Naproxen Sodium + Esomeprazole Magnesium interactions
Checked as Naproxen + Esomeprazole in this data source.
Full monograph for Naproxen Sodium + Esomeprazole MagnesiumCheck it against another medicine
Medicines
703 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Acalabrutinibvia Naproxen, Esomeprazole | Major | Absorption · Synergy | Coadministration of acalabrutinib and drugs that interfere with platelet function or coagulation may potentiate the risk of bleeding complications.2 documented mechanisms | 5 sources — open the full entry |
| Adefovir Dipivoxilvia Naproxen | Major | Excretion | Coadministration of adefovir dipivoxil with other nephrotoxic agents may increase the risk and severity of renal impairment due to additive effects on the… | 1 sources — open the full entry |
| Apixabanvia Naproxen | Major | Synergy | Concomitant use of apixaban with other agents that alter hemostasis such as aspirin, nonsteroidal anti-inflammatory drugs (NSAIDs), platelet aggregation… | 39 sources — open the full entry |
| Betrixabanvia Naproxen | Major | Synergy | Concomitant use of betrixaban with other agents that alter hemostasis such as aspirin, nonsteroidal anti-inflammatory drugs (NSAIDs), platelet aggregation… | 39 sources — open the full entry |
| Cabozantinibvia Naproxen | Major | Synergy | Coadministration of cabozantinib and drugs that interfere with platelet function or coagulation may potentiate the risk of bleeding complications. Treatment… | 39 sources — open the full entry |
| Citalopram Hydrobromidevia Naproxen, Esomeprazole | Major | Metabolism · Synergy | Coadministration with CYP450 2C19 inhibitors may increase the plasma concentrations of citalopram, which is partially metabolized by the isoenzyme. Cases of QT…2 documented mechanisms | 51 sources — open the full entry |
| Clopidogrel + Aspirinvia Naproxen, Esomeprazole | Major | Absorption · Metabolism · Others | Coadministration with proton pump inhibitors (PPIs) may reduce the cardioprotective effects of clopidogrel. The proposed mechanism is PPI inhibition of the…4 documented mechanisms | 58 sources — open the full entry |
| Clopidogrel Bisulphatevia Naproxen, Esomeprazole | Major | Metabolism · Others | Coadministration with proton pump inhibitors (PPIs) may reduce the cardioprotective effects of clopidogrel. The proposed mechanism is PPI inhibition of the…2 documented mechanisms | 25 sources — open the full entry |
| Dabigatran Etexilate Mesylatevia Naproxen, Esomeprazole | Major | Synergy | Coadministration of thrombin inhibitors with drugs that affect platelet function may potentiate the risk of bleeding due to additive or synergistic effects on…2 documented mechanisms | 6 sources — open the full entry |
| Dacomitinibvia Esomeprazole | Major | Absorption | Coadministration with proton pump inhibitors (PPIs) may decrease the plasma concentrations of dacomitinib. The proposed mechanism is a pH-dependent reduction… | 2 sources — open the full entry |
| Dalteparin Sodiumvia Naproxen | Major | Synergy | In patients receiving neuraxial anesthesia or spinal puncture, the risk of developing an epidural or spinal hematoma during low molecular weight heparin (LMWH)… | 12 sources — open the full entry |
| Dasatinibvia Naproxen, Esomeprazole | Major | Absorption · Synergy | Coadministration of dasatinib and drugs that interfere with platelet function or coagulation may potentiate the risk of bleeding complications. Treatment with…2 documented mechanisms | 9 sources — open the full entry |
| Deferasiroxvia Naproxen | Major | Synergy | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase the risk of gastrointestinal bleeding associated with the use of deferasirox… | 3 sources — open the full entry |
| Enoxaparin Sodiumvia Naproxen | Major | Synergy | In patients receiving neuraxial anesthesia or spinal puncture, the risk of developing an epidural or spinal hematoma during low molecular weight heparin (LMWH)… | 12 sources — open the full entry |
| Erlotinibvia Naproxen, Esomeprazole | Major | Absorption · Unknown | Concurrent administration of agents that increase gastric pH such as proton pump inhibitors may decrease the oral bioavailability of erlotinib and reduce its…2 documented mechanisms | 6 sources — open the full entry |
| Everolimusvia Naproxen | Major | Synergy | Coadministration of macrolide immunosuppressants with other nephrotoxic agents may increase the risk and/or severity of renal impairment due to additive… | 4 sources — open the full entry |
| Fondaparinux Sodiumvia Naproxen | Major | Synergy | In patients receiving neuraxial anesthesia or spinal puncture, the risk of developing an epidural or spinal hematoma during LMWH, heparinoid, or fondaparinux… | 1 sources — open the full entry |
| Human Anti-D Immunoglobulinsvia Naproxen | Major | Synergy | Coadministration of intravenous immune globulin preparations with nephrotoxic agents may potentiate the risk of renal impairment. Many commercially available… | 11 sources — open the full entry |
| Ibrutinibvia Naproxen | Major | Synergy | Coadministration of ibrutinib and drugs that interfere with platelet function or coagulation may potentiate the risk of bleeding complications. | 6 sources — open the full entry |
