Inflammatory Agents. Management: Consider alternatives to nonsteroidal anti-inflammatory agents (NSAIDs). Monitor for evidence of nephrotoxicity, as well as increased serum cyclosporine concentrations and systemic effects (eg, hypertension) during concomitant therapy with NSAIDs. Risk D: Consider Therapy Modification

CYP2C9 Inhibitors (Moderate): May increase serum concentration of Meloxicam. Risk C: Monitor

Dasatinib: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Deferasirox: Nonsteroidal Anti-Inflammatory Agents may increase adverse/toxic effects of Deferasirox. Specifically, the risk for GI ulceration/irritation or GI bleeding may be increased. Risk C: Monitor

Deoxycholic Acid: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Desirudin: Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase anticoagulant effects of Desirudin. Risk C: Monitor

Desmopressin: Nonsteroidal Anti-Inflammatory Agents may increase hyponatremic effects of Desmopressin. Risk C: Monitor

Direct Oral Anticoagulants (DOACs): Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase anticoagulant effects of Direct Oral Anticoagulants (DOACs). Risk C: Monitor

Drospirenone-Containing Products: May increase hyperkalemic effects of Nonsteroidal Anti-Inflammatory Agents. Risk C: Monitor

Enoxaparin: Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase anticoagulant effects of Enoxaparin. Management: Discontinue nonselective NSAIDs prior to initiation of enoxaparin whenever possible. If coadministration cannot be avoided, monitor patients closely for clinical and laboratory evidence of bleeding. Risk D: Consider Therapy Modification

Eplerenone: Nonsteroidal Anti-Inflammatory Agents may decrease antihypertensive effects of Eplerenone. Nonsteroidal Anti-Inflammatory Agents may increase hyperkalemic effects of Eplerenone. Risk C: Monitor

Fondaparinux: Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase anticoagulant effects of Fondaparinux. Management: Discontinue nonselective nonsteroidal anti-inflammatory agents prior to the initiation of fondaparinux, if possible. If coadministration is required, monitor patients closely for signs and symptoms of bleeding. Risk D: Consider Therapy Modification

Glycoprotein IIb/IIIa Inhibitors: Agents with Antiplatelet Effects may increase antiplatelet effects of Glycoprotein IIb/IIIa Inhibitors. Risk C: Monitor

Heparin: Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase anticoagulant effects of Heparin. Risk C: Monitor

Heparins (Low Molecular Weight): Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase anticoagulant effects of Heparins (Low Molecular Weight). Risk C: Monitor

Herbal Products with Anticoagulant/Antiplatelet Effects: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

HydrALAZINE: Nonsteroidal Anti-Inflammatory Agents may decrease antihypertensive effects of HydrALAZINE. Risk C: Monitor

Ibritumomab Tiuxetan: Agents with Antiplatelet Effects may increase antiplatelet effects of Ibritumomab Tiuxetan. Risk C: Monitor

Ibrutinib: Agents with Antiplatelet Effects may increase adverse/toxic effects of Ibrutinib. Specifically, the risk of bleeding and hemorrhage may be increased. Risk C: Monitor

Inotersen: Agents with Antiplatelet Effects may increase adverse/toxic effects of Inotersen. Specifically, the risk of bleeding may be increased. Risk C: Monitor

Itraconazole: May decrease serum concentration of Meloxicam. Risk C: Monitor

Ketorolac (Nasal): May increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents. Risk X: Avoid

Ketorolac (Systemic): Nonsteroidal Anti-Inflammatory Agents may increase adverse/toxic effects of Ketorolac (Systemic). Risk X: Avoid

Limaprost: May increase adverse/toxic effects of Agents with Antiplatelet Effects. Specifically, the risk of bleeding may be increased. Risk C: Monitor

Lithium: Nonsteroidal Anti-Inflammatory Agents may increase serum concentration of Lithium. Management: Consider reducing the lithium dose when initiating a NSAID. Monitor for increased lithium therapeutic/toxic effects if a NSAID is initiated/dose increased, or decreased effects if a NSAID is discontinued/dose decreased. Risk D: Consider Therapy Modification

Loop Diuretics: Nonsteroidal Anti-Inflammatory Agents may decrease diuretic effects of Loop Diuretics. Loop Diuretics may increase nephrotoxic effects of Nonsteroidal Anti-Inflammatory Agents. Management: Monitor for evidence of kidney injury or decreased therapeutic effects of loop diuretics with concurrent use of an NSAID. Consider avoiding concurrent use in CHF or cirrhosis. Concomitant use of bumetanide with indomethacin is not recommended. Risk D: Consider Therapy Modification

Lumacaftor and Ivacaftor: May decrease serum concentration of CYP2C9 Substrates (High Risk with Inhibitors or Inducers). Lumacaftor and Ivacaftor may increase serum concentration of CYP2C9 Substrates (High Risk with Inhibitors or Inducers). Risk C: Monitor

Macimorelin: Coadministration of Nonsteroidal Anti-Inflammatory Agents and Macimorelin may alter diagnostic results. Risk X: Avoid

