Alpelisib interactions
Full monograph for AlpelisibCheck it against another medicine
Medicines
234 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Apalutamide | Major | Metabolism | Coadministration of alpelisib with potent inducers of CYP450 3A4 may significantly reduce the plasma concentrations of alpelisib. The proposed mechanism, based… | 8 sources — open the full entry |
| Carbamazepine | Major | Metabolism | Coadministration of alpelisib with potent inducers of CYP450 3A4 may significantly reduce the plasma concentrations of alpelisib. The proposed mechanism, based… | 8 sources — open the full entry |
| Enzalutamide | Major | Metabolism | Coadministration of alpelisib with potent inducers of CYP450 3A4 may significantly reduce the plasma concentrations of alpelisib. The proposed mechanism, based… | 8 sources — open the full entry |
| Fosphenytoin Sodium | Major | Metabolism | Coadministration of alpelisib with potent inducers of CYP450 3A4 may significantly reduce the plasma concentrations of alpelisib. The proposed mechanism, based… | 8 sources — open the full entry |
| Phenobarbital | Major | Metabolism | Coadministration of alpelisib with potent inducers of CYP450 3A4 may significantly reduce the plasma concentrations of alpelisib. The proposed mechanism, based… | 8 sources — open the full entry |
| Phenytoin Sodium | Major | Metabolism | Coadministration of alpelisib with potent inducers of CYP450 3A4 may significantly reduce the plasma concentrations of alpelisib. The proposed mechanism, based… | 8 sources — open the full entry |
| Primidone | Major | Metabolism | Coadministration of alpelisib with potent inducers of CYP450 3A4 may significantly reduce the plasma concentrations of alpelisib. The proposed mechanism, based… | 8 sources — open the full entry |
| Rifampicin | Major | Metabolism | Coadministration of alpelisib with potent inducers of CYP450 3A4 may significantly reduce the plasma concentrations of alpelisib. The proposed mechanism, based… | 8 sources — open the full entry |
| Rifampicin + Isoniazid | Major | Metabolism | Coadministration of alpelisib with potent inducers of CYP450 3A4 may significantly reduce the plasma concentrations of alpelisib. The proposed mechanism, based… | 8 sources — open the full entry |
| Rifampicin + Isoniazid + Pyrazinamide + Ethambutol | Major | Metabolism | Coadministration of alpelisib with potent inducers of CYP450 3A4 may significantly reduce the plasma concentrations of alpelisib. The proposed mechanism, based… | 8 sources — open the full entry |
| Abametapir | 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… | 1 sources — open the full entry |
| Acarbose | Moderate | Antagonism | The efficacy of insulin and other antidiabetic agents may be diminished by certain drugs, including atypical antipsychotics, corticosteroids, diuretics… | 95 sources — open the full entry |
| Afatinib Dimaleate | Moderate | Others | Coadministration of inhibitors of the breast cancer resistance protein (BCRP) transporter with alpelisib may increase the plasma concentrations and risk of… | 3 sources — open the full entry |
| Alendronic acid | Moderate | Synergy | Coadministration of alpelisib with bisphosphonates or denosumab may increase the risk of developing osteonecrosis of the jaw (ONJ). The condition can occur… | 3 sources — open the full entry |
| Alendronic Acid + Vitamin D3 | Moderate | Synergy | Coadministration of alpelisib with bisphosphonates or denosumab may increase the risk of developing osteonecrosis of the jaw (ONJ). The condition can occur… | 3 sources — open the full entry |
| Alogliptin Benzoate | Moderate | Antagonism | The efficacy of insulin and other antidiabetic agents may be diminished by certain drugs, including atypical antipsychotics, corticosteroids, diuretics… | 95 sources — open the full entry |
| Amitriptyline Hydrochloride | 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 |
| Amitriptyline Hydrochloride + Chlordiazepoxide | 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 |
| Amlodipine Besilate + Atorvastatin | Moderate | Excretion | Coadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)… | 5 sources — open the full entry |
| Apixaban | Moderate | Metabolism | Coadministration with inducers of CYP450 3A4 and/or P-glycoprotein (P-gp) may decrease the plasma concentrations of apixaban, which is a substrate of both the… | 11 sources — open the full entry |
| Armodafinil | Moderate | Metabolism | Coadministration of alpelisib with inducers of CYP450 3A4 may reduce the plasma concentrations of alpelisib. The proposed mechanism, based on in vitro data, is… | 2 sources — open the full entry |
| Artesunate | Moderate | Excretion | Coadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)… | 5 sources — open the full entry |
| Atorvastatin + Ezetimibe | Moderate | Excretion | Coadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)… | 5 sources — open the full entry |
| Atorvastatin Calcium | Moderate | Excretion | Coadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)… | 5 sources — open the full entry |
| Betrixaban | Moderate | Absorption | Coadministration with inhibitors of P-glycoprotein (P-gp) may increase the plasma concentrations of betrixaban, which is a substrate of the efflux transporter. | 4 sources — open the full entry |