| Iodixanolvia Naproxen | Major | Synergy | Concomitant use of intravascular radiocontrast media with other nephrotoxic agents may potentiate the risk of contrast-induced nephropathy and renal… | 7 sources — open the full entry |
| Iohexolvia Naproxen | Major | Synergy | Concomitant use of intravascular radiocontrast media with other nephrotoxic agents may potentiate the risk of contrast-induced nephropathy and renal… | 7 sources — open the full entry |
| Iopamidolvia Naproxen | Major | Synergy | Concomitant use of intravascular radiocontrast media with other nephrotoxic agents may potentiate the risk of contrast-induced nephropathy and renal… | 7 sources — open the full entry |
| Ketorolac Tromethaminevia Naproxen | Major | Synergy | The use of ketorolac in combination with other nonsteroidal anti-inflammatory drugs (NSAIDs) may increase the risk of serious adverse effects such as renal… | 1 sources — open the full entry |
| Leflunomidevia Naproxen | Major | Synergy | The recent, concomitant, or subsequent use (without the recommended leflunomide washout period or procedure) of other agents known to induce hepatotoxicity… | 3 sources — open the full entry |
| Lithium Carbonatevia Naproxen | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase serum lithium levels and induce toxicity in some patients. The exact mechanism… | 48 sources — open the full entry |
| Mavacamtenvia Naproxen, Esomeprazole | Major | Metabolism | Coadministration with inhibitors of CYP450 2C19 or CYP450 3A4 may increase the plasma concentrations of mavacamten. Because mavacamten reduces systolic…2 documented mechanisms | 2 sources — open the full entry |
| Methotrexatevia Naproxen, Esomeprazole | Major | Excretion | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase the plasma concentrations and toxicities of methotrexate. The proposed…2 documented mechanisms | 37 sources — open the full entry |
| Monobasic Sodium Phosphate + Dibasic Sodium Phosphatevia Naproxen | Major | Others | The following interaction applies only to products containing sodium biphosphate that are used for bowel cleansing. It does not apply to products containing… | 3 sources — open the full entry |
| Nelfinavirvia Esomeprazole | Major | Absorption | Concurrent use of proton pump inhibitors may decrease the oral bioavailability of nelfinavir and reduce its concentrations in plasma. Nelfinavir solubility may… | 2 sources — open the full entry |
| Neratinib Maleatevia Esomeprazole | Major | Absorption | Coadministration with proton pump inhibitors or H2-receptor antagonists may significantly decrease the oral bioavailability of neratinib. The solubility of… | 5 sources — open the full entry |
| Pazopanib Hydrochloridevia Esomeprazole | Major | Absorption | Coadministration with proton pump inhibitors or H2-receptor antagonists may significantly decrease the oral bioavailability of pazopanib and reduce its… | 7 sources — open the full entry |
| Ponatinib Hydrochloridevia Naproxen, Esomeprazole | Major | Absorption · Synergy | Coadministration of ponatinib and drugs that interfere with platelet function or coagulation may potentiate the risk of bleeding complications. Treatment with…2 documented mechanisms | 6 sources — open the full entry |
| Prasugrel Hydrochloridevia Naproxen, Esomeprazole | Major | Absorption · Synergy | Concomitant use of prasugrel with other agents that affect hemostasis such as anticoagulants, platelet inhibitors, thrombin inhibitors, thrombolytic agents…2 documented mechanisms | 4 sources — open the full entry |
| Ramucirumabvia Naproxen | Major | Synergy | Theoretical concerns exist that nonsteroid anti-inflammatory drugs (NSAIDs) and salicylates may potentiate the risk of bleeding and gastrointestinal… | 1 sources — open the full entry |
| Regorafenib Monohydratevia Naproxen | Major | Synergy | Coadministration of regorafenib and drugs that interfere with platelet function or coagulation may potentiate the risk of bleeding complications. Treatment… | 5 sources — open the full entry |
| Rivaroxabanvia Naproxen | Major | Synergy | Concomitant use of rivaroxaban with other agents that alter hemostasis such as aspirin, nonsteroidal anti-inflammatory drugs (NSAIDs), platelet aggregation… | 1 sources — open the full entry |
| Selpercatinibvia Naproxen, Esomeprazole | Major | Absorption · Metabolism | Coadministration with drugs that increase gastric pH may significantly decrease the oral bioavailability of selpercatinib and reduce its concentrations in…2 documented mechanisms | 4 sources — open the full entry |
| Sofosbuvir + Velpatasvirvia Esomeprazole | Major | Absorption | Coadministration of velpatasvir with proton pump inhibitors may reduce its gastrointestinal absorption. Velpatasvir exhibits pH-dependent solubility, with…2 documented mechanisms | 4 sources — open the full entry |
| Sotorasibvia Esomeprazole | Major | Absorption | Coadministration with drugs that increase gastric pH may significantly decrease the oral bioavailability of sotorasib and reduce its concentrations in plasma. | 2 sources — open the full entry |