MetFORMIN: Nonsteroidal Anti-Inflammatory Agents may increase adverse/toxic effects of MetFORMIN. Risk C: Monitor

Methotrexate: Nonsteroidal Anti-Inflammatory Agents may increase serum concentration of Methotrexate. Management: Avoid coadministration of higher dose methotrexate (such as that used for the treatment of oncologic conditions) and NSAIDs. Use caution if coadministering lower dose methotrexate and NSAIDs. Risk D: Consider Therapy Modification

Methoxsalen (Systemic): Photosensitizing Agents may increase photosensitizing effects of Methoxsalen (Systemic). Risk C: Monitor

Methoxyflurane: Nonsteroidal Anti-Inflammatory Agents may increase nephrotoxic effects of Methoxyflurane. Risk X: Avoid

Mifamurtide: Nonsteroidal Anti-Inflammatory Agents may decrease therapeutic effects of Mifamurtide. Risk X: Avoid

Miscellaneous Antiplatelets: Agents with Antiplatelet Effects may increase antiplatelet effects of Miscellaneous Antiplatelets. Risk C: Monitor

Nadroparin: Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase anticoagulant effects of Nadroparin. Management: Coadministration of NSAIDs and nadroparin is not recommended due to an increased risk of bleeding. If coadministration is required, monitor patients closely for clinical and laboratory signs of bleeding. Risk D: Consider Therapy Modification

Naftazone: May increase antiplatelet effects of Nonsteroidal Anti-Inflammatory Agents. Risk C: Monitor

Nonsteroidal Anti-Inflammatory Agents (Topical): Nonsteroidal Anti-Inflammatory Agents (Topical) may increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents. Specifically, the risk of gastrointestinal (GI) toxicity is increased. Management: Coadministration of systemic nonsteroidal anti-inflammatory drugs (NSAIDs) and topical NSAIDs is not recommended. If systemic NSAIDs and topical NSAIDs, ensure the benefits outweigh the risks and monitor for increased NSAID toxicities. Risk D: Consider Therapy Modification

Nonsteroidal Anti-Inflammatory Agents: May increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents. Specifically, the risk for gastrointestinal toxicity is increased. Risk X: Avoid

Obinutuzumab: Agents with Antiplatelet Effects may increase adverse/toxic effects of Obinutuzumab. Specifically, the risk of bleeding may be increased. Management: Consider avoiding coadministration of obinutuzumab and agents with antiplatelet effects, especially during the first cycle of obinutuzumab therapy. Risk D: Consider Therapy Modification

Omacetaxine: Nonsteroidal Anti-Inflammatory Agents may increase adverse/toxic effects of Omacetaxine. Specifically, the risk for bleeding-related events may be increased. Risk C: Monitor

Pentosan Polysulfate Sodium: Agents with Antiplatelet Effects may increase adverse/toxic effects of Pentosan Polysulfate Sodium. Specifically, the risk of hemorrhage may be increased. Risk C: Monitor

Phenylbutazone: May increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents. Risk X: Avoid

Pirtobrutinib: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Polyethylene Glycol-Electrolyte Solution: Nonsteroidal Anti-Inflammatory Agents may increase nephrotoxic effects of Polyethylene Glycol-Electrolyte Solution. Risk C: Monitor

Porfimer: Photosensitizing Agents may increase photosensitizing effects of Porfimer. Risk X: Avoid

Potassium Salts: Nonsteroidal Anti-Inflammatory Agents may increase hyperkalemic effects of Potassium Salts. Risk C: Monitor

Potassium-Sparing Diuretics: Nonsteroidal Anti-Inflammatory Agents may increase hyperkalemic effects of Potassium-Sparing Diuretics. Nonsteroidal Anti-Inflammatory Agents may decrease antihypertensive effects of Potassium-Sparing Diuretics. Risk C: Monitor

PRALAtrexate: Nonsteroidal Anti-Inflammatory Agents may increase serum concentration of PRALAtrexate. More specifically, NSAIDS may decrease the renal excretion of pralatrexate. Management: Avoid coadministration of pralatrexate with nonsteroidal anti-inflammatory drugs (NSAIDs). If coadministration cannot be avoided, closely monitor for increased pralatrexate serum levels or toxicity. Risk D: Consider Therapy Modification

Probenecid: May increase serum concentration of Nonsteroidal Anti-Inflammatory Agents. Risk C: Monitor

Prostaglandins (Ophthalmic): Nonsteroidal Anti-Inflammatory Agents may decrease therapeutic effects of Prostaglandins (Ophthalmic). Nonsteroidal Anti-Inflammatory Agents may also enhance the therapeutic effects of Prostaglandins (Ophthalmic). Risk C: Monitor

Quinolones: Nonsteroidal Anti-Inflammatory Agents may increase neuroexcitatory and/or seizure-potentiating effects of Quinolones. Nonsteroidal Anti-Inflammatory Agents may increase serum concentration of Quinolones. Risk C: Monitor

Salicylates: Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase adverse/toxic effects of Salicylates. An increased risk of bleeding may be associated with use of this combination. Risk X: Avoid

