Deferasirox interactions
Full monograph for DeferasiroxCheck it against another medicine
Medicines
428 documented
Mechanism
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Acalabrutinib | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Acyclovir + Hydrocortisone | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Adefovir Dipivoxil | Major | Synergy | Theoretical concerns exist regarding the potential for increased risk of renal impairment during coadministration of deferasirox with other nephrotoxic agents. | 2 sources — open the full entry |
| Alendronic acid | Major | Synergy | Coadministration with oral bisphosphonates may increase the risk of gastrointestinal bleeding associated with the use of deferasirox. Fatal gastrointestinal… | 3 sources — open the full entry |
| Alendronic Acid + Vitamin D3 | Major | Synergy | Coadministration with oral bisphosphonates may increase the risk of gastrointestinal bleeding associated with the use of deferasirox. Fatal gastrointestinal… | 3 sources — open the full entry |
| Allium cepa + Heparin + Allantoin | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Alteplase | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Amikacin | Major | Synergy | Theoretical concerns exist regarding the potential for increased risk of renal impairment during coadministration of deferasirox with other nephrotoxic agents… | 3 sources — open the full entry |
| Aminophylline | Major | Metabolism | Coadministration with deferasirox may significantly increase the plasma concentrations of theophylline. The proposed mechanism is deferasirox inhibition of… | 5 sources — open the full entry |
| Amphotericin B | Major | Synergy | Theoretical concerns exist regarding the potential for increased risk of renal impairment during coadministration of deferasirox with other nephrotoxic agents… | 3 sources — open the full entry |
| Apixaban | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Aspirin | 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 |
| Aspirin + Dipyridamole | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of…2 documented mechanisms | 6 sources — open the full entry |
| Bacitracin Zinc + Polymyxin B Sulfate | Major | Synergy | Theoretical concerns exist regarding the potential for increased risk of renal impairment during coadministration of deferasirox with other nephrotoxic agents…2 documented mechanisms | 3 sources — open the full entry |
| Benzoic Acid + Salicylic Acid | Major | Synergy | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase the risk of gastrointestinal bleeding associated with the use of deferasirox. | 2 sources — open the full entry |
| Betamethasone | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Betamethasone + Calcipotriol | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Betamethasone + Clotrimazole | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Betamethasone + Clotrimazole + Gentamicin | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of…2 documented mechanisms | 6 sources — open the full entry |
| Betamethasone + Neomycin Sulphate (Ophthalmic) | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of…2 documented mechanisms | 6 sources — open the full entry |
| Betamethasone + Phenylephrine + Lignocaine | Major | Metabolism · Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of…2 documented mechanisms | 7 sources — open the full entry |
| Betamethasone Dipropionate | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Betamethasone Dipropionate + Salicylic Acid | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of…2 documented mechanisms | 5 sources — open the full entry |
| Betamethasone Sodium Phosphate | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Betamethasone Valerate | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Betrixaban | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Bismuth Subsalicylate | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Bivalirudin | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Bromfenac Sodium | 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 |
| Cabozantinib | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Calcium Dobesilate + Lidocaine + Dexamethasone | Major | Metabolism · Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of…2 documented mechanisms | 7 sources — open the full entry |
| Cetalkonium Chloride + Choline Salicylate | 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 |
| Cilostazol | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Cinchocaine + Hydrocortisone + Framycetin + Esculin | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of…2 documented mechanisms | 6 sources — open the full entry |
| Cinchocaine + Hydrocortisone + Neomycin + Esculin | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of…2 documented mechanisms | 6 sources — open the full entry |
| Ciprofloxacin + Dexamethasone | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Cisplatin | Major | Synergy | Theoretical concerns exist regarding the potential for increased risk of renal impairment during coadministration of deferasirox with other nephrotoxic agents… | 3 sources — open the full entry |
| Clobetasol Propionate + Neomycin Sulphate + Nystatin | Major | Synergy | Theoretical concerns exist regarding the potential for increased risk of renal impairment during coadministration of deferasirox with other nephrotoxic agents… | 3 sources — open the full entry |
| Clobetasol Propionate + Salicylic Acid | Major | Synergy | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase the risk of gastrointestinal bleeding associated with the use of deferasirox. | 2 sources — open the full entry |
| Clopidogrel + Aspirin | Major | Synergy | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase the risk of gastrointestinal bleeding associated with the use of deferasirox…2 documented mechanisms | 6 sources — open the full entry |
| Clopidogrel Bisulphate | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Clotrimazole + Hydrocortisone | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Clozapine | Major | Synergy | Coadministration of clozapine with other agents that can cause neutropenia or agranulocytosis may increase the risk and/or severity of hematologic toxicity. | 9 sources — open the full entry |
| Coal Tar + Precipitated Sulphur + Salicylic Acid | Major | Synergy | Coadministration with nonsteroidal anti-inflammatory drugs (NSAIDs) may increase the risk of gastrointestinal bleeding associated with the use of deferasirox. | 2 sources — open the full entry |
| Colistimethate Sodium | Major | Synergy | Theoretical concerns exist regarding the potential for increased risk of renal impairment during coadministration of deferasirox with other nephrotoxic agents… | 3 sources — open the full entry |
| Cyclosporine (Oral) | Major | Synergy | Theoretical concerns exist regarding the potential for increased risk of renal impairment during coadministration of deferasirox with other nephrotoxic agents… | 3 sources — open the full entry |
| Dabigatran Etexilate Mesylate | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 1 sources — open the full entry |
| Dalteparin Sodium | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
| Daprodustat | Major | Metabolism | Coadministration with moderate inhibitors of CYP450 2C8 may significantly increase the plasma concentrations and the risk of adverse effects associated with… | 1 sources — open the full entry |
| Dasatinib | Major | Synergy | Coadministration with drugs that have known ulcerogenic or hemorrhagic potential may increase the risk of gastrointestinal bleeding associated with the use of… | 3 sources — open the full entry |
Food & lifestyle
food
ModerateAbsorption
According to product labeling, the bioavailability of deferasirox was variably increased when taken with a meal.
