Summary of Product Characteristics Updated 07-Jun-2016 | Pfizer Limited
Patients over 12 years and adultsThe recommended starting dose is 5 mg per day. If required, this dosage can later be increased up to 20 mg, and then to 40 mg daily (given as a single dose or in two divided doses). Dose increases should be made at increments of 5 mg to 10 mg minoxidil per day at intervals of three or more days. If a dose of 50 mg of minoxidil has been reached, the dose may be increased by 25 mg minoxidil per day to a maximum dose of 100 mg per day.If the desired decrease of diastolic blood pressure exceeds 30 mmHg, dosage should be divided to two daily doses to keep daily blood pressure fluctuations as low as possible.
Patients younger than 12 years of ageThe use of minoxidil in children is restricted to children with severe hypertension associated with target organ damage where other treatment has failed. The data regarding the use of minoxidil in children is very limited, especially in infants. The dosage recommendations can only be considered as a rough guide to treatment at present as this is based on the publication of a few case reports and studies involving a small number of children. The starting dose used basing on these reports is 0.2 mg/kg of minoxidil as a single or divided dose. Careful titration increasing in steps of 0.1 to 0.2 mg/kg/day at intervals of at least 3 days is essential. The effective dose range is 0.25 to 1.0 mg/kg/day. The maximum dose is 50 mg/day.Treatment of children with minoxidil should only be initiated under the close supervision of a specialist in hospital.
Elderly patientsAt present there are no extensive clinical studies with minoxidil in patients over age 65. There is data indicating that elevated systolic and diastolic pressures are important risk factors for cardiovascular disease in individuals over age 65. However, elderly patients may be sensitive to the blood pressure lowering effect of minoxidil and thus caution is urged in initiating therapy as orthostatic hypotension may occur. It is suggested that 2.5 mg per day be used as the initial starting dose in patients over 65 years of age.
Renal failure or dialysis patientsDosage requirements may be lower in dialysis patients. Minoxidil is removed from the blood by dialysis, but its pharmacological action, once established is not reversed. Therefore haemodialysis patients should take minoxidil either after or at least two hours before dialysis.
Rapid reduction of blood pressureUnder hospital monitoring conditions, rapid reduction of blood pressure can be achieved using continuous blood pressure monitoring and incremental doses of 5 mg every six hours.
Concomitant antihypertensive therapyIt is recommended that, where possible, antihypertensive therapy, other than a beta-adrenergic blocking agent and a diuretic be discontinued before minoxidil treatment is started. It is recognised that some antihypertensive agents should not be abruptly discontinued. These drugs should be gradually discontinued during the first week of minoxidil treatment.Minoxidil causes sodium retention and if used alone can result in several hundred milli-equivalents of salt being retained together with a corresponding volume of water.Therefore, in all patients who are not on dialysis, minoxidil must be given in conjunction with a diuretic in sufficient dosage to maintain salt and water balance. Examples of the daily dosages of diuretics commonly used when starting therapy with minoxidil include:1. Hydrochlorothiazide (100 mg) - or other thiazides at equi-effective dosage.2. Chlortalidone (100 mg).3. Furosemide (80 mg).If excessive water retention results in a weight gain of more than 3 pounds when a thiazide or chlortalidone is being used, diuretic therapy should be changed to furosemide, the dose of which may be increased in accordance with the patient's requirements. Diuretic dosage in children should be proportionally less in relation to weight.Patients will require a sympathetic nervous system suppressant to limit a minoxidil-induced rise in heart rate. The preferred agent is a beta-blocker equivalent to an adult propranolol dosage of 80 - 160 mg/day. Higher doses may be required when pre-treated patients have an increase in heart rate exceeding 20 beats per minute or when simultaneous introduction causes an increase exceeding 10 beats per minute. When beta-blockers are contra-indicated, alternatives such as methyldopa may be used instead and should be started 24 hours prior to minoxidil.
Method of AdministrationOral administration
Salt and water retentionIf used alone, minoxidil can cause a significant retention of salt and water leading to physical signs such as oedema, and to clinical deterioration of some patients with heart failure. Diuretic treatment alone, or in combination with restricted salt intake is, therefore, necessary for all patients taking minoxidil. Haemodilution may occur leading to temporary decrease in haematocrit, haemoglobin, and erythrocyte count (by approximately 7% initially which then recovers to pre-treatment levels). The patient's bodyweight, fluid and electrolyte balance should be monitored for evidence of fluid retention.Salt and water retention in excess of 1 to 1.5 kg may diminish the effectiveness of minoxidil. Patients should, therefore, be carefully instructed about compliance with diuretic therapy and a detailed record of body weight should be maintained. The product should be used with particular attention to maintenance of salt and water balance in patients with renal impairment, but who are not on dialysis.