| Tacrolimus MonohydrateOralTopicalvia Naproxen, Esomeprazole | Major | Metabolism · Synergy | Coadministration of macrolide immunosuppressants with other nephrotoxic agents may increase the risk and/or severity of renal impairment due to additive…2 documented mechanisms | 29 sources — open the full entry |
| Tenofovir Alafenamidevia Naproxen | Major | Excretion | Coadministration of tenofovir with other nephrotoxic agents may increase the risk of renal impairment due to additive effects on the kidney. Additionally… | 8 sources — open the full entry |
| Tenofovir Disoproxilvia Naproxen | Major | Excretion | Coadministration of tenofovir with other nephrotoxic agents may increase the risk of renal impairment due to additive effects on the kidney. Additionally… | 8 sources — open the full entry |
| Warfarin Sodiumvia Naproxen, Esomeprazole | Major | Metabolism · Synergy | Nonsteroidal anti-inflammatory drugs (NSAIDs) may potentiate the hypoprothrombinemic effect and bleeding risk associated with oral anticoagulants.2 documented mechanisms | 126 sources — open the full entry |
| Abametapirvia Naproxen, Esomeprazole | Moderate | Metabolism | Based on in vitro inhibition data, a single topical application of abametapir lotion may increase plasma concentrations of drugs that are substrates of CYP450…2 documented mechanisms | 1 sources — open the full entry |
| Acyclovir + Hydrocortisonevia Naproxen | Moderate | Synergy · Unknown | The combined use of corticosteroids and nonsteroidal anti-inflammatory drugs (NSAIDs) may increase the potential for serious gastrointestinal (GI) toxicity…2 documented mechanisms | 11 sources — open the full entry |
| Alendronic acidvia Naproxen | Moderate | Synergy | Theoretical concerns exist regarding the potential for increased risk and severity of gastrointestinal toxicity during coadministration of oral bisphosphonates… | 12 sources — open the full entry |
| Alendronic Acid + Vitamin D3via Naproxen | Moderate | Synergy | Theoretical concerns exist regarding the potential for increased risk and severity of gastrointestinal toxicity during coadministration of oral bisphosphonates… | 12 sources — open the full entry |
| Allium cepa + Heparin + Allantoinvia Naproxen | Moderate | Synergy | Theoretically, the coadministration of nonsteroidal anti-inflammatory drugs (NSAIDs) and heparin or low molecular weight heparin (LMWH) may potentiate the risk… | 6 sources — open the full entry |
| Alpelisibvia Naproxen | Moderate | Metabolism | Coadministration with alpelisib may decrease the plasma concentrations and therapeutic effects of drugs that are substrates of CYP450 2C9, such as warfarin… | 36 sources — open the full entry |
| Alteplasevia Naproxen | Moderate | Synergy | Systemically and topically administered nonsteroidal anti-inflammatory drugs (NSAIDs) may potentiate the risk of bleeding in patients treated with… | 3 sources — open the full entry |
Food & lifestyle
alcohol
ModerateSynergy
The concurrent use of aspirin or nonsteroidal anti-inflammatory drugs (NSAIDs) and ethanol may lead to gastrointestinal (GI) blood loss. The mechanism may be due to a combined local effect as well as inhibition of prostaglandins leading to decreased integrity of the GI lining.
What to do: Patients should be counseled on this potential interaction and advised to refrain from alcohol consumption while taking aspirin or NSAIDs.
1 source
- "Product Information. Motrin (ibuprofen)." Pharmacia and Upjohn (2002):
food
ModerateAbsorption
Food may interfere with the absorption of esomeprazole. The manufacturer reports that the area under the concentration-time curve for esomeprazole following a single 40 mg dose was 33% to 53% lower when administered after food intake as opposed to during fasting conditions.
What to do: Esomeprazole should be taken at least one hour before meals. When administered to patients receiving continuous enteral nutrition, some experts recommend that the tube feeding should be interrupted for at least 1 hour before and 1 hour after the dose of esomeprazole is given.
2 sources
- "Product Information. Nexium (esomeprazole)." Astra-Zeneca Pharmaceuticals (2001):
- Wohlt PD, Zheng L, Gunderson S, Balzar SA, Johnson BD, Fish JT "Recommendations for the use of medications with continuous enteral nutrition." Am J Health Syst Pharm 66 (2009): 1438-67
Conditions
Conditions in which Naproxen Sodium + Esomeprazole Magnesium needs care, as documented in this source.
Asthma
MajorNonsteroidal anti-inflammatory drugs (NSAIDs) are contraindicated in patients with history of asthma, urticaria, or other allergic-type reactions after taking aspirin or other NSAIDs; severe, sometimes fatal, anaphylactic reactions to NSAIDs have been reported in such patients. A subpopulation of patients with asthma may have aspirin-sensitive asthma which may include chronic rhinosinusitis complicated by nasal polyps, severe potentially fatal bronchospasm, and/or intolerance to aspirin and other NSAIDs. Since cross-reactivity between aspirin and other NSAIDs has been reported in such aspirin-sensitive patients, therapy with any NSAID should be avoided in patients with this form of aspirin sensitivity. NSAIDs should be used with caution in patients with preexisting asthma (without known aspirin sensitivity), and these patients should be monitored for changes in the signs and symptoms of asthma.
