ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : -8 مورد

Indomethacin: Pediatric drug information

Indomethacin: Pediatric drug information
2025© UpToDate, Inc. and its affiliates and/or licensors. All Rights Reserved.
For additional information see "Indomethacin: Drug information" and "Indomethacin: 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.

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

Serious gastrointestinal bleeding, ulceration, and perforation:

NSAIDs cause an increased risk of serious gastrointestinal (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
  • Indocin;
  • Tivorbex [DSC]
Brand Names: Canada
  • AURO-Indomethacin;
  • MINT-Indomethacin;
  • ODAN-Indomethacin;
  • TEVA-Indomethacin
Therapeutic Category
  • Analgesic, Nonopioid;
  • Anti-inflammatory Agent;
  • Antipyretic;
  • Nonsteroidal Anti-inflammatory Drug (NSAID), Oral;
  • Nonsteroidal Anti-inflammatory Drug (NSAID), Parenteral
Dosing: Neonatal

Dosage guidance:

Safety: Due to potential adverse effects with indomethacin therapy, consider discontinuing indomethacin if any of the following occur: Clinical evidence of excessive bleeding (from IV sites or GI or pulmonary systems); grade 3 or 4 intraventricular hemorrhage (IVH); platelets <50,000/mm3; evidence of necrotizing enterocolitis; SCr >1.8 mg/dL; urine output <0.5 mL/kg/hour; serum K >7 mEq/L with EKG changes and/or Na <120 or >150 mEq/L (Ref).

Patent ductus arteriosus (PDA), treatment (Ref): Preterm neonates:

Initial: IV: 0.2 mg/kg/dose, followed by 2 doses depending on PNA:

PNA at time of first dose <48 hours: IV: 0.1 mg/kg at 12- to 24-hour intervals.

PNA at time of first dose 2 to 7 days: IV: 0.2 mg/kg at 12- to 24-hour intervals.

PNA at time of first dose >7 days: IV: 0.25 mg/kg at 12- to 24-hour intervals.

Note: In general, may use 12-hour dosing interval if urine output >1 mL/kg/hour after prior dose; use 24-hour dosing interval if urine output is <1 mL/kg/hour but >0.6 mL/kg/hour; doses should be withheld if patient has oliguria (urine output <0.6 mL/kg/hour) or anuria.

Intraventricular hemorrhage (IVH), prevention: Limited data available, efficacy results variable. Note: Although indomethacin has been shown to reduce the incidence of IVH, no change was seen in the long-term neurodevelopmental outcomes (eg, cerebral palsy, deaf, blind). Indomethacin is not recommended for routine prophylactic use; use may be warranted depending on comorbid conditions (Ref).

Preterm neonates weighing <1.25 kg: IV: Initial: 0.1 mg/kg administered within 6 to 12 hours of birth, followed by 2 additional doses of 0.1 mg/kg every 24 hours for a total of 3 doses (Ref).

Dosing: Altered Kidney Function: Neonatal: IV: If significant decrease in urine output occurs after a dose, hold additional dose until the urine output returns to normal. Use is contraindicated in preterm infants with significant kidney impairment.

Dosing: Pediatric
Inflammatory/Rheumatoid disorders

Inflammatory/Rheumatoid disorders: Note: Use lowest effective dose for the shortest duration:

Immediate release: Children ≥2 years and Adolescents (limited data available in ages <15 years): Oral (immediate release [excluding Tivorbex]): Initial: 1 to 2 mg/kg/day in 3 to 4 divided doses; usual initial adult dose range: 50 to 75 mg/day; maximum daily dose: 4 mg/kg/day or 200 mg/day, whichever is less (Ref).

Extended release: Adolescents ≥15 years: Oral: Initial: 75 mg once daily, may increase to 75 mg twice daily; maximum daily dose: 150 mg/day (Ref).

Gout, acute flares

Gout, acute flares (alternative agent): Adolescents ≥15 years: Immediate release (capsules [excluding Tivorbex], suspension, suppository): Oral, Rectal: 50 mg 3 times daily; once pain is tolerable, rapidly reduce until completely discontinued; pain relief begins 2 to 4 hours after initiating therapy with tenderness and warmth beginning to subside in 24 to 36 hours and swelling gradually resolving in 3 to 5 days (Ref).

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

Oral, Rectal: There are no specific pediatric dosage adjustments provided in the manufacturer's labeling, not recommended in patients with advanced renal disease; some experts have suggested the following:

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

Oral, Rectal: There are no dosage adjustments provided in the manufacturer's labeling; use with caution.

Dosing: Adult

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

Note: Safety: Use the lowest effective dose for the shortest duration of time. 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 administering in combination with a proton pump inhibitor in patients at risk for GI bleeding (eg, taking dual antiplatelet therapy or an anticoagulant, ≥60 years of age, high indomethacin doses) (Ref).

Acute pain

Acute pain (mild to moderate): Note: Indomethacin 20 mg capsules (brand and generic) have been discontinued in the United States for >1 year.

Oral (Tivorbex only): 20 mg 3 times daily or 40 mg 2 or 3 times daily.

Ankylosing spondylosis, osteoarthritis, or rheumatoid arthritis

Ankylosing spondylosis, osteoarthritis, or rheumatoid arthritis: Note: Use lowest effective dose for the shortest duration possible.

Oral (immediate release [excluding Tivorbex]), rectal: 25 mg 2 to 3 times daily; if well tolerated, increase daily dosage by 25 or 50 mg at weekly intervals until satisfactory response or a total daily dose of 150 to 200 mg/day (maximum dose: 200 mg/day) is reached. In patients with arthritis and persistent night pain and/or morning stiffness may give the larger portion (up to maximum of 100 mg) of the total daily dose at bedtime.

Oral (ER capsules): Initial: 75 mg once daily, may increase to 75 mg twice daily (maximum dose: 150 mg/day).

Bursitis/tendinopathy of the shoulder

Bursitis/tendinopathy of the shoulder: Oral (excluding Tivorbex), rectal: Initial dose: 75 to 150 mg/day in 3 to 4 divided doses or 1 to 2 divided doses for extended release; usual treatment is 7 to 14 days; discontinue after signs/symptoms of inflammation have been controlled for several days.

Gout, treatment, acute flares

Gout, treatment, acute flares:

Oral (generic IR capsules, suspension), rectal (suppository): 50 mg 3 times daily 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).

Pericarditis, acute or recurrent

Pericarditis, acute or recurrent (off-label use):

Note: In patients with an indication for aspirin (eg, coronary artery disease), aspirin is preferred over other nonsteroidal anti-inflammatory drugs (NSAIDs). Non-aspirin NSAIDs should be avoided in patients with pericarditis secondary to acute myocardial infarction given lack of benefit and potential harm (Ref).

Oral: Initial: 25 to 50 mg every 8 hours until resolution of symptoms for at least 24 hours and normalization of inflammatory biomarkers (eg, C-reactive protein) if monitored; initial therapy typically lasts for ≥1 to 2 weeks. Gradually taper by decreasing each dose by 25 mg every 1 to 2 weeks (eg, if initially 50 mg every 8 hours, taper to 25 mg every 8 hours, then discontinue); some clinicians may taper more slowly before discontinuing therapy (eg, if inititally 25 mg every 8 hours, taper to 25 mg every 12 hours, then 25 mg once daily, then discontinue); during taper, ensure patient remains asymptomatic and inflammatory biomarkers remain normal (if monitored). Use in combination with colchicine. In patients at risk of NSAID-related GI toxicity, prophylaxis (generally with a proton pump inhibitor) is recommended (Ref).

Prevention of pancreatitis post-endoscopic retrograde cholangiopancreatography

Prevention of pancreatitis post-endoscopic retrograde cholangiopancreatography (off-label use): Rectal: 100 mg immediately before or after endoscopic retrograde cholangiopancreatography (Ref).

Tocolysis

Tocolysis (off-label use): Oral, rectal: Initial: 50 to 100 mg orally or rectally, followed by 25 mg every 4 to 6 hours orally in women between 24 and 32 weeks' gestation. Duration of treatment is generally limited to 48 to 72 hours (Ref).

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.

Altered kidney function:

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

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

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

Hemodialysis, intermittent (thrice weekly): Slightly dialyzable (20%) (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: Unlikely to be significantly dialyzable (high protein binding): 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 (may worsen kidney injury) (Ref).

PIRRT (eg, sustained, low-efficiency diafiltration): Avoid use (may worsen kidney injury) (Ref).

Acute kidney injury while on indomethacin therapy: Discontinue use (Ref).

Dosing: Liver Impairment: Adult

There are no dosage adjustments provided in the manufacturer's labeling; use with caution to avoid adverse effects and discontinue if hepatic function worsens.