Selective Serotonin Reuptake Inhibitor: May increase antiplatelet effects of Nonsteroidal Anti-Inflammatory Agents (Nonselective). Nonsteroidal Anti-Inflammatory Agents (Nonselective) may decrease therapeutic effects of Selective Serotonin Reuptake Inhibitor. Management: Consider alternatives to NSAIDs. Monitor for evidence of bleeding and diminished antidepressant effects. It is unclear whether COX-2-selective NSAIDs reduce risk. Risk D: Consider Therapy Modification

Selumetinib: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Serotonin/Norepinephrine Reuptake Inhibitor: May increase antiplatelet effects of Nonsteroidal Anti-Inflammatory Agents (Nonselective). Risk C: Monitor

Sincalide: Drugs that Affect Gallbladder Function may decrease therapeutic effects of Sincalide. Management: Consider discontinuing drugs that may affect gallbladder motility prior to the use of sincalide to stimulate gallbladder contraction. Risk D: Consider Therapy Modification

Sodium Phosphates: May increase nephrotoxic effects of Nonsteroidal Anti-Inflammatory Agents. Specifically, the risk of acute phosphate nephropathy may be enhanced. Risk C: Monitor

Sodium Polystyrene Sulfonate: Meloxicam may increase adverse/toxic effects of Sodium Polystyrene Sulfonate. More specifically, concomitant use of meloxicam oral suspension (which contains sorbitol) may increase the risk for intestinal necrosis. Risk X: Avoid

Sulprostone: Nonsteroidal Anti-Inflammatory Agents may decrease therapeutic effects of Sulprostone. Risk X: Avoid

Tacrolimus (Systemic): Nonsteroidal Anti-Inflammatory Agents may increase nephrotoxic effects of Tacrolimus (Systemic). Risk C: Monitor

Tenofovir Products: Nonsteroidal Anti-Inflammatory Agents may increase nephrotoxic effects of Tenofovir Products. Management: Seek alternatives to these combinations whenever possible. Avoid use of tenofovir with multiple NSAIDs or any NSAID given at a high dose due to a potential risk of acute renal failure. Diclofenac appears to confer the most risk. Risk D: Consider Therapy Modification

Tenoxicam: May increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents. Risk X: Avoid

Thiazide and Thiazide-Like Diuretics: Nonsteroidal Anti-Inflammatory Agents may decrease therapeutic effects of Thiazide and Thiazide-Like Diuretics. Thiazide and Thiazide-Like Diuretics may increase nephrotoxic effects of Nonsteroidal Anti-Inflammatory Agents. Risk C: Monitor

Thrombolytic Agents: Agents with Antiplatelet Effects may increase adverse/toxic effects of Thrombolytic Agents. Specifically, the risk of bleeding may be increased. Risk C: Monitor

Tipranavir: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Tolperisone: Nonsteroidal Anti-Inflammatory Agents may increase adverse/toxic effects of Tolperisone. Specifically, the risk of hypersensitivity reactions may be increased. Tolperisone may increase therapeutic effects of Nonsteroidal Anti-Inflammatory Agents. Risk C: Monitor

Tricyclic Antidepressants: May increase antiplatelet effects of Nonsteroidal Anti-Inflammatory Agents. Tricyclic Antidepressants may increase adverse/toxic effects of Nonsteroidal Anti-Inflammatory Agents. Specifically, the risk of major adverse cardiac events (MACE), hemorrhagic stroke, ischemic stroke, and heart failure may be increased. Risk C: Monitor

Vancomycin: Nonsteroidal Anti-Inflammatory Agents may increase serum concentration of Vancomycin. Risk C: Monitor

Vanzacaftor, Tezacaftor, and Deutivacaftor: May increase serum concentration of CYP2C9 Substrates (High risk with Inhibitors). Risk C: Monitor

Verteporfin: Photosensitizing Agents may increase photosensitizing effects of Verteporfin. Risk C: Monitor

Vitamin E (Systemic): May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Vitamin K Antagonists: Nonsteroidal Anti-Inflammatory Agents (Nonselective) may increase anticoagulant effects of Vitamin K Antagonists. Management: Consider alternatives to this combination when possible. If the combination must be used, monitor coagulation status closely and advise patients to promptly report any evidence of bleeding or bruising. Risk D: Consider Therapy Modification

Volanesorsen: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Zanubrutinib: May increase antiplatelet effects of Agents with Antiplatelet Effects. Risk C: Monitor

Dietary Considerations

Oral: May be taken with food or milk to minimize GI irritation.

Reproductive Considerations

Nonsteroidal anti-inflammatory drugs (NSAIDs) may delay or prevent rupture of ovarian follicles. This may be associated with infertility that is reversible upon discontinuation of the medication. Consider discontinuing use in patients having difficulty conceiving or those undergoing investigation of fertility.

Based on available information, NSAIDs can be continued in males with rheumatic and musculoskeletal diseases who are planning to father a child (ACR [Sammaritano 2020]).

Pregnancy Considerations

The use of nonsteroidal anti-inflammatory drugs (NSAIDs) close to conception may be associated with an increased risk of miscarriage due to cyclooxygenase-2 inhibition interfering with implantation (Bermas 2014; Bloor 2013).