Renal failure or dialysis patientsThose patients with renal failure or on haemodialysis may require smaller doses of minoxidil (see section 4.2).
Myocardial infarctionPatients who have had myocardial infarction should only be treated with minoxidil after a stable post-infarction state has been established.
TachycardiaBecause minoxidil is a vasodilator, reflex tachycardia may occur and possibly angina pectoris may occur in patients at risk; it is recommended that minoxidil be used in combination with beta-adrenergic blocking agent or other sympathetic nervous system suppressants to blunt or prevent such a response.
HypertrichosisHypertrichosis occurs in most patients treated with minoxidil and all patients should be warned of this possibility before starting therapy. Most patients will experience an elongation, thickening and enhanced pigmentation of fine body hair. Usually these signs will emerge 3 to 6 weeks after starting treatment. They initially emerge in the face, and they may slightly subside with continued treatment. However, hypertrichosis was hardly or not at all tolerable in less than 10% of patients. Spontaneous reversal to the pre-treatment state can be expected one to six months after cessation of therapy.
ECG alterationsSoon after starting minoxidil therapy approximately 60% of patients exhibit ECG alterations in the direction and magnitude of their T waves. Large changes may encroach on the ST segment, unaccompanied by evidence of ischaemia. These asymptomatic changes usually disappear with continuing minoxidil treatment. The ECG reverts to the pre-treatment state when minoxidil is discontinued.
Thrombocytopenia and leucopoeniaThrombocytopenia and leucopoenia have been rarely reported.
Pericarditis, Pericardial Effusion and TamponadePericarditis, Pericardial Effusion and Tamponade Although there is no evidence of a causal relationship, there have been multiple reports of pericarditis occurring in association with minoxidil.Pericardial effusion and occasionally tamponade, has been observed in about 3% - 5% of treated patients not on dialysis. While in many cases, the pericardial effusion is associated with other potential aetiologies, there have been cases in which these potential causes of effusion were not present. Patients should be observed closely for any suggestion of a pericardial effusion and pericardiocentesis, or surgery may be required. If the effusion persists, withdrawal of minoxidil should be considered in light of other means of controlling the hypertension and the patient's clinical status.
Galactose intolerancePatients with rare hereditary problems of galactose intolerance, the Lapp lactose deficiency or glucose-galactose malabsorption should not take this medicine.
Paediatric populationChildren strictly require appropriate and individualised dosing of minoxidil, beta-blockers and diuretics. They should be under close specialist supervision in hospital. Caution is required when there is significant renal impairment. The development of peripheral oedema or any signs suggestive of congestive heart failure or of pericardial or pleural effusion should be carefully watched for. Renal function should be monitored. Body weight and urine output should be monitored.Regular follow up must be ensured during treatment with minoxidil. Before starting treatment parents and carers should be warned of the likely occurrence of hypertrichosis.
PregnancyThere is limited data from the use of minoxidil in pregnant women. Studies in animals have shown reproductive toxicity (see section 5.3). Minoxidil is not recommended during pregnancy and in women of childbearing potential not using contraception. Neonatal hirsutism has been reported following exposure of minoxidil during pregnancy.
Breast-feedingMinoxidil has been reported to be excreted in human milk. A risk to the suckling child cannot be excluded. A decision must be made whether to discontinue breast-feeding or to discontinue/abstain from minoxidil therapy taking into account the benefit of breast-feeding for the child and the benefit of therapy for the woman.
FertilityThere are no fertility data from the use of minoxidil in humans. In a fertility study with male and female rats, a dose-dependent reduction of the conception rate was found. The dose corresponded to one to five times the maximum dose used in humans to treat hypertension.