Adverse Reactions

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

>10%:

Gastrointestinal: Vomiting (≤12%)

Hematologic & oncologic: Postoperative hemorrhage (≤11%)

Nervous system: Headache (12% to 16%)

1% to 10%:

Cardiovascular: Presyncope (≤3%), syncope (≤2%)

Dermatologic: Hyperhidrosis (2%), pruritus (1% to 4%), skin rash (1% to 2%)

Endocrine & metabolic: Hot flash (2%)

Gastrointestinal: Abdominal distress (1% to 3%), abdominal pain (<3%), constipation (≤6%), decreased appetite (≥2%), diarrhea (<3%), dyspepsia (2% to 9%), epigastric pain (3% to 9%), heartburn (3% to 9%), nausea (3% to 9%)

Nervous system: Depression (1% to 3%), dizziness (3% to 9%), drowsiness (1% to 3%), fatigue (1% to 3%), malaise (1% to 3%), vertigo (1% to 3%)

Otic: Tinnitus (>1%)

Miscellaneous: Swelling (3%; postprocedural)

<1%:

Cardiovascular: Cardiac arrhythmia, chest pain, edema, flushing, heart failure, hypertension, hypotension, palpitations, shock, tachycardia, vasculitis

Dermatologic: Alopecia, diaphoresis, ecchymoses, erythema multiforme, erythema nodosum, exfoliative dermatitis, fixed drug eruption, skin photosensitivity, Stevens-Johnson syndrome, toxic epidermal necrolysis, urticaria

Endocrine & metabolic: Fluid retention, gynecomastia, hyperglycemia, hyperkalemia, weight gain

Gastrointestinal: Anorexia, aphthous stomatitis, bloating, dry mucous membranes, flatulence, gastroenteritis, gastrointestinal hemorrhage, gastrointestinal perforation, gastrointestinal ulcer, ileitis (regional), intestinal obstruction, intestinal stenosis, pancreatitis, peptic ulcer, proctitis, rectal hemorrhage, stomatitis, ulcerative colitis

Genitourinary: Breast hypertrophy, breast tenderness, glycosuria, hematuria, proteinuria, vaginal hemorrhage

Hematologic & oncologic: Agranulocytosis, anemia, aplastic anemia, bone marrow depression, disseminated intravascular coagulation, hemolytic anemia, immune thrombocytopenia, leukopenia, nonthrombocytopenic purpura, petechia, purpuric disease

Hepatic: Hepatic failure, hepatic necrosis, jaundice, toxic hepatitis

Hypersensitivity: Anaphylaxis, angioedema

Nervous system: Anxiety, coma, confusion, depersonalization, dysarthria, exacerbation of epilepsy, exacerbation of Parkinson disease, insomnia, involuntary muscle movements, myasthenia, nervousness, paresthesia, peripheral neuropathy, psychic disturbance, psychosis, seizure

Ophthalmic: Blurred vision, corneal deposits, diplopia, maculopathy, retinal disturbance

Otic: Auditory disturbance, deafness

Renal: Increased blood urea nitrogen, interstitial nephritis, kidney failure, kidney impairment, nephrotic syndrome

Respiratory: Acute respiratory distress, asthma, dyspnea, epistaxis, pulmonary edema

Miscellaneous: Fever

Frequency not defined:

Cardiovascular: Acute myocardial infarction, coronary thrombosis

Gastrointestinal: Gastrointestinal inflammation

Hepatic: Increased serum alanine aminotransferase, increased serum aspartate aminotransferase

Nervous system: Cerebrovascular accident

Postmarketing:

Gastrointestinal: Tenesmus (rectal)

Hepatic: Hepatotoxicity (idiosyncratic) (Chalasani 2021)

Hypersensitivity: Drug reaction with eosinophilia and systemic symptoms

Contraindications

Hypersensitivity (eg, anaphylactic reactions, serious skin reactions) to indomethacin or any component of the formulation; use in the setting of coronary artery bypass graft (CABG) surgery; history of asthma, urticaria, or allergic-type reactions after taking aspirin or other NSAID agents; patients with a history of proctitis or recent rectal bleeding (suppositories).

Neonates (IV only): Necrotizing enterocolitis (proven or suspected); significant kidney impairment; active bleeding (including intracranial hemorrhage and gastrointestinal bleeding), thrombocytopenia, coagulation defects; untreated infection (proven or suspected); congenital heart disease where patency of the ductus arteriosus is necessary for adequate pulmonary or systemic blood flow (eg, pulmonary atresia, severe tetralogy of Fallot, severe coarctation of the aorta)

Canadian labeling: Additional contraindications (not in US labeling): Severe uncontrolled heart failure; known hyperkalemia; active gastric/duodenal/peptic ulcer; active GI bleed; history of recurrent GI ulceration; active GI inflammatory disease; cerebrovascular bleeding or other bleeding disorders; severe hepatic impairment or active liver disease; severe kidney impairment (CrCl <30 mL/minute) or deteriorating kidney function; concurrent use with other NSAIDs; complete or partial syndrome of nasal polyps; children and adolescents <14 years of age; breast-feeding; pregnancy (third trimester)

Warnings/Precautions

Concerns related to adverse effects:

• Anaphylactoid reactions: Even in patients without prior exposure anaphylactoid reactions may occur; patients with "aspirin triad" (bronchial asthma, aspirin intolerance, rhinitis) may be at increased risk.

• Cardiovascular events:Relative risk appears to be similar in those with and without known cardiovascular disease or risk factors for cardiovascular disease; however, absolute incidence of serious cardiovascular thrombotic events (which may occur early during treatment) was higher in patients with known cardiovascular disease or risk factors and in those receiving higher doses. New-onset hypertension or exacerbation of hypertension may occur (NSAIDs may also impair response to ACE inhibitors, thiazide diuretics, or loop diuretics); may contribute to cardiovascular events; monitor blood pressure; use with caution in patients with hypertension. May cause sodium and fluid retention, use with caution in patients with edema. Avoid use in heart failure (FDA 2015). Avoid use in patients with recent MI unless benefits outweigh risk of cardiovascular thrombotic events. Use the lowest effective dose for the shortest duration of time, consistent with individual patient goals, to reduce risk of cardiovascular events; alternate therapies should be considered for patients at high risk.

• CNS effects: May cause drowsiness, dizziness, blurred vision, and other neurologic effects, which may impair physical or mental abilities; patients must be cautioned about performing tasks that require mental alertness (eg, operating machinery, driving). Headache may occur; cessation of therapy required if headache persists after dosage reduction.

• Drug reaction with eosinophilia and systemic symptoms: Potentially serious, sometimes fatal, drug reaction with eosinophilia and systemic symptoms (DRESS), also known as multiorgan hypersensitivity reactions, has been reported with NSAIDs. Monitor for signs and symptoms (eg, fever, rash, lymphadenopathy, eosinophilia) in association with other organ system involvement (eg, hepatitis, nephritis, hematological abnormalities, myocarditis, myositis). Early symptoms of hypersensitivity reaction (eg, lymphadenopathy, fever) may occur without rash; discontinue therapy and further evaluate if DRESS is suspected.

• GI events: Avoid use in patients with active GI bleeding. In patients with a history of acute lower GI bleeding, avoid use of non-aspirin NSAIDs, especially if due to angioectasia or diverticulosis (Strate 2016). Use caution with a history of GI ulcers, concurrent therapy known to increase the risk of GI bleeding (eg, aspirin, anticoagulants and/or corticosteroids, selective serotonin reuptake inhibitors), advanced hepatic disease, coagulopathy, smoking, use of alcohol, or in older or debilitated patients. Use the lowest effective dose for the shortest duration of time, consistent with individual patient goals, to reduce risk of GI adverse events; alternate therapies should be considered for patients at high risk. When used concomitantly with aspirin, a substantial increase in the risk of GI complications (eg, ulcer) occurs; concomitant gastroprotective therapy (eg, proton pump inhibitors) is recommended (Bhatt 2008).

• Hematologic effects: Platelet adhesion and aggregation may be decreased; may prolong bleeding time; patients with coagulation disorders or who are receiving anticoagulants should be monitored closely. Anemia may occur; patients on long-term NSAID therapy should be monitored for anemia. Rarely, NSAID use has been associated with potentially severe blood dyscrasias (eg, agranulocytosis, thrombocytopenia, aplastic anemia).

• Hepatic effects: Transaminase elevations have been reported with use; closely monitor patients with any abnormal liver function test (LFT). Rare, sometimes fatal severe hepatic reactions (eg, fulminant hepatitis, hepatic necrosis, hepatic failure) have occurred with NSAID use; discontinue immediately if clinical signs or symptoms of liver disease develop or if systemic manifestations occur.

• Hyperkalemia: NSAID use may increase the risk of hyperkalemia, particularly in older patients, diabetic patients, patients with kidney disease, and with concomitant use of other agents capable of inducing hyperkalemia (eg, ACE inhibitors). Monitor potassium closely.

