Drug Interactions between Revatio and vericiguat
This report displays the potential drug interactions for the following 2 drugs:
- Revatio (sildenafil)
- vericiguat
Interactions between your drugs
sildenafil vericiguat
Applies to: Revatio (sildenafil) and vericiguat
CONTRAINDICATED: Coadministration of vericiguat and phosphodiesterase type 5 (PDE-5) inhibitors may result in additive hypotension. PDE-5 inhibitors prevent degradation of cyclic guanosine monophosphate (cGMP), a messenger that plays a role in the regulation of vascular tone, while vericiguat promotes cGMP synthesis. In a study involving healthy subjects, concomitant use of vericiguat (10 mg) with sildenafil (25, 50, or 100 mg single dose) led to an additional decrease in seated blood pressure of up to 5.4 mmHg compared to vericiguat alone. No clinically significant differences in vericiguat or sildenafil pharmacokinetics were observed during coadministration. There is limited experience with concomitant use of vericiguat and PDE-5 inhibitors in patients with heart failure.
MANAGEMENT: Due to potential hypotension, concomitant use of vericiguat with PDE-5 inhibitors is considered contraindicated.
References (10)
- (2001) "Product Information. Viagra (sildenafil)." Pfizer U.S. Pharmaceuticals
- (2003) "Product Information. Cialis (tadalafil)." Lilly, Eli and Company
- (2005) "Product Information. Revatio (sildenafil)." Pfizer U.S. Pharmaceuticals Group
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- Cerner Multum, Inc. "Australian Product Information."
- (2009) "Product Information. Adcirca (tadalafil)." United Therapeutics Corporation
- (2012) "Product Information. Stendra (avanafil)." Vivus LLC.
- (2014) "Product Information. Staxyn (vardenafil)." Merck & Co., Inc
- (2021) "Product Information. Verquvo (vericiguat)." Merck & Co., Inc
- Boettcher M, Gerisch M, Lobmeyer M, et al. (2020) "Metabolism and pharmacokinetic drug–drug interaction profile of vericiguat, a soluble guanylate cyclase stimulator: Results from preclinical and phase I healthy volunteer studies." Clin Pharmacokinet, 59, p. 1407-18
Drug and food interactions
sildenafil food
Applies to: Revatio (sildenafil)
GENERALLY AVOID: Coadministration with grapefruit juice may slightly increase the oral bioavailability and delay the onset of action of sildenafil. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruits. In a randomized, crossover study with 24 healthy male volunteers, ingestion of 250 mL of grapefruit juice one hour before and concurrently with a 50 mg dose of sildenafil increased the mean area under the plasma concentration-time curve (AUC) of sildenafil and its pharmacologically active N-desmethyl metabolite by 23% and 24%, respectively, compared to water. Peak plasma concentrations (Cmax) were unaltered, but the time to reach sildenafil Cmax was prolonged by 0.25 hour. The observed increase in sildenafil bioavailability is unlikely to be of clinical significance in most individuals. However, pharmacokinetic interactions involving grapefruit juice are often subject to a high degree of interpatient variability and may be significant in the occasional susceptible patient. Indeed, one subject in the study had a 2.6-fold increase in sildenafil concentrations.
MANAGEMENT: It may be advisable to avoid administration of sildenafil with grapefruit juice to prevent potential toxicity and delay in onset of action.
References (1)
- Jetter A, Kinzig-Schippers M, Walchner-Bonjean M, et al. (2002) "Effects of grapefruit juice on the pharmacokinetics of sildenafil." Clin Pharmacol Ther, 71, p. 21-29
vericiguat food
Applies to: vericiguat
ADJUST DOSING INTERVAL: Administration of vericiguat with food reduces its pharmacokinetic variability and increases its exposure. Vericiguat is less soluble at neutral pH than at acidic pH. Administration of vericiguat with a high-fat, high-calorie meal or low-fat, high-carbohydrate meal increased time to reach peak plasma concentration (Tmax) from about 1 hour (fasted) to about 4 hours (fed) and increased vericiguat systemic exposure (AUC) by 19% and peak plasma concentration (Cmax) by 9% for the 5 mg tablet and by 44% (AUC) and 41% (Cmax) for the 10 mg tablet as compared with the fasted state. Concurrent treatment with drugs that increase gastric pH, such as proton pump inhibitors or antacids, decrease vericiguat AUC by about 30%. Co-treatment with drugs that increase gastric pH did not affect vericiguat exposure in patients with heart failure when vericiguat was taken as directed with food.
MANAGEMENT: Administer vericiguat with food to ensure maximal exposure and decrease pharmacokinetic variability.
References (2)
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- (2021) "Product Information. Verquvo (vericiguat)." Merck & Co., Inc
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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