| Biphasic Insulin Aspart | Moderate | Antagonism | The efficacy of insulin and other antidiabetic agents may be diminished by certain drugs, including atypical antipsychotics, corticosteroids, diuretics… | 95 sources — open the full entry |
| Bortezomib | 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 |
| Bosentan Monohydrate | 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 |
| Brigatinib | Moderate | Metabolism | Coadministration of alpelisib with inducers of CYP450 3A4 may reduce the plasma concentrations of alpelisib. The proposed mechanism, based on in vitro data, is… | 2 sources — open the full entry |
| Bupropion Hydrochloride | Moderate | Metabolism | Coadministration with alpelisib may decrease the plasma concentrations and therapeutic effects of drugs that are substrates of CYP450 2B6. The proposed… | 15 sources — open the full entry |
| Calcium Dobesilate + Lidocaine + Dexamethasone | Moderate | Excretion | Coadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)… | 5 sources — open the full entry |
| Canagliflozin Hemihydrate | Moderate | Antagonism | The efficacy of insulin and other antidiabetic agents may be diminished by certain drugs, including atypical antipsychotics, corticosteroids, diuretics… | 95 sources — open the full entry |
| Candesartan Cilexetil | Moderate | Metabolism | Coadministration with alpelisib may decrease the plasma concentrations and therapeutic effects of drugs that are substrates of CYP450 2C9, such as warfarin. | 1 sources — open the full entry |
| Candesartan Cilexetil + Hydrochlorothiazide | Moderate | Metabolism | Coadministration with alpelisib may decrease the plasma concentrations and therapeutic effects of drugs that are substrates of CYP450 2C9, such as warfarin. | 1 sources — open the full entry |
| Carvedilol | 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 |
| Cenobamate | Moderate | Metabolism | Coadministration of alpelisib with inducers of CYP450 3A4 may reduce the plasma concentrations of alpelisib. The proposed mechanism, based on in vitro data, is… | 2 sources — open the full entry |
| Ceritinib | Moderate | Others | Coadministration of inhibitors of the breast cancer resistance protein (BCRP) transporter with alpelisib may increase the plasma concentrations and risk of… | 3 sources — open the full entry |
| Ciprofloxacin + Dexamethasone | Moderate | Excretion | Coadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)… | 5 sources — open the full entry |
| Clobetasol Propionate + Ofloxacin + Ornidazole + Terbinafine | 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 |
| Colchicine | Moderate | Excretion | Coadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)… | 5 sources — open the full entry |
| Cyclophosphamide | 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 |
| Cyclosporine (Oral) | Moderate | Others | Coadministration of inhibitors of the breast cancer resistance protein (BCRP) transporter with alpelisib may increase the plasma concentrations and risk of… | 3 sources — open the full entry |
| Dabigatran Etexilate Mesylate | Moderate | Excretion | Coadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)… | 2 sources — open the full entry |
| Daclatasvir | Moderate | Excretion | Coadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)… | 5 sources — open the full entry |
| Daclatasvir + Sofosbuvir | Moderate | Excretion | Coadministration with alpelisib may theoretically increase the plasma concentrations of drugs that are substrates of organic anion transporter (OAT3)… | 5 sources — open the full entry |
| Dapagliflozin Propanediol | Moderate | Antagonism | The efficacy of insulin and other antidiabetic agents may be diminished by certain drugs, including atypical antipsychotics, corticosteroids, diuretics… | 95 sources — open the full entry |
| Dapsone | 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 |
| Darolutamide | Moderate | Others | Coadministration of inhibitors of the breast cancer resistance protein (BCRP) transporter with alpelisib may increase the plasma concentrations and risk of… | 3 sources — open the full entry |
| Daunorubicin | Moderate | Absorption | Coadministration with inhibitors of P-glycoprotein (P-gp) may increase the plasma concentrations of daunorubicin and idarubicin, both of which are substrates… | 5 sources — open the full entry |
| Deferasirox | Moderate | Metabolism | Coadministration of alpelisib with inducers of CYP450 3A4 may reduce the plasma concentrations of alpelisib. The proposed mechanism, based on in vitro data, is… | 2 sources — open the full entry |
Food & lifestyle
high-fat foods
ModerateAbsorption
Food significantly enhances the oral absorption and bioavailability of alpelisib. When administered with a high-fat high-calorie meal (985 calories with 58.1 g of fat) or a low-fat low-calorie meal (334 calories with 8.7 g of fat) the AUC and Cmax of a single dose of alpelisib was increased by 73% and 84% and 77% and 145%, respectively. There were no clinically significant differences in alpelisib AUC between the two types of meals. In addition, food appears to have a more pronounced effect on the solubility of alpelisib than gastric pH.