15 sources
- "Product Information. Motrin (ibuprofen)." Pharmacia and Upjohn (2002):
- "Product Information. Nalfon (fenoprofen)." Xspire Pharma (2002):
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Orudis (ketoprofen)." Wyeth-Ayerst Laboratories (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Clinoril (sulindac)." Merck & Co., Inc (2001):
- "Product Information. Tolectin (tolmetin)." McNeil Pharmaceutical (2001):
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
Show all 15 sourcesShow fewer sources
- "Product Information. Relafen (nabumetone)." SmithKline Beecham (2001):
- "Product Information. Feldene (piroxicam)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Daypro (oxaprozin)." Searle (2001):
- "Product Information. Celebrex (celecoxib)." Searle (2001):
- "Product Information. Mobic (meloxicam)." Boehringer-Ingelheim (2001):
Clostridium Infections
MajorPublished observational studies suggest that proton pump inhibitor (PPI) use may be associated with an increased risk of Clostridium difficile-associated diarrhea (CDAD), especially in hospitalized patients. This diagnosis should be considered for diarrhea that does not improve. It is recommended that patients should use the lowest dose and shortest duration of PPI therapy appropriate to the condition being treated. Close monitoring is recommended in patients with diarrhea and in those taking antibacterial agents as CDAD has been reported with the use of nearly all these agents. Treatment with antibacterial agents alters the normal flora of the colon, leading to overgrowth of C. difficile. C. difficile produces toxins A and B, which contribute to the development of CDAD. Appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of C. difficile, and surgical evaluation should be instituted as clinically indicated.
8 sources
- "Product Information. PriLOSEC (omeprazole)." Merck & Co., Inc (2022):
- "Product Information. Prevacid (lansoprazole)." TAP Pharmaceuticals Inc (2001):
- "Product Information. Aciphex (rabeprazole)." Janssen Pharmaceuticals (2001):
- "Product Information. Protonix (pantoprazole)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Protonix IV (pantoprazole)." Wyeth-Ayerst Laboratories
- "Product Information. Kapidex (dexlansoprazole)." Takeda Pharmaceuticals America (2009):
- "Product Information. NexIUM I.V. (esomeprazole)." Astra-Zeneca Pharmaceuticals (2014):
- "Product Information. Esomeprazole Strontium (esomeprazole)." Amneal Pharmaceuticals (2014):
Exanthema
MajorNonsteroidal anti-inflammatory drugs (NSAIDs) can cause serious skin adverse reactions (e.g., Stevens-Johnson syndrome, toxic epidermal necrolysis, and exfoliative dermatitis), which can be fatal. These serious events may occur without warning. Patients should be advised to discontinue the NSAID and seek medical attention promptly at the first sign of skin rash or any other sign of hypersensitivity. NSAIDs are contraindicated in patients with previous serious skin reactions to these drugs.
16 sources
- "Product Information. Motrin (ibuprofen)." Pharmacia and Upjohn (2002):
- "Product Information. Nalfon (fenoprofen)." Xspire Pharma (2002):
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Orudis (ketoprofen)." Wyeth-Ayerst Laboratories (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Clinoril (sulindac)." Merck & Co., Inc (2001):
- "Product Information. Tolectin (tolmetin)." McNeil Pharmaceutical (2001):
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
Show all 16 sourcesShow fewer sources
- "Product Information. Relafen (nabumetone)." SmithKline Beecham (2001):
- "Product Information. Feldene (piroxicam)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Daypro (oxaprozin)." Searle (2001):
- "Product Information. Celebrex (celecoxib)." Searle (2001):
- "Product Information. Mobic (meloxicam)." Boehringer-Ingelheim (2001):
- "Product Information. Meclofenamate Sodium (meclofenamate)." Mylan Pharmaceuticals Inc (2012):
Kidney Diseases
MajorLong-term use of nonsteroidal anti-inflammatory drugs (NSAIDs) has resulted in renal papillary necrosis and other renal injury. Renal toxicity has been seen in patients in whom renal prostaglandins have a compensatory role in the maintenance of renal perfusion: in such patients, NSAIDs may cause a dose-dependent reduction in prostaglandin synthesis and, secondarily, in renal blood flow, which may precipitate overt renal decompensation. Patients at greatest risk for this reaction include the elderly, those with impaired renal function, dehydration, hypovolemia, heart failure, or liver dysfunction, and those taking diuretics, angiotensin-converting enzyme inhibitors, or angiotensin receptor blockers; discontinuation of NSAID therapy will usually lead to recovery to the pretreatment state. No information is available regarding use NSAIDs in patients with advanced renal disease; the renal effects of NSAIDs may hasten the progression of renal dysfunction in patients with preexisting renal disease. Volume status should be corrected in dehydrated or hypovolemic patients prior to initiating treatment. Renal function should be monitored during therapy in patients with renal or liver dysfunction, heart failure, dehydration, or hypovolemia. NSAIDs should be avoided in patients with advanced renal disease unless the benefits are expected to outweigh the risk of worsening renal function; if an NSAID is used in such patients, they should be monitored for signs of worsening renal function.