• Kidney effects: NSAID use may compromise existing kidney function; dose-dependent decreases in prostaglandin synthesis may result from NSAID use, reducing renal blood flow which may cause kidney decompensation (usually reversible). Patients with impaired kidney function, dehydration, hypovolemia, heart failure, hepatic impairment, those taking diuretics, and ACE inhibitors, and older patients are at greater risk of kidney toxicity. Rehydrate patient before starting therapy; monitor kidney function closely. Long-term NSAID use may result in renal papillary necrosis and other kidney injury.

• Ophthalmic effects: Prolonged therapy may cause corneal deposits and retinal disturbances, including those of the macula. Discontinue use with blurred or diminished vision and perform ophthalmologic exam. Periodically evaluate vision in all patients receiving long-term therapy.

• Skin reactions: NSAIDs may cause potentially fatal serious skin adverse events, including drug reaction with eosinophilia and systemic symptoms, exfoliative dermatitis, Stevens-Johnson syndrome, and toxic epidermal necrolysis. Fixed drug eruption, including a life-threatening generalized bullous fixed drug eruption, may also occur with NSAIDs. These reactions may occur without warning; discontinue use at first sign of skin rash (or any other hypersensitivity).

Disease-related concerns:

• Aseptic meningitis: May increase the risk of aseptic meningitis, especially in patients with systemic lupus erythematosus (SLE) and mixed connective tissue disorders.

• Asthma: Contraindicated in patients with aspirin-sensitive asthma; severe and 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).

• Coronary artery bypass graft surgery: Risk of MI and stroke may be increased with use following CABG surgery.

• Depression: Use caution with depression; use may aggravate depression or other psychiatric disorders.

• Epilepsy: Use caution with epilepsy; use may aggravate this condition.

• Hepatic impairment: Use with caution in patients with hepatic impairment; patients with advanced hepatic disease are at an increased risk of GI bleeding and kidney failure with NSAIDs (AASLD [Biggins 2021]; AASLD [Runyon 2013]).

• Kidney impairment: Avoid use in patients with advanced kidney disease; discontinue use with persistent or worsening abnormal kidney function tests. The injection formulation is contraindicated in neonates with significant kidney impairment.

• Parkinsonism: Use caution with Parkinson disease; use may aggravate this condition.

Special populations:

• Older adult: Older adult patients are at greater risk for serious GI, cardiovascular, and/or kidney adverse events; use with caution. Indomethacin may cause confusion or, rarely, psychosis; remain alert to the possibility of such adverse reactions in older adult patients.

• Pediatric: Oral: There have been cases of hepatotoxicity reported in pediatric patients with juvenile rheumatoid arthritis, including fatalities. Closely monitor if needed in pediatric patients ≥2 years and periodically assess liver function.

Other warnings/precautions:

• Appropriate use: Tivorbex is not indicated for long-term use.

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

Warnings: Additional Pediatric Considerations

A single-center, 10-year, retrospective review of pediatric patients diagnosed with acute kidney injury (AKI) (n=1,015; ages: ≤18 years) reported nonsteroidal anti-inflammatory drugs (NSAIDs) as a potential cause of AKI in 2.7% of patients (n=27); a higher incidence (6.6%) was reported when additional exclusion factors were included in the data analysis. Dosing information was available for 74% of the NSAID-associated AKI cases (n=20); dosing was within the recommended range in 75% (n=15) of these cases. The median age of children with NSAID-associated AKI was 14.7 years (range: 0.5 to 17.7 years) and 15% of patients were <5 years and more likely to require dialysis than the older patients. Some experts suggest the incidence of NSAID-associated AKI found in this study is conservative due to aggressive exclusion criteria (eg, concurrent aminoglycoside or other nephrotoxic therapy) and the actual incidence may be higher (Brophy 2013; Misurac 2013).

Product Availability

Indomethacin 20 mg capsules (brand and generic) 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:

Tivorbex: 20 mg [DSC] [contains fd&c blue #1 (brilliant blue), fd&c blue #2 (indigotine,indigo carmine), fd&c red #40 (allura red ac dye)]

Generic: 20 mg [DSC], 25 mg, 50 mg

Capsule Extended Release, Oral:

Generic: 75 mg

Solution Reconstituted, Intravenous:

Generic: 1 mg (1 ea)

Solution Reconstituted, Intravenous [preservative free]:

Generic: 1 mg (1 ea)

Suppository, Rectal:

Indocin: 50 mg (30 ea)

Generic: 50 mg (1 ea, 30 ea)

Suspension, Oral:

Indocin: 25 mg/5 mL (237 mL) [contains alcohol, usp; pineapple-coconut-mint flavor]

Generic: 25 mg/5 mL (237 mL)

Generic Equivalent Available: US

Yes

Pricing: US

Capsule Extended Release (Indomethacin ER Oral)

75 mg (per each): $3.00 - $3.04

Capsules (Indomethacin Oral)

25 mg (per each): $0.38 - $0.55

50 mg (per each): $0.64 - $0.78

Solution (reconstituted) (Indomethacin Sodium Intravenous)

1 mg (per each): $445.49 - $634.73

Suppository (Indocin Rectal)

50 mg (per each): $434.29

Suppository (Indomethacin Rectal)

50 mg (per each): $412.57

Suspension (Indocin Oral)

25 mg/5 mL (per mL): $11.99

Suspension (Indomethacin Oral)

25 mg/5 mL (per mL): $10.78

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.

Capsule, Oral:

Generic: 25 mg, 50 mg

Suppository, Rectal:

Generic: 50 mg (30 ea); 100 mg (30 ea)

Administration: Pediatric

Oral: Capsule, oral suspension: Administer with food, milk, or antacids to decrease GI adverse effects; extended-release capsules must be swallowed whole; do not crush or chew.

Parenteral: IV: Administer IV over 20 to 30 minutes. Do not administer via IV bolus or IV infusion via an umbilical catheter into vessels near the superior mesenteric artery, as these may cause vasoconstriction and can compromise blood flow to the intestines.

Rectal: Suppository: For rectal use only; not for oral or intravaginal use.

Administration: Adult

Oral: Administer with food, immediately after meals, or with milk or antacids to decrease GI adverse effects. ER capsules must be swallowed whole; do not crush.

Bariatric surgery: Capsule, extended release. Some institutions may have specific protocols that conflict with these recommendations; refer to institutional protocols as appropriate. Do not cut, crush, or chew. Nonsteroidal anti-inflammatory drugs are not recommended for routine use after bariatric surgery. Where possible, cyclooxygenase-2 selective therapy should be used.

Rectal: For rectal use only; not for oral or intravaginal use.

Storage/Stability

Capsules: Store at 20°C to 25°C (68°F to 77°F); excursions permitted to 15°C to 30°C (59°F to 86°F).

Tivorbex: Store at 20°C to 25°C (68°F to 77°F); excursions permitted to 15°C to 30°C (59°F to 86°F). Store in the original container; protect from moisture and light.

IV: Store at 25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F). Protect from light. Store vials in original carton until contents used.

Oral suspension: Store below 30°C (86°F). Avoid temperatures above 50°C (122°F). Protect from freezing.

Suppositories: Store at 2°C to 8°C (36°F to 46°F).

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:

Indocin capsules: https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/016059s102lbl.pdf#page=25

Indocin oral suspension: https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/018332s043lbl.pdf

Indocin rectal suppository: https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/017814s045lbl.pdf

Indocin SR: https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/018185s059lbl.pdf#page=26

Tivorbex: https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/204768s008lbl.pdf#page=25

Use

Oral: Treatment of moderate to severe ankylosing spondylitis, acute painful bursitis and/or tendinitis of the shoulder, moderate to severe rheumatoid arthritis (including acute flares of chronic disease), and moderate to severe osteoarthritis (Immediate-release capsule [excluding Tivorbex], Extended-release capsule, Oral suspension: FDA approved in ages ≥15 years and adults); treatment of acute gouty arthritis (Immediate-release capsule [excluding Tivorbex], Oral suspension: FDA approved in ages ≥15 years and adults); treatment of mild to moderate pain (Oral capsule: Tivorbex only: FDA approved in adults).

Rectal: Treatment of moderate to severe ankylosing spondylitis, acute painful bursitis and/or tendinitis of the shoulder, moderate to severe rheumatoid arthritis (including acute flares of chronic disease), moderate to severe osteoarthritis, and acute gouty arthritis (FDA approved in ages ≥15 years and adults).

Parenteral: Closure of hemodynamically significant patent ductus arteriosus (PDA) (FDA approved in premature neonates weighing 0.5 to 1.75 kg); has also been used for prophylaxis of PDA and prevention of intraventricular hemorrhage in very low birth weight neonates.

Medication Safety Issues
Sound-alike/look-alike issues:

Indocin may be confused with Imodium, Lincocin, Minocin, Vicodin

Older Adult: High-Risk Medication:

Beers Criteria: Indomethacin is identified in the Beers Criteria as a potentially inappropriate medication to be avoided in patients 65 years and older (independent of diagnosis or condition) due to an increased risk of GI bleeding, peptic ulcer disease and acute kidney injury in older adults. Indomethacin is more likely to have NSAID-related adverse events and adverse CNS effects in older adults compared to other NSAIDs (Beers Criteria [AGS 2023]).