What to do: To ensure maximal oral absorption, alpelisib should be administered with a meal.
1 source
- "Product Information. Piqray (alpelisib)." Novartis Pharmaceuticals (2019):
Conditions
Conditions in which Alpelisib needs care, as documented in this source.
Bisphosphonate-Associated Osteonecrosis of the Jaw
ModerateOsteonecrosis of the jaw (ONJ) has been reported in patients using alpelisib. Caution is advised when this drug and bisphosphonates or denosumab are used either simultaneously or sequentially. Do not initiate treatment with alpelisib in patients with ongoing osteonecrosis of the jaw from previous or concurrent treatment with bisphosphonates or denosumab. Patients experiencing ONJ should be managed according to clinical practice.
1 source
- "Product Information. Piqray (alpelisib)." Novartis Pharmaceuticals (2019):
Diabetes Mellitus
ModerateSevere hyperglycemia, including ketoacidosis, has been reported in patients treated with alpelisib. Before initiating treatment with alpelisib it is recommend to test, optimize and monitor blood glucose as clinically indicated. Care should be exercised when using this agent in diabetic patients. Patients with a history of diabetes mellitus may require intensified diabetic treatment. Based on the severity of the hyperglycemia, alpelisib may require dose interruption, reduction, or discontinuation. Advise patients of the signs and symptoms of hyperglycemia. Closely monitor patients with diabetes.
1 source
- "Product Information. Piqray (alpelisib)." Novartis Pharmaceuticals (2019):
Diarrhea
ModerateSevere diarrhea, including dehydration and acute kidney injury, occurred in patients treated with alpelisib. Based on the severity of the diarrhea, alpelisib may require dose interruption, reduction, or discontinuation. Care should be exercised when using this agent in patients with diarrhea. Advise patients to start antidiarrheal treatment, increase oral fluids, and notify their healthcare provider if diarrhea occurs while taking alpelisib.
1 source
- "Product Information. Piqray (alpelisib)." Novartis Pharmaceuticals (2019):
Kidney Diseases
ModerateNo dose adjustment is recommended for patients with mild to moderate renal impairment (CrCl 30 to < 90 mL/min). Close monitoring is recommended when using alpelisib in patients with severe renal impairment (CrCl < 30 mL/min) as its effect on the pharmacokinetics is unknown.
1 source
- "Product Information. Piqray (alpelisib)." Novartis Pharmaceuticals (2019):
Pneumonia
ModerateSevere pneumonitis, including acute interstitial pneumonitis and interstitial lung disease, has been reported in patients treated with alpelisib. It is recommended to interrupt alpelisib immediately and evaluate the patient for pneumonitis in patients who have new or worsening respiratory symptoms or are suspected to have developed pneumonitis. Advise patients to immediately report new or worsening respiratory symptoms. Permanently discontinue alpelisib in all patients with confirmed pneumonitis.
1 source
- "Product Information. Piqray (alpelisib)." Novartis Pharmaceuticals (2019):
Skin Diseases
ModerateSevere cutaneous reactions, including Stevens-Johnson Syndrome (SJS) and Erythema Multiforme (EM) were reported in patients treated with alpelisib. Do not initiate alpelisib treatment in patients with a history of SJS, EM, or Toxic Epidermal Necrolysis (TEN). If signs or symptoms of severe cutaneous reactions occur, interrupt treatment until the etiology of the reaction has been determined. Consultation with a dermatologist is recommended. If SJS, TEN, or EM is confirmed, permanently discontinue alpelisib. Do not reintroduce alpelisib in patients who have experienced previous severe cutaneous reactions during treatment.
1 source
- "Product Information. Piqray (alpelisib)." Novartis Pharmaceuticals (2019):