What to do: To ensure consistent plasma drug levels, deferasirox should be taken on an empty stomach 30 minutes before eating preferably at the same time everyday.
1 source
- "Product Information. Exjade (deferasirox)." Novartis Pharmaceuticals (2005):
Conditions
Conditions in which Deferasirox needs care, as documented in this source.
Bone Marrow Failure Disorders
MajorThe use of deferasirox is contraindicated in patients with platelet counts below 50 x 109/L. Cytopenias, worsening anemia, and thrombocytopenia, including fatal events, have been reported in patients treated with deferasirox. Preexisting hematologic disorders may increase this risk. It is recommended to monitor blood counts in all patients and to interrupt treatment in patients who develop cytopenias until the cause of the cytopenia has been determined.
1 source
- "Product Information. Exjade (deferasirox)." Novartis Pharmaceuticals (2005):
Hepatic Insufficiency
MajorThe use of deferasirox should be avoided in patients with severe hepatic impairment. The starting dose of deferasirox should be reduced by 50% in patients with moderate hepatic impairment. It is recommended to measure serum transaminases and bilirubin in all patients prior to initiating treatment, every 2 weeks during the first month, and at least monthly or more frequently as clinically appropriate. Closely monitor patients with mild or moderate hepatic impairment for efficacy and adverse reactions that may require dose titration.
1 source
- "Product Information. Exjade (deferasirox)." Novartis Pharmaceuticals (2005):
Kidney Diseases
MajorThe use of deferasirox is contraindicated in patients with serum creatinine greater than two times the age-appropriate upper limit of normal or creatinine clearance less than 40 mL/min. The starting dose of deferasirox should be reduced by 50% in patients with creatine clearance 40 to 60 mL/min. It is recommended to measure serum creatine and calculate clearance in duplicate prior to initiating treatment in all patients and monitor renal function at least monthly or more frequently as clinically appropriate. Consider dose reduction, interruption, or discontinuation of deferasirox based on increases in serum creatinine.
1 source
- "Product Information. Exjade (deferasirox)." Novartis Pharmaceuticals (2005):
Stevens-Johnson Syndrome
MajorFatal cases of severe cutaneous reactions, including Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and erythema multiforme have occurred in patients treated with deferasirox. The risk of other skin reactions cannot be excluded. It is recommended that if SJS or TEN is suspected to interrupt therapy until the etiology of the reaction has been determined, and if SJS or TEN is confirmed to permanently discontinue treatment with deferasirox. Monitor patients for the development of these severe cutaneous reactions, discontinue deferasirox if clinically appropriate and do not reintroduce therapy. For severe cases of rash, interrupt treatment and consider reintroducing therapy after resolution of the rash at a lower dose with dose escalation as appropriate.
1 source
- "Product Information. Exjade (deferasirox)." Novartis Pharmaceuticals (2005):
Auditory Diseases, Central
ModerateAuditory disturbances (high-frequency hearing loss, decreased hearing), and ocular disturbances (lens opacities, cataracts, elevations in intraocular pressure, and retinal disorders) have been reported in patients using deferasirox. It is recommended to perform auditory and ophthalmic testing (including slit lamp examinations and dilated fundoscopy) before starting therapy with deferasirox and thereafter as clinically indicated. If disturbances are noted, consider dose reduction or interruption if appropriate.
1 source
- "Product Information. Exjade (deferasirox)." Novartis Pharmaceuticals (2005):
Gastrointestinal Diseases
ModerateGastrointestinal hemorrhage, ulcerations, perforations, including deaths have been documented in patients using deferasirox, especially in elderly patients who had advanced hematologic malignancies and/or low platelet counts. The risk of gastrointestinal hemorrhage may be increased when administering deferasirox in combination with drugs that have ulcerogenic or hemorrhagic potential, such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, oral bisphosphonates, or anticoagulants. It is recommended to monitor patients and discontinue therapy for suspected GI ulceration or hemorrhage. Care is recommended when using this agent in patients at risk of GI complications.
1 source
- "Product Information. Exjade (deferasirox)." Novartis Pharmaceuticals (2005):