Metabolism/Transport Effects

Substrate of CYP2C19 (Minor), CYP2C9 (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

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

Bremelanotide: May decrease serum concentration of Indomethacin. Risk C: Monitor

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

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

Diflunisal: May increase adverse/toxic effects of Indomethacin. Specifically, the risk for gastrointestinal hemorrhage may be increased. Diflunisal may increase antiplatelet effects of Indomethacin. Diflunisal may increase serum concentration of Indomethacin. Risk X: Avoid

Dihydralazine: Indomethacin may decrease therapeutic effects of Dihydralazine. 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

Glucagon and Glucagon Analogs: Indomethacin may decrease therapeutic effects of Glucagon and Glucagon Analogs. Risk C: Monitor

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

Haloperidol: Indomethacin may increase CNS depressant effects of Haloperidol. 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

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

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

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

Triamterene: May increase adverse/toxic effects of Indomethacin. Specifically, the risk for renal failure and hyperkalemia may be increased. Management: Consider alternatives to concomitant treatment with triamterene and indomethacin. If the combination cannot be avoided, monitor for development of renal failure and hyperkalemia. Risk D: Consider Therapy Modification

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

Vasopressin: Indomethacin may increase therapeutic effects of Vasopressin. Specifically, vasopressin effects on cardiac index and systemic vascular resistance may be enhanced. 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

Food Interactions

Food may decrease the rate but not the extent of absorption. Indomethacin peak serum levels may be delayed if taken with food. Management: Administer with food or milk to minimize GI upset.

Dietary Considerations

May cause GI upset; take with food or milk to minimize

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

Indomethacin crosses the placenta.

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, kidney 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 kidney 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 indomethacin specifically states use should be avoided starting at ~30 weeks' gestation.

Due to pregnancy-induced physiologic changes, the clearance of indomethacin may be increased during pregnancy. Additional studies are needed to evaluate the influence of maternal CYP2C9 genotype, BMI, and if dosing adjustment is required (Balevic 2024; Pillai 2022; Rytting 2014; Shah 2019).

NSAIDs, such as indomethacin, are an effective short-term (≤48 hours) treatment option for the management of preterm labor to prolong pregnancy and allow for the administration of antenatal steroids. When choosing a specific agent, the benefits of the available tocolytic agents should be weighed against the potential risks for the individual person. Use >48 hours may increase the risk of in utero constriction of the ductus arteriosus and oligohydramnios (ACOG 2016).

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]).

NSAIDs may be used as part of a multimodal approach to pain relief following cesarean delivery (ACOG 2019; Murdoch 2023).

Monitoring Parameters

BUN, SCr, potassium, liver enzymes, CBC with differential; in addition, in neonates treated for patent ductus arteriosus: Heart rate, heart murmur, blood pressure, urine output, echocardiogram, serum sodium and glucose, platelet count, and serum concentrations of concomitantly administered drugs which are renally eliminated (eg, aminoglycosides, digoxin); periodic ophthalmic exams with chronic use. Evaluate for rash, skin eruptions, or other signs of drug reaction with eosinophilia and systemic symptoms (DRESS) (fever, lymphadenopathy, or eosinophilia).

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)

Onset of action: ~30 minutes

Duration: 4 to 6 hours

Absorption: Oral: Immediate release: Neonates: Formulation specific; Adults: Prompt and extensive; Extended release: Adults: 90% over 12 hours (Note: 75 mg product is designed to initially release 25 mg and then 50 mg over an extended period of time)

Distribution: Crosses blood-brain barrier; Neonates: PDA: 0.36 L/kg; Post-PDA closure: 0.26 L/kg; Adults: 0.34-1.57 L/kg

Protein binding: 99%

Metabolism: Hepatic; significant enterohepatic recirculation; metabolites include desmethyl, desbenzoyl and desmethyl-desbenzoyl (all in unconjugated form)

Bioavailability:

Neonates, premature: Percent bioavailability reported in the literature is highly variable and may be influenced by formulation components and indomethacin physicochemical properties (Scanlon 1982); some have suggested that aqueous formulations are less bioavailable compared to ethanol based formulations (Mrongovious 1982; Scanlon 1982); aqueous suspension (in saline): 13% to 20% (Mrongovious 1982; Sharma 2003); ethanol based (96% v/v) suspension: 98.6% (Al Za'abi 2007)

Adults: Oral: 100%; rectal: 80% to 90% (than that absorbed from capsule form)

Half-life elimination:

Neonates: Postnatal age (PNA) <2 weeks: ∼20 hours; PNA >2 weeks: ∼11 hours

Adults: 2.6-11.2 hours; 7.6 hours (Tivorbex)

Time to peak: Oral: Immediate release: 2 hours; Tivorbex capsules: 1.67 hours

Excretion: Urine (60%, primarily as glucuronide conjugates); feces (33%, primarily as metabolites; 1.5% as unchanged drug)

Clearance: Preterm neonates: ~19 mL/hour/kg (range: 4.7-45.5 mL/hour/kg) (Al Za'abi 2007)

