No pharmaceutical opinion available for this interaction.
Lopinavir / ritonavir may possibly inhibit the metabolism (CYP 3A4) and consequently increase the plasma concentration of Nifedipine.
3A4 (major), 13 identified metabolites, 5 of these metabolites are linked to the metabolism of ritonavir, transporters: MRP1, MRP2, OATP1A2, OATP1B1, P-gp
2C19 (strong), 1A2, 2C9 (moderate) UGT (moderate)
3A4 and 2D6 (strong), transporters: BCRP, MRP2, OATP1A2, OATP1B1, OATP1B3, OATP2B1, P-gp
3A4 (major) > 2D6 (minor)
1A2 (moderate) > 2C9, 3A4et 2D6 (weak)
Possible increase of adverse effects.
Use this combination with caution.
Start treatment with lower dose possible.
Reduce the dose of the CCB if judged necessary and gradually increase according to clinical response and tolerance.
In patients already being treated with this combination and tolerating it, if deemed appropriate, keep actual treatment and exercise close monitoring of adverse effects.
Or choose an alternative.
Diuretics, ACE inhibitors and some ARBs (if no contranindications).
Adverse effects associated with CCB : headache, peripheral edema, flushing, dyspnea, chest pain/oppression, gastrointestinal effects, fatigue, hypotension, palpitations, tachycardia or bradycardia (diltiazem and verapamil), dizziness, nervousness, vertigo and drowsiness.
When possible, monitor the effects on blood pressure, heart rate and ECG.
Advise patient to consult quickly if lower limb edema, sudden weight gain, difficulty breathing, chest pain or tightness, or hypotension (dizziness, orthostatic effects).
Lopinavir can prolong the PR interval of the ECG as do the BCC. Use cautiously . Potentially additive effect.
Follow the effect on the blood pressure, the heart beat and the ECG.
Ref #2773 : Concomitant administration of nifedipine with cimetidine or ranitidine caused an increase of about 80% with cimetidine and 70% with ranitidine. The monograph recommends avoiding the combination of felodipine with potent CYP3A4 inhibitors.
Ref #2407: In one study, patients who received indinavir 800 mg + ritonavir 100 mg BID with amlodipine 5 mg QD had an increase in amlodipine AUC of approximately 90%. Other patients received indinavir 800 mg + ritonavir 100 mg BID with diltiazem 120 mg QD and a 26.5% increase in diltiazem AUC was observed. 13 patients in the study, two subjects had an increase in diltiazem AUC of 4 times the normal. By cons, no serious adverse effects on the cardiovascular system was observed.
The searchers therefore recommend, if co-administration is indicated, to initiate treatment with low doses increasing doses with caution according to clinical response and the occurrence of adverse effects.
Ref #2110 : Patient Case. The patient has developed hypotension and progressive kidney insufficiency with the association of Lopinavir/ritonavir with nifedipine (long action). When the patient stopped the intake, the symptoms also stopped. Symptoms started again with an edema several years later when the association was taken again.
Ref #1938: A patient case showed with the association nelfinavir with nifedipine (long action): the patient has shown symptomatic orthostatic hypotension, fatigue, dizziness and a complet heart blocking after the start of nefedipine administration. An improvement of the EKG was noted 24 hours after stopping the intake of nelfinavir. Symptoms started again when nelfinavir was administrated again. This patient showed again orthostatic hypotension with the association indinavir-ritonavir and no symptom with the association efavirenz and nifedipine.