Birth defects have been observed following in utero NSAID exposure in some studies; however, data are conflicting (Bloor 2013). Nonteratogenic effects, including prenatal constriction of the ductus arteriosus, persistent pulmonary hypertension of the newborn, oligohydramnios, necrotizing enterocolitis, renal dysfunction or failure, and intracranial hemorrhage have been observed in the fetus/neonate following in utero NSAID exposure (Bermas 2014; Bloor 2013). Maternal NSAID use may cause fetal renal dysfunction leading to oligohydramnios. Although rare, this may occur as early as 20 weeks' gestation and is more likely to occur with prolonged maternal use. Oligohydramnios may be reversible following discontinuation of the NSAID (Dathe 2019; FDA 2020). In addition, nonclosure of the ductus arteriosus postnatally may occur and be resistant to medical management (Bermas 2014; Bloor 2013).

Maternal use of NSAIDs should be avoided beginning at 20 weeks' gestation. If NSAID use is necessary between 20 and 30 weeks' gestation, limit use to the lowest effective dose and shortest duration possible; consider ultrasound monitoring of amniotic fluid if treatment extends beyond 48 hours and discontinue the NSAID if oligohydramnios is found (FDA 2020). Because NSAIDs may cause premature closure of the ductus arteriosus, product labeling for meloxicam specifically states use should be avoided starting at 30 weeks' gestation.

Based on available information, NSAIDs can be continued during the first 2 trimesters of pregnancy in patients with rheumatic and musculoskeletal diseases; use in the third trimester is not recommended (ACR [Sammaritano 2020]).

Monitoring Parameters

CBC and chemistry profile; occult blood loss and periodic liver function tests; renal function (urine output, serum BUN and creatinine); signs or symptoms of GI bleeding; blood pressure; periodic ophthalmologic exam with long-term therapy.

Mechanism of Action

Reversibly inhibits cyclooxygenase-1 and 2 (COX-1 and 2) enzymes, which results in decreased formation of prostaglandin precursors; has antipyretic, analgesic, and anti-inflammatory properties

Other proposed mechanisms not fully elucidated (and possibly contributing to the anti-inflammatory effect to varying degrees), include inhibiting chemotaxis, altering lymphocyte activity, inhibiting neutrophil aggregation/activation, and decreasing proinflammatory cytokine levels.

Pharmacokinetics (Adult Data Unless Noted)

Distribution:

Children 2 to 6 years (n=7): Oral: Apparent Vd: Mean: 0.19 L/kg (Burgos-Vargas 2004).

Children and Adolescents 7 to 16 years (n=11): Oral: Apparent Vd: Mean: 0.13 L/kg (Burgos-Vargas 2004).

Adults: IV: Vz: 9.63 L; Oral: Vdss~10 L.

Protein binding: ~99%, primarily to albumin; Note: Free fraction was higher in adult patients with renal failure who were receiving chronic dialysis.

Metabolism: Hepatic via CYP2C9 and CYP3A4 (minor); forms 4 metabolites (inactive).

Bioavailability: 89% (capsule).

Half-life elimination:

Children 2 to 6 years (n=7): Oral: Mean: 13.4 hours (Burgos-Vargas 2004).

Children and Adolescents 7 to 16 years (n=11): Oral: Mean: 12.7 hours (Burgos-Vargas 2004).

Adults: IV: ~24 hours; Oral: ~15 to 22 hours.

Time to peak:

IV: 0.12 ± 0.04 hours.

Oral: Initial: Within 2 hours (capsule); 4 to 5 hours (tablet); 4 to 12 hours (orally disintegrating tablet; prolonged with food); ~7 hours (suspension; following a high-fat meal [75 g of fat]); Secondary: ~8 hours (capsule); 12 to 14 hours (tablet).

Excretion: Urine (predominantly as inactive metabolites; <1% unchanged drug); feces (predominantly as inactive metabolites; 1.6% as unchanged drug).

Clearance: Oral:

Children 2 to 6 years (n=7): Mean: 0.17 mL/minute/kg (Burgos-Vargas 2004).

Children and Adolescents 7 to 16 years (n=11): Mean: 0.12 mL/minute/kg (Burgos-Vargas 2004).

Adults: 7 to 9 mL/minute.

Pharmacokinetics: Additional Considerations (Adult Data Unless Noted)

Altered kidney function:

IV: Cmax and AUC increased 5% and 7%, respectively, in elderly subjects with mild renal impairment (eGFR 60 to 90 mL/minute/1.73 m2) compared to young healthy controls.

Oral: Meloxicam plasma concentration is decreased and total clearance increased in patients with renal impairment.