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

  • (AE) United Arab Emirates: Bonidon | Confortid | Indocid | Indogesic | Indolag | Indomethacin | Indylon | Metacen | Methacin | Rothacin;
  • (AR) Argentina: Agilex | I.m. 75 montpellier | Im 75 montpellier | Indocid | Indogesic | Indometacina lafedar | Indotex | Klonametacina;
  • (AT) Austria: Amuno | Indobene | Indocid | Indohexal | Indomelan;
  • (AU) Australia: Arthrexin | Indocid | Indomethacin Agila | Indoptol;
  • (BD) Bangladesh: Imet | Incin | Indo-A | Indocap | Indocid | Indocin | Indofex | Indomet | Indomin | Indorex | Indoseem | Indotec | Indylon | Methacin | Methocid | Reumacap | Reumacid | Rheumet | Rindocin | Servimeta;
  • (BE) Belgium: Dolcidium | Indocid | Indoptol;
  • (BR) Brazil: Indocid | Indocid colirio | Metacidil;
  • (CH) Switzerland: Confortid | Indocid | Indometacin Helvepharm;
  • (CI) Côte d'Ivoire: Idol;
  • (CL) Chile: Indometacina;
  • (CN) China: Indomethacin | Jupocin | Xiao yan tong;
  • (CO) Colombia: Indoblan | Indocid | Indocierr | Indomet | Indometacina | Pexail | Servimeta;
  • (CZ) Czech Republic: Apo indomethacin | Confortid | Indobene | Indocid | Indometacinum | Indomethacin | Metindol;
  • (DE) Germany: Amuno | Confortid | Durametacin | Indo | Indo paed | Indo phlogont | Indohexal | Indomet | Indometacin Sandoz | Indometacinum | Indomisal | Indorektal;
  • (DO) Dominican Republic: Indocid | Indolgina | Indotero | Malival;
  • (EC) Ecuador: Bonidon | Indocid | Indometacina;
  • (EE) Estonia: Indocid | Indomet | Indometacin Actavis | Indometacine cf | Indometatsiin ns | Indomethacin | Indometin | Indoxen | Indylon | Liometacen | Metindol;
  • (EG) Egypt: Bonidon | Indacin | Indocid | Indomethacin | Indomin | Liometacen | Rheumacid | Rothacin;
  • (ES) Spain: Aliviosin | Artrinovo | Flogoter | Inacid | Inacid dap | Indolgina | Indonilo | Mederreumol | Reusin;
  • (ET) Ethiopia: Indol | Indomethacin;
  • (FI) Finland: Indetrit | Indocal | Indocid | Indomesal | Indometin | Inmetsin;
  • (FR) France: Ainscrid | Chrono indocid | Dolcidium | Indocid;
  • (GB) United Kingdom: Artracin | Berlind | Imbrilon | Indocid | Indocid pda | Indoflex | Indolar | Indomax | Indomethacin | Indomethacin berk | Indomethacin boots | Indomethacin cox | Indomethacin kent | Indomod | Indotard | Kap ind | Maximet | Mobilan | Pardelprin | Rheumacin la | Rimacid | Tannex;
  • (GR) Greece: Afardin | Bavilon | Begincalm | Bonatol | Cindol | Fortathrin | Indocid | Indocid pda | Indomethol | Intobutaz | Itapredin | Reumacid | Reumadolor | Reumastop | Rheumafar;
  • (HK) Hong Kong: Apo-Indomethacine | Indocaps | Indocid | Indomethacin | Indoxen | Indylon | Jarkims | Methacin | Rheumaxin;
  • (HR) Croatia: Indometacin belupo;
  • (HU) Hungary: Indometacinum;
  • (ID) Indonesia: Areumatin | Benocid | Confortid | Dialon | Indocid | Indomethacin;
  • (IE) Ireland: Cidomel | Indocid | Indocid pda | Indolar;
  • (IL) Israel: Indomed | Indotard | Indovis;
  • (IN) India: Ancap | Artisid | Donica | Endocin-sr | Idicin | Imacin | Indocap | Indofen | Indoflam | Indogo | Indometh | Indonet | Inmecin | Inmeth | Inocin | Microcid | Recticin;
  • (IQ) Iraq: Indomethacin | Indomethacin b p;
  • (IT) Italy: Indoxen | Liometacen | Metacen;
  • (JO) Jordan: Bonidon | Indocent | Indocid | Indogesic | Indomin | Indopharm | Indorem | Indylon | Metacen | Methacin;
  • (JP) Japan: Abanyu | Aindaxin | Arsetin | Bistep | Doilin | Endsin | Idomethine | Igecin | Indacin | Indepearl | Inderanic taiyo | Inderapollon | Indome | Indometacin amel | Indometacin arax | Indometacin hexal | Indometacin hisamitsu | Indometacin hk | Indometacin isei | Indometacin maruko | Indometacin merck | Indometacin nichiiko | Indometacin r sato | Indometacin s kyorin | Indometacin s teisan | Indometacin sawai | Indometacin showa | Indometacin sioe | Indometacin sv | Indometacin takeshima | Indometacin teika | Indometacin towa | Indometacin tp | Indometacin tsuruhara | Indometacin wakodo | Indometacin yamano | Inflazon | Infree | Inmecin | Inmecin amel | Inmecin maruko | Inmecin merck hoei | Inmecin nissin | Inmecin towa | Inmetan | Inmetocin | Inpucin | Inteban | Inteban sp | Intedaru | Intedaru choseido | Intedaru kayaku | Intedaru nisshin kyorin sei | Lausit | Methalicin | Methazin sankyo | Mezolin | Mikametan | Proarisin merck hoei | Salinac | Sifolin | Taihothacin s | Zalbico;
  • (KE) Kenya: Caredomet | Cindomet | Dinlacin | Dometin | Indocid | Indomethacin | Indopac | Indos | Indosha | Indosyn | Indowin;
  • (KR) Korea, Republic of: Indocin | Indometa | Indomethacin | Inteban spansule | Intevan | Methacin | Rheumametacin;
  • (KW) Kuwait: Indocid | Rothacin;
  • (LB) Lebanon: Dolovin | Indocid | Indomel;
  • (LT) Lithuania: Indo | Indobene | Indocin | Indomelan | Indomet | Indometacin bc | Indometacine | Indotard | Metindol;
  • (LU) Luxembourg: Dolcidium | Indocid | Indomet | Indoptol;
  • (LV) Latvia: Bonidon | Indobene | Indomelan | Indomet | Metindol;
  • (MA) Morocco: Apo-methacine | Chrono indocid | Di Indo | Idol | Indocid | Indolan | Indopharm | Liometacen;
  • (MX) Mexico: Antalgin | Artaxol | Artilen | Biometacin | Draxil | Indanet | Indocid | Indometacina | Indometacina gi se | Indometacina Silanes | Indosan | Indotrin | Italon | Labymetacyn | Malival | Malival AP | Minudoc p | Neoleina | Stratasin;
  • (MY) Malaysia: Arthrexin | Asimet | Domicap | Ductaclose | Imc | Indecin | Indo | Indocap | Indocid | Indomen | Indometha | Indomethacin | Indomin | Indylon | Methacid | Methacin;
  • (NG) Nigeria: Athralon | Maxindo | New divine indomethacin;
  • (NL) Netherlands: Dometin | Indocid | Indometacine | Indometacine A | Indometacine flx;
  • (NO) Norway: Confortid | Indo | Indo ct | Indo paed | Indocid | Indomet | Indometacin accord | Indometacin Actavis | Indometacin crescent | Indometacine aurobindo | Indometacine cf | Indomethacin Sandoz | Indoxen;
  • (NZ) New Zealand: Arthrexin | Indocid | Indometacin Actavis | Indomethacin IV Mylan | Rheumacin;
  • (PE) Peru: Indatacin | Indocid | Indometacina;
  • (PH) Philippines: Indocid | Infree;
  • (PK) Pakistan: Arthrocid | Camocid | Incin | Indobid | Indomethacin | Indosone | Liometacen | Matindol | Methacid;
  • (PL) Poland: Indo paed | Indomet | Indomethacin | Liometacen | Metindol;
  • (PR) Puerto Rico: Indocin | Indomethacin | Indomethacin extended release;
  • (PT) Portugal: Dolovin | Indocid | Indometacina | Reumacide;
  • (PY) Paraguay: Xantomicin forte;
  • (QA) Qatar: Elmetacin | Indocid | Indogesic | Rothacin;
  • (RO) Romania: Indocid | Indometacin arena | Indometacin laropharm | Indometacin terapia | Indometacin zentiva;
  • (RU) Russian Federation: Indobene | Indometacin biosyn | Indometacin Biosyntez | Indometacin sopharma | Indomethacin | Indomin | Metindol;
  • (SA) Saudi Arabia: Confortid | Indocid | Indogesic | Indomethacin | Liometacen | Rothacin;
  • (SE) Sweden: Confortid;
  • (SG) Singapore: Apo-Indomethacine | Eldocid | Indo | Indocap | Indocid | Indoflam TR | Indomen | Methacin;
  • (SI) Slovenia: Indometacinum | Liometacen;
  • (SK) Slovakia: Indobene | Indocid | Indometacin Galvex | Indometacinum | Metindol;
  • (SL) Sierra Leone: Indomethacin;
  • (SR) Suriname: Apo indomethacin | Indometacine | Indometacine aurobindo | Indometacine cf;
  • (TH) Thailand: Ammi-indocin | Andocit | Api Pyrin | Busolon S | Cocid | Confortid | Docid | Docin | Dome | Dometa | Findo | Fob | Fob Indo C | Idc | Idomet | Incosit | Indo | Indo-q | Indocap | Indocid | Indocin | Indocit | Indogesic | Indohim | Indoin | Indoman | Indomed | Indomen | Indomet | Indometh | Indomethacin | Indono | Indostar | Indotrustman | Inflamed | Inflamet | Inmed | Inthacine | K.B. Indomethacin | Neocid | Phardomet | Pybucid | S Docid;
  • (TN) Tunisia: Chrono indocid | Indocid | Indocine | Indometacine Ips | Indomin | Indopal | Methacin | Rothacin | Tendinyl;
  • (TR) Turkey: Endol | Endosetin | Indocid | Romacid;