16 sources
- "Product Information. Motrin (ibuprofen)." Pharmacia and Upjohn (2002):
- "Product Information. Nalfon (fenoprofen)." Xspire Pharma (2002):
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Orudis (ketoprofen)." Wyeth-Ayerst Laboratories (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Clinoril (sulindac)." Merck & Co., Inc (2001):
- "Product Information. Tolectin (tolmetin)." McNeil Pharmaceutical (2001):
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
Show all 16 sourcesShow fewer sources
- "Product Information. Relafen (nabumetone)." SmithKline Beecham (2001):
- "Product Information. Feldene (piroxicam)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Dolobid (diflunisal)." Merck & Co., Inc (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Daypro (oxaprozin)." Searle (2001):
- "Product Information. Celebrex (celecoxib)." Searle (2001):
- "Product Information. Mobic (meloxicam)." Boehringer-Ingelheim (2001):
Peptic Ulcer
MajorNonsteroidal anti-inflammatory drugs (NSAIDs) can cause serious gastrointestinal (GI) adverse events including inflammation, bleeding, ulceration, and perforation of the esophagus, stomach, small intestine, or large intestine, which can be fatal. These serious adverse events can develop at any time, with or without warning symptoms. Only 1 in 5 patients who develop a serious upper GI side effect on NSAIDs is symptomatic. NSAIDs should be used with caution in patients with history of peptic ulcer disease and/or GI bleeding, as these patients had a greater than 10-fold increased risk for developing a GI bleed compared to patients without these risk factors. Caution is also advised if NSAIDs are prescribed to patients with other factors that increase risk of GI bleeding, such as: prolonged NSAID therapy; concomitant use of oral corticosteroids, antiplatelet agents (e.g., aspirin), anticoagulants, selective serotonin reuptake inhibitors; alcohol use; smoking; history of gastrointestinal surgery or anastomosis, older age; poor general health status; and advanced liver disease and/or coagulopathy. Particular vigilance is necessary when treating elderly or debilitated patients since most postmarketing reports of fatal GI events occurred in these patients.
16 sources
- "Product Information. Motrin (ibuprofen)." Pharmacia and Upjohn (2002):
- "Product Information. Nalfon (fenoprofen)." Xspire Pharma (2002):
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Orudis (ketoprofen)." Wyeth-Ayerst Laboratories (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Clinoril (sulindac)." Merck & Co., Inc (2001):
- "Product Information. Tolectin (tolmetin)." McNeil Pharmaceutical (2001):
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
Show all 16 sourcesShow fewer sources
- "Product Information. Relafen (nabumetone)." SmithKline Beecham (2001):
- "Product Information. Feldene (piroxicam)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Dolobid (diflunisal)." Merck & Co., Inc (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Daypro (oxaprozin)." Searle (2001):
- "Product Information. Celebrex (celecoxib)." Searle (2001):
- "Product Information. Mobic (meloxicam)." Boehringer-Ingelheim (2001):
Thrombosis
MajorNonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal. This risk may occur early in treatment and may increase with duration of use. Clinical trials of several cyclooxygenase-2 (COX-2) selective and nonselective NSAIDs of up to 3 years duration have supported this increased risk. It is unclear from available data if the risk for cardiovascular thrombotic events is similar for all NSAIDs. Therapy with NSAIDs should be administered cautiously in patients with a history of cardiovascular or cerebrovascular disease. Patients should be treated with the lowest effective dosage for the shortest duration necessary. Appropriate antiplatelet therapy should be administered to patients requiring cardioprotection; however, there is no consistent evidence that concurrent use of aspirin mitigates the increased risk of serious cardiovascular thrombotic events associated with NSAID use, while the risk of serious gastrointestinal events is increased. Physicians and patients should remain alert for the development of adverse cardiovascular events throughout the entire duration of therapy, even without prior cardiovascular symptoms. Patients should be advised to promptly seek medical attention if they experience symptoms of cardiovascular thrombotic events (including chest pain, shortness of breath, weakness, or slurring of speech).NSAIDs are contraindicated in the setting of coronary artery bypass graft (CABG) surgery. Two large clinical trials of a COX-2 selective NSAID for the treatment of pain in the first 10 to 14 days following CABG surgery found an increased incidence of myocardial infarction and stroke.The use of NSAIDs should be avoided in patients with a recent myocardial infarction unless the benefits are expected to outweigh the risk of recurrent cardiovascular thrombotic events. If an NSAID is used in patients with a recent myocardial infarction, they should be monitored for signs of cardiac ischemia.