Brand Names: International
International Brand Names by Country
For country code abbreviations (show table)

  • (AE) United Arab Emirates: Coxicam | Medoxicam | Meflam | Mel od | Melflam | Melocam | Meloxydar | Mobic | Moven | Neoxicam;
  • (AR) Argentina: Aldoron M | Apo meloxicam | Bronax | Bronax cb | Dominadol | Flexidol | Flexidol cb | Flexium | Flogoten | Labsycam | Loxitenk | Mell | Meloxicam denver farma | Meloxicam Northia | Meloxicam teva | Mextran | Miogesil | Miolox | Mobic | Nemdol | Skudal | Tenaron | Virobron;
  • (AT) Austria: Meloxicam alternova | Meloxicam arcana | Meloxicam G L | Meloxicam interpharm | Meloxicam Ranbaxy | Metosan | Movalis;
  • (AU) Australia: Apo meloxicam | Apx meloxicam | Chemmart Meloxicam | Cipla meloxicam | GenRx Meloxicam | Melobic | Melox | Meloxiauro | Meloxibell | Meloxicam an | Meloxicam pfizer | Meloxicam Ranbaxy | Meloxicam sandoz | Meloxicam viatris | Mobic | Movalis | Moxicam | Pharmacor Meloxicm | Terry White Chemists Meloxicam | Tw Meloxicam;
  • (BD) Bangladesh: Melcam;
  • (BE) Belgium: Docmeloxi | Meloxicam Aurobindo Pharma | Meloxicam EG | Meloxicam ratiopharm | Meloxicam sandoz | Meloxicam teva | Mobic;
  • (BG) Bulgaria: Loximed | Melbek fort | Melox | Movalis | Movix | Noflamen | Recoxa | Trosicam;
  • (BR) Brazil: Alivian | Artritec | Beflox | Bioflac | Cicloxx | Diaden | Dormelox | Flamatec | Inicox | Leutrol | Lonaflam | Loxam | Loxiflan | Melocox | Meloflan | Melotec | Melovac | Meloxigran | Meloxil | Menoxiton | Mevamox | Movacox | Movatec | Movoxicam;
  • (CH) Switzerland: Mobicox;
  • (CI) Côte d'Ivoire: M cam | Meflam | Mefsal;
  • (CL) Chile: Anposel | Ecax | Hyflex | Isox | Melic | Melodol | Mexan | Mexilal | Mobex | Tenaron | Zix;
  • (CN) China: AN LI QING | He chang | Hong qiang | Jie zong | Ke yi | Keyi | Lao guan jian | Luo ke | Mai jie | Mai li ke | Mei er tong | Mo ke lin | Mobic | Qing qing | Sai ke si | Si lai mei | Tong ke | Wu yan | You ni | Ze li;
  • (CO) Colombia: Algiflex | Artriclox | Artricure | Bienex | Bienex fast | Butazolidina nf | Coxamer | Coxxin | Cronodol forte | Desinbal | Flexidyn | Flexol | Froben | Gesflamar | Henoclox | Impomel x | Inoxicam | Inzelk | Isavan | Lesflis | Leuxicam | Loxac tridex | Loxicam | Mediflex | Melcox | Melocam | Meloflex | Meloxaine | Meltocram | Meprogal | Mevican | Mexican | Mibloc ft | Mobic | Movalis | Mowin | Niflamin | Niflamin pl | Niflamin pl forte | Novoxican | Nulox | Ocam | Rodiflex | Rumonal | Xicandol | Xiclomelan | Xiloxim;
  • (CR) Costa Rica: Mobicox;
  • (CZ) Czech Republic: Apo meloxicam | Artrilom | Melovis | Meloxistad | Movalis | Noflamen | Oramellox | Recoxa;
  • (DE) Germany: Galoxiway | Meloxicam 1 A Pharma | Meloxicam Aaa | Meloxicam AL | Meloxicam CT | Meloxicam Hexal | Meloxicam ratiopharm | Meloxicam sandoz | Meloxicam stada | Meloxicam Winthrop | Mobec | Mobic | Movalis;
  • (DO) Dominican Republic: Acticam | Alentum | Alidrex | Amix | Bienex | Dicorp | Ilacox | Leutrol | Lexicox | Mecanyl NF | Megaflex | Melatax | Melican | Melocox | Melonax | Melonex | Melosteral | Meloxicam lam | Meloxicam mamey | Meloxil | Mexor | Mibloc ft | Mobicox | Mobicox Vr | Movix | Noragel | Permitil | Rumonal | Suimax | Tenaron;
  • (EC) Ecuador: 15 mel | 15mel | Alivcam | Aremil | Artrox | Autdol | Bexican | Bienex | Bienex sl | Bienexflex | Booxicam | Camdol | Coxamer | Coxicam | Desinflamex | Elocox flash | Flamacoxine | Flexol | Ideloxan | Lamocox | Loxem | Loxihelab | Loximel | M loxsa | Medoxicam | Melbicox | Melcan | Melixflam | Meloara | Melocam | Melor | Melorex | Melox letic | Meloxi | Meloxicam MK | Meloxicam nifa | Meloxid | Meloxifem | Meloxigran | Meloxim | Meloxistar | Meloxsa | Mexan | Mibloc ft | Mikalex | Mikalex Direct | Miolox | Mioloxen | Mobic | Mowin | Niflamin | Nodolex | Nordicox | Oxa | Oxipan | Relmex nf | Tenaron | Trisedam | Xiarax | Xicandol;