  • (TW) Taiwan: Antirheumatic | Cedric | Cyeda Cin | Defever | Goncid | Indalgin | Indecin | Indershin | Indetole | Indocaps | Indocid | Indocin | Indocine | Indome | Indomecin | Indomen | Indomesa | Indomethacin | Indothan | Indoy | Inpan | Intean | Inteban | Intedaru | Inthacid | Inthacin | Intocin | Kindocid | Lausit | Li Shin Ning | Methatin | Neo-Tonfonrin | Patetin | Pisulou | Referlas | Servimeta | Tenton;
  • (UA) Ukraine: Metindol | Movilon;
  • (UG) Uganda: Indol | Indomethacin | Indoren | Indos | Indosim | Indosupp | Rectin;
  • (UY) Uruguay: Artrilona S | Indoartril | Indocid | Indometacina Winpharm | Indopert LA | Sinartril;
  • (VE) Venezuela, Bolivarian Republic of: Cevimin | Indocid | Indometacina | Romazulan;
  • (VN) Viet Nam: Axomecin;
  • (ZA) South Africa: Adco-indomethacin | Aflamin | Amdocin | Arthrexin | Aspen-Indomethacin | Betacin | Flamaret | Flamecid | Gulf Indomethacin | Indocid | Indomethacin | Indomethacin oethmaan | Methamax | Methocaps | Nisaid | Restameth-sr | Rolab-indomethacin;
  • (ZM) Zambia: Arthrexin | Cindomet | Flamcid | Indoflam | Indomethacin | Indosule | Methocid | Recticin | Tissop;
  • (ZW) Zimbabwe: Arthrexin | Indomethacin | Methocid
  1. 2023 American Geriatrics Society Beers Criteria Update Expert Panel. American Geriatrics Society 2023 updated AGS Beers Criteria for potentially inappropriate medication use in older adults. J Am Geriatr Soc. 2023;71(7):2052-2081. doi:10.1111/jgs.18372 [PubMed 37139824]
  2. Abraham NS, Hlatky MA, Antman EM, et al; ACCF/ACG/AHA. ACCF/ACG/AHA 2010 expert consensus document on the concomitant use of proton pump inhibitors and thienopyridines: a focused update of the ACCF/ACG/AHA 2008 expert consensus document on reducing the gastrointestinal risks of antiplatelet therapy and NSAID use: a report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents. Circulation. 2010;122(24):2619-2633. doi:10.1161/CIR.0b013e318202f701 [PubMed 21060077]
  3. Adler Y, Charron P, Imazio M, et al; ESC Scientific Document Group. 2015 ESC Guidelines for the diagnosis and management of pericardial diseases: The Task Force for the Diagnosis and Management of Pericardial Diseases of the European Society of Cardiology (ESC) endorsed by: The European Association for Cardio-Thoracic Surgery (EACTS). Eur Heart J. 2015;36(42):2921-2964. doi:10.1093/eurheartj/ehv318 [PubMed 26320112]
  4. Al Za'abi M, Donovan T, Tudehope D, et al. Orogastric and intravenous indomethacin administration to very premature neonates with patent ductus arteriosus: population pharmacokinetics, absolute bioavailability, and treatment outcome. Ther Drug Monit. 2007;29(6):807-814. [PubMed 18043480]
  5. Alabed S, Cabello JB, Irving GJ, Qintar M, Burls A. Colchicine for pericarditis. Cochrane Database Syst Rev. 2014;(8):CD010652. doi:10.1002/14651858.CD010652.pub2 [PubMed 25164988]
  6. American College of Obstetricians and Gynecologists (ACOG). ACOG practice bulletin no. 209: obstetric analgesia and anesthesia. Obstet Gynecol. 2019;133(3):e208‐e225. doi:10.1097/AOG.0000000000003132 [PubMed 30801474]
  7. American College of Obstetricians and Gynecologists (ACOG). Committee on Practice Bulletins—Obstetrics. Practice Bulletin No. 171: Management of preterm labor. Obstet Gynecol. 2016;128(4):e155-e164. doi: 10.1097/AOG.0000000000001711 [PubMed 27661654]
  8. American Pain Society (APS). Principles of Analgesic Use. 7th ed. American Pain Society; 2016.
  9. Anderson PO, Sauberan JB. Modeling drug passage into human milk. Clin Pharmacol Ther. 2016;100(1):42-52. [PubMed 27060684]
  10. ASGE Standards of Practice Committee, Chandrasekhara V, Khashab MA, et al. Adverse events associated with ERCP. Gastrointest Endosc. 2017;85(1):32-47. doi:10.1016/j.gie.2016.06.051 [PubMed 27546389]
  11. Baker M, Perazella MA. NSAIDs in CKD: are they safe? Am J Kidney Dis. 2020;76(4):546-557. doi:10.1053/j.ajkd.2020.03.023 [PubMed 32479922]
  12. Balevic SJ, Weiner D, Hornik CP, et al. Indomethacin pharmacokinetics and pharmacodynamics in pregnancies with preterm labor: the need for dose-ranging trials. J Clin Pharmacol. 2024;64(6):728-736. doi:10.1002/jcph.2412 [PubMed 38315120]
  13. Ballabh P. Pathogenesis and prevention of intraventricular hemorrhage. Clin Perinatol. 2014;41(1):47-67. doi:10.1016/j.clp.2013.09.007 [PubMed 24524446]
  14. Bell AD, Roussin A, Cartier R, et al, “The Use of Antiplatelet Therapy in the Outpatient Setting: Canadian Cardiovascular Society Guidelines,” Can J Cardiol, 2011, 27(Suppl A):1-59. [PubMed 21640290]
  15. Bermas BL. Non-steroidal anti inflammatory drugs, glucocorticoids and disease modifying anti-rheumatic drugs for the management of rheumatoid arthritis before and during pregnancy. Curr Opin Rheumatol. 2014;26(3):334-340. [PubMed 24663106]
  16. Bhangu A, Singh P, Fitzgerald JE, Slesser A, Tekkis P. Postoperative nonsteroidal anti-inflammatory drugs and risk of anastomotic leak: meta-analysis of clinical and experimental studies. World J Surg. 2014;38(9):2247-2257. doi: 10.1007/s00268-014-2531-1. [PubMed 24682313]
  17. Bhatt DL, Scheiman J, Abraham NS, et al; American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents. ACCF/ACG/AHA 2008 expert consensus document on reducing the gastrointestinal risks of antiplatelet therapy and NSAID use: a report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents. J Am Coll Cardiol. 2008;52(18):1502-1517. doi:10.1016/j.jacc.2008.08.002 [PubMed 19017521]
  18. Biggins SW, Angeli P, Garcia-Tsao G, et al. Diagnosis, evaluation, and management of ascites, spontaneous bacterial peritonitis and hepatorenal syndrome: 2021 practice guidance by the American Association for the Study of Liver Diseases. Hepatology. 2021;74(2):1014-1048. doi:10.1002/hep.31884 [PubMed 33942342]
  19. Bilimoria Y, Moy J, and Yu B, “Nephrotic Syndrome, Exfoliative Dermatitis, Eosinophilia, and Elevated IgE Associated With Indomethacin,” J Allergy Clin Immunol, 2095, 95(2):287.
  20. Bloor M, Paech M. Nonsteroidal anti-inflammatory drugs during pregnancy and the initiation of lactation. Anesth Analg. 2013;116(5):1063-1075. [PubMed 23558845]
  21. Brooks PM and Day RO, “Nonsteroidal Anti-inflammatory Drugs - Differences and Similarities,” N Engl J Med, 1991, 324(24):1716-25. [PubMed 2034249]
  22. Brophy PD. Changing the paradigm in pediatric acute kidney injury. J Pediatr. 2013;162(6):1094-1096. [PubMed 23453549]
  23. Capone ML, Sciulli MG, Tacconelli S, et al, “Pharmacodynamic Interaction of Naproxen With Low-Dose Aspirin in Healthy Subjects,” J Am Coll Cardiol, 2005, 45(8):1295-1301. [PubMed 15837265]
  24. Catella-Lawson F, Reilly MP, Kapoor SC, et al, “Cyclooxygenase Inhibitors and the Antiplatelet Effects of Aspirin,” N Engl J Med, 2001, 345(25):1809-17. [PubMed 11752357]
  25. Chalasani NP, Hayashi PH, Bonkovsky HL, et al. ACG Clinical Guideline: the diagnosis and management of idiosyncratic drug-induced liver injury. Am J Gastroenterol. 2014;109(7):950-966. [PubMed 24935270]
  26. Chalasani NP, Maddur H, Russo MW, Wong RJ, Reddy KR; Practice Parameters Committee of the American College of Gastroenterology. ACG clinical guideline: diagnosis and management of idiosyncratic drug-induced liver injury. Am J Gastroenterol. 2021;116(5):878-898. doi:10.14309/ajg.0000000000001259 [PubMed 33929376]
  27. Chou R, Gordon DB, de Leon-Casasola OA, et al. Management of postoperative pain: a clinical practice guideline from the American Pain Society, the American Society of Regional Anesthesia and Pain Medicine, and the American Society of Anesthesiologists' Committee on Regional Anesthesia, Executive Committee, and Administrative Council [published correction appears in J Pain. 2016;17(4):508-510]. J Pain. 2016;17(2):131-157. doi: 10.1016/j.jpain.2015.12.008. [PubMed 26827847]
  28. Clunie M, Crone LA, Klassen L, et al, "Psychiatric Side Effects of Indomethacin in Parturients," Can J Anaesth, 2003, 50(6):586-8. [PubMed 12826551]
  29. Clyman RI, Saha S, Jobe A, Oh W. Indomethacin prophylaxis for preterm infants: the impact of 2 multicentered randomized controlled trials on clinical practice. J Pediatr. 2007;150(1):46-50. [PubMed 17188612]