8 sources
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Celebrex (celecoxib)." Searle (2001):
- "Product Information. Ponstel (mefenamic acid)." Pfizer U.S. Pharmaceuticals Group (2006):
- "Product Information. Meclofenamate Sodium (meclofenamate)." Mylan Pharmaceuticals Inc (2012):
Water-Electrolyte Imbalance
MajorFluid retention and edema have been reported in association with the use of nonsteroidal anti-inflammatory drugs (NSAIDs). Therapy with NSAIDs should be administered cautiously in patients with preexisting fluid retention, hypertension, or a history of heart failure. Blood pressure and cardiovascular status should be monitored closely during the initiation of NSAID treatment and throughout the course of therapy.
14 sources
- "Product Information. Motrin (ibuprofen)." Pharmacia and Upjohn (2002):
- "Product Information. Nalfon (fenoprofen)." Xspire Pharma (2002):
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Orudis (ketoprofen)." Wyeth-Ayerst Laboratories (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Anaprox (naproxen)." Roche Laboratories (2006):
- "Product Information. Clinoril (sulindac)." Merck & Co., Inc (2001):
- "Product Information. Tolectin (tolmetin)." McNeil Pharmaceutical (2001):
Show all 14 sourcesShow fewer sources
- "Product Information. Relafen (nabumetone)." SmithKline Beecham (2001):
- "Product Information. Feldene (piroxicam)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Daypro (oxaprozin)." Searle (2001):
- "Product Information. Mobic (meloxicam)." Boehringer-Ingelheim (2001):
Anemia
ModerateAnemia has been reported in patients treated with nonsteroidal anti-inflammatory drugs (NSAIDs). This may be due to fluid retention, occult/gross blood loss, or an incompletely described effect on erythropoiesis. Hemoglobin or hematocrit should be monitored in patients with any signs/symptoms of anemia or blood loss, especially during long-term therapy. NSAIDs may increase risk of bleeding events; comorbid conditions (e.g., coagulation disorders; concomitant use of warfarin/other anticoagulants, antiplatelet agents, serotonin/serotonin norepinephrine reuptake inhibitors) may increase this risk, and patients with these conditions should be monitored for signs of bleeding. Therapy with NSAIDs should be administered cautiously in patients with or predisposed to anemia. Clinical monitoring of hematopoietic function may be appropriate, particularly during chronic therapy.
17 sources
- "Product Information. Motrin (ibuprofen)." Pharmacia and Upjohn (2002):
- "Product Information. Nalfon (fenoprofen)." Xspire Pharma (2002):
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Orudis (ketoprofen)." Wyeth-Ayerst Laboratories (2002):
- "Product Information. Toradol (ketorolac)." Roche Laboratories (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Clinoril (sulindac)." Merck & Co., Inc (2001):
- "Product Information. Tolectin (tolmetin)." McNeil Pharmaceutical (2001):
Show all 17 sourcesShow fewer sources
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
- "Product Information. Relafen (nabumetone)." SmithKline Beecham (2001):
- "Product Information. Feldene (piroxicam)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Dolobid (diflunisal)." Merck & Co., Inc (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Daypro (oxaprozin)." Searle (2001):
- "Product Information. Celebrex (celecoxib)." Searle (2001):
- "Product Information. Mobic (meloxicam)." Boehringer-Ingelheim (2001):
Blood Platelet Disorders
ModerateNonsteroidal anti-inflammatory drugs (NSAIDs) reversibly inhibit platelet adhesion and aggregation and may prolong bleeding time in some patients. With the exception of aspirin, the platelet effects seen with most NSAIDs at usual recommended dosages are generally slight and of relatively short duration but may be more pronounced in patients with underlying hemostatic abnormalities. Thrombocytopenia has also been reported rarely during NSAID use. Therapy with NSAIDs should be administered cautiously in patients with significant active bleeding or a hemorrhagic diathesis, including hemostatic and/or coagulation defects associated with hemophilia, vitamin K deficiency, hypoprothrombinemia, thrombocytopenia, thrombocytopathy, or severe hepatic impairment. NSAIDs that selectively inhibit cyclooxygenase-2 (i.e., COX-2 inhibitors) do not appear to affect platelet function or bleeding time at indicated dosages and may be preferable if risk of bleeding is a concern.
16 sources
- "Product Information. Motrin (ibuprofen)." Pharmacia and Upjohn (2002):
- "Product Information. Nalfon (fenoprofen)." Xspire Pharma (2002):
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Orudis (ketoprofen)." Wyeth-Ayerst Laboratories (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Clinoril (sulindac)." Merck & Co., Inc (2001):
- "Product Information. Tolectin (tolmetin)." McNeil Pharmaceutical (2001):
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
Show all 16 sourcesShow fewer sources
- "Product Information. Relafen (nabumetone)." SmithKline Beecham (2001):
- "Product Information. Feldene (piroxicam)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Dolobid (diflunisal)." Merck & Co., Inc (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Daypro (oxaprozin)." Searle (2001):
- "Product Information. Mobic (meloxicam)." Boehringer-Ingelheim (2001):
- "Product Information. Flector Patch (diclofenac topical)." Actavis U.S. (Alpharma USPD) (2016):
Fractures, Bone
ModerateVarious published observational studies have reported that PPI therapy may be associated with an increased risk for osteoporosis related fractures of the hip, wrist or spine. The risk was increased in patients who received high doses (multiple daily doses), and long term treatment (a year or longer). Patients should use the lowest dose and shortest duration of PPI therapy appropriate to the condition being treated. Caution should be used in patients at risk for osteoporosis related fractures and should be managed according to established treatment guidelines.