  • (EE) Estonia: Melox | Meloxicam ratiopharm | Mexolan | Movalis | Recoxa;
  • (EG) Egypt: Anti-cox II | Coxicam | Medexaflam | Melocam | Meloflam | Mexicam | Mobic | Mobitil | Moxen;
  • (ES) Spain: Aliviodol | Meloxicam asol | Meloxicam bayvit | Meloxicam bexal | Meloxicam kern | Meloxicam merck | Meloxicam Normon | Meloxicam Pensa | Meloxicam ratiopharm | Meloxicam sandoz | Meloxicam sumol | Movalis | Parocin | Uticox;
  • (ET) Ethiopia: Mebilax | Melocam | Melonax;
  • (FI) Finland: Latonid | Meloxicam alternova | Meloxicam BMM Pharma | Meloxicam Hexal | Meloxicam Orion | Meloxicam pfizer | Meloxicam ratiopharm | Meloxicam sandoz | Meloxicam teva | Meloxicam Winthrop | Meloxikam Ivax | Mobic;
  • (FR) France: Meloxicam Biogaran | Meloxicam EG | Meloxicam pfizer | Meloxicam sandoz | Mobic;
  • (GB) United Kingdom: Meloxicam Almus | Meloxicam Chanelle | Meloxicam Ivax | Meloxicam Kent | Mobic;
  • (GR) Greece: Auroxicam | Brosiral | Doctinon | Examel | Farmelox | Iamaxicam | Iaten | Iconal | Infomel | Loxitan | Medoxicam | Melocalm | Melock | Melocox | Melodim | Meloprol | Melorem | Melotec | Melotop | Melox Raldex | Meloxicam/mylan | Meloxicam/SM | Meloxil | Melus | Meomel | Movatec | Movaxin | Notpel | Parogal | Partial | Philipon S | Reumotec | Reumotherm | Saniflam | Starmelox | Supercad | Transantor | Tropofin | Vexicam | Zametrixal | Zerelin;
  • (HK) Hong Kong: Amoria | Apo meloxicam | Arthcam | Mecon | Melanic | Melcam | Melflam | Melocam | Melocan | Melox | Meloxicam cinfa | Meloxicam stada | Meloxin | Meosicam | Mobic | Moxic | Newsicam | Nulox | Partial | Symelocam | Synloxicam;
  • (HR) Croatia: Meliam | Movalis;
  • (HU) Hungary: Borbin | Camelox | Melodyn | Meloxep | Meloxicam pfizer | Meloxicam ratiopharm | Meloxicam teva | Meloxicam Zentiva | Movalis | Moxicam | Noflamen | Trosicam;
  • (ID) Indonesia: Artrilox | Denilox | Flamoxi | Flasicox | Fri art | Futamel | Hexcam | Loxicox | Loxil | Loximei | Loxinic | Mecox | Meflam | Melogra | Meloxin | Mevilox | Mexpharm | Mobiflex | Movicox | Movix | Moxam | Moxic | Ostelox | Paxicam | Relox | Remelox | Rhemacox | Velcox | X-Cam;
  • (IE) Ireland: Areloger | Melcam | Mobic | Mobicam | Mobiglan | Movox;
  • (IN) India: Artaz | Ecwin | M cam | Mel od | Melflam | Melo | Meloflam | Melogesic | Melone | Melosuganril | Meloxi | Mexam | Mobix | Movac | Movacam | Movel-old | Muvera | Rafree | Tmel;
  • (IQ) Iraq: Fubic | Meloxicam awa | Movineer | Mubek;
  • (IT) Italy: Gixal | Leutrol | Meloxicam arrow | Meloxicam EG | Meloxicam Mylan | Meloxicam Ranbaxy | Meloxicam Winthrop | Mobic;
  • (JO) Jordan: Coxicam | Fixol | Loxicam | Miloxam | Mobic | Motion | Moven | Neo cam | Selektine;
  • (JP) Japan: Meloxicam Emec | Meloxicam Kunihiro | Meloxicam Nippon-zoki | Meloxicam towa | Mobic;
  • (KE) Kenya: Anti-cox II | Benacam | Bettam | Camola | M cam | Mel od | Melbix | Melcam | Melflam | Melgesic | Melonac | Meloxee | Meloz | Mexic | Mobic | Mocam | Mofic | Muvera | Neoxicam | Sucentis | Uxim;
