Drug Interactions between cabotegravir and tipranavir
This report displays the potential drug interactions for the following 2 drugs:
- cabotegravir
- tipranavir
Interactions between your drugs
tipranavir cabotegravir
Applies to: tipranavir and cabotegravir
CONTRAINDICATED: Coadministration with inducers of uridine diphosphate glucuronosyltransferase (UGT)1A1 or 1A9 may decrease the plasma concentrations of cabotegravir. Cabotegravir is primarily metabolized by UGT1A1 and to a lesser extent by UGT 1A9. In 15 study subjects given a single 30 mg dose of cabotegravir with the UGT 1A1 inducer rifampin (600 mg once daily), mean cabotegravir peak plasma concentration (Cmax) and systemic exposure (AUC) were reduced by 6% and 59%, respectively. Loss of therapeutic efficacy of cabotegravir may occur.
MANAGEMENT: According to the manufacturer of cabotegravir, due to the potential for loss of therapeutic efficacy, its concomitant use with UGT 1A1 inducers including, but not limited to carbamazepine, oxcarbazepine, phenobarbital, phenytoin, rifampin, and rifapentine is considered contraindicated.
References (7)
- (2021) "Product Information. Cabenuva (cabotegravir-rilpivirine)." ViiV Healthcare ULC
- (2021) "Product Information. Vocabria (cabotegravir)." ViiV Healthcare
- Lee LSU, Pham PA, Flexner C (2012) "Unexpected drug-drug interactions in human immunodeficiency virus (HIV) therapy: induction of UGT1A1 and bile efflux transporters by Efavirenz" National Library of Medicine, 41, p. 559-562
- Miners JO, Polasek TM, Hulin JA, Rowland A, Meech R (2023) "Drug-drug interactions that alter the exposure of glucuronidated drugs: Scope, UDP-glucuronosyltransferase (UGT) enzyme selectivity, mechanisms (inhibition and induction), and clinical significance" Pharmacol Ther, 248, p. 108459
- Song I, Borland J, Chen S, Guta P, Lou Y, Wilfret D, Wajima T, Savina P, Peppercorn AF, castellino s, wagner d, Hosking L, Mosteller M, Rubio JP (2014) "Effects of enzyme inducers efavirenz and tipranavir/ritonavir on the pharmacokinetics of the HIV integrase inhibitor dolutegravir" Eur J Clin Pharmacol, 70, p. 1173-1179
- Marvanova M (2016) "Pharmacokinetic characteristics of antiepileptic drugs (AEDs)" National Library of Medicine, 6, p. 8-20
- Lemaitre F, Grégoire M, Monchaud C, Bouchet S, Saint-Salvi B, Polard E (2022) "Management of drug-drug interactions with nirmatrelvir/ritonavir in patients treated for Covid-19: Guidelines from the French Society of Pharmacology and Therapeutics (SFPT)" National Library of Medicine, 77, p. 509-521
Drug and food interactions
tipranavir food
Applies to: tipranavir
ADJUST DOSING INTERVAL: Food does not appear to substantially alter the pharmacokinetics of tipranavir. When tipranavir capsules or oral solution was coadministered with ritonavir capsules at steady-state, no clinically significant changes in tipranavir peak plasma concentration (Cmax) and systemic exposure (AUC) were observed under fed conditions (500 to 682 kcal, 23% to 25% calories from fat) relative to fasted conditions. The effect of food on tipranavir exposure during coadministration with ritonavir tablets has not been evaluated. High-fat foods may enhance the gastrointestinal absorption of tipranavir. In a multiple-dose study, administration of tipranavir capsules with a high-fat meal (868 kcal, 53% from fat, 31% from carbohydrates) increased the oral bioavailability of tipranavir by 31% compared to administration with toast and skimmed milk, but did not significantly affect tipranavir Cmax. Thus, tipranavir may be safely taken with standard or high-fat meals.
MANAGEMENT: Tipranavir coadministered with low-dose ritonavir should be taken with food to improve the gastrointestinal tolerability of ritonavir. According to the product labeling, tipranavir coadministered with ritonavir capsules or solution can be taken with or without meals, whereas tipranavir coadministered with ritonavir tablets must be taken with meals.
References (4)
- (2005) "Product Information. Aptivus (tipranavir)." Boehringer-Ingelheim
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- Canadian Pharmacists Association (2006) e-CPS. http://www.pharmacists.ca/function/Subscriptions/ecps.cfm?link=eCPS_quikLink
- Cerner Multum, Inc. "Australian Product Information."
Therapeutic duplication warnings
No warnings were found for your selected drugs.
Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
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