6 sources
- "Product Information. Prevacid (lansoprazole)." TAP Pharmaceuticals Inc (2001):
- "Product Information. Aciphex (rabeprazole)." Janssen Pharmaceuticals (2001):
- "Product Information. Protonix (pantoprazole)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Nexium (esomeprazole)." Astra-Zeneca Pharmaceuticals (2001):
- "Product Information. Omeprazole (omeprazole)." Mylan Pharmaceuticals Inc (2003):
- "Product Information. Kapidex (dexlansoprazole)." Takeda Pharmaceuticals America (2009):
Heart Failure
ModerateAnaprox and Anaprox DS (brands of naproxen sodium) contain 25 mg and 50 mg of sodium per tablet (approximately 1 mEq/250 mg naproxen), respectively, and Naprosyn suspension contains 39 mg per teaspoonful (approximately 1.5 mEq/125 mg naproxen). The sodium content should be considered when these products are used in patients with conditions that may require sodium restriction, such as congestive heart failure, hypertension, and fluid retention.
2 sources
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Anaprox (naproxen)." Roche Laboratories (2006):
Heart Failure
ModerateFluid retention and edema have been observed in patients treated with nonsteroidal anti-inflammatory drugs (NSAIDs), including some topical formulations. These drugs should be avoided in patients with severe heart failure unless the benefits are expected to outweigh the risk of worsening heart failure. If an NSAID is used in patients with severe heart failure, they should be monitored for signs of worsening heart failure.
12 sources
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
- "Product Information. Relafen (nabumetone)." SmithKline Beecham (2001):
- "Product Information. Feldene (piroxicam)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Dolobid (diflunisal)." Merck & Co., Inc (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
Show all 12 sourcesShow fewer sources
- "Product Information. Daypro (oxaprozin)." Searle (2001):
- "Product Information. Celebrex (celecoxib)." Searle (2001):
- "Product Information. Meclofenamate Sodium (meclofenamate)." Mylan Pharmaceuticals Inc (2012):
- "Product Information. Flector Patch (diclofenac topical)." Actavis U.S. (Alpharma USPD) (2016):
Hyperkalemia
ModerateIncreases in serum potassium concentration (including hyperkalemia) have been reported with use of nonsteroidal anti-inflammatory drugs (NSAIDs), even in some patients without renal impairment. In patients with normal renal function, these effects have been attributed to a hyporeninemic-hypoaldosteronism state. Caution is advised in patients with hyperkalemia.
3 sources
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
- "Product Information. Celebrex (celecoxib)." Searle (2001):
Hypertension
ModerateNonsteroidal anti-inflammatory drugs (NSAIDs), including topicals, can lead to new onset of hypertension or worsening of preexisting hypertension, either of which can contribute to the increased incidence of cardiovascular events. NSAIDs should be used with caution in patients with hypertension. Blood pressure should be monitored closely during the initiation of NSAID therapy and throughout the course of therapy.
12 sources
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
- "Product Information. Relafen (nabumetone)." SmithKline Beecham (2001):
- "Product Information. Feldene (piroxicam)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Dolobid (diflunisal)." Merck & Co., Inc (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
Show all 12 sourcesShow fewer sources
- "Product Information. Daypro (oxaprozin)." Searle (2001):
- "Product Information. Celebrex (celecoxib)." Searle (2001):
- "Product Information. Meclofenamate Sodium (meclofenamate)." Mylan Pharmaceuticals Inc (2012):
- "Product Information. Flector Patch (diclofenac topical)." Actavis U.S. (Alpharma USPD) (2016):
Hypomagnesemia 1, Intestinal
ModerateSymptomatic and asymptomatic hypomagnesemia has been reported rarely in patients treated with PPIs for at least 3 months, in most cases after a year of therapy. Serious adverse events can include tetany, seizures, and arrhythmias. Caution should be used in patients prone to magnesium imbalances such as patients taking other medications that can cause hypomagnesemia (e.g., diuretics). Regular monitoring is recommended.
