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Drug Interactions between Prezcobix and sildenafil

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Major

sildenafil darunavir

Applies to: sildenafil and Prezcobix (cobicistat / darunavir)

Talk to your doctor before using sildenafil together with darunavir. Combining these medications may significantly increase the blood levels and effects of sildenafil. Depending on your condition, you may not be able to use these medications together, or you may need a dose adjustment or more frequent monitoring by your doctor to safely use both medications. Contact your doctor if your condition changes or you experience nausea, shortness of breath, dizziness, lightheadedness, fainting, visual disturbances, ringing in the ears, vision or hearing loss, chest pain or tightness, irregular heartbeat, and/or priapism (prolonged and painful erection unrelated to sexual activity), as these may be signs and symptoms of excessive sildenafil levels. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.

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Major

sildenafil cobicistat

Applies to: sildenafil and Prezcobix (cobicistat / darunavir)

Consumer information for this interaction is not currently available.

CONTRAINDICATED: Coadministration with protease inhibitors (PIs) may significantly increase the plasma concentrations and effects of sildenafil. The mechanism is PI inhibition of CYP450 3A4, the isoenzyme primarily responsible for the metabolic clearance of sildenafil. This interaction also extends to cobicistat, a potent and selective mechanism-based CYP450 3A4 inhibitor. Pharmacokinetic models predict that this interaction may be more significant for oral rather than intravenous formulations of sildenafil, due at least partly to effects from first pass metabolism. In healthy adult volunteers (n=14), administration of a single dose of sildenafil (100 mg) during treatment with ritonavir (500 mg twice a day for 7 days) increased the mean sildenafil peak plasma concentration (Cmax) and systemic exposure (AUC) by 300% and 1000%, respectively, compared to administration alone. At 24 hours, sildenafil plasma levels were approximately 200 ng/mL as opposed to about 5 ng/mL with sildenafil alone. No change in safety or tolerability of sildenafil was observed. In HIV-infected patients (n=6) stabilized on triple antiretroviral therapy containing indinavir (800 mg three times a day), the AUC of a single dose of sildenafil (25 mg) was 4.4 times higher than dose-normalized data from historical controls. These patients experienced headache, flushing, dyspepsia and rhinitis, as well as a mean maximal decrease in blood pressure of 14/10 mmHg. This interaction was also suspected in the death of a 47-year-old man who used sildenafil (25 mg) during treatment with both ritonavir and saquinavir. However, there are a few case studies available in the literature which describe the successful use of sildenafil in combination with ritonavir and 1 case study of use in combination with cobicistat in HIV-infected patients being treated for pulmonary arterial hypertension (PAH). These cases report the use of therapeutic drug monitoring for sildenafil. Data regarding this interaction in pediatric patients has not been reported by the manufacturers of sildenafil.

MANAGEMENT: A safe and effective dosage of sildenafil has not been established for the treatment of pulmonary arterial hypertension (PAH) when used in the presence of protease inhibitors (PIs) or cobicistat. Some professional guidelines and product labeling consider its use with PIs and/or cobicistat in this setting to be contraindicated. Some authorities advise monitoring and a reduction of sildenafil dosing to 20 mg oral (10 mg intravenous) once daily in adult patients receiving potent CYP450 3A4 inhibitors like clarithromycin, telithromycin, or nefazodone. Although generally considered contraindicated, there are some case reports available in the literature which describe initiating sildenafil at reduced doses (10 mg orally every 8 hours for example) in combination with therapeutic drug monitoring for PAH in HIV-infected patients receiving ritonavir or cobicistat-boosted antiretroviral regimens. When used for erectile dysfunction, a lower starting dose of 25 mg is generally recommended with a warning that the maximum dosage of sildenafil should not exceed 25 mg in 48-hours. Regardless of indication, the product labeling for both medications involved should be consulted to ensure the most up to date dosing recommendations are being followed. Additionally, all patients should be monitored closely for adverse effects and advised to promptly notify their doctor if they experience pain or tightness in the chest or jaw, irregular heartbeat, nausea, shortness of breath, hypotension, sudden decrease or loss of hearing, visual disturbances, syncope, or prolonged erection (greater than 4 hours).

Drug and food interactions

Moderate

sildenafil food

Applies to: sildenafil

If you are receiving therapy with sildenafil you should avoid the regular consumption of large amounts of grapefruits and grapefruit juice. Grapefruit can raise the levels of sildenafil in your body and delay the time it takes for the medication to work. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.

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Moderate

darunavir food

Applies to: Prezcobix (cobicistat / darunavir)

Food can enhance the levels of darunavir in your body. Take darunavir with food. The type of food does not matter. This will make it easier for your body to absorb the medication. Swallow the whole tablets with a drink such as water or milk. Do not chew the tablets. Darunavir must be always be taken together at the same time as another medication called ritonavir (Norvir).

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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.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor 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.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.