  • (KR) Korea, Republic of: Amelox | Amolex | Amoria | Anycox | Aprogen meloxicam | Bomic | Boryung meloxicam | C bic | Camlox | Camrox | Cioex | Cmg Meloxicam | Coxicam | Daewoongbio meloxicam | Exicam | Hamobic | Hamobig | Hanall meloxicam | Huons meloxicam | Icox | Inoxicam | Keibic | Kwangdong meloxicam | Locam | Loxical | Loxicam | Maccam | Mccam | Mebicam | Mecaron | Medicox | Melax | Melbic | Melbicam | Melbigcam | Melbix | Melbrex | Melcam | Melcams | Melcox | Melcoxi | Melica | Melix | Mellox | Melnox | Melo d | Melobic | Meloca m | Melocam | Melocan | Melocap | Melocox | Melodex | Melodin | Melogreen | Melotex | Melotin | Melovic | Melowin | Melox | Meloxam | Meloxcaf | Meloxcam | Meloxi | Meloxica | Meloxid | Meloxifen | Meloxigen | Meloxim | Meloxin | Meloxipen | Meloxone | Meloxt | Melxibic | Memobic | Meranza | Merobic | Merocam | MEROKCAM | Mexi | Moacamxi | Mobex | Mobic | Mobicam | Mobicicam | Mobicox | Mobicxicam | Mobid gju | Mobiden | Mobirocam | Mobixcam | Mocox | Molexel | Moloxcam | Moloxicam | Molvic | Morbic | Morexel | Moricam | Morix | Moscam | Moxicam | Newlocam | Newroxicam | Newsicam | Newvic | Pharmabic | Reumel | Samsung meloxicam | Seoul meloxicam | Troxicam | Unicam | Unicox | Woncox;
  • (KW) Kuwait: Coxicam | Melgesic | Meloxydar | Mobic | Neoxicam | Rafree;
  • (LB) Lebanon: Loxicam | Miloxam | Mobic | Mobitil | Moven | Neoxicam | Oximal | Penocam | Selektine;
  • (LT) Lithuania: Lormed | Melobax | Melox | Meloxicam ratiopharm | Meloxicam teva | Meloxistad | Movalis | Noflamen | Normelox | Recoxa;
  • (LU) Luxembourg: Meloxicam Hexal | Meloxicam sandoz | Mobic;
  • (LV) Latvia: Lormed | Melflam | Melobax | Melox | Meloxicam Cipla | Meloxicam ratiopharm | Meloxicam teva | Meloxistad | Mobic | Movalis | Noflamen | Normelox | Recoxa;
  • (MA) Morocco: Aloxia | Artyx | Flamix | Ibermox | Lomax | Mefsal | Melicam | Meloxam | Mobic | Osmal | Raviva | Zenoxia;
  • (MX) Mexico: Aflamid | Anflatox | Anpre | Apocox | Auricam | Dolocam | Exel | Flexiver | Flexol | Indager | Loxam | Loxibach | Masflex | Mavicam | Maxoflam | Meflen | Melhexal | Melican | Melosteral | Meloxicam gi | Meloxicam landsteiner | Menflixil | Mobicox | Nacoflar | Oxart | Pliris | Promotion | Rafitex | Reosan | Retoflam | Tobansa;
  • (MY) Malaysia: Apo meloxicam | Aroxicam | Arrox | Avegesic | Dyna meloxicam | Mel od | Melartin | Melflam | Melocam | Melonex | Melox | Meloxim | Mobic | Quicktra | Rafree;
  • (NG) Nigeria: Artrosan | Celomoxicaps | Dabic | Flexaid | Meflex | Melocap | Melorem | Mexpharm | Orthopain | Zilocam;
  • (NL) Netherlands: Meloxicam a | Meloxicam apotex | Meloxicam PCH | Meloxicam ratiopharm | Meloxicam sandoz | Mobic | Movalis | Movicox;
  • (NO) Norway: Meloxicam Actavis | Meloxicam bluefish | Meloxicam BMM Pharma | Meloxicam Mylan | Mobic;
  • (NZ) New Zealand: Arrow meloxicam | Melorex | Mobic;
  • (PE) Peru: Afloxx | Anaxicam | Aremil | Areuma | Artricam | Artriflam | Artrigan | Artritin max | Atiflam | Axius | Bexx | Bioxicam | Cimelox | Coxamer | Coxicam | Dolocam | Dolorit | Dolxicam | Flamelox | Flexaid | Flexol | Flexomycin nf | Flodin | Hynoflex | Ilacox | Isox | Laboxicam | Melbrand | Melixflam | Meloflex | Melonex | Meloxartril | Meloxed | Meloxen | Meloxic | Meloximek | Meloxx | Melsol | Mexifar | Mibloc ft | Mobic | Mowin | Moxicax | Profel | Quimoflan | Talflam | Telaren | Telaren NF | Urzac;
  • (PH) Philippines: Beramex | Bexxam | Caxlem | Cloxim | Domelox | Eloxim | Flamicxine | Loflam | Loxaid | Loxibic | Meflam | Mel od | Melart | Melcom | Melocam | Melocox | Melofar | Meloflam | Melora | Melox | Meloxicam sandoz | Mexx | Mobic | Newsicam | Osteolax | Pharex Meloxicam | Syloxicam | Teracam | Unicox | Winthrop Meloxicam | Xicam;
  • (PK) Pakistan: Abidacam | Altoxicam | Aponip | Armex | Arsocam | Artex | Articam | Artipro | Brilox | Camilox | Coxicam | Coxlan | Eroxx | Freda | Healcam | Jorr | Lexicon | Loxatec | Loxic | Loxicam | Loxidol | Loxigood | Loxitan | M lox | Magix | Mecam | Megit | Mel 2 Cox | Melfax | Melor | Melow | Melox | Meloximed | Meloxistar | Meloxsel | Melpar | Melrun | Mesocam | Metrocam | Mexicam | Mexiran | Mexofin | Micam | Mits | Miws | Miws plus | Mo tu | Mobilex | Mobix | Movera | Mozta | Mubik | Nalcam | Nilem | Orthicam | Osteocam | Oxitic | Ravina | Talgesic | Xetza | Xobix | Xoxilum | Zeloxin | Zoxicam;