6 sources
- "Product Information. Prevacid (lansoprazole)." TAP Pharmaceuticals Inc (2001):
- "Product Information. Aciphex (rabeprazole)." Janssen Pharmaceuticals (2001):
- "Product Information. Protonix (pantoprazole)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Nexium (esomeprazole)." Astra-Zeneca Pharmaceuticals (2001):
- "Product Information. Omeprazole (omeprazole)." Mylan Pharmaceuticals Inc (2003):
- "Product Information. Kapidex (dexlansoprazole)." Takeda Pharmaceuticals America (2009):
Liver Diseases
ModerateBorderline elevations of 1 or more liver tests may occur in up to 15% of patients treated with nonsteroidal anti-inflammatory drugs (NSAIDs). These laboratory abnormalities may progress, remain unchanged, or regress with continuing therapy. Elevations of ALT or AST (at least 3 times the upper limit of normal) have been reported in about 1% of patients in clinical trials. In addition, rare (sometimes fatal) cases of severe hepatotoxicity, including liver necrosis, hepatic failure, jaundice, and fulminant hepatitis have been reported. Therapy with NSAIDs should be administered cautiously in patients with preexisting liver disease. Periodic monitoring of liver function is recommended during prolonged therapy. NSAIDs are also highly protein-bound and some are extensively metabolized by the liver. Metabolic activity and/or plasma protein binding may be altered in patients with hepatic impairment. A dosage reduction may be required in some cases.
17 sources
- "Product Information. Motrin (ibuprofen)." Pharmacia and Upjohn (2002):
- "Product Information. Nalfon (fenoprofen)." Xspire Pharma (2002):
- "Product Information. Indocin (indomethacin)." Merck & Co., Inc (2002):
- "Product Information. Orudis (ketoprofen)." Wyeth-Ayerst Laboratories (2002):
- "Product Information. Toradol (ketorolac)." Roche Laboratories (2002):
- "Product Information. Naprosyn (naproxen)." Syntex Laboratories Inc (2002):
- "Product Information. Clinoril (sulindac)." Merck & Co., Inc (2001):
- "Product Information. Tolectin (tolmetin)." McNeil Pharmaceutical (2001):
Show all 17 sourcesShow fewer sources
- "Product Information. Voltaren (diclofenac)." Novartis Pharmaceuticals (2001):
- "Product Information. Relafen (nabumetone)." SmithKline Beecham (2001):
- "Product Information. Feldene (piroxicam)." Pfizer U.S. Pharmaceuticals (2001):
- "Product Information. Dolobid (diflunisal)." Merck & Co., Inc (2001):
- "Product Information. Ansaid (flurbiprofen)." Pharmacia and Upjohn (2001):
- "Product Information. Lodine (etodolac)." Wyeth-Ayerst Laboratories (2001):
- "Product Information. Daypro (oxaprozin)." Searle (2001):
- "Product Information. Celebrex (celecoxib)." Searle (2001):
- "Product Information. Mobic (meloxicam)." Boehringer-Ingelheim (2001):
Liver Diseases
ModerateEsomeprazole is primarily metabolized by the liver. In patients with mild to moderate hepatic impairment (Child Pugh Class A and B), little drug accumulation has been observed following once-daily, multiple-dose administration. No dosage adjustments are necessary in these patients. In severe hepatic impairment (Child Pugh Class C), however, substantial increases in plasma drug concentrations have been demonstrated. The manufacturer recommends a maximum dosage of 20 mg once daily in patients with severe liver disease.
1 source
- "Product Information. Nexium (esomeprazole)." Astra-Zeneca Pharmaceuticals (2001):
Therapeutic duplication
Drug classes that overlap with Naproxen Sodium + Esomeprazole Magnesium, so taking both doubles up the same effect. This source publishes no per-row citations for duplication.
acid suppressant agents
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Example product in the source data (US market): Prevpac
acid suppressant agents
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acid suppressant agents
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acid suppressant agents
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nonsteroidal anti-inflammatories
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nonsteroidal anti-inflammatories
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Example product in the source data (US market): Consensi
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Example product in the source data (US market): Synalgos-dc
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Phosphasal
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Chlorpheniramine/ibuprofen/pseudoephedrine
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Orphengesic forte
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Combunox
nonsteroidal anti-inflammatories
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nonsteroidal anti-inflammatories
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Example product in the source data (US market): Aspirin/citric acid/sodium bicarbonate
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Ibuprofen/pseudoephedrine
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Soma compound with codeine
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Stanback
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Example product in the source data (US market): Aspirin/methocarbamol
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Diphenhydramine/ibuprofen
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Example product in the source data (US market): Aspirin/carisoprodol
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Example product in the source data (US market): Aspirin/butalbital/caffeine/codeine
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Micrainin
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Acetaminophen/ibuprofen
nonsteroidal anti-inflammatories
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nonsteroidal anti-inflammatories
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Example product in the source data (US market): Ibuprofen/phenylephrine
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Seglentis
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Zynrelef
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Percodan
nonsteroidal anti-inflammatories
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nonsteroidal anti-inflammatories
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Example product in the source data (US market): Aspirin/dipyridamole
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Migraine relief
nonsteroidal anti-inflammatories
The recommended maximum number of medicines in the 'nonsteroidal anti-inflammatories' category to be taken concurrently is usually one.Your list includes two medicines belonging to the 'nonsteroidal anti-inflammatories' category.
Example product in the source data (US market): Aspirin/chlorpheniramine/phenylephrine
nonsteroidal anti-inflammatories
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Example product in the source data (US market): Aspirin/hydrocodone
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nonsteroidal anti-inflammatories
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Example product in the source data (US market): Laniroif