Source: European Medicines Agency (EU) Revision Year: 2013 Publisher: Astellas Pharma Europe B.V., Sylviusweg 62, 2333 BE Leiden, The Netherlands
Hypersensitivity to the active substance (or to any dihydropyridine) or to any of the excipients.
Hepatic impairment.
Severe renal impairment (creatinine clearance < 10 ml/min).
Unstable angina pectoris and acute myocardial infarction (in the first 4 weeks).
Untreated heart failure.
Blood levels of barnidipine may be increased when used in combination with strong CYP3A4 inhibitors (results in vitro interaction studies). Therefore, antiproteases, ketoconazole, itraconazole, erythromycin and clarithromycin should not be used concomitantly.
Vasexten should be used with caution in patients with mild to moderate renal impairment (creatinine clearance between 10 and 80 ml/min) (see section 4.2 “Posology and method of administration”).
The combination of a calcium antagonist with a drug that exerts a negative inotropic effect may lead to cardiac decompensation, hypotension or an (additional) myocardial infarction in high-risk patients (e.g. patients with a history of myocardial infarction).
As with all other dihydropyridines, Vasexten should be used with caution in patients with left ventricular dysfunction, in patients suffering from obstruction of the outflow channel of the left ventricle and patients with isolated right-sided cardiac decompensation, e.g. cor pulmonale. Barnidipine has not been studied in NYHA class III or IV patients.
Caution is recommended also when barnidipine is administered to patients with sick sinus (if a pacemaker is not in situ).
In vitro studies indicate that barnidipine is metabolised by cytochrome P450 3A4 (CYP3A4). No in vivo interaction studies on the effect of drugs that inhibit or induce the cytochrome P450 3A4 enzyme on the pharmacokinetics of barnidipine, have been carried out. Based on the results of in vitro interaction studies, care should be taken when barnidipine is prescribed concomitantly with mild CYP3A4 inhibitors or inducers (see the “Interactions with other medicinal products and other forms of interaction” section).
The capsules contain sucrose. Patients with rare hereditary problems of fructose intolerance, glucosegalactose malabsorption or sucrase-isomaltase insufficiency should not take this medicine.
The concurrent administration of barnidipine and other antihypertensive drugs may result in an additional antihypertensive effect.
Vasexten can be used concurrently with betablockers or ACE inhibitors.
The pharmacokinetic interaction profile of barnidipine has not been studied in full. In vitro studies show that barnidipine is metabolised by cytochrome P450 3A4 (CYP3A4).
No elaborate in vivo interaction studies on the effect of drugs which inhibit or induce the CYP3A4 enzyme on the pharmacokinetics of barnidipine, have been carried out.
In vitro data show that cyclosporin may inhibit the metabolism of barnidipine. Until in vivo information is available, barnidipine should not be prescribed concomitantly with the strong CYP3A4 inhibitors: antiproteases, ketoconazole, itraconazole, erythromycin and clarithromycin (see section 4.3 Contraindications). Care should be taken with concomitant use of mild CYP3A4 inhibitors or inducers. In case of concomitant use of CYP3A4 inhibitors it is discouraged to increase the dosage of barnidipine to 20 mg.
Concurrent dosing of cimetidine in a specific interaction study led on average to a doubling of barnidipine plasma levels. Care should therefore be exercised when using barnidipine concomitantly with cimetidine.
A higher dose of barnidipine may be necessary when barnidipine is administered concomitantly with enzyme inducing drugs, such as phenytoin, carbamazepine and rifampicin. Should a patient stop using an enzyme inducing drug, lowering the dosage of barnidipine should be considered.
Based on the results of in vitro interaction studies with, among other things, simvastatin, metoprolol, diazepam and terfenadine, it is considered unlikely that barnidipine has any effect on the pharmacokinetics of other drugs which are metabolised by cytochrome P450 isoenzymes.
An in vivo interaction study showed that barnidipine does not influence the pharmacokinetics of digoxin. In a specific interaction study alcohol led to an increase of barnidipine plasma levels (40%), which increase may be considered clinically not relevant. As with all vasodilating and antihypertensive agents, caution should be exercised when alcohol is taken concomitantly as it may potentiate their effect. Although barnidipine kinetics was not significantly altered by administration with grapefruit juice, a modest effect was observed.
No clinical experience with barnidipine in pregnancy or lactation is present. Animal studies do not indicate direct harmful effects with respect to pregnancy, embryonal/foetal or postnatal development. Only indirect effects are observed (see 5.3). The class of dihydropyridines has shown the potential to prolong delivery and parturition, which was not observed with barnidipine. As a consequence, barnidipine could be used in pregnancy only if the benefit justifies the potential risk to the fetus.
The results of animal tests have shown that barnidipine (or its metabolites) is excreted in human milk. Therefore, breast feeding is not advised during use of barnidipine.
No studies on the effects on the ability to drive and use machines have been performed Vasexten. However, caution should be exercised because dizziness/vertigo may occur during antihypertensive treatment.
| System organ class | 10 mg dosage | 20 mg dosage |
|---|---|---|
| Immune system disorders | ||
| Anaphylactoid reaction | Not known (frequency cannot be estimated from the available data) | Not known (frequency cannot be estimated from the available data) |
| Nervous system disorders | ||
| Headache | Common (≥1/100 to <1/10) | Very common (≥1/10) |
| Dizziness/vertigo | Common (≥1/100 to <1/10) | Common (≥1/100 to <1/10) |
| Cardiac disorders | ||
| Palpitations | Common (≥1/100 to <1/10) | Common (≥1/100 to <1/10) |
| Tachycardia, sinus tachycardia, heart rate increased | Not known (frequency cannot be estimated from the available data) | Not known (frequency cannot be estimated from the available data) |
| Vascular disorders | ||
| Flushing | Common (≥1/100 to <1/10) | Very common (≥1/10) |
| Hepato-biliary disorders | ||
| Liver function test abnormal | Not known (frequency cannot be estimated from the available data) | Not known (frequency cannot be estimated from the available data) |
| Skin and subcutaneous tissue disorders | ||
| Rash | Not known (frequency cannot be estimated from the available data) | Not known (frequency cannot be estimated from the available data) |
| General and administration site conditions | ||
| Peripheral oedema | Common (≥1/100 to <1/10) | Very common (≥1/10) |
The symptoms tend to diminish or disappear during treatment (within one month for peripheral oedema and two weeks for flushing, headache and palpitations).
Although never observed, the following adverse event may be of interest, as it is in the use of other dihydropyridines: gingival hyperplasia.
Some dihydropyridines may rarely lead to precordial pain or angina pectoris. Very rarely patients with preexisting angina pectoris may experience increased frequency, duration or severity of these attacks. Isolated cases of myocardial infarction may be observed.
Not applicable.
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