  30. Coombs RC, Morgan ME, Durbin GM, et al, “Gut Blood Flow Velocities in the Newborn: Effects of Patent Ductus Arteriosus and Parenteral Indomethacin,” Arch Dis Child, 1990, 65(10 Spec No):1067-71. [PubMed 2241229]
  31. Dathe K, Hultzsch S, Pritchard LW, Schaefer C. Risk estimation of fetal adverse effects after short-term second trimester exposure to non-steroidal anti-inflammatory drugs: a literature review. Eur J Clin Pharmacol. 2019;75(10):1347-1353. doi:10.1007/s00228-019-02712-2 [PubMed 31273431]
  32. Dumonceau JM, Andriulli A, Elmunzer BJ, et al. Prophylaxis of post-ERCP pancreatitis: European Society of Gastrointestinal Endoscopy (ESGE) guideline - updated June 2014. Endoscopy. 2014;46(9):799-815. doi:10.1055/s-0034-1377875 [PubMed 25148137]
  33. Eeg-Olofsson O, Malmros I, Elwin CE, et al, "Convulsions in a Breast-Fed Infant After Maternal Indomethacin," Lancet, 1978, 2(8082):215. [PubMed 78421]
  34. Eichenwald EC, ed. Cloherty and Stark's Manual of Neonatal Care. 8th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2017.
  35. Elmunzer BJ, Scheiman JM, Lehman GA, et al, “A Randomized Trial of Rectal Indomethacin to Prevent Post-ERCP Pancreatitis,” N Engl J Med, 2012, 366(15):1414-22. [PubMed 22494121]
  36. Expert opinion. Senior Renal Editorial Team: Bruce Mueller, PharmD, FCCP, FASN, FNKF; Jason A. Roberts, PhD, BPharm (Hons), B App Sc, FSHP, FISAC; Michael Heung, MD, MS.
  37. Ferraris VA, Saha SP, Oestreich JH, et al, “2012 Update to the Society of Thoracic Surgeons Guideline on Use of Antiplatelet Drugs in Patients Having Cardiac and Noncardiac Operations,” Ann Thorac Surg, 2012, 94(5):1761-81. [PubMed 23098967]
  38. FitzGerald JD, Dalbeth N, Mikuls T, et al. 2020 American College of Rheumatology guideline for the management of gout. Arthritis Care Res (Hoboken). 2020;72(6):744-760. doi:10.1002/acr.24180 [PubMed 32391934]
  39. Fowlie PW, Davis PG, McGuire W. Prophylactic intravenous indomethacin for preventing mortality and morbidity in preterm infants. Cochrane Database Syst Rev. 2010;(7):CD000174. [PubMed 20614421]
  40. Fowlie PW, Davis PG. Prophylactic indomethacin for preterm infants: a systematic review and meta-analysis. Arch Dis Child Fetal Neonatal Ed. 2003;88(6):F464-466. [PubMed 14602691]
  41. Funder JW, Carey RM, Mantero F, et al. The management of primary aldosteronism: case detection, diagnosis, and treatment: an Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab. 2016;101(5):1889-1916. doi:10.1210/jc.2015-4061 [PubMed 26934393]
  42. Gaffo AL. Treatment of gout flares. Post TW, ed. UpToDate. Waltham, MA: UpToDate Inc. http://www.uptodate.com. Accessed October 9, 2023.
  43. Garg R, Mohan BP, Krishnamoorthi R, Rustagi T. Pre-endoscopic retrograde cholangiopancreatography (ERCP) administration of rectal indomethacin in unselected patients to reduce post-ERCP pancreatitis: a systematic review and meta-analysis. Indian J Gastroenterol. 2018;37(2):120-126. doi:10.1007/s12664-018-0841-1 [PubMed 29619673]
  44. Gersony WM, Peckham GJ, Ellison RC, et al, “Effects of Indomethacin in Premature Infants With Patent Ductus Arteriosus: Results of a National Collaborative Study,” J Pediatr, 1983, 102(6):895-906. [PubMed 6343572]
  45. Haas DM, Caldwell DM, Kirkpatrick P, McIntosh JJ, Welton NJ. Tocolytic therapy for preterm delivery: systematic review and network meta-analysis. BMJ. 2012;345:e6226. doi: 10.1136/bmj.e6226 [PubMed 23048010]
  46. Haas DM, Imperiale TF, Kirkpatrick PR, Klein RW, Zollinger TW, Golichowski AM. Tocolytic therapy: a meta-analysis and decision analysis. Obstet Gynecol. 2009;113(3):585-594. doi: 10.1097/AOG.0b013e318199924a [PubMed 19300321]
  47. Helleberg L. Clinical pharmacokinetics of indomethacin. Clin Pharmacokinet. 1981;6(4):245-258. doi:10.2165/00003088-198106040-00001 [PubMed 7249487]
  48. Hoppmann RA, Peden JG, and Ober SK, “Central Nervous System Side Effects of Nonsteroidal Anti-inflammatory Drugs. Aseptic Meningitis, Psychosis, and Cognitive Dysfunction,” Arch Intern Med, 1991, 151(7):1309-13. [PubMed 2064481]
  49. Horsley RD, Vogels ED, McField DAP, et al. Multimodal postoperative pain control is effective and reduces opioid use after laparoscopic Roux-en-Y gastric bypass. Obes Surg. 2019;29(2):394-400. doi: 10.1007/s11695-018-3526-z. [PubMed 30317488]
  50. Imazio M. Acute pericarditis: Treatment and prognosis. Post TW, ed. UpToDate. Waltham, MA: UpToDate Inc. http://www.uptodate.com. Accessed September 27, 2022.
  51. Imazio M, Belli R, Brucato A, et al. Efficacy and safety of colchicine for treatment of multiple recurrences of pericarditis (CORP-2): a multicentre, double-blind, placebo-controlled, randomised trial. Lancet. 2014;383(9936):2232-2237. doi:10.1016/S0140-6736(13)62709-9 [PubMed 24694983]
  52. Indocin Oral Suspension (indomethacin) [prescribing information]. Wayne, PA: Zyla Life Sciences US Inc; April 2021.
  53. Indocin Oral Suspension (indomethacin) [prescribing information]. Wayne, PA: Zyla Life Sciences US Inc; December 2019.
  54. Indocin Suppositories (indomethacin) [prescribing information]. South Plainfield, NJ: Cosette Pharmaceuticals, Inc; September 2019.
  55. Indocin Suppositories (indomethacin) [prescribing information]. Lincolnton, NC: Cosette Pharmaceuticals Inc; April 2021.
  56. Indomethacin capsules [prescribing information]. Cranford, NJ: Viona Pharmaceuticals Inc; October 2024.
  57. Indomethacin extended-release capsules [prescribing information]. Newtown, PA: KVK-Tech Inc; April 2021.
  58. Indomethacin injection [prescribing information]. Lake Zurich, IL: Fresenius Kabi; March 2023.
  59. Ito S. Drug therapy for breast-feeding women. N Engl J Med. 2000;343(2):118-126. [PubMed 10891521]
  60. Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. KDIGO 2012 clinical practice guidelines for the evaluation and management of chronic kidney disease. Kidney Int Suppl. 2013;3(1):1-150.
  61. Kim KN. Treatment of juvenile rheumatoid arthritis. Korean J Pediatr. 2010;53(11):936-941. doi:10.3345/kjp.2010.53.11.936 [PubMed 21218015]
  62. Koncicki HM, Unruh M, Schell JO. Pain management in CKD: a guide for nephrology providers. Am J Kidney Dis. 2017;69(3):451-460. doi:10.1053/j.ajkd.2016.08.039 [PubMed 27881247]
  63. Kurella M, Bennett WM, Chertow GM. Analgesia in patients with ESRD: a review of available evidence. Am J Kidney Dis. 2003;42(2):217-228. doi:10.1016/s0272-6386(03)00645-0 [PubMed 12900801]
  64. Lebedevs TH, Wojnar-Horton RE, Yapp P, et al. Excretion of indomethacin in breast milk. Br J Clin Pharmacol. 1991;32(6):751-754. [PubMed 1768569]
  65. LeWinter MM. Pericardial complications of myocardial infarction. Post TW, ed. UpToDate. Waltham, MA: UpToDate Inc. http://www.uptodate.com. Accessed August 2, 2022.
  66. Litalien C, Jacqz-Aigrain E. Risks and benefits of nonsteroidal anti-inflammatory drugs in children: a comparison with paracetamol. Paediatr Drugs. 2001;3(11):817-858. [PubMed 11735667]
  67. Luo H, Zhao L, Leung J, et al. Routine pre-procedural rectal indometacin versus selective post-procedural rectal indometacin to prevent pancreatitis in patients undergoing endoscopic retrograde cholangiopancreatography: a multicentre, single-blinded, randomised controlled trial. Lancet. 2016;387(10035):2293-2301. doi:10.1016/S0140-6736(16)30310-5 [PubMed 27133971]
  68. Makris A, Thornton C, and Hennessy A, "Postpartum Hypertension and Nonsteroidal Analgesia," Am J Obstet Gynecol, 2004, 190(2):577-8. [PubMed 14981414]
  69. Martin E, Vickers B, Landau R, Reece-Stremtan S. ABM clinical protocol #28, peripartum analgesia and anesthesia for the breastfeeding mother. Breastfeed Med. 2018;13(3):164-171. [PubMed 29595994]
  70. Mechanick JI, Apovian C, Brethauer S, et al. Clinical practice guidelines for the perioperative nutrition, metabolic, and nonsurgical support of patients undergoing bariatric procedures - 2019 update: cosponsored by American Association of Clinical Endocrinologists/American College of Endocrinology, the Obesity Society, American Society for Metabolic & Bariatric Surgery, Obesity Medicine Association, and American Society of Anesthesiologists. Surg Obes Relat Dis. 2020;16(2):175-247. doi:10.1016/j.soard.2019.10.025 [PubMed 31917200]