|Very common Common Uncommon Rare Very rare Not known||(≥1/10) (≥1/100 to <1/10) (≥1/1,000 to <1/100) (≥1/10,000 to <1/1,000) (<1/10,000) (cannot be estimated from the available data).|
|MedDRA System Organ Class||Frequency||Undesirable Effects|
|Blood and Lymphatic System Disorders||Rare||Leucopoenia, thrombocytopenia|
|Metabolism and Nutrition Disorders||Common||Fluid retention, oedema|
|Cardiac Disorders||Very Common||Tachycardia, pericarditis|
|Common||Pericardial effusion, cardiac tamponade|
|Not Known||Angina pectoris|
|Respiratory, Thoracic and Mediastinal Disorders||Not Known||Pleural effusion|
|Gastrointestinal Disorders||Not known||Gastrointestinal disorder|
|Skin and Subcutaneous Tissue Disorders||Very Common||Hypertrichosis, hair colour changes|
|Rare||Stevens-Johnson syndrome, dermatitis bullous, rash,|
|Reproductive System and Breast Disorders||Not known||Breast tenderness|
|General Disorders and Administration Site Conditions||Not known||Peripheral oedema associated with or independent of weight gain|
|Investigations||Very Common||ECG abnormal|
|Not Known||Blood creatinine increased Blood urea increased|
Reporting of suspected adverse reactionsReporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.
Mechanism of actionMinoxidil lowers the elevated systolic and diastolic blood pressure by decreasing peripheral vascular resistance via vasodilation. The smooth musculature of the resistance vessels must be regarded as the site of action for the relaxant effect of minoxidil. The active metabolite of minoxidil activates the ATP-modulated potassium (K+ATP) channel causing K+ efflux, hyperpolarization, and smooth muscle relaxation.
Pharmacodynamic effectsSympathetic reflexes mediated by baroreceptors secondarily increase heart rate and myocardial contractility, thereby increasing cardiac output. In addition, the plasma renin activity is increased via sympathetic nervous system stimulation, which results in an increased angiotensin II concentration with subsequent increased aldosterone secretion. In this way, the renal sodium excretion is reduced and extracellular volume increased. The pulmonary artery pressure may occasionally increase after the administration of minoxidil alone, but it decreases with the recommended concomitant therapy (beta-blocker plus diuretic).
Paediatric populationAs severe hypertension requiring multi-drug therapy is uncommon in children, paediatric use of minoxidil was limited in the development programme and has remained so in published literature. Data available in children younger than 10 years of age is very limited; it involves approximately 40 patients, eight of whom were under one year of age.
Absorption and distributionAfter oral administration in humans, at least 90% of minoxidil is absorbed in the gastrointestinal tract. Minoxidil is detected within 30 minutes in the plasma. Maximum plasma levels are reached 60 minutes after administration.Based on results from a relative bioavailability study, tablet and oral solution formulations have similar values in area under the serum concentration-time curve (AUC), maximum serum concentration, time to reach maximum serum concentration (approximately 40 minutes), and the type of effect (antihypertensive). There is no accumulation following chronic administration of oral tablets compared with single dose.Minoxidil is not bound to plasma proteins.Minoxidil does not cross the blood-brain barrier.
MetabolismAt least 90% of the administered minoxidil is metabolized in the liver. The primary metabolite in humans is the minoxidil O-glucuronide. Some polar metabolites are also produced. The known metabolites have a weaker antihypertensive effect than the active ingredient itself.
EliminationIn humans, minoxidil plasma concentrations decrease with an average half-life of approximately 4 hours. However, the duration of action is over several days.Minoxidil and its metabolites are dialyzable.The renal clearance of minoxidil corresponds to the glomerular filtration rate. No substantial changes in the glomerular filtration rate and the renal plasma flow could be detected under minoxidil.
Paediatric populationNo pharmacokinetic data regarding minoxidil in the paediatric population is currently available.
Hepatic impairmentNo data are available.
Cardiac lesions in animalsIn non-clinical studies in a variety of species, minoxidil induces several types of cardiac lesions including necrotic and hemorrhagic lesions of the myocardium and papillary muscles, and cardiac hypertrophy and dilation. These changes occur only in the context of profound hypotension and tachycardia and reflect haemodynamic and/or hypoxic stress rather than direct cytotoxicity. As greater experience with the drug has accumulated, it has become apparent that these cardiac lesions do not occur in humans treated with minoxidil.
CarcinogenicityIn carcinogenicity studies in rats and mice dosed via oral or dermal routes of administration no findings considered relevant to humans were found.
Reproductive toxicityIn a fertility study with male and female rats, a dose-dependent reduction of the conception rate was found. The no observed adverse effect level (NOAEL) for this finding was 1 mg/kg per day in treated rats.Teratogenicity has been demonstrated in the rat at doses above 80 mg/kg/day. Oral administration of minoxidil has been associated with evidence of increased foetal resorption in rabbits at doses associated with maternal toxicity. Teratogenicity was not demonstrated in the rabbit.No data regarding juvenile animal toxicity studies is currently available.
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