  • (PL) Poland: Aglan | Aspicam | Lormed | Mel | Mel forte | Meloksam | Melokssia | Melotev | Meloxic | Meloxicam adamed | Meloxilek | Meloxistad | Moilec | Movalis | Movmax | Opokan | Opokan forte | Ortopedina Forte (Meloxicam Arrow 15) | Remolexam | Reumelox | Trosicam;
  • (PR) Puerto Rico: Anjeso | Mobic | Qmiiz odt | Vivlodex;
  • (PT) Portugal: Marlex | Meloxicam APceuticals | Meloxicam aurobindo | Meloxicam Azevedos | Meloxicam bluepharma | Meloxicam Lador | Melpor | Movalis | Ziloxican;
  • (PY) Paraguay: Algioflex | Anaflax | Bexx | Coxifar | Dolimax | Foldox nf | Forenol nf | Huesobone | Hyflex | Letex | Melocox | Meloxicam la sante | Meloxican empa | Mobic | Sinartrol | Supracam | Telarid;
  • (QA) Qatar: Aroxicam | Coxicam | Melox | Meloxydar | Mobic | Moven | Neoxicam | Oximal | Selektine;
  • (RO) Romania: Antrend | Aspiflex | Celomix | Valzer;
  • (RU) Russian Federation: Amelotex | Bi ksikam | Bi-xikam | Cadimelcox | Exen sanovel | Flexibon | Genitron | Lem | Liberum | M cam | Mataren | Medsikam | Melbek | Meloflam | Melox | Meloxicam akrikhin | Meloxicam Avexima | Meloxicam ds | Meloxicam Obl | Meloxicam pfizer | Meloxicam prana | Meloxicam sandoz | Meloxicam stada | Meloxicam teva | Meloxicam velfarm | Meloxicam vertex | Meloxicam xantis | Mesipol | Mirlox | Mixol OD | Movageyn Express | Movalis | Movasin | Movix | Oxicamox | Revmart;
  • (SA) Saudi Arabia: Apo meloxicam | Coxicam | Mobic | Neoxicam | Oximal | Pms-meloxicam | Selektine;
  • (SE) Sweden: Meloxicam BMM Pharma | Meloxicam ebb | Meloxicam Hexal | Meloxicam Mylan | Meloxicam teva | Meloxikam MA | Mobic;
  • (SG) Singapore: Arrox | Melox | Mobic | Nulox;
  • (SI) Slovenia: Celomix | Lormed | Meloksikam Arrow | Melokssia | Meloxan | Movalis | Moxicam;
  • (SK) Slovakia: Antrend | Lormed | Meloxan | Meloxicam teva | Meloxikam saneca | Meloxistad | Movalis | Oramellox | Recoxa;
  • (TH) Thailand: Cambic | M.p. | Mel od | Melcam | Melobic | Melox | Mobic | Xidane;
  • (TN) Tunisia: Mobic | Moven | Oximal | Xicalm;
  • (TR) Turkey: Enflar | Exen | Meksun | Melcam | Melox | Melurjin | Mobic | Runomex | Zeloxim;
  • (TW) Taiwan: Bon Jour | Loxu | Mecon | Melicam | Melocam | Melox | Meloxicam Shyh Dar | Meloxin | Meosicam | Merocam | Mobic | Mobicam | Mopik | Subic;
  • (TZ) Tanzania, United Republic of: Muvera;
  • (UA) Ukraine: Algezicam | Existen sanovel | Loxidol | Melox | Meloxan | Meloxicam kv | Meloxicam ratiopharm | Meloxicam sopharma | Melsi | Movalgin | Movalis | Movixicam odt | Recoxa | Reumalgin | Reumoxicam | Revmoxicamum | Zeloxim;
  • (UG) Uganda: M cam | Melonax | Melox | Mobic | Sunflam;
  • (UY) Uruguay: Devincan | Dolcox | Meloxicam Servimedic | Meloxicam teva | Mobic | Nopain | Racotil | Tenaron | Xicane;
  • (VE) Venezuela, Bolivarian Republic of: Calmox | Mecox | Melocox | Melonax | Melovax | Meloxican | Mobic | Mowin | Pundol | Quicktra | Solican | Taucaron;
  • (VN) Viet Nam: Arthamin | Arthrobic | Ausxicam | Bexis | Bicapain | Bixicam | Brawnime | Ceteco melocen | Cophamlox | Coxnis | Fenxicam m | Mealphin | Melgez | Melorich | Mibelcam fort | Mobimed | Zixocam;
  • (ZA) South Africa: ADCO Meloxicam | Apex Meloxicam | Arrow meloxicam | Arthrocox | Coxflam | Flamaryx | Flexocam | Glenmark meloxicam | Loxiflam | Medoxicam | Meloxicam Unicorn | Melzy | Mobic;
  • (ZM) Zambia: Aroxicam | M cam
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