  71. Ment LR, Oh W, Ehrenkranz RA, et al. Low-dose indomethacin and prevention of intraventricular hemorrhage: a multicenter randomized trial. Pediatrics. 1994;93(4):543-550. [PubMed 8134206]
  72. Ment LR, Vohr B, Allan W, et al. Outcome of children in the indomethacin intraventricular hemorrhage prevention trial. Pediatrics. 2000;105(3 Pt 1):485-491. [PubMed 10699097]
  73. Mint-Indomethacin [product monograph]. Mississauga, Ontario, Canada: Mint Pharmaceuticals Inc; February 2017.
  74. Mirza H, Oh W, Laptook A, Vohr B, Tucker R, Stonestreet BS. Indomethacin prophylaxis to prevent intraventricular hemorrhage: association between incidence and timing of drug administration. J Pediatr. 2013;163(3):706-710. [PubMed 23522865]
  75. Misurac JM, Knoderer CA, Leiser JD, et al. Nonsteroidal anti-inflammatory drugs are an important cause of acute kidney injury in children. J Pediatr. 2013;162(6):1153-1159. [PubMed 23360563]
  76. Mrongovius R, Imbeck H, Wille L, et al. Variability of serum indomethacin concentrations after oral and intravenous administration to preterm infants. Eur J Pediatr. 1982;138(2):151-153. [PubMed 7094936]
  77. Murdoch I, Carver AL, Sultan P, et al. Comparison of different nonsteroidal anti-inflammatory drugs for cesarean section: a systematic review and network meta-analysis. Korean J Anesthesiol. 2023;76(6):597-616. doi:10.4097/kja.23014 [PubMed 37066603]
  78. O'Gara PT, Kushner FG, Ascheim DD, et al. 2013 ACCF/AHA guideline for the management of ST-elevation myocardial infarction: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2013;61(4):e78-e140. doi:10.1016/j.jacc.2012.11.019 [PubMed 23256914]
  79. Patai Á, Solymosi N, Mohácsi L, Patai ÁV. Indomethacin and diclofenac in the prevention of post-ERCP pancreatitis: a systematic review and meta-analysis of prospective controlled trials. Gastrointest Endosc. 2017;85(6):1144-1156.e1. doi:10.1016/j.gie.2017.01.033 [PubMed 28167118]
  80. Petty RE, Laxer RM, Lindsley CB, Wedderburn LR. Textbook of Pediatric Rheumatology. 7th ed. Elsevier; 2016.
  81. Pillai VC, Shah M, Rytting E, et al. Prediction of maternal and fetal pharmacokinetics of indomethacin in pregnancy. Br J Clin Pharmacol. 2022;88(1):271-281. doi:10.1111/bcp.14960 [PubMed 34185331]
  82. Rath W, Kehl S. Acute tocolysis - a critical analysis of evidence-based data. Geburtshilfe Frauenheilkd. 2018;78(12):1245-1255. doi: 10.1055/a-0717-5329 [PubMed 30655648]
  83. ratio-Indomethacin [product monograph]. Toronto, Ontario, Canada: Teva Canada Limited; June 2013.
  84. Reece-Stremtan S, Campos M, Kokajko L; Academy of Breastfeeding Medicine. ABM clinical protocol #15: analgesia and anesthesia for the breastfeeding mother, revised 2017. Breastfeed Med. 2017;12(9):500-506. [PubMed 29624435]
  85. Refer to manufacturer’s labeling.
  86. Reinebrant HE, Pileggi-Castro C, Romero CL, et al. Cyclo-oxygenase (COX) inhibitors for treating preterm labour. Cochrane Database Syst Rev. 2015;(6):CD001992. doi: 10.1002/14651858.CD001992.pub3 [PubMed 26042617]
  87. Runyon BA; AASLD. Introduction to the revised American Association for the Study of Liver Diseases practice guideline management of adult patients with ascites due to cirrhosis 2012. Hepatology. 2013;57(4):1651-1653. doi:10.1002/hep.26359 [PubMed 23463403]
  88. Rytting E, Nanovskaya TN, Wang X, et al. Pharmacokinetics of indomethacin in pregnancy. Clin Pharmacokinet. 2014;53(6):545-551. [PubMed 24493205]
  89. Sammaritano LR, Bermas BL, Chakravarty EE, et al. 2020 American College of Rheumatology guideline for the management of reproductive health in rheumatic and musculoskeletal diseases. Arthritis Rheumatol. 2020;72(4):529‐556. doi:10.1002/art.41191 [PubMed 32090480]
  90. Sandoz-Indomethacin [product monograph]. Boucherville, Quebec, Canada: Sandoz Canada Inc; March 2007.
  91. Scanlon JW. Oral aqueous suspension of indomethacin should be abandoned. Pediatrics. 1982;69(4):507. [PubMed 7070912]
  92. Schmidt B, Davis P, Moddemann D, et al. Long-term effects of indomethacin prophylaxis in extremely-low-birth-weight infants. N Engl J Med. 2001;344(26):1966-1972. [PubMed 11430325]
  93. Shah M, Xu M, Shah P, et al. Effect of CYP2C9 polymorphisms on the pharmacokinetics of indomethacin during pregnancy. Eur J Drug Metab Pharmacokinet. 2019;44(1):83-89. doi:10.1007/s13318-018-0505-7 [PubMed 30159654]
  94. Sharma PK, Garg SK, Narang A. A preliminary study on pharmacokinetics of oral indomethacin in premature infants in North India. Indian J Med Res. 2003;117:164-169. [PubMed 14604305]
  95. Sivera F, Andres M, Carmona L, et al. Multinational evidence-based recommendations for the diagnosis and management of gout: integrating systematic literature review and expert opinion of a broad panel of rheumatologists in the 3e initiative. Ann Rheum Dis. 2014;73(2):328-335. [PubMed 23868909]
  96. Skoutakis VA, Acchiardo SR, Carter CA, Wojciechowski NJ, Straughn AB, Meyer MC. Dialyzability and pharmacokinetics of indomethacin in adult patients with end-stage renal disease. Drug Intell Clin Pharm. 1986;20(12):956-960. doi:10.1177/106002808602001208 [PubMed 3816544]
  97. Smolinske SC, Hall AH, Vandenberg SA, et al, “Toxic Effects of Nonsteroid Anti-inflammatory Drugs in Overdose. An Overview of Recent Evidence on Clinical Effects and Dose-Response Relationships,” Drug Saf, 1990, 5(4):252-74. [PubMed 2198051]
  98. Strate LL, Gralnek IM. ACG clinical guideline: management of patients with acute lower gastrointestinal bleeding. Am J Gastroenterol. 2016;111(4):459-474. doi: 10.1038/ajg.2016.41. [PubMed 26925883]
  99. Teva-Indomethacin [product monograph]. Toronto, Ontario, Canada: Teva Canada Limited; February 2022.
  100. The International Agranulocytosis and Aplastic Anemia Study, “Risks of Agranulocytosis and Aplastic Anemia. A First Report of Their Relation to Drug Use With Special Reference to Analgesics,” JAMA, 1986, 256(13):1749-57. [PubMed 3747087]
  101. Thorell A, MacCormick AD, Awad S, et al. Guidelines for perioperative care in bariatric surgery: Enhanced Recovery After Surgery (ERAS) Society recommendations. World J Surg. 2016;40(9):2065-2083. doi: 10.1007/s00268-016-3492-3. [PubMed 26943657]
  102. Tivorbex (indomethacin) [prescribing information]. Madisonville, LA: Basiem LLC; September 2021.
  103. US Food and Drug Administration (FDA). FDA Drug Safety Communication: FDA strengthens warning that non-aspirin nonsteroidal anti-inflammatory drugs (NSAIDs) can cause heart attacks or strokes. 2015. https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-fda-strengthens-warning-non-aspirin-nonsteroidal-anti-inflammatory.
  104. US Food and Drug Administration (FDA). FDA recommends avoiding use of NSAIDs in pregnancy at 20 weeks or later because they can result in low amniotic fluid. https://www.fda.gov/drugs/drug-safety-and-availability/fda-recommends-avoiding-use-nsaids-pregnancy-20-weeks-or-later-because-they-can-result-low-amniotic. Published October 15, 2020. Accessed October 20, 2020.
  105. Weiss PF. Diagnosis and treatment of enthesitis-related arthritis. Adolesc Health Med Ther. 2012;2012(3):67-74. doi:10.2147/AHMT.S25872 [PubMed 23236258]
  106. Wong F, Massie D, and Hsu P, “The Effect of Misoprostol on Indomethacin-Induced Renal Dysfunction in Well-Compensated Cirrhosis,” J Hepatol, 1995, 23(1):1-7. [PubMed 8530800]
  107. Zhang W, Doherty M, Bardin T, et al; EULAR Standing Committee for International Clinical Studies Including Therapeutics. EULAR evidence based recommendations for gout. Part II: Management. Report of a task force of the EULAR Standing Committee for International Clinical Studies Including Therapeutics (ESCISIT). Ann Rheum Dis. 2006;65(10):1312-1324. [PubMed 16707532]
Topic 